Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2 (Q21092497)

15 August 2022

7

James Lespinasse

James

Lespinasse

1 reference

15 August 2022

Slawomir Wolczynski

14

Slawomir

Wolczynski

1 reference

15 August 2022

18

Jean-Pierre Hardelin

Jean-Pierre

Hardelin

1 reference

15 August 2022

6

Marie-Laure Kottler

Marie-Laure

Kottler

1 reference

15 August 2022

Jacques Young

17

Jacques

Young

2 references

ORCID Public Data File 2021

15 August 2022

Luis Teixeira

2

Luis

Teixeira

2 references

ORCID Public Data File 2021

15 August 2022

Catherine Dodé

1

Catherine

Dodé

1 reference

15 August 2022

Jacqueline Levilliers

3

Jacqueline

Levilliers

1 reference

15 August 2022

Corinne Fouveaut

4

Corinne

Fouveaut

1 reference

15 August 2022

Philippe Bouchard

5

Philippe

Bouchard

1 reference

15 August 2022

Anne Lienhardt-Roussie

8

Anne

Lienhardt-Roussie

1 reference

15 August 2022

Michèle Mathieu

9

Michèle

Mathieu

1 reference

15 August 2022

Alexandre Moerman

10

Alexandre

Moerman

1 reference

15 August 2022

Graeme Morgan

11

Graeme

Morgan

1 reference

15 August 2022

Arnaud Murat

12

Arnaud

Murat

1 reference

15 August 2022

Jean-Edmont Toublanc

13

Jean-Edmont

Toublanc

1 reference

15 August 2022

Marc Delpech

15

Marc

Delpech

1 reference

Creative Commons Attribution 4.0 International

15 August 2022

language of work or name

English

0 references

publication date

20 October 2006

0 references

published in

PLOS Genetics

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volume

2

0 references

issue

10

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page(s)

e175

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copyright license

start time

20 October 2006

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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The endocrine-gland-derived VEGF homologue Bv8 promotes angiogenesis in the testis: Localization of Bv8 receptors to endothelial cells

19 March 2017

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Identification of two prokineticin cDNAs: recombinant proteins potently contract gastrointestinal smooth muscle

19 March 2017

1 reference

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Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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Molecular cloning and characterization of prokineticin receptors

19 March 2017

1 reference

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Isolation and identification of EG-VEGF/prokineticins as cognate ligands for two orphan G-protein-coupled receptors

19 March 2017

1 reference

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Prokineticin 2 transmits the behavioural circadian rhythm of the suprachiasmatic nucleus

19 March 2017

1 reference

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Identification and molecular characterization of two closely related G protein-coupled receptors activated by prokineticins/endocrine gland vascular endothelial growth factor

19 March 2017

1 reference

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Molecular modelling and experimental studies of mutation and cell-adhesion sites in the fibronectin type III and whey acidic protein domains of human anosmin-1

19 March 2017

1 reference

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

19 March 2017

1 reference

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

12 September 2017

1 reference

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Prokineticin 2 and circadian clock output

12 September 2017

1 reference

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Regulation of translation via mRNA structure in prokaryotes and eukaryotes

12 September 2017

1 reference

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Dependence of olfactory bulb neurogenesis on prokineticin 2 signaling

12 September 2017

1 reference

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Structural basis for fibroblast growth factor receptor activation

12 September 2017

1 reference

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Bv8, the amphibian homologue of the mammalian prokineticins, modulates ingestive behaviour in rats

12 September 2017

1 reference

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

12 September 2017

1 reference

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Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome

12 September 2017

1 reference

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Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts).

12 September 2017

1 reference

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Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1617130

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

30 May 2018

1 reference

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Extended and flexible domain solution structure of the extracellular matrix protein anosmin-1 by X-ray scattering, analytical ultracentrifugation and constrained modelling.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1617130

Identification and pharmacological characterization of prokineticin 2 beta as a selective ligand for prokineticin receptor 1.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1617130

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

29 November 2018

1 reference

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Structural determinants required for the bioactivities of prokineticins and identification of prokineticin receptor antagonists

29 November 2018

1 reference

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Median craioencephalic dysraphias and olfactogenital dysplasia

29 November 2018

1 reference

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

29 November 2018

1 reference

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FGF signaling through FGFR1 is required for olfactory bulb morphogenesis

29 November 2018

1 reference

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Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome

29 November 2018

1 reference

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10.1371/JOURNAL.PGEN.0020175

29 November 2018

Identifiers

DOI

1 reference

1 reference

1 reference

1 reference