Impaired FGF signaling contributes to cleft lip and palate (Q24683257)

2

M Adela

Mansilla

1 reference

19 October 2023

Jinghong Ma

3

Jinghong

Ma

1 reference

19 October 2023

Brion S Maher

5

Brion S

Maher

1 reference

19 October 2023

Lisa M Raffensperger

6

Lisa M

Raffensperger

1 reference

19 October 2023

Erilynn T Russo

7

Erilynn T

Russo

1 reference

19 October 2023

Alexandre R Vieira

8

Alexandre R

Vieira

1 reference

19 October 2023

Catherine Dodé

9

Catherine

Dodé

1 reference

19 October 2023

Jeffrey C Murray

12

Jeffrey C

Proceedings of the National Academy of Sciences of the United States of America

Murray

1 reference

19 October 2023

language of work or name

English

0 references

publication date

13 March 2007

0 references

published in

0 references

volume

104

0 references

issue

11

0 references

page(s)

4512-7

0 references

cites work

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Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism

7 April 2017

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Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis

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Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands

7 April 2017

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

7 April 2017

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Promotion and attenuation of FGF signaling through the Ras-MAPK pathway

7 April 2017

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The endogenous fibroblast growth factor-2 antisense gene product regulates pituitary cell growth and hormone production

7 April 2017

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Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate

7 April 2017

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Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

7 April 2017

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NMR structure of the first Ig module of mouse FGFR1

28 September 2017

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Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

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p53 Mutation analysis in breast tumors by a DNA microarray method

28 September 2017

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The Pittsburgh Oral-Facial Cleft study: expanding the cleft phenotype. Background and justification.

28 September 2017

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Progress toward discerning the genetics of cleft lip

28 September 2017

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Sequencing arrays for screening multiple genes associated with early-onset human retinal degenerations on a high-throughput platform

28 September 2017

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Orofacial clefting: recent insights into a complex trait

28 September 2017

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28 September 2017

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Kallmann syndrome: fibroblast growth factor signaling insufficiency?

28 September 2017

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

28 September 2017

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

28 September 2017

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Long term follow up study of survival associated with cleft lip and palate at birth

28 September 2017

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28 September 2017

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28 September 2017

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Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome

28 September 2017

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Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

28 September 2017

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An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis.

28 September 2017

1 reference

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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

30 May 2018

1 reference

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The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

1 reference

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A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

21 January 2018

1 reference

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Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0607956104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0607956104

The Endogenous Fibroblast Growth Factor-2 Antisense Gene Product Regulates Pituitary Cell Growth and Hormone Production

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0607956104

Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1810508

The oral manifestations of Apert syndrome

28 November 2018

1 reference

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

28 November 2018

1 reference

12 December 2020

Signal transduction by fibroblast growth factor receptors

1 reference

12 December 2020

Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2)

1 reference

12 December 2020

Extensive sequencing of the CFTR gene: lessons learned from the first 157 patient samples

1 reference

12 December 2020

Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0607956104

1 reference

release_ns7m2cndbjapjeqqfev6u4bsaq

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ns7m2cndbjapjeqqfev6u4bsaq

24 November 2022

mapped directly with Wikidata item

4172727

1 reference

1 reference

1 reference