Deficiency of the tensin2 gene in the ICGN mouse: An animal model for congenital nephrotic syndrome

Mammalian Genome

Volumn 17, Issue 5, 2006, Pages 407-416

  Cho, A Ri ^a,b   Uchio Yamada, Kozue ^c   Torigai, Takeshi ^a   Miyamoto, Tomomi ^a   Miyoshi, Ichiro ^a   Matsuda, Junichiro ^c   Kurosawa, Tsutomu ^d   Kon, Yasuhiro ^b   Asano, Atsushi ^b   Sasaki, Nobuya ^b   Agui, Takashi ^a,b  

^a NAGOYA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCES   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

^c NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

^d OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALBUMINURIA; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHROMOSOME 15; CODON; CONGENITAL NEPHROTIC SYNDROME; CONTROLLED STUDY; EPITHELIUM CELL; EXON; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE EXPRESSION; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENETIC DISORDER; GENETIC LINKAGE; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; KIDNEY FUNCTION; MALE; MOUSE; MOUSE STRAIN; NONHUMAN; NUCLEOTIDE SEQUENCE; PODOCYTE; PROGENY; QUANTITATIVE TRAIT LOCUS; TELOMERE;

ALBUMINURIA; ANIMALS; CROSSES, GENETIC; DISEASE MODELS, ANIMAL; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; IMMUNOHISTOCHEMISTRY; KIDNEY; MALE; MICE; MICE, INBRED ICR; NEPHROTIC SYNDROME; PHOSPHOPROTEIN PHOSPHATASE; QUANTITATIVE TRAIT LOCI;

ANIMALIA;

EID: 33745736730     PISSN: 09388990     EISSN: 14321777     Source Type: Journal    
DOI: 10.1007/s00335-005-0167-z     Document Type: Article

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