(Q35510647)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

2

1 reference

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7 February 2020

Wasiu L. Adeyemo

3

1 reference

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7 February 2020

Chika K Onwuamah

5

1 reference

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7 February 2020

author name string

A Butali

1

1 reference

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7 February 2020

P A Jezewski

4

1 reference

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7 February 2020

M O Ogunlewe

6

1 reference

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7 February 2020

V I Ugboko

7

1 reference

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7 February 2020

O Adejuyigbe

8

1 reference

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7 February 2020

A I Adigun

9

1 reference

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7 February 2020

L O Abdur-Rahman

10

1 reference

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7 February 2020

I I Onah

11

1 reference

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7 February 2020

R A Audu

12

1 reference

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7 February 2020

E O Idigbe

13

1 reference

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7 February 2020

M A Mansilla

14

1 reference

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7 February 2020

E A Dragan

15

1 reference

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7 February 2020

A L Petrin

16

1 reference

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7 February 2020

S A Bullard

17

1 reference

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7 February 2020

A O Uduezue

18

1 reference

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7 February 2020

O Akpata

19

1 reference

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7 February 2020

A O Osaguona

20

1 reference

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7 February 2020

H O Olasoji

21

1 reference

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7 February 2020

T O Ligali

22

1 reference

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7 February 2020

B M Kejeh

23

1 reference

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7 February 2020

K R Iseh

24

1 reference

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7 February 2020

P B Olaitan

25

1 reference

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7 February 2020

A R Adebola

26

1 reference

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7 February 2020

E Efunkoya

27

1 reference

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7 February 2020

O A Adesina

28

1 reference

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7 February 2020

O M Oluwatosin

29

1 reference

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7 February 2020

J C Murray

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

NigeriaCRAN Collaboration

31

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

language of work or name

English

0 references

publication date

8 July 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

Cleft Palate: Craniofacial Journal

7 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

volume

48

1 reference

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7 February 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

page(s)

646-653

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

Epidemiology of Orofacial clefts in Africa: Methodological challenges in ascertainment.

7 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Challenges of cleft care in Africa

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

The genetics of isolated orofacial clefts: from genotypes to subphenotypes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Molecular mechanisms underlying polyalanine diseases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Bilateral transverse facial cleft as an isolated deformity: case report.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Cleft lip and palate repair: the experience from two West African sub-regional centres

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Impaired FGF signaling contributes to cleft lip and palate

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

MSX1 and orofacial clefting with and without tooth agenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Requirement of the forkhead gene Foxe1, a target of sonic hedgehog signaling, in hair follicle morphogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

The role of MSX1 in human tooth agenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Evidence of a sex-dependent association between the MSX1 locus and nonsyndromic cleft lip with or without cleft palate in the Chilean population

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

A role for the Msx-1 homeodomain in transcriptional regulation: residues in the N-terminal arm mediate TATA binding protein interaction and transcriptional repression

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Transcriptional repression by Msx-1 does not require homeodomain DNA-binding sites

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

The incidence of cleft lip and palate in Nigeria.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Culture, rehabilitation, and facial birth defects: international case studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Knowledge and cultural beliefs about the etiology and management of orofacial clefts in Nigeria's major ethnic groups

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Mutation analysis of CLPTM 1 and PVRL 1 genes in patients with non-syndromic clefts of lip, alveolus and palate

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Classification and birth prevalence of orofacial clefts

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

Incidence of cleft lip and palate in a newborn Zairian sample.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

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

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1597%2F10-133

Genes causing clefting syndromes as candidates for non-syndromic cleft lip with or without cleft palate: a family-based association study

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3206991

A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families

26 September 2018

1 reference

PubMed

12 December 2020

MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population

1 reference

PubMed

12 December 2020

1 reference

12 December 2020

A novelMSX1 mutation in hypodontia

1 reference

PubMed

12 December 2020

Identifiers

DOI

10.1597/10-133

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21740177%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

PubMed publication ID

21740177

1 reference