(Q37383066)

20 August 2017

1 reference

title

The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models (English)

1 reference

cleft lip and cleft palate

20 August 2017

main subject

1 reference

1 reference

1 reference

Amel Gritli-Linde

1

1 reference

20 August 2017

publication date

1 January 2008

1 reference

Current Topics in Developmental Biology

20 August 2017

published in

1 reference

20 August 2017

volume

84

1 reference

20 August 2017

page(s)

37-138

1 reference

Phenotypic changes in dentition of Runx2 homozygote-null mutant mice

20 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Runx2 mediates FGF signaling from epithelium to mesenchyme during tooth morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mechanisms of palatal epithelial seam disintegration by transforming growth factor (TGF) beta3

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The cellular and molecular etiology of the cleft secondary palate in Fgf10 mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

SUMO1 haploinsufficiency leads to cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Histone H2AX-dependent GABA(A) receptor regulation of stem cell proliferation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Menin molecular interactions: insights into normal functions and tumorigenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Eph/ephrin signaling: networks.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cleft palate and decreased brain gamma-aminobutyric acid in mice lacking the 67-kDa isoform of glutamic acid decarboxylase

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Deletion of CASK in mice is lethal and impairs synaptic function

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Expression of members of the Fgf family and their receptors during midfacial development.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Zebrafish DeltaNp63 is a direct target of Bmp signaling and encodes a transcriptional repressor blocking neural specification in the ventral ectoderm

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Sp8 is crucial for limb outgrowth and neuropore closure

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

TGF-beta3-induced palatogenesis requires matrix metalloproteinases

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A locus for isolated cleft palate, located on human chromosome 2q32

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Novel transcription factor Satb2 interacts with matrix attachment region DNA elements in a tissue-specific manner and demonstrates cell-type-dependent expression in the developing mouse CNS

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Associated anomalies in multi-malformed infants with cleft lip and palate: An epidemiologic study of nearly 6 million births in 23 EUROCAT registries

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller-Dieker syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

p63 regulates an adhesion programme and cell survival in epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Craniofacial dysmorphogenesis including cleft palate in mice with an insertional mutation in the discs large gene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Jag2-Notch1 signaling regulates oral epithelial differentiation and palate development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Recent advances in craniofacial morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Ovca1 regulates cell proliferation, embryonic development, and tumorigenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Facial clefting and psychiatric diseases: a follow-up of the Danish 1936-1987 Facial Cleft cohort

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Long term follow up study of survival associated with cleft lip and palate at birth

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The complex genetics of cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cleft palate in mice with a targeted mutation in the gamma-aminobutyric acid-producing enzyme glutamic acid decarboxylase 67

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Oxysterols stimulate Sonic hedgehog signal transduction and proliferation of medulloblastoma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Tshz1 is required for axial skeleton, soft palate and middle ear development in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Overexpression of Smad2 in Tgf-beta3-null mutant mice rescues cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Deficiency of the beta 3 subunit of the type A gamma-aminobutyric acid receptor causes cleft palate in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Nf2/Merlin: a coordinator of receptor signalling and intercellular contact

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Ski is involved in transcriptional regulation by the repressor and full-length forms of Gli3

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A mouse model for hereditary thyroid dysgenesis and cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Genome scan for teratogen-induced clefting susceptibility loci in the mouse: evidence of both allelic and locus heterogeneity distinguishing cleft lip and cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Signaling pathways are focused at specialized regions of the plasma membrane by scaffolding proteins of the MAGUK family

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

SUMO modification of a novel MAR-binding protein, SATB2, modulates immunoglobulin mu gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Frontal nasal prominence expression driven by Tcfap2a relies on a conserved binding site for STAT proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Tgf-beta superfamily and mouse craniofacial development: interplay of morphogenetic proteins and receptor signaling controls normal formation of the face.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Tgf-beta3-induced palatal fusion is mediated by Alk-5/Smad pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Craniofacial defects in mice lacking BMP type I receptor Alk2 in neural crest cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Epithelial and ectomesenchymal role of the type I TGF-beta receptor ALK5 during facial morphogenesis and palatal fusion

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Palatal fusion - where do the midline cells go? A review on cleft palate, a major human birth defect

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Severe facial clefting in Insig-deficient mouse embryos caused by sterol accumulation and reversed by lovastatin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Menin is required in cranial neural crest for palatogenesis and perinatal viability

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Regulation of sterol synthesis in eukaryotes.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

CHD7 gene and non-syndromic cleft lip and palate.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

7-Dehydrocholesterol-dependent proteolysis of HMG-CoA reductase suppresses sterol biosynthesis in a mouse model of Smith-Lemli-Opitz/RSH syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Identification of SATB2 as the cleft palate gene on 2q32-q33.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The cellular basis of epithelial morphogenesis. A review

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

p57 and Hes1 coordinate cell cycle exit with self-renewal of pancreatic progenitors

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Palatal development in Twirler mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Bmp4 gene is expressed at the putative site of fusion in the midfacial region

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The Twirler mouse, a model for the study of cleft lip and palate.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Molecular control of secondary palate development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The whereabouts of a morphogen: direct evidence for short- and graded long-range activity of hedgehog signaling peptides

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mice with an anterior cleft of the palate survive neonatal lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Modification of Msx1 by SUMO-1

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Nonneuronal expression of the GABA(A) beta3 subunit gene is required for normal palate development in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Adult Apaf-1-deficient mice exhibit male infertility

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Regional regulation of palatal growth and patterning along the anterior-posterior axis in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cell-cell signaling via Eph receptors and ephrins

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Altered sumoylation of p63alpha contributes to the split-hand/foot malformation phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Association of the GABRB3 gene with nonsyndromic oral clefts

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Experimental induction of palate shelf elevation in glutamate decarboxylase 67-deficient mice with cleft palate due to vertically oriented palatal shelf.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Development of the upper lip: morphogenetic and molecular mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Analysis of Meox-2 mutant mice reveals a novel postfusion-based cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Analysis of cell migration, transdifferentiation and apoptosis during mouse secondary palate fusion.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Prenatal craniofacial development: new insights on normal and abnormal mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Orofacial clefting: recent insights into a complex trait

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mouse genetic models of cleft lip with or without cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Association between nonsyndromic cleft lip with or without cleft palate and the glutamic acid decarboxylase 67 gene in the Japanese population.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Sprouty genes control diastema tooth development via bidirectional antagonism of epithelial-mesenchymal FGF signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Lathosterolosis: an inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Murine CASK is disrupted in a sex-linked cleft palate mouse mutant

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

PIAS1 confers DNA-binding specificity on the Msx1 homeoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Wnt11/Fgfr1b cross-talk modulates the fate of cells in palate development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A mutation of the p63 gene in non-syndromic cleft lip.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

IKK1-deficient mice exhibit abnormal development of skin and skeleton

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Coordination of chondrogenesis and osteogenesis by fibroblast growth factor 18

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Activation of transforming growth factor-beta signaling by SUMO-1 modification of tumor suppressor Smad4/DPC4

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Distinct functions for Bmp signaling in lip and palate fusion in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Identification and developmental expression analysis of a novel homeobox gene closely linked to the mouse Twirler mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Chemical rescue of cleft palate and midline defects in conditional GSK-3beta mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Function of Rieger syndrome gene in left-right asymmetry and craniofacial development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mammalian Ryk is a Wnt coreceptor required for stimulation of neurite outgrowth

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

1 reference

7 January 2021

Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Contributions of PTCH gene variants to isolated cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

TBX22 mutations are a frequent cause of cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Molecular genetics of multiple endocrine neoplasia types 1 and 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The Nf2 tumor suppressor regulates cell-cell adhesion during tissue fusion

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Developmental roles and clinical significance of hedgehog signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

1 reference

7 January 2021

Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

p63 is a p53 homologue required for limb and epidermal morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

TFAP2A mutations result in branchio-oculo-facial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Transforming growth factor alpha locus and nonsyndromic cleft lip with or without cleft palate: a reappraisal

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Exclusive paternal origin of new mutations in Apert syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The pit, the cleft and the web

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Genetics of ventral forebrain development and holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cleft palate in domestic animals: epidemiologic features.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Multiple functions of Snail family genes during palate development in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mouse R-spondin2 is required for apical ectodermal ridge maintenance in the hindlimb

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

FGF signalling in craniofacial development and developmental disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

BMP signalling in craniofacial development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

FGF18 is required for normal cell proliferation and differentiation during osteogenesis and chondrogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cardiovascular and craniofacial defects in Crk-null mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Loss of the Sall3 gene leads to palate deficiency, abnormalities in cranial nerves, and perinatal lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Eph-ephrin bidirectional signaling in physiology and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cholesterol precursors and facial clefting

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Transforming growth factor-beta 3 is required for secondary palate fusion

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Sterol-regulated transport of SREBPs from endoplasmic reticulum to Golgi: oxysterols block transport by binding to Insig

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

PTCH mutations in four Brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Craniofacial anomalies: from development to molecular pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Expression patterns of Hedgehog signalling pathway members during mouse palate development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A targeted mutation in the mouse E-cadherin gene results in defective preimplantation development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Impaired FGF signaling contributes to cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Filamin A: phenotypic diversity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

SUMO-1 modification activates the transcriptional response of p53

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Anteriorization of neural fate by inhibitor of beta-catenin and T cell factor (ICAT), a negative regulator of Wnt signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Multiplex relative risk and estimation of the number of loci underlying an inherited disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Study of the PVRL1 gene in Italian nonsyndromic cleft lip patients with or without cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

PDGF signaling specificity is mediated through multiple immediate early genes

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Molecular mechanisms of epithelial morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Transcription factor AP-2 essential for cranial closure and craniofacial development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Experimental induction of an incomplete hard-palate cleft in the rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The many faces and factors of orofacial clefts

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Pygo1 and Pygo2 roles in Wnt signaling in mammalian kidney development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Gas1 is a modifier for holoprosencephaly and genetically interacts with sonic hedgehog

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Craniofacial abnormalities resulting from targeted disruption of the murine Sim2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Gene targeting reveals a widespread role for the high-mobility-group transcription factor Sox11 in tissue remodeling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Bone morphogenetic proteins induce apoptosis and growth factor dependence of cultured sympathoadrenal progenitor cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Embryonic development of folate binding protein-1 (Folbp1) knockout mice: Effects of the chemical form, dose, and timing of maternal folate supplementation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Exploiting protein destruction for constructive use.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Interaction of the Ski oncoprotein with Smad3 regulates TGF-beta signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Role of the Bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cell autonomous requirement for PDGFRalpha in populations of cranial and cardiac neural crest cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Neural and orofacial defects in Folp1 knockout mice [corrected]

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

SoxE factors function equivalently during neural crest and inner ear development and their activity is regulated by SUMOylation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Conditional targeting of E-cadherin in skin: insights into hyperproliferative and degenerative responses

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Loss of the Max-interacting protein Mnt in mice results in decreased viability, defective embryonic growth and craniofacial defects: relevance to Miller-Dieker syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

RYK, a catalytically inactive receptor tyrosine kinase, associates with EphB2 and EphB3 but does not interact with AF-6

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Fgfr1 regulates patterning of the pharyngeal region

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

1 reference

7 January 2021

Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

GABA signalling during development: new data and old questions

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Fate-mapping of the epithelial seam during palatal fusion rules out epithelial-mesenchymal transformation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Stage of palate closure as one indication of “liability” to cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Unraveling human cleft lip and palate research

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Ski represses bone morphogenic protein signaling in Xenopus and mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Forkhead transcription factor Foxf2 (LUN)-deficient mice exhibit abnormal development of secondary palate.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Shifting paradigms in Hedgehog signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Genetic evidence for the role of loci at 19q13 in cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith--Lemli--Opitz syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Initial sequencing and comparative analysis of the mouse genome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

GABA uptake in embryonic palate mesenchymal cells of two mouse strains

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A dosage-dependent role for Spry2 in growth and patterning during palate development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

A shared vesicular carrier allows synaptic corelease of GABA and glycine

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Ski acts as a co-repressor with Smad2 and Smad3 to regulate the response to type beta transforming growth factor

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Cell autonomous requirement for Tgfbr2 in the disappearance of medial edge epithelium during palatal fusion

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Role of TBX1 in human del22q11.2 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Effect of ENU (ethylnitrosourea) mutagenesis in cleft lip and/or palate pathogenesis in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Tgfb1 expressed in the Tgfb3 locus partially rescues the cleft palate phenotype of Tgfb3 null mutants

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Wnt5a and Wnt5b exhibit distinct activities in coordinating chondrocyte proliferation and differentiation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Interaction between fidgetin and protein kinase A-anchoring protein AKAP95 is critical for palatogenesis in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Tissue-specific expression of Cre recombinase from the Tgfb3 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Miller-Dieker syndrome: analysis of a human contiguous gene syndrome in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Apaf1 is required for mitochondrial pathways of apoptosis and brain development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Wnt-mediated axon guidance via the Drosophila Derailed receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Shox2-deficient mice exhibit a rare type of incomplete clefting of the secondary palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Shox2 is required for chondrocyte proliferation and maturation in proximal limb skeleton

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Targeted disruption of Kir2.1 and Kir2.2 genes reveals the essential role of the inwardly rectifying K(+) current in K(+)-mediated vasodilation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Isolated cleft palate in mice with a targeted mutation of the LIM homeobox gene lhx8

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Tbx1 is expressed at multiple sites of epithelial-mesenchymal interaction during early development of the facial complex.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

DEVELOPMENTAL GENETICS OF A LETHAL MUTATION, MUSCULAR DYSGENESIS (MDG), IN THE MOUSE. I. GENETIC ANALYSIS AND GROSS MORPHOLOGY

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2808%2900602-9

7 January 2021

10.1016/S0070-2153(08)00602-9

Identifiers

DOI

1 reference

20 August 2017

1 reference