Developmental disorders of the midbrain and hindbrain. - Wikidata - awgldk - TriplyDB

Developmental disorders of the midbrain and hindbrain.

Developmental disorders of the midbrain and hindbrain.

http://www.wikidata.org/entity/Q37992627

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Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities Blake's pouch cyst Inferior cerebellar hypoplasia resembling a Dandy-Walker-like malformation in purebred Eurasier dogs with familial non-progressive ataxia: a retrospective and prospective clinical cohort study Magnetic resonance imaging of anterior temporal lobe cysts in children: discriminating special imaging features in a particular group of diseases.Update on neuroimaging phenotypes of mid-hindbrain malformations.Cellular and molecular basis of cerebellar development.Role of Shh in the development of molecularly characterized tegmental nuclei in mouse rhombomere 1.Challenges of diagnostic exome sequencing in an inbred founder population.The cerebellum: from development to structural complexity and motor learning.The fetal vermis, pons and brainstem: normal longitudinal development as shown by dedicated neurosonography.Caudal Fossa Ratio in Normal Dogs and Eurasier Dogs with VLDLR-Associated Genetic Cerebellar Hypoplasia.

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Developmental disorders of the midbrain and hindbrain.

http://www.wikidata.org/entity/Q37992627

description

article científic

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article scientifique

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articolo scientifico

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Developmental disorders of the midbrain and hindbrain.

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Developmental disorders of the midbrain and hindbrain.

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Developmental disorders of the midbrain and hindbrain.

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Developmental disorders of the midbrain and hindbrain.

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Developmental disorders of the midbrain and hindbrain.

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Developmental disorders of the midbrain and hindbrain.

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FNANA.2012.00007

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Frontiers in Neuroanatomy

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Developmental disorders of the midbrain and hindbrain.

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A James Barkovich

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Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

Reelin is a ligand for lipoprotein receptors

Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation

Disease-associated GPR56 mutations cause bilateral frontoparietal polymicrogyria via multiple mechanisms

Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis

Mouse disabled (mDab1): a Src binding protein implicated in neuronal development

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