Nuclear factor I X deficiency causes brain malformation and severe skeletal defects

Molecular and Cellular Biology

Volumn 27, Issue 10, 2007, Pages 3855-3867

  Driller, Katrin ^a   Pagenstecher, Axel ^b,e   Uhl, Markus ^c   Omran, Heymut ^c   Berlis, Ansgar ^d   Gründer, Albert ^a,f   Sippel, Albrecht E ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b Abteilung Neuropathologie   (Germany)

^c UNIVERSITY OF FREIBURG   (Germany)

^d Neuroradiologie   (Germany)

^e PHILIPPS UNIVERSITY MARBURG   (Germany)

^f MAX PLANCK INSTITUTE OF IMMUNOBIOLOGY AND EPIGENETICS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; NFIX PROTEIN; NUCLEAR FACTOR; NUCLEAR FACTOR 9; PLASMINOGEN; PROTEIN DERIVATIVE; TETRANECTIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BONE MINERALIZATION; CORPUS CALLOSUM AGENESIS; DOWN REGULATION; EMBRYO; ENCHONDRAL OSSIFICATION; FEMALE; FEMUR; GENE LOSS; HYDROCEPHALUS; INTERVERTEBRAL DISK DEGENERATION; KNOCKOUT GENE; MALE; MOUSE; MULTIGENE FAMILY; NONHUMAN; OSSIFICATION; PERINATAL PERIOD; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN EXPRESSION; SPINE MALFORMATION; VERTEBRA BODY;

ANIMALS; BIOLOGICAL MARKERS; BRAIN; COLLAGEN TYPE II; CORPUS CALLOSUM; FEMUR; GENE TARGETING; HUMANS; HYDROCEPHALUS; LECTINS, C-TYPE; MICE; MICE, KNOCKOUT; NFI TRANSCRIPTION FACTORS; OSTEOCALCIN; OSTEOGENESIS; PHENOTYPE; SPINE;

MUS;

EID: 34248168145     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.02293-06     Document Type: Article

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