Genetic modifiers that aggravate the neurological phenotype of the wobbler mouse

NeuroReport

Volumn 13, Issue 4, 2002, Pages 535-539

  Ulbrich, Michael ^a   Schmidt, Volker C ^a,b   Ronsiek, Melanie ^a   Mussmann, Anke ^a   Bartsch, Jrg W ^a   Augustin, Martin ^a,b   Jockusch, Harald ^a   Schmitt John, Thomas ^a  

^a BIELEFELD UNIVERSITY   (Germany)

^b Ingenium Pharmaceuticals AG   (Germany)

Author keywords

Astrogliosis; Modifier locus; Neurodegeneration; QTL; Wobbler mouse

Indexed keywords

CHOLINERGIC RECEPTOR; MESSENGER RNA; RECEPTOR SUBUNIT;

ALPHA CHAIN; ANIMAL TISSUE; ARTICLE; ASTROCYTOSIS; AUTOSOMAL RECESSIVE INHERITANCE; BACKCROSSING; CHROMOSOME 13Q; CHROMOSOME 14; CONTROLLED STUDY; DISEASE SEVERITY; DNA MODIFICATION; FORELIMB; GENE LOCUS; GENE MUTATION; GENETIC RECOMBINATION; GENOTYPE; HEREDITARY SPINAL MUSCULAR ATROPHY; HINDLIMB; HISTOLOGY; HYBRID; LEG MUSCLE; MICROSATELLITE MARKER; MOTONEURON; MOUSE; MUSCLE ATROPHY; NERVE CELL DEGENERATION; NEUROLOGIC DISEASE; NONHUMAN; PENETRANCE; PHENOTYPE; PRIORITY JOURNAL; RAT STRAIN; SEGREGATION ANALYSIS; SEQUENCE HOMOLOGY; SPINAL CORD VENTRAL HORN;

EID: 0037171031     PISSN: 09594965     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001756-200203250-00035     Document Type: Article

References (23)