(Q24533993)

4 July 2017

title

Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome (English)

1 reference

4 July 2017

Ilse Wieland

1

1 reference

4 July 2017

Sibylle Jakubiczka

2

1 reference

4 July 2017

Petra Muschke

3

1 reference

4 July 2017

Monika Cohen

4

1 reference

4 July 2017

Hannelore Thiele

5

1 reference

4 July 2017

Klaus L Gerlach

6

1 reference

4 July 2017

Ralf H Adams

7

1 reference

4 July 2017

Peter Wieacker

8

1 reference

4 July 2017

language of work or name

English

0 references

publication date

29 April 2004

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

74

1 reference

4 July 2017

issue

6

1 reference

4 July 2017

page(s)

1209-1215

1 reference

Crystal structure of an Eph receptor-ephrin complex

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Crystal structure of an ephrin ectodomain

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

'Eph'ective signaling: forward, reverse and crosstalk

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Mechanisms and functions of Eph and ephrin signalling

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Multiple roles of EPH receptors and ephrins in neural development

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Nuk controls pathfinding of commissural axons in the mammalian central nervous system

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Control of skeletal patterning by ephrinB1-EphB interactions

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

A first-generation X-inactivation profile of the human X chromosome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Metabolic interference and the + - heterozygote. a hypothetical form of simple inheritance which is neither dominant nor recessive

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Mapping of a further locus for X-linked craniofrontonasal syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

An ephrin mimetic peptide that selectively targets the EphA2 receptor

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Craniofrontonasal syndrome: study of 41 patients

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182084

Craniofrontonasal dysplasia: more severe expression in the mother than in her son

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15124102

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/421532

1 reference

OpenCitations bibliographic resource ID

4 July 2017

1969682

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

4 July 2017

1 reference