Pages that link to "Q34142314"
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The following pages link to GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. (Q34142314):
Displaying 50 items.
- Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities (Q24323215) (← links)
- Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development (Q26770788) (← links)
- A developmental and genetic classification for malformations of cortical development: update 2012 (Q26858999) (← links)
- Congenital muscular dystrophies: a brief review (Q28255519) (← links)
- International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors (Q28257710) (← links)
- G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination (Q28512264) (← links)
- Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning (Q28513831) (← links)
- Growth and folding of the mammalian cerebral cortex: from molecules to malformations (Q28655454) (← links)
- Polymicrogyria: pathology, fetal origins and mechanisms. (Q34109022) (← links)
- Loss of Col3a1, the gene for Ehlers-Danlos syndrome type IV, results in neocortical dyslamination (Q34123887) (← links)
- A novel GPR56 mutation causes bilateral frontoparietal polymicrogyria (Q34196998) (← links)
- GPR56 and the developing cerebral cortex: cells, matrix, and neuronal migration (Q34301363) (← links)
- Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype (Q34320039) (← links)
- GPR56 functions together with α3β1 integrin in regulating cerebral cortical development (Q34359060) (← links)
- G-protein coupled receptor 56 promotes myoblast fusion through serum response factor- and nuclear factor of activated T-cell-mediated signalling but is not essential for muscle development in vivo (Q34376127) (← links)
- The adhesion G protein-coupled receptor GPR56 is a cell-autonomous regulator of oligodendrocyte development. (Q34458989) (← links)
- The adhesion GPCR Gpr56 regulates oligodendrocyte development via interactions with Gα12/13 and RhoA (Q34459009) (← links)
- Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly (Q34462730) (← links)
- Polymicrogyria includes fusion of the molecular layer and decreased neuronal populations but normal cortical laminar organization (Q35041227) (← links)
- Morphological and functional aspects of progenitors perturbed in cortical malformations (Q35077279) (← links)
- Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly (Q37396892) (← links)
- Neuropathology of brain and spinal malformations in a case of monosomy 1p36. (Q37485274) (← links)
- Characterization of G protein-coupled receptor 56 protein expression in the mouse developing neocortex (Q37537269) (← links)
- Development and Dysgenesis of the Cerebral Cortex: Malformations of Cortical Development (Q37909671) (← links)
- Cerebellar cysts in children: a pattern recognition approach (Q38287439) (← links)
- Disease-associated extracellular loop mutations in the adhesion G protein-coupled receptor G1 (ADGRG1; GPR56) differentially regulate downstream signaling (Q38706852) (← links)
- Adhesion G protein-coupled receptors in nervous system development and disease (Q38910702) (← links)
- Adhesion GPCR-Related Protein Networks (Q39004694) (← links)
- Adhesion G-protein coupled receptors and extracellular matrix proteins: Roles in myelination and glial cell development (Q39012388) (← links)
- Recognizable phenotypes associated with intracranial calcification (Q39526484) (← links)
- Structural Basis for Regulation of GPR56/ADGRG1 by Its Alternatively Spliced Extracellular Domains (Q41182997) (← links)
- Ultra-high-field MR imaging in polymicrogyria and epilepsy (Q41299267) (← links)
- Tubulinopathies and Their Brain Malformation Syndromes: Every TUB on Its Own Bottom (Q42405349) (← links)
- Terminology in morphological anomalies of the cerebellum does matter (Q42930599) (← links)
- Ataxia, intellectual disability, and ocular apraxia with cerebellar cysts: a new disease? (Q46160898) (← links)
- Developing guinea pig brain as a model for cortical folding. (Q46355654) (← links)
- Homozygous nonsense mutation in SCHIP1/IQCJ-SCHIP1 causes a neurodevelopmental brain malformation syndrome. (Q47979112) (← links)
- GPR56-Related Polymicrogyria: Clinicoradiologic Profile of 4 Patients (Q48203864) (← links)
- Bilateral frontoparietal polymicrogyria (Q48449990) (← links)
- Neuronal migration disorders: Focus on the cytoskeleton and epilepsy (Q50346016) (← links)
- Cerebellar Bottom-of-Fissure Dysplasia-a Novel Cerebellar Gray Matter Neuroimaging Pattern (Q50551588) (← links)
- The histopathology of polymicrogyria: a series of 71 brain autopsy studies (Q50577595) (← links)
- Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities. (Q52089031) (← links)
- Whole‐exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria (Q55054741) (← links)
- Three Mutations in the Bilateral Frontoparietal Polymicrogyria Gene in Pakistani Intellectual Disability Families (Q56232629) (← links)
- Malformations of cortical development and epilepsy (Q56770849) (← links)
- The Genetics of Brain Malformations (Q57252972) (← links)
- A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis (Q57809058) (← links)
- Delineating syndrome: From congenital microcephaly to hyperkinetic encephalopathy (Q59798714) (← links)
- Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: neuroimaging and clinical findings (Q64091383) (← links)