(Q52609939)

English

FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy-Walker malformation carrying a de novo 8p deletion.

scientific article published on 12 April 2011

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy-Walker malformation carrying a de novo 8p deletion. (English)

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

1

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

Bruno Dallapiccola

14

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

15

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

object named as

Sabina Barresi

2

0 references

Lorena Travaglini

object named as

Lorena Travaglini

3

0 references

Stefano Cianfarani

object named as

Stefano Cianfarani

8

0 references

Antonio Novelli

object named as

Antonio Novelli

12

0 references

Enza Maria Valente

object named as

Enza Maria Valente

13

0 references

5

object named as

Teresa Rizza

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

Laura Bernardini

4

object named as

Laura Bernardini

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

author name string

Maria Cristina Digilio

6

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

Eugenio Mercuri

7

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

Massimiliano Valeriani

9

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

Alessandro Ferraris

10

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

Letizia Da Sacco

11

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

publication date

12 April 2011

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

12

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

3

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

241-245

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

https://scigraph.springernature.com/pub.10.1007/s10048-011-0283-8

0 references

Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Human malformations of the midbrain and hindbrain: review and proposed classification scheme

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Genomic profile of copy number variants on the short arm of human chromosome 8.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Fibroblast growth factors 1, 2, 17, and 19 are the predominant FGF ligands expressed in human fetal growth plate cartilage

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Transcriptional control of chondrocyte fate and differentiation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Expression of the Nkx3.1 homobox gene during pre and postnatal development.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Fibroblast growth factor signaling is required for the proliferation and patterning of progenitor cells in the developing anterior pituitary.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Relative impact of nucleotide and copy number variation on gene expression phenotypes

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Cis-regulation and chromosomal rearrangement of the fgf8 locus after the teleost/tetrapod split.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Specific regions within the embryonic midbrain and cerebellum require different levels of FGF signaling during development.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Glypican-1 controls brain size through regulation of fibroblast growth factor signaling in early neurogenesis

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Expanding CEP290 mutational spectrum in ciliopathies

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0283-8

21 January 2018

Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ADAM7, a member of the ADAM (a disintegrin and metalloprotease) gene family is specifically expressed in the mouse anterior pituitary and epididymis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-011-0283-8

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

release_ehyhaebt5bfmzdhzpdhm2xqrii

1 reference

https://api.fatcat.wiki/v0/release/ehyhaebt5bfmzdhzpdhm2xqrii

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21484435

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q52609939&oldid=1842891742"