About: G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination

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About: G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination Goto Sponge NotDistinct Permalink

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description	artículu científicu espublizáu en 2011 (ast) vědecký článek publikovaný v roce 2011 (cs) наукова стаття, опублікована в серпні 2011 (uk) 2011 թվականի օգոստոսին հրատարակված գիտական հոդված (hy) 2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած (hyw) 2011年學術文章 (zh) vedecký článok (publikovaný 2011/08/02) (sk) مقالة علمية (نشرت في 2-8-2011) (ar) article publié dans les Proceedings of the National Academy of Sciences of the United States of America (fr) scientific journal article (en) im August 2011 veröffentlichter wissenschaftlicher Artikel (de) wetenschappelijk artikel (gepubliceerd op 2011/08/02) (nl)
publication date	wds:Q28512264-62F47376-80DB-4C98-AEAB-D5C98399C3EC
publication date	2011-08-02 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28512264-2E6EB850-AB85-43AD-881E-7D8E2225D557
language of work or name	English
cites work	wds:Q28512264-0B8D79C9-CBAA-414D-BCF2-DB67892F784D wds:Q28512264-0BDCF76F-B730-401C-A76E-9863641B553C wds:Q28512264-0CE26660-7192-4EBB-BD4F-650E8139E420 wds:Q28512264-0E5BD311-6E21-4157-8DDC-E2002FD3020C wds:Q28512264-0E7D17C2-2A61-4402-87C1-060384F3EB82 wds:Q28512264-0FA85CFC-258D-43B3-ADD4-99E8F94E58D7 wds:Q28512264-22694600-EFC6-44A5-821B-AF82766B8FC7 wds:Q28512264-258131F3-011D-4A92-82F6-4564A7F6F549 wds:Q28512264-29867956-3F5B-4044-91F7-7F3C415A6B5A wds:Q28512264-2B5410B0-E2C6-45F9-B5EB-DE2E31C96A2A wds:Q28512264-2C2B0FEE-5F6E-4136-AA08-C99E83D6990B wds:Q28512264-2EFA0BE8-D196-437A-964E-31908189B19A wds:Q28512264-3525B440-9826-40D1-AF1D-A117B4C09EE2 wds:Q28512264-36492BD1-10BA-4F0A-9F82-A56F061101F2 wds:Q28512264-3F3E00AA-C2E7-4D44-AA67-845CC47FEBA5 wds:Q28512264-3FA17869-9BBB-45EB-865F-E6F9FE0A650B wds:Q28512264-47CDA363-6078-4B9C-9AE0-DC7C56DFC50B wds:Q28512264-4EA649AA-0D4B-444C-9277-83DA685501A4 wds:Q28512264-5B1F1F53-89DD-4219-B759-243BB7C4D502 wds:Q28512264-5FCA25AA-52D6-484E-8021-37059CE78EF3 wds:Q28512264-6433F981-4C33-43FB-81B0-A4A13B91FDFF wds:Q28512264-656EAC0E-4471-41AB-B623-BCC5BE40C4DD wds:Q28512264-6576D428-1491-44D4-BBBF-16307EF701BA wds:Q28512264-6AE594AF-CF38-41A3-98D2-5207BB117DEE wds:Q28512264-6DFC0716-5E3C-4DA0-BE78-52004461DB9F wds:Q28512264-88CF8493-E366-4AB6-BBF3-91525F58BDDF wds:Q28512264-8B60EA90-7108-495D-A3AF-F877EE7ABA06 wds:Q28512264-8D16ADE5-50E0-4849-B858-A8A30DDF8E87 wds:Q28512264-8F974437-1B2F-41B3-B181-5E118D57326C wds:Q28512264-9084D0EF-E7AC-4E35-9ABA-D520D3C54045 wds:Q28512264-9105DFD4-EA47-491D-99AE-193B506C2FD8 wds:Q28512264-926FBC24-8854-4C6B-9932-CCC455661AEF wds:Q28512264-A348FD64-AEAF-4843-B406-C36E2357CBA1 wds:Q28512264-AA7842A7-8FC3-485F-A86C-F213BF5C15E9 wds:Q28512264-ADC78F33-6D60-4FC6-A945-82CB585CF5FA wds:Q28512264-AFA5D4DE-5D87-4747-A3FC-F4B2C03E5E92 wds:Q28512264-B271C2AA-85E1-4B9D-824B-FC25FB14D641 wds:Q28512264-B4598D11-2E69-47B5-97B1-18B2B1A4D95B wds:Q28512264-B61CE3EC-AFDE-4603-9837-9D4176D0CC7B wds:Q28512264-B97C63F7-5E79-4AF9-A1C4-56F0F35DDD6C wds:Q28512264-BDECEF43-E3CB-494D-8E18-255D8FFEAF13 wds:Q28512264-C36559EE-92CF-4635-853E-FEA5C85DF59C wds:Q28512264-C4DACBCD-4877-4D4F-9179-DA6A2C76E5C1 wds:Q28512264-D75C08A0-02D3-49C5-8807-362D814B2326 wds:Q28512264-DA5B2000-0A8D-4B39-90C5-91A06EE4DA7B wds:Q28512264-E4BDCCF6-363A-4F1E-AC2B-6A94C420F5A6 wds:Q28512264-F472901B-C097-4B6B-9270-A027CEC5587B wds:Q28512264-F7639FA7-D453-4636-A17D-63B8B560F0FE wds:Q28512264-F9CB98CB-F170-4B2F-B92F-01AA3D23D7BA wds:Q28512264-FE3D881B-D59D-4457-97A0-99A89D5BF94D
cites work	Trekking across the brain: the journey of neuronal migration Ehlers-Danlos Syndrome Type IV: A Single Base Substitution of the Last Nucleotide of Exon 34 in COL3A1 Leads to Exon Skipping The multipolar stage and disruptions in neuronal migration Development of the human cerebral cortex: Boulder Committee revisited Perlecan maintains the integrity of cartilage and some basement membranes FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. Smooth, rough and upside-down neocortical development Beta1-class integrins regulate the development of laminae and folia in the cerebral and cerebellar cortex Essential role of alpha 6 integrins in cortical and retinal lamination. Heritable diseases of collagen A novel binding site in collagen type III for integrins alpha1beta1 and alpha2beta1 Fezl is required for the birth and specification of corticospinal motor neurons Mechanisms of Cortical Development: A View From Mutations in Mice Galpha12/Galpha13 deficiency causes localized overmigration of neurons in the developing cerebral and cerebellar cortices Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development Rho signaling, ROCK and mDia1, in transformation, metastasis and invasion Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex Platelet-activating factor receptor stimulation disrupts neuronal migration In vitro. Ehlers-Danlos syndrome type IV GPR56, an atypical G protein-coupled receptor, binds tissue transglutaminase, TG2, and inhibits melanoma tumor growth and metastasis G protein-coupled receptor-dependent development of human frontal cortex An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21 GPR56 is a GPCR that is overexpressed in gliomas and functions in tumor cell adhesion GPR56 regulates pial basement membrane integrity and cortical lamination GPR56-regulated granule cell adhesion is essential for rostral cerebellar development Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV. A mutation in the gene for type III procollagen (COL3A1) in a family with aortic aneurysms Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes Disease-associated mutations affect GPR56 protein trafficking and cell surface expression. Orphan G protein-coupled receptor GPR56 regulates neural progenitor cell migration via a G alpha 12/13 and Rho pathway. Genetics of disorders of cortical development MEKK4 signaling regulates filamin expression and neuronal migration.

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