메뉴 건너뛰기




Volumn 22, Issue 5, 2005, Pages 595-604

The Tennessee Mouse Genome Consortium: Identification of ocular mutants

Author keywords

Ethylnitrosourea; Mouse; Mutagenesis; Ocular phenotyping; Retina

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BIOMICROSCOPY; EYE; GENE FUNCTION; GENE MAPPING; GENE MUTATION; GENOMICS; HISTOLOGY; IMMUNOHISTOCHEMISTRY; MEDICAL RESEARCH; MOUSE; NONHUMAN; OPHTHALMOLOGY; PHOTOGRAPHY; PRIORITY JOURNAL; SCIENCE; SCREENING; SLIT LAMP;

EID: 26244462607     PISSN: 09525238     EISSN: 14698714     Source Type: Journal    
DOI: 10.1017/S0952523805225087     Document Type: Article
Times cited : (13)

References (15)
  • 2
    • 0038708118 scopus 로고    scopus 로고
    • Age-related macular degeneration: Etiology, pathogenesis, and therapeutic strategies
    • AMBATI, J., AMBATI, B.K., YOO, S.H., IANCHULEV, S. & ADAMIS, A.P. (2003). Age-related macular degeneration: Etiology, pathogenesis, and therapeutic strategies. Survey Ophthalmologyl 48, 257-293.
    • (2003) Survey Ophthalmologyl , vol.48 , pp. 257-293
    • Ambati, J.1    Ambati, B.K.2    Yoo, S.H.3    Ianchulev, S.4    Adamis, A.P.5
  • 5
    • 12144288188 scopus 로고    scopus 로고
    • Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice
    • DU, X., TABETA, K., HOEBE, K., LIU, H., MANN, N., MUDD, S., CROZAT, K., SOVATH, S., GONG, X. & BEUTLER, B. (2004). Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice. Genetics 166, 331-340.
    • (2004) Genetics , vol.166 , pp. 331-340
    • Du, X.1    Tabeta, K.2    Hoebe, K.3    Liu, H.4    Mann, N.5    Mudd, S.6    Crozat, K.7    Sovath, S.8    Gong, X.9    Beutler, B.10
  • 7
    • 0036672646 scopus 로고    scopus 로고
    • Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract
    • GRAW, J., NEUHAUSER-KLAUS, A., LOSTER, J., KLOPP, N. & FAVOR, J. (2002). Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract. Genetics 161, 1633-1640.
    • (2002) Genetics , vol.161 , pp. 1633-1640
    • Graw, J.1    Neuhauser-Klaus, A.2    Loster, J.3    Klopp, N.4    Favor, J.5
  • 8
    • 0033520641 scopus 로고    scopus 로고
    • Histopathology of age-related macular degeneration
    • GREEN, W. (1999). Histopathology of age-related macular degeneration. Molecular Vision 5, 27.
    • (1999) Molecular Vision , vol.5 , pp. 27
    • Green, W.1
  • 13
    • 0038683341 scopus 로고    scopus 로고
    • An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina
    • SEMENOVA, E., WANG, X.F., JABLONSKI, M.M., LEVORSE, J. & TILGHMAN, S.M. (2003). An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina. Human Molecular Genetics 12, 1301-1312.
    • (2003) Human Molecular Genetics , vol.12 , pp. 1301-1312
    • Semenova, E.1    Wang, X.F.2    Jablonski, M.M.3    Levorse, J.4    Tilghman, S.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.