An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21
about
Disease-associated mutations prevent GPR56-collagen III interactionCerebral cortex expansion and folding: what have we learned?A developmental and genetic classification for malformations of cortical development: update 2012Genetic malformations of the cerebral cortex and epilepsyInternational Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptorsG protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and laminationGPR56 regulates pial basement membrane integrity and cortical laminationGPR56-regulated granule cell adhesion is essential for rostral cerebellar development.Genetics of the polymicrogyria syndromes.Neuronal migration disorders, genetics, and epileptogenesis.Current concepts of polymicrogyria.Loss of Col3a1, the gene for Ehlers-Danlos syndrome type IV, results in neocortical dyslamination.GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex.A novel GPR56 mutation causes bilateral frontoparietal polymicrogyriaGPR56 and the developing cerebral cortex: cells, matrix, and neuronal migrationGPR56 functions together with α3β1 integrin in regulating cerebral cortical development.The adhesion G protein-coupled receptor GPR56 is a cell-autonomous regulator of oligodendrocyte development.The adhesion GPCR Gpr56 regulates oligodendrocyte development via interactions with Gα12/13 and RhoABilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations.Cortical malformation and pediatric epilepsy: a molecular genetic approach.Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions.Autosomal recessive bilateral frontal polymicrogyria with ectopia lentis and chorioretinal dystrophy.Quantification and discrimination of abnormal sulcal patterns in polymicrogyriaCharacterization of G protein-coupled receptor 56 protein expression in the mouse developing neocortexAssociation between copy number variation losses and alcohol dependence across African American and European American ethnic groups.A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.Adhesion GPCR-Related Protein Networks.Adhesion GPCRs Govern Polarity of Epithelia and Cell Migration.Adhesion GPCRs as Novel Actors in Neural and Glial Cell Functions: From Synaptogenesis to Myelination.MRI analysis of sulcation morphology in polymicrogyria.Excitatory and inhibitory postsynaptic currents in a rat model of epileptogenic microgyria.GPR56-Related Polymicrogyria: Clinicoradiologic Profile of 4 Patients.Malformations of cortical development
P2860
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P2860
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21
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2002 nî lūn-bûn
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2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2002年の論文
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2002年論文
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2002年論文
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2002年論文
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2002年論文
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2002年論文
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name
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@ast
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@en
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@nl
type
label
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@ast
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@en
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@nl
prefLabel
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@ast
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@en
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@nl
P2093
P2860
P3181
P356
P1476
An autosomal recessive form of ...... maps to chromosome 16q12.2-21
@en
P2093
Betty Doan
Christopher A Walsh
Elizabeth W Pugh
Kim Doheny
P Ellen Grant
Rachel Straussberg
Susan E Hong
Yin Yao Shugart
P2860
P304
P3181
P356
10.1086/339552
P407
P577
2002-04-01T00:00:00Z