Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities

Human Molecular Genetics

Volumn 10, Issue 23, 2001, Pages 2717-2726

  Seznec, Hervé ^a   Agbulut, Onnik ^b   Sergeant, Nicolas ^a   Savouret, Cédric ^a   Ghestem, Antoine ^a   Tabti, Nacira ^b   Willer, Jean Claude ^b   Ourth, Lucie ^a   Duros, Chantal ^a   Brisson, Edith ^a   Fouquet, Coralie ^a   Butler Browne, Gillian ^b   Delacourte, André ^a   Junien, Claudine ^a   Gourdon, Geneviève ^a  

^a INSERM   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; CYTOSINE; GUANINE; HOMEODOMAIN PROTEIN; MESSENGER RNA; PROTEIN KINASE; RNA; TAU PROTEIN;

3' UNTRANSLATED REGION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN DISEASE; CATARACT; COGNITIVE DEFECT; CONTROLLED STUDY; DISEASE COURSE; ELECTROPHYSIOLOGY; ENDOCRINE DISEASE; GENE EXPRESSION; GENE MUTATION; HEART MUSCLE CONDUCTION DISTURBANCE; MOUSE; MUSCLE ATROPHY; MUSCLE DISEASE; MUSCLE WEAKNESS; MYOPATHY; MYOTONIA; MYOTONIC DYSTROPHY; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SKELETAL MUSCLE; SYMPTOMATOLOGY; TESTIS ATROPHY; TRANSGENE; TRINUCLEOTIDE REPEAT;

EID: 0035510133     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.23.2717     Document Type: Article

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