(Q24321656)

Wnt family member 3A

1 reference

Wnt family member 5A

1 reference

Wnt family member 11

1 reference

Wnt family member 8A

1 reference

secondary palate development

1 reference

cleft lip with or without cleft palate

1 reference

1 reference

7

Jacqueline T Hecht

0 references

author name string

Brett T Chiquet

1

0 references

Susan H Blanton

2

0 references

Amber Burt

3

0 references

Deqiong Ma

4

0 references

Samuel Stal

5

0 references

John B Mulliken

Impaired FGF signaling contributes to cleft lip and palate

6

0 references

language of work or name

English

0 references

publication date

15 July 2008

0 references

published in

Human Molecular Genetics

0 references

volume

17

0 references

issue

14

0 references

page(s)

2212-8

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Variation in IRF6 contributes to nonsyndromic cleft lip and palate

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Wnt signaling mediates regional specification in the vertebrate face

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Development of the upper lip: morphogenetic and molecular mechanisms

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Gene Expression Profiling of Rat Uterus at Different Stages of Parturition

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Wnt signaling: a common theme in animal development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

A "silent" polymorphism in the MDR1 gene changes substrate specificity

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

CRISPLD2: a novel NSCLP candidate gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Recent advances in craniofacial morphogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Association between the transforming growth factor alpha gene and nonsyndromic oral clefts: a HuGE review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Progress toward discerning the genetics of cleft lip

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Expression of all Wnt genes and their secreted antagonists during mouse blastocyst and postimplantation development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Wnt signaling in disease and in development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Reiterated Wnt signaling during zebrafish neural crest development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

T (Brachyury) is a direct target of Wnt3a during paraxial mesoderm specification.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: A possible new lethal syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852032

Essential role of non-canonical Wnt signalling in neural crest migration.

30 May 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

FGF Signaling Regulates Mesoderm Cell Fate Specification and Morphogenetic Movement at the Primitive Streak

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

Association of chromosomal regions 3p21.2, 10p13, and 16p13.3 with nonsyndromic cleft lip and palate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

Genotype‐based association test for general pedigrees: The genotype‐PDT

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

The APL test: extension to general nuclear families and haplotypes and examination of its robustness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

Nonsyndromic cleft lip and palate: four chromosomal regions of interest

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN121

A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18413325

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of nonsyndromic oral clefts in Texas: 1995-1999

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18413325

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

GOLD--graphical overview of linkage disequilibrium

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18413325

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDN121

1 reference

2978219

2978219

1 reference

1 reference

1 reference