Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

Nature Genetics

Volumn 45, Issue 11, 2013, Pages 1300-1310

  Cappello, Silvia ^a   Gray, Mary J ^b   Badouel, Caroline ^c,d   Lange, Simona ^a   Einsiedler, Melanie ^a   Srour, Myriam ^e   Chitayat, David ^c,f   Hamdan, Fadi F ^e   Jenkins, Zandra A ^b   Morgan, Tim ^b   Preitner, Nadia ^b   Uster, Tami ^c   Thomas, Jackie ^c   Shannon, Patrick ^c   Morrison, Victoria ^g   Di Donato, Nataliya ^h   Van Maldergem, Lionel ⁱ   Neuhann, Teresa ^j   Newbury Ecob, Ruth ^k   Swinkells, Marielle ^l   Terhal, Paulien ^l   Wilson, Louise C ^m   Zwijnenburg, Petra J G ⁿ   Sutherland Smith, Andrew J ^o   Black, Michael A ^p   Markie, David ^b   Michaud, Jacques L ^e   Simpson, Michael A ^q   Mansour, Sahar ^r   McNeill, Helen ^c,d   Götz, Magdalena ^a,s,t   Robertson, Stephen P ^b   more..

^a INSTITUTE OF EPIDEMIOLOGY   (Germany)

^b UNIVERSITY OF OTAGO   (New Zealand)

^c MOUNT SINAI HOSPITAL   (Canada)

^d UNIVERSITY OF TORONTO   (Canada)

^e UNIVERSITY OF MONTREAL   (Canada)

^f HOSPITAL FOR SICK CHILDREN   (Canada)

^g UNIVERSITY COLLEGE LONDON   (United Kingdom)

^h DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

ⁱ UNIVERSITÉ DE FRANCHE COMTÉ   (France)

^j Medizinisch Genetisches Zentrum   (Germany)

^k ST MICHAEL'S HOSPITAL   (United Kingdom)

^l UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^m GREAT ORMOND STREET HOSPITAL   (United Kingdom)

ⁿ VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^o MASSEY UNIVERSITY   (New Zealand)

^p UNIVERSITY OF OTAGO   (New Zealand)

^q GUY S HOSPITAL   (United Kingdom)

^r KING'S COLLEGE LONDON   (United Kingdom)

^s UNIVERSITY OF MUNICH   (Germany)

^t Germany 3 Munich Cluster for Systems Neurology   (Germany)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; DCHS1 PROTEIN; FAT4 PROTEIN; LIGAND; SHORT HAIRPIN RNA; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRAIN CORTEX; BRAIN DEVELOPMENT; CELL ADHESION; CELL CYCLE G1 PHASE; CELL PROLIFERATION; CELLULAR DISTRIBUTION; CLINICAL ARTICLE; CONTROLLED STUDY; ELECTROPORATION; FEMALE; G1 PHASE CELL CYCLE CHECKPOINT; GENE EXPRESSION; GENE MUTATION; GENE SILENCING; GENETIC CODE; HETEROTOPIA; HUMAN; INTELLECTUAL IMPAIRMENT; MALE; NERVE CELL DIFFERENTIATION; NEURAL STEM CELL; NEUROEPITHELIUM; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SUBVENTRICULAR ZONE; VAN MALDERGEM SYNDROME;

ABNORMALITIES, MULTIPLE; ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; BASE SEQUENCE; CADHERINS; CELL DIFFERENTIATION; CELL PROLIFERATION; CEREBRAL CORTEX; CRANIOFACIAL ABNORMALITIES; FOOT DEFORMITIES, CONGENITAL; GENE KNOCKDOWN TECHNIQUES; HAND DEFORMITIES, CONGENITAL; HUMANS; INTELLECTUAL DISABILITY; JOINT INSTABILITY; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NEURAL STEM CELLS; NEUROGENESIS; NEURONS; PERIVENTRICULAR NODULAR HETEROTOPIA; PHOSPHOPROTEINS; SEQUENCE ANALYSIS, DNA; SIGNAL TRANSDUCTION; TUMOR SUPPRESSOR PROTEINS;

MAMMALIA;

EID: 84887085013     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2765     Document Type: Article

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