| P50 | author | Sue Brown | Q43179657 |
| P2093 | author name string | Mark Hopkinson | |
| | Helen S Booler | |
| | Josie L Williams | |
| P2860 | cites work | Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1 | Q24291905 |
| | Disease-associated GPR56 mutations cause bilateral frontoparietal polymicrogyria via multiple mechanisms | Q24294181 |
| | Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan | Q24294992 |
| | Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE | Q24301093 |
| | Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy | Q24308069 |
| | ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome | Q24316024 |
| | Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan | Q24316123 |
| | SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function | Q24316126 |
| | Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan | Q24321692 |
| | Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan | Q24535942 |
| | Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome | Q24561808 |
| | Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies | Q24651944 |
| | POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome | Q24674153 |
| | A stoichiometric complex of neurexins and dystroglycan in brain | Q26269938 |
| | Endocytic trafficking of laminin is controlled by dystroglycan and is disrupted in cancers | Q27342661 |
| | Reelin induces a radial glial phenotype in human neural progenitor cells by activation of Notch-1 | Q27496548 |
| | Neurons derived from radial glial cells establish radial units in neocortex | Q28202112 |
| | Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan | Q28206027 |
| | Mode of cell migration to the superficial layers of fetal monkey neocortex | Q28243757 |
| | Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor | Q28254849 |
| | Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies | Q28256756 |
| | LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation | Q28288934 |
| | Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix | Q28296676 |
| | Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly | Q39849372 |
| | Fukutin-related protein localizes to the Golgi apparatus and mutations lead to mislocalization in muscle in vivo | Q40122746 |
| | Cajal-Retzius cells and the development of the neocortex | Q41719474 |
| | DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. | Q41933116 |
| | Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies | Q42524150 |
| | Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. | Q42524154 |
| | Investigating the functions of LARGE: lessons from mutant mice | Q42917952 |
| | Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome. | Q43073716 |
| | Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders | Q44159158 |
| | Zic deficiency in the cortical marginal zone and meninges results in cortical lamination defects resembling those in type II lissencephaly | Q46617677 |
| | Brain lipid-binding protein (BLBP): a novel signaling system in the developing mammalian CNS. | Q48083537 |
| | Molecular heterogeneity in fetal forms of type II lissencephaly. | Q48142018 |
| | Breaches of the pial basement membrane and disappearance of the glia limitans during development underlie the cortical lamination defect in the mouse model of muscle-eye-brain disease | Q48179008 |
| | LIS1-related isolated lissencephaly: spectrum of mutations and relationships with malformation severity | Q48489735 |
| | Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies | Q48666364 |
| | Fukutin-related protein alters the deposition of laminin in the eye and brain | Q48911848 |
| | Simulation studies of phase inversion in agitated vessels using a Monte Carlo technique. | Q51320181 |
| | Exposure to in utero irradiation produces disruption of radial glia in rats. | Q52528864 |
| | Disruption of neuronal migration and radial glia in the developing cerebral cortex following ablation of Cajal-Retzius cells. | Q52539654 |
| | Ectopia of meningeal fibroblasts and reactive gliosis in the cerebral cortex of the mouse model of muscle-eye-brain disease. | Q52582691 |
| | Reelin binds alpha3beta1 integrin and inhibits neuronal migration. | Q55034150 |
| | Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy | Q28303419 |
| | Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation | Q28478647 |
| | Reelin signaling directly affects radial glia morphology and biochemical maturation | Q28505272 |
| | Functional requirements for fukutin-related protein in the Golgi apparatus | Q28505367 |
| | Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation | Q28507319 |
| | Characterization of CNS precursor subtypes and radial glia | Q28508337 |
| | Radial glia regulate Cajal-Retzius cell positioning in the early embryonic cerebral cortex | Q28512286 |
| | GPR56 regulates pial basement membrane integrity and cortical lamination | Q28590062 |
| | Developmental roles of p73 in Cajal-Retzius cells and cortical patterning | Q28590271 |
| | LARGE2 generates the same xylose- and glucuronic acid-containing glycan structures as LARGE | Q28591175 |
| | Xylosyl- and glucuronyltransferase functions of LARGE in α-dystroglycan modification are conserved in LARGE2 | Q28592706 |
| | A genetic model for muscle-eye-brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1) | Q28593129 |
| | Karl Pribram, The James Arthur lectures, and what makes us human | Q28764730 |
| | Dystroglycan versatility in cell adhesion: a tale of multiple motifs | Q30156956 |
| | Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations | Q33845128 |
| | Interference with the development of early generated neocortex results in disruption of radial glia and abnormal formation of neocortical layers | Q33860000 |
| | Radial glia is a progenitor of neocortical neurons in the developing cerebral cortex | Q34089225 |
| | Malformation of the radial glial scaffold in the dentate gyrus of reeler mice, scrambler mice, and ApoER2/VLDLR-deficient mice | Q34189780 |
| | Primary cellular meningeal defects cause neocortical dysplasia and dyslamination | Q34250989 |
| | Meninges control tangential migration of hem-derived Cajal-Retzius cells via CXCL12/CXCR4 signaling | Q34565048 |
| | Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome | Q34722788 |
| | A dystroglycan mutation associated with limb-girdle muscular dystrophy. | Q34767085 |
| | Mutation of Large, which encodes a putative glycosyltransferase, in an animal model of muscular dystrophy | Q34989520 |
| | Breaches of the pial basement membrane are associated with defective dentate gyrus development in mouse models of congenital muscular dystrophies | Q35627405 |
| | Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome. | Q35880856 |
| | A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. | Q36232550 |
| | Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome | Q36439344 |
| | Dystroglycan on radial glia end feet is required for pial basement membrane integrity and columnar organization of the developing cerebral cortex. | Q36439974 |
| | Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly | Q36451494 |
| | Sticky situations: recent advances in control of cell adhesion during neuronal migration | Q36551557 |
| | Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome. | Q36731388 |
| | Diagnostic criteria for Walker-Warburg syndrome | Q38221850 |
| | Development, evolution and pathology of neocortical subplate neurons | Q38361885 |
| | Distinct functions of glial and neuronal dystroglycan in the developing and adult mouse brain. | Q38426779 |
| P433 | issue | 4 | |
| P921 | main subject | Cajal–Retzius cell | Q2299284 |
| P304 | page(s) | 465-478 | |
| P577 | publication date | 2015-08-26 | |
| P1433 | published in | Brain Pathology | Q4955776 |
| P1476 | title | Degree of Cajal-Retzius Cell Mislocalization Correlates with the Severity of Structural Brain Defects in Mouse Models of Dystroglycanopathy. | |
| P478 | volume | 26 | |