(Q51963826)

19 April 2018

title

Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome. (English)

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19 April 2018

9

Jean-Pierre Hardelin

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19 April 2018

Chrystel Leroy

1

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19 April 2018

Corinne Fouveaut

2

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19 April 2018

Sandrine Leclercq

3

1 reference

19 April 2018

Sébastien Jacquemont

4

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19 April 2018

Hélène Du Boullay

5

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19 April 2018

James Lespinasse

6

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19 April 2018

Marc Delpech

7

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19 April 2018

Jean-Michel Dupont

8

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19 April 2018

Catherine Dodé

10

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19 April 2018

publication date

20 February 2008

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19 April 2018

European Journal of Human Genetics

published in

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19 April 2018

volume

16

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19 April 2018

issue

7

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19 April 2018

page(s)

865-868

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19 April 2018

https://scigraph.springernature.com/pub.10.1038/ejhg.2008.15

exact match

0 references

cites work

Effect of Purified Luteinizing Hormone Releasing Factor on Normal and Hypogonadotrophic Anosmic Men

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Anosmin-1 modulates fibroblast growth factor receptor 1 signaling in human gonadotropin-releasing hormone olfactory neuroblasts through a heparan sulfate-dependent mechanism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Abnormal development of the olfactory bulb and reproductive system in mice lacking prokineticin receptor PKR2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Dependence of olfactory bulb neurogenesis on prokineticin 2 signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.15

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/EJHG.2008.15

1 reference

19 April 2018

1 reference

19 April 2018