(Q56266838)

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

author name string

Ana Laura Fernández-Perrone

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Daniel Martín Fernández-Mayoralas

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Beatriz Calleja-Pérez

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

María Del Carmen Sánchez-Hombre

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Ester Corbacho Fernández

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Sara López-Martín

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

publication date

December 2014

0 references

published in

Child's Nervous System

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

volume

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

page(s)

2157-2161

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24980605%20AND%20SRC:MED&resulttype=core&format=json

Craniosynostosis genetics: The mystery unfolds

1 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Cranial sutures: a brief review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Genetic study of nonsyndromic coronal craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Molecular analysis of patients with synostotic frontal plagiocephaly (unilateral coronal synostosis).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Craniosynostosis: genes and mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Genetic study of scaphocephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

The FGF family: biology, pathophysiology and therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

FGF2 stimulation of the pyrophosphate-generating enzyme, PC-1, in pre-osteoblast cells is mediated by RUNX2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Effect of fibroblast growth factor on cultured fetal rat calvaria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

In vivo modulation of FGF biological activity alters cranial suture fate

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Twist1 homodimers enhance FGF responsiveness of the cranial sutures and promote suture closure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Runx2 regulates FGF2-induced Bmp2 expression during cranial bone development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Fibroblast growth factor 2 control of vascular tone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Expression of alternatively spliced FGF-2 antisense RNA transcripts in the central nervous system: regulation of FGF-2 mRNA translation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

CAP-1A is a novel linker that binds clathrin and the voltage-gated sodium channel Na(v)1.8

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Major channels involved in neuropsychiatric disorders and therapeutic perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Neurological perspectives on voltage-gated sodium channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Cadherins and neuropsychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

The misdiagnosis of craniosynostosis as deformational plagiocephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative g

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-014-2474-8

Vertebrate Sprouty genes are induced by FGF signaling and can cause chondrodysplasia when overexpressed.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24980605

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24980605

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Integration of FGF and TWIST in calvarial bone and suture development.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24980605