(Q47917792)

English

Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice.

scientific article published on 2 March 2017

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scholarly article

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice. (English)

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

Jean-Pierre Hardelin

8

object named as

Jean-Pierre Hardelin

1 reference

Europe PubMed Central

6 February 2018

Nelly Pitteloud

5

object named as

Nelly Pitteloud

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

author name string

Séverine Marcos

1

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

Carine Monnier

2

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

Corinne Fouveaut

4

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

Fabrice Ango

6

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

Catherine Dodé

7

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

publication date

2 March 2017

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

Human Molecular Genetics

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

26

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

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Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

2006-2017

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Development of the neurons controlling fertility in humans: new insights from 3D imaging and transparent fetal brains

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Mutations in FEZF1 cause Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Semaphorin signalling during development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Neuropilin Functions as an Essential Cell Surface Receptor

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Structural Basis for Plexin Activation and Regulation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Origin of luteinizing hormone-releasing hormone neurons

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Evidence that cells expressing luteinizing hormone-releasing hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Immunocytochemical demonstration of neural cell adhesion molecule (NCAM) along the migration route of luteinizing hormone-releasing hormone (LHRH) neurons in mice.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Defective gonadotropin-releasing hormone neuron migration in mice lacking SEMA3A signalling through NRP1 and NRP2: implications for the aetiology of hypogonadotropic hypogonadism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Neuropilins and their ligands are important in the migration of gonadotropin-releasing hormone neurons

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Neuropilin-2 is required in vivo for selective axon guidance responses to secreted semaphorins.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Composition of the migratory mass during development of the olfactory nerve

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Olfactory epithelium progenitors: insights from transgenic mice and in vitro biology

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Olfactory ensheathing glia are required for embryonic olfactory axon targeting and the migration of gonadotropin-releasing hormone neurons

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

PlexinA1 signaling directs the segregation of proprioceptive sensory axons in the developing spinal cord

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Nipple attachment and survival in neonatal olfactory bulbectomized rats.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Opposite-sex attraction in male mice requires testosterone-dependent regulation of adult olfactory bulb neurogenesis.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Crystal structure of the plexin A3 intracellular region reveals an autoinhibited conformation through active site sequestration

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Semaphorins command cells to move

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Plexin structures are coming: opportunities for multilevel investigations of semaphorin guidance receptors, their cell signaling mechanisms, and functions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Plexina1 autoinhibition by the plexin sema domain.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Semaphorin 4D regulates gonadotropin hormone-releasing hormone-1 neuronal migration through PlexinB1-Met complex

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Plexin-A3 mediates semaphorin signaling and regulates the development of hippocampal axonal projections

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

A simple and efficient procedure for non-isotopic in situ hybridization to sectioned material.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Comparative protein modelling by satisfaction of spatial restraints

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

UniProt: a hub for protein information

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Clustal W and Clustal X version 2.0

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Statistical potential for assessment and prediction of protein structures

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

UCSF Chimera--a visualization system for exploratory research and analysis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Jalview Version 2--a multiple sequence alignment editor and analysis workbench

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Neuropilin-1 extracellular domains mediate semaphorin D/III-induced growth cone collapse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDX080

21 January 2018

Identifiers

10.1093/HMG/DDX080

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

1 reference

Europe PubMed Central

6 February 2018

http://europepmc.org/abstract/MED/28334861

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