Identification of a rat model for Usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward genetics

Genetics

Volumn 170, Issue 4, 2005, Pages 1887-1896

  Smits, Bart M G ^a   Peters, Theo A ^b   Mul, Joram D ^a   Croes, Huib J ^b   Fransen, Jack A M ^b   Beynon, Andy J ^b   Guryev, Victor ^a   Plasterk, Ronald H A ^a   Cuppen, Edwin ^a,c  

^a NETHERLANDS CANCER INSTITUTE   (Netherlands)

^b RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

^c HUBRECHT INSTITUTE   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ETHYLNITROSOUREA;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHEMICAL MUTAGENESIS; CHROMOSOME 1; CIRCLING BEHAVIOR; CONTROLLED STUDY; CORTI ORGAN; DNA SEQUENCE; EVOKED BRAIN STEM AUDITORY RESPONSE; FEMALE; GENE; GENE IDENTIFICATION; GENE MAPPING; GENETIC LINKAGE; GENETIC VARIABILITY; HEARING IMPAIRMENT; HYPERACTIVITY; MALE; MYO7A GENE; NONHUMAN; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RAT; RECESSIVE GENE; SCANNING ELECTRON MICROSCOPY; SINGLE NUCLEOTIDE POLYMORPHISM; SPONTANEOUS MUTATION; STEREOTYPY; USHER SYNDROME; VESTIBULAR DISORDER;

ANIMALS; CHROMOSOME DISORDERS; CODON, TERMINATOR; DISEASE MODELS, ANIMAL; DYNEIN ATPASE; ETHYLNITROSOUREA; GENES, RECESSIVE; HUMANS; LINKAGE (GENETICS); MALE; MUTAGENESIS; MUTAGENS; MYOSINS; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RATS; RATS, WISTAR; USHER SYNDROMES;

RATTUS NORVEGICUS;

EID: 25444525667     PISSN: 00166731     EISSN: None     Source Type: Journal    
DOI: 10.1534/genetics.105.044222     Document Type: Article

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