Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members

EMBO Journal

Volumn 23, Issue 20, 2004, Pages 4106-4115

  Herms, Jochen ^a   Anliker, Brigitte ^b,d   Heber, Sabine ^b   Ring, Sabine ^b   Fuhrmann, Martin ^a   Kretzschmar, Hans ^a   Sisodia, Sangram ^c   Müller, Ulrike ^b  

^a UNIVERSITY OF MUNICH   (Germany)

^b MAX PLANCK INSTITUTE FOR BRAIN RESEARCH   (Germany)

^c UNIVERSITY OF CHICAGO   (United States)

^d SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

amyloid precursor protein; Alzheimer's disease; APLP; Lissencephaly; Triple knockout

Indexed keywords

AMYLOID PRECURSOR LIKE PROTEIN 1; AMYLOID PRECURSOR LIKE PROTEIN 2; AMYLOID PRECURSOR PROTEIN; UNCLASSIFIED DRUG;

AGYRIA; ALZHEIMER DISEASE; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BASEMENT MEMBRANE; BRAIN DEVELOPMENT; CELL ADHESION; CELL MIGRATION; CELL SURVIVAL; CONTROLLED STUDY; CORTICAL DYSPLASIA; EMBRYO; EMBRYO DEVELOPMENT; HUMAN; NEUROBLAST; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FAMILY; SKULL MALFORMATION;

AMYLOID BETA-PROTEIN PRECURSOR; ANIMALS; ANIMALS, NEWBORN; CEREBRAL CORTEX; CROSSES, GENETIC; EMBRYONIC DEVELOPMENT; HUMANS; IMMUNOHISTOCHEMISTRY; MICE; MICE, KNOCKOUT; MUTATION; SKULL; SURVIVAL RATE;

ANIMALIA;

EID: 8144230876     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.emboj.7600390     Document Type: Article

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