CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration

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Arachnoid cyst: a further anomaly associated with Kallmann syndrome?Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism.CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism.

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CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration

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2016 nî lūn-bûn

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CCDC141 Mutation Identified in ...... Alters GnRH Neuronal Migration

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CCDC141 Mutation Identified in ...... Alters GnRH Neuronal Migration

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CCDC141 Mutation Identified in ...... Alters GnRH Neuronal Migration

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CCDC141 Mutation Identified in ...... Alters GnRH Neuronal Migration

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A Kemal Topaloglu

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Carol Taylor-Burds

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Jean D R Tiong

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Paul J Cheng

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Yusuf Ozkan

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Capture of microtubule plus-ends at the actin cortex promotes axophilic neuronal migration by enhancing microtubule tension in the leading process

Cholecystokinin modulates migration of gonadotropin-releasing hormone-1 neurons

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

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

Calcium release-dependent actin flow in the leading process mediates axophilic migration

Novel gene expressed in nasal region influences outgrowth of olfactory axons and migration of luteinizing hormone-releasing hormone (LHRH) neurons

Kinesin-5, a mitotic microtubule-associated motor protein, modulates neuronal migration

From nose to brain: development of gonadotrophin-releasing hormone-1 neurones

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

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1956-1966

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scholarly article

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10.1210/EN.2015-1846

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English

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157

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2016-03-25T00:00:00Z

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anosmia

hypogonadism

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4870868

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CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration

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P2860

P2860

CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration

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type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932