Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases. - Wikidata - awgldk - TriplyDB

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

http://www.wikidata.org/entity/Q41967721

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Dcc Mediates Functional Assembly of Peripheral Auditory Circuits Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline.Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature Amphetamine in adolescence disrupts the development of medial prefrontal cortex dopamine connectivity in a DCC-dependent manner Supplementary Motor Complex and Disturbed Motor Control - a Retrospective Clinical and Lesion Analysis of Patients after Anterior Cerebral Artery Stroke.A novel role for the DNA repair gene Rad51 in Netrin-1 signalling.One hand clapping: lateralization of motor control.Biallelic mutations in human DCC cause developmental split-brain syndrome.The corticospinal tract: Evolution, development, and human disorders.Resilience to amphetamine in mouse models of netrin-1 haploinsufficiency: role of mesocortical dopamine.Dcc haploinsufficiency regulates dopamine receptor expression across postnatal lifespan.Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.Mutations in the netrin-1 gene cause congenital mirror movements.Is one motor cortex enough for two hands?Congenital mirror movements caused by a mutation in the DCC gene.

P2860

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P2860

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

http://www.wikidata.org/entity/Q41967721

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

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Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

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Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

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Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

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Alessandra Borgheresi

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Chloé Quélin

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Christel Depienne

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Delphine Bouteiller

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Diane Doummar

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Emmanuel Roze

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Florence Riant

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Ghislaine Plessis

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Isabelle Lagroua

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Jean-Louis Golmard

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P2860

Identification of a novel human Rad51 variant that promotes DNA strand exchange

The netrin 1 receptors Unc5h3 and Dcc are necessary at multiple choice points for the guidance of corticospinal tract axons.

Developmental and benign movement disorders in childhood.

RAD51 haploinsufficiency causes congenital mirror movements in humans.

RAD51 deficiency disrupts the corticospinal lateralization of motor control.

Mirror movements after childhood hemiparesis.

Mutations in DCC cause congenital mirror movements.

A novel DCC mutation and genetic heterogeneity in congenital mirror movements.

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