메뉴 건너뛰기




Volumn 38, Issue 12, 1997, Pages 2502-2507

Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16

Author keywords

Candidate genes; Congenital cataracts; Genetic locus; Genetic map; Mouse cataracts

Indexed keywords

MICROSATELLITE DNA;

EID: 0030731478     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (14)

References (40)
  • 1
    • 1842266297 scopus 로고    scopus 로고
    • Ophthalmic Pathology. 4th Ed.
    • Philadelphia: WB Saunders
    • Spencer WH. Lens. In: Ophthalmic Pathology. 4th ed. Philadelphia: WB Saunders; 1996:372-437.
    • (1996) Philadelphia: WB Saunders , pp. 372-437
    • Spencer, W.H.1
  • 2
    • 0026570323 scopus 로고
    • Cataract; linkage relations: Clinical and genetic heterogeneity
    • Lund AM, Eiberg H, Rosenberg T, Warburg M. Cataract; linkage relations: Clinical and genetic heterogeneity. Clin Genet. 1992;41:65-69.
    • (1992) Clin Genet. , vol.41 , pp. 65-69
    • Lund, A.M.1    Eiberg, H.2    Rosenberg, T.3    Warburg, M.4
  • 4
    • 0023889728 scopus 로고
    • Genetic linkage analysis of autosomal dominant congenital cataracts with lens specific DNA probes and polymorphic phenotypic markers
    • Barrett DJ, Sparkes RS, Gorin MB, et al. Genetic linkage analysis of autosomal dominant congenital cataracts with lens specific DNA probes and polymorphic phenotypic markers. Ophthalmology. 1988;95:538-544.
    • (1988) Ophthalmology , vol.95 , pp. 538-544
    • Barrett, D.J.1    Sparkes, R.S.2    Gorin, M.B.3
  • 5
    • 0029002373 scopus 로고
    • Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36
    • Eiberg H, Lund AM, Warburg M, Rosenberg T. Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36. Hum Genet. 1995;96:33-38.
    • (1995) Hum Genet. , vol.96 , pp. 33-38
    • Eiberg, H.1    Lund, A.M.2    Warburg, M.3    Rosenberg, T.4
  • 6
    • 0002288531 scopus 로고
    • Probable linkage between a congenital cataract locus and the Duffy blood group locus
    • Renwick JH, Lawler SD. Probable linkage between a congenital cataract locus and the Duffy blood group locus. Ann Hum Genet. 1963;27:67-84.
    • (1963) Ann Hum Genet. , vol.27 , pp. 67-84
    • Renwick, J.H.1    Lawler, S.D.2
  • 7
    • 9244251074 scopus 로고    scopus 로고
    • Linkage of polymorphic congenital cataract to the γ-crystallin gene locus on human chromosome 2q33-35
    • Rogaev EI, Rogaeva EA, Korovaitseva GI, et al. Linkage of polymorphic congenital cataract to the γ-crystallin gene locus on human chromosome 2q33-35. Hum Mol Genet. 1996;6:699-703.
    • (1996) Hum Mol Genet. , vol.6 , pp. 699-703
    • Rogaev, E.I.1    Rogaeva, E.A.2    Korovaitseva, G.I.3
  • 8
    • 0024334955 scopus 로고
    • Autosomal dominant congenital cataract: Morphology and genetic mapping
    • Marner E, Rosenberg T, Eiberg H. Autosomal dominant congenital cataract: Morphology and genetic mapping. Acta Ophthalmol. 1989;67:151-158.
    • (1989) Acta Ophthalmol. , vol.67 , pp. 151-158
    • Marner, E.1    Rosenberg, T.2    Eiberg, H.3
  • 10
    • 0029095859 scopus 로고
    • Autosomal dominant zonular cataract with suturai opacities localized to chromosome 17q11-12
    • Padma T, Ayyagari R, Murty JS, et al. Autosomal dominant zonular cataract with suturai opacities localized to chromosome 17q11-12. Am J Hum Genet. 1995; 57:840-845.
    • (1995) Am J Hum Genet. , vol.57 , pp. 840-845
    • Padma, T.1    Ayyagari, R.2    Murty, J.S.3
  • 11
    • 0028835546 scopus 로고
    • A progressive early onset cataract gene maps to human chromosome 17q24
    • Armitage MM, Kivlin JD, Ferrell RE. A progressive early onset cataract gene maps to human chromosome 17q24. Nat Genet. 1995;9:36-40.
    • (1995) Nat Genet. , vol.9 , pp. 36-40
    • Armitage, M.M.1    Kivlin, J.D.2    Ferrell, R.E.3
  • 12
    • 0030217901 scopus 로고    scopus 로고
    • A second gene for cerulean cataracts maps to the γ crystallin region on chromosome 22
    • Kramer P, Yount J, Mitchell T, et al. A second gene for cerulean cataracts maps to the γ crystallin region on chromosome 22. Genomics. 1996;35:539-542.
    • (1996) Genomics , vol.35 , pp. 539-542
    • Kramer, P.1    Yount, J.2    Mitchell, T.3
  • 14
    • 0028308664 scopus 로고
    • Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly
    • Hanson IM, Fletcher JM, Jordan T, Brown A, et al. Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly. Nat Genetics. 1994;6:168-73.
    • (1994) Nat Genetics , vol.6 , pp. 168-173
    • Hanson, I.M.1    Fletcher, J.M.2    Jordan, T.3    Brown, A.4
  • 15
    • 0006792422 scopus 로고    scopus 로고
    • Linkage and synteny homologies in mouse and man
    • Lyon MF, Rastan S, Brown SDM, eds. New York: Oxford University Press
    • Peters J, Searle AG. Linkage and synteny homologies in mouse and man. In: Lyon MF, Rastan S, Brown SDM, eds. Genetic Variants and Strains of the Laboratory Mouse. New York: Oxford University Press; 1996:1256-1312.
    • (1996) Genetic Variants and Strains of the Laboratory Mouse , pp. 1256-1312
    • Peters, J.1    Searle, A.G.2
  • 16
    • 1842385794 scopus 로고    scopus 로고
    • The mouse genome database
    • The Jackson Laboratory. The mouse genome database. In: Mouse Genome Informatics. 1996. http:// www.informatics.jax.org.
    • (1996) Mouse Genome Informatics
  • 17
    • 1842303978 scopus 로고
    • Mouse models for studying cataracts
    • Bar Harbor: The Jackson Laboratory
    • Smith RS, Linder CC, Sunberg JP. Mouse models for studying cataracts. Ophthalmology News. Bar Harbor: The Jackson Laboratory 1995;July:1-9.
    • (1995) Ophthalmology News , vol.JULY , pp. 1-9
    • Smith, R.S.1    Linder, C.C.2    Sunberg, J.P.3
  • 19
    • 0022571975 scopus 로고
    • Dominant cataract and recessive specific locus mutations in offspring of X-irradiated male mice
    • Graw J, Favor J, Neuhäuser-Klaus A, Ehling UH. Dominant cataract and recessive specific locus mutations in offspring of X-irradiated male mice. Mutat Res. 1986;159:47-54.
    • (1986) Mutat Res. , vol.159 , pp. 47-54
    • Graw, J.1    Favor, J.2    Neuhäuser-Klaus, A.3    Ehling, U.H.4
  • 20
    • 0023787187 scopus 로고
    • Phenotypic characterization and genetic analysis of twenty dominant cataract mutations detected in offspring of irradiated male mice
    • Kratochvilova J, Favor J. Phenotypic characterization and genetic analysis of twenty dominant cataract mutations detected in offspring of irradiated male mice. Genet Res. 1988;52:125-134.
    • (1988) Genet Res. , vol.52 , pp. 125-134
    • Kratochvilova, J.1    Favor, J.2
  • 21
    • 0026717906 scopus 로고
    • Allelism tests of 15 dominant cataract mutations in mice
    • Kratochvilova J, Favor J. Allelism tests of 15 dominant cataract mutations in mice. Genet Res. 1992;5:199-203.
    • (1992) Genet Res. , vol.5 , pp. 199-203
    • Kratochvilova, J.1    Favor, J.2
  • 23
    • 0027355585 scopus 로고
    • A Macintosh program for storage and analysis of experimental genetic mapping data
    • Manly KF. A Macintosh program for storage and analysis of experimental genetic mapping data. Mamm Genome. 1993;4:303-13.
    • (1993) Mamm Genome. , vol.4 , pp. 303-313
    • Manly, K.F.1
  • 24
    • 0026645062 scopus 로고
    • A genetic map of the mouse suitable for typing intraspecific crosses
    • Dietrich W, Katz H, Lincoln SE, et al. A genetic map of the mouse suitable for typing intraspecific crosses. Genetics. 1992;131:423-445.
    • (1992) Genetics , vol.131 , pp. 423-445
    • Dietrich, W.1    Katz, H.2    Lincoln, S.E.3
  • 25
    • 13344287050 scopus 로고    scopus 로고
    • A comprehensive genetic map of the mouse genome
    • Dietrich WF, Miller J, Steen R, et al. A comprehensive genetic map of the mouse genome. Nature. 1996; 380:149-152.
    • (1996) Nature , vol.380 , pp. 149-152
    • Dietrich, W.F.1    Miller, J.2    Steen, R.3
  • 27
    • 0029188455 scopus 로고
    • Targeted disruption of mammalian hairy and enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects
    • Ishibashi M, Ang SL, Shiota K, Nakanishi S, Kageyama R, Guillemot F. Targeted disruption of mammalian hairy and enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects. Genes Dev. 1995;9:3136-48.
    • (1995) Genes Dev. , vol.9 , pp. 3136-3148
    • Ishibashi, M.1    Ang, S.L.2    Shiota, K.3    Nakanishi, S.4    Kageyama, R.5    Guillemot, F.6
  • 28
    • 0029977614 scopus 로고    scopus 로고
    • Mammalian hairy and enhancer of split homolog 1 regulates differentiation of retial neurons and is essential for eye morphogenesis
    • Tomita K, Ishibashi M, Nakahara K, Ang S-L, Nakanishi S, Kageyama R. Mammalian hairy and enhancer of split homolog 1 regulates differentiation of retial neurons and is essential for eye morphogenesis. Neuron. 1996;16:723-734.
    • (1996) Neuron. , vol.16 , pp. 723-734
    • Tomita, K.1    Ishibashi, M.2    Nakahara, K.3    Ang, S.-L.4    Nakanishi, S.5    Kageyama, R.6
  • 30
    • 0018959579 scopus 로고
    • Murine lymphocyte alloantigens. II. The Ly-7 locus
    • Potter TA, Morgan GM, McKenzie IF. Murine lymphocyte alloantigens. II. The Ly-7 locus. J Immunol. 1980;125:546-50.
    • (1980) J Immunol. , vol.125 , pp. 546-550
    • Potter, T.A.1    Morgan, G.M.2    McKenzie, I.F.3
  • 32
    • 0024407347 scopus 로고
    • Structure of the bovine lens γS-crystallin gene (formerly βS)
    • van Rens GLM, Raats JMH, Driessen HPC, et al. Structure of the bovine lens γS-crystallin gene (formerly βS). Gene. 1989;78:225-233.
    • (1989) Gene. , vol.78 , pp. 225-233
    • Van Rens, G.L.M.1    Raats, J.M.H.2    Driessen, H.P.C.3
  • 33
    • 0031154010 scopus 로고    scopus 로고
    • The mouse Cat4a locus maps to chromosome 8 and mutants express lens-corneal adhesion
    • Favor J, Grimes P, Neuhäuser-Klaus A, Pretsch W, Stambolian D. The mouse Cat4a locus maps to chromosome 8 and mutants express lens-corneal adhesion. Mamm Genome. 1997;8:403-406.
    • (1997) Mamm Genome. , vol.8 , pp. 403-406
    • Favor, J.1    Grimes, P.2    Neuhäuser-Klaus, A.3    Pretsch, W.4    Stambolian, D.5
  • 34
    • 0030586841 scopus 로고    scopus 로고
    • Two new cataract loci, Ccw, and To3, and further mapping of the Npp and Opj cataracts in the mouse
    • Kerscher S, Glinister PH, Favor J, Lyon MF. Two new cataract loci, Ccw, and To3, and further mapping of the Npp and Opj cataracts in the mouse. Genomics. 1996;36:17-21.
    • (1996) Genomics , vol.36 , pp. 17-21
    • Kerscher, S.1    Glinister, P.H.2    Favor, J.3    Lyon, M.F.4
  • 35
    • 0022620395 scopus 로고
    • Further experience of the mouse dominant cataract mutation test from an experiment with ethylnitrosourea
    • West JD, Fisher G. Further experience of the mouse dominant cataract mutation test from an experiment with ethylnitrosourea. Mutat Res. 1986;164:127-136.
    • (1986) Mutat Res. , vol.164 , pp. 127-136
    • West, J.D.1    Fisher, G.2
  • 36
    • 0030031158 scopus 로고    scopus 로고
    • Mutations in the founder of the MIP gene family underlie cataract development in the mouse
    • Shiels A, Bassnett S. Mutations in the founder of the MIP gene family underlie cataract development in the mouse. Nat Genet. 1996;12:212-215.
    • (1996) Nat Genet. , vol.12 , pp. 212-215
    • Shiels, A.1    Bassnett, S.2
  • 37
    • 0030447981 scopus 로고    scopus 로고
    • The mouse Pax2 (1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney
    • Favor J, Sandulache R, Neuhäuser-Klaus A, et al. The mouse Pax2 (1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Proc Natl Acad Sci USA. 1996;93:13870-5.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 13870-13875
    • Favor, J.1    Sandulache, R.2    Neuhäuser-Klaus, A.3
  • 38
    • 0026345992 scopus 로고
    • Mouse small eye results from mutations in a paired-like homeobox-containing gene
    • Hill RE, Favor J, Hogan BLM, et al. Mouse small eye results from mutations in a paired-like homeobox-containing gene. Nature. 1990;354:522-525.
    • (1990) Nature , vol.354 , pp. 522-525
    • Hill, R.E.1    Favor, J.2    Hogan, B.L.M.3
  • 39
    • 0025778685 scopus 로고
    • Deletion mutation in an eye lens β-crystallin
    • Chambers C, Russell P. Deletion mutation in an eye lens β-crystallin. J Biol Chem. 1991;66:6742-6746.
    • (1991) J Biol Chem. , vol.66 , pp. 6742-6746
    • Chambers, C.1    Russell, P.2
  • 40
    • 0031089330 scopus 로고    scopus 로고
    • Genetic mapping of a mouse ocular malformation locus, Tcm, on chromosome 4
    • Zhou E, Grimes P, Favor J, et al. Genetic mapping of a mouse ocular malformation locus, Tcm, on chromosome 4. Mamm Genome. 1997;8:178-181.
    • (1997) Mamm Genome. , vol.8 , pp. 178-181
    • Zhou, E.1    Grimes, P.2    Favor, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.