(Q81505360)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Sequence evaluation of FGF and FGFR gene conserved non-coding elements in non-syndromic cleft lip and palate cases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

Bridget M Riley

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Jeffrey C Murray

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

publication date

1 December 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics

9 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

143A

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

24

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9 January 2020

page(s)

3228-3234

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

Dlx5 regulates regional development of the branchial arches and sensory capsules

9 January 2020

cites work

1 reference

12 December 2020

A model of the statistical power of comparative genome sequence analysis

1 reference

12 December 2020

Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction.

1 reference

12 December 2020

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

1 reference

12 December 2020

Orofacial clefting: recent insights into a complex trait

1 reference

12 December 2020

Small fitness effect of mutations in highly conserved non-coding regions

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12 December 2020

Progress toward discerning the genetics of cleft lip

1 reference

12 December 2020

Conservation of RET regulatory function from human to zebrafish without sequence similarity

1 reference

12 December 2020

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

1 reference

12 December 2020

Clinical and epidemiologic studies of cleft lip and palate in the Philippines.

1 reference

12 December 2020

Ancient noncoding elements conserved in the human genome

1 reference

12 December 2020

Impaired FGF signaling contributes to cleft lip and palate

1 reference

12 December 2020

A combinatorial code for gene expression generated by transcription factor Bach2 and MAZR (MAZ-related factor) through the BTB/POZ domain

1 reference

12 December 2020

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

1 reference

12 December 2020

The transcription factors L-Sox5 and Sox6 are essential for cartilage formation

1 reference

12 December 2020

The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development

1 reference

12 December 2020

FGF signaling regulates expression of Tbx2, Erm, Pea3, and Pax3 in the early nasal region.

1 reference

12 December 2020

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

1 reference

12 December 2020

Regulation of the FGF-4 gene by a complex distal enhancer that functions in part as an enhanceosome

1 reference

12 December 2020

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families

1 reference

12 December 2020

SOX7 and GATA-4 are competitive activators of Fgf-3 transcription

1 reference

12 December 2020

Significant association between nonsyndromic oral clefts and arylhydrocarbon receptor nuclear translocator (ARNT)

1 reference

12 December 2020

Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome

1 reference

12 December 2020

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

1 reference

12 December 2020

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

1 reference

12 December 2020

Signatures of adaptive evolution within human non-coding sequence

1 reference

12 December 2020

Identifiers

DOI

10.1002/AJMG.A.31965

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17963255%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

PubMed publication ID

17963255

1 reference