(Q35150807)

6 August 2017

1 reference

title

Genetically altered mouse models: the good, the bad, and the ugly (English)

1 reference

6 August 2017

Tamizchelvi Thyagarajan

1

1 reference

6 August 2017

Satish Totey

2

1 reference

6 August 2017

Mary Jo S Danton

3

1 reference

6 August 2017

Ashok B Kulkarni

4

1 reference

6 August 2017

language of work or name

English

0 references

publication date

1 January 2003

1 reference

Journal of Dental Research

6 August 2017

1 reference

6 August 2017

14

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6 August 2017

3

1 reference

6 August 2017

154-174

1 reference

Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation

6 August 2017

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Perlecan is essential for cartilage and cephalic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mouse and hamster mutants as models for Waardenburg syndromes in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A mouse model for Zellweger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mouse models of human disease. Part I: techniques and resources for genetic analysis in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mouse models of human disease. Part II: recent progress and future directions

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Functional analysis of the p57KIP2 gene mutation in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Anhidrosis and absence of sweat glands in mice hemizygous for the Tabby gene: supportive evidence for the hypothesis of homology between Tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Insertion of Inhbb into the Inhba locus rescues the Inhba-null phenotype and reveals new activin functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The PTH/PTHrP receptor in Jansen's metaphyseal chondrodysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Abnormal bone growth and selective translational regulation in basic fibroblast growth factor (FGF-2) transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Perlecan maintains the integrity of cartilage and some basement membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mouse models of human single gene disorders. I: Nontransgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Human/mouse homology relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Fibroblast growth factor receptor 3 is a negative regulator of bone growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Early-onset multifocal inflammation in the transforming growth factor beta 1-null mouse is lymphocyte mediated

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Cystic fibrosis in the mouse by targeted insertional mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutations of the TWIST gene in the Saethre-Chotzen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mouse models of human genetic disease: which mouse is more like a man?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Transforming growth factor beta 1 (TGF-beta 1) controls expression of major histocompatibility genes in the postnatal mouse: aberrant histocompatibility antigen expression in the pathogenesis of the TGF-beta 1 null mouse phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Gene-targeting studies of mammalian behavior: is it the mutation or the background genotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Amelogenin-deficient mice display an amelogenesis imperfecta phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The broken mouse: the role of development, plasticity and environment in the interpretation of phenotypic changes in knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Palatal development in Twirler mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Incidence of cleft lip and palate and risks of additional malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Synthetic fibronectin peptides interrupt inflammatory cell infiltration in transforming growth factor beta 1 knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s)

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Molecular and developmental genetics of mouse coat color

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Dominant mutation of the murine Hox-2.2 gene results in developmental abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A novel murine homeobox gene isolated by a tissue specific PCR cloning strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The murine homeo domain protein Hox 1.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Structure and chromosomal localization of a murine LIM/homeobox gene, Lhx8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Lef1 expression is activated by BMP-4 and regulates inductive tissue interactions in tooth and hair development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Transforming growth factor beta 1 null mutation in mice causes excessive inflammatory response and early death

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Function of cytokines within the TGF-beta superfamily as determined from transgenic and gene knockout studies in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Genetic study of nonsyndromic coronal craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The mechanism of palatal clefting in the Col11a1 mutant mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Strain-dependent myeloid hyperplasia, growth deficiency, and accelerated cell cycle in mice lacking the Rb-related p107 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Maternal rescue of transforming growth factor-beta 1 null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Autoimmunity associated with TGF-beta1-deficiency in mice is dependent on MHC class II antigen expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Normal development and growth of mice carrying a targeted disruption of the alpha 1 retinoic acid receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Growth retardation and cysteine deficiency in gamma-glutamyl transpeptidase-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A targeted mutation at the known collagenase cleavage site in mouse type I collagen impairs tissue remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Function of retinoic acid receptor gamma in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The Gy mutation: another cause of X-linked hypophosphatemia in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The genetic control of early tooth development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Chondrodysplasia in transgenic mice harboring a 15-amino acid deletion in the triple helical domain of pro alpha 1(II) collagen chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

TGF-beta: a balancing act.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Ectopic expression of Hox-2.3 induces craniofacial and skeletal malformations in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mouse models of abnormal skeletal development and homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Legless, a Novel Mutation Found in PHT1-1 Transgenic Mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Retinoic acid receptor beta 2 (RAR beta 2) null mutant mice appear normal.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Genetic disorders of the elastic fiber system

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Insight into the microphthalmia gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Placental failure in mice lacking the homeobox gene Dlx3

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Fibroblast-growth-factor receptor mutations in human skeletal disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Molecular genetics of craniosynostotic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

MSX-1 gene expression and regulation in embryonic palatal tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

alpha-Galactosidase A deficient mice: a model of Fabry disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The mouse homeobox gene, S8, is expressed during embryogenesis predominantly in mesenchyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Regulated gene expression dictates enamel structure and tooth function

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Parathyroid hormone-related protein is a developmental regulatory molecule

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Collagens: molecular biology, diseases, and potentials for therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Fibrillln mutations in Marfan syndrome and related phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Altered mandibular development precedes the time of palate closure in mice homozygous for disproportionate micromelia: an oral clefting model supporting the Pierre-Robin sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Insertion of a targeting construct in a Hoxd-10 allele can influence the control of Hoxd-9 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Abnormal craniofacial growth and early mandibular osteoarthritis in mice harbouring a mutant type II collagen transgene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Physiological actions and clinical applications of transforming growth factor-beta (TGF-beta).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Homeobox genes and orofacial development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Fish scale development: Hair today, teeth and scales yesterday?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Targeted disruption of the mouse transforming growth factor-beta 1 gene results in multifocal inflammatory disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

legless insertional mutation: morphological, molecular, and genetic characterization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Molecular biology experimental strategies for craniofacial-oral-dental dysmorphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

An animal model for cystic fibrosis made by gene targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Odontoblast-specific expression of cre recombinase successfully deletes gene segments flanked by loxP sites in mouse teeth.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutation of PAX9 is associated with oligodontia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mandibulofacial dysostosis (Treacher Collins syndrome): a new proposal for its pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Long-term enzyme correction and lipid reduction in multiple organs of primary and secondary transplanted Fabry mice receiving transduced bone marrow cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Chimeras of the native form or achondroplasia mutant (G375C) of human fibroblast growth factor receptor 3 induce ligand-dependent differentiation of PC12 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mutations in holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A mouse model for achondroplasia produced by targeting fibroblast growth factor receptor 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Mice lacking link protein develop dwarfism and craniofacial abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Craniosynostosis: genes and mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

DiGeorge syndrome: part of CATCH 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Genetic and teratogenic approaches to craniofacial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

DSPP mutation in dentinogenesis imperfecta Shields type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Fibroblast growth factor 2 control of vascular tone

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154411130301400302

10.1177/154411130301400302

21 January 2018

Identifiers

DOI

1 reference

6 August 2017

1 reference