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 (Q81399102)

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scientific article published on 25 October 2005

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English	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	scientific article published on 25 October 2005

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scholarly article

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8 January 2020

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 (English)

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8 January 2020

cleft lip with or without cleft palate

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based on heuristic

inferred from title

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based on heuristic

inferred from title

10

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Norio Niikawa

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8 January 2020

Akira Kinoshita

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Akira Kinoshita

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8 January 2020

Koh-ichiro Yoshiura

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Koh-ichiro Yoshiura

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8 January 2020

Tatsuya Kishino

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Tatsuya Kishino

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8 January 2020

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Sadanori Akita

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8 January 2020

3

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Yoko Nakano

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8 January 2020

Takeshi Uchiyama

9

object named as

Takeshi Uchiyama

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8 January 2020

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Shinji Kondo

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8 January 2020

author name string

Eisaburo Ichikawa

1

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8 January 2020

Akira Watanabe

2

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8 January 2020

Akiyoshi Hirano

5

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8 January 2020

publication date

25 October 2005

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8 January 2020

Journal of Human Genetics

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8 January 2020

51

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8 January 2020

1

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8 January 2020

38-46

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Europe PubMed Central

PubMed publication ID

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8 January 2020

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent developments in orofacial cleft genetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: summary report from a Workshop of the International Consortium for Oral Clefts Genetics.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessing the impact of population stratification on genetic association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TBX10, a member of the Tbx1-subfamily of conserved developmental genes, is located at human chromosome 11q13 and proximal mouse chromosome 19

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of cleft lip, cleft palate, and cleft lip and palate among races: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The many faces and factors of orofacial clefts

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mammalian Dlx homeobox gene control of craniofacial and inner ear morphogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Dlx3 protein harbors basic residues required for nuclear localization, transcriptional activity and binding to Msx1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between transforming growth factor beta 3 and cleft lip and/or palate in the Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The complex genetics of cleft lip and palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of cleft lip or palate in 303738 Japanese babies born between 1994 and 1995

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the candidate genes responsible for non-syndromic cleft lip and palate in Japanese people

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transforming growth factor-beta3 gene SfaN1 polymorphism in Korean nonsyndromic cleft lip and palate patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unravelling the complex genetics of cleft lip in the mouse model

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive ectodermal dysplasia: I. An undescribed dysplasia/malformation syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The T-box gene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TBX22 mutations are a frequent cause of cleft palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transgenic expression of a novel thymic epithelial cell antigen stimulates abberant development of thymocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beyond Mendel: an evolving view of human genetic disease transmission

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of PAX9 is associated with oligodontia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testing candidate genes for non-syndromic oral clefts using a case-parent trio design

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16247549

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-005-0319-8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16247549%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16247549%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

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