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Results: 1-10 |
Results: 10
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene
Authors: Cook, SA Akeson, EC Calvano, C Johnson, KR Mandell, J Hawes, NL Bronson, RT Roderick, TH Davisson, MT
Citation: Sa. Cook et al., Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene, CYTOG C GEN, 93(1-2), 2001, pp. 77-82
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract
Authors: Smith, RS Hawes, NL Chang, B Roderick, TH Akeson, EC Heckenlively, JR Gong, XH Wang, X Davisson, MT
Citation: Rs. Smith et al., Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract, GENOMICS, 63(3), 2000, pp. 314-320
Retinal degeneration 6 (rd6): A new mouse model for human retinitis punctata albescens
Authors: Hawes, NL Chang, B Hageman, GS Nusinowitz, S Nishina, PM Schneider, BS Smith, RS Roderick, TH Davisson, MT Heckenlively, JR
Citation: Nl. Hawes et al., Retinal degeneration 6 (rd6): A new mouse model for human retinitis punctata albescens, INV OPHTH V, 41(10), 2000, pp. 3149-3157
The Bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization
Authors: Smith, RS John, SWM Zabeleta, A Davisson, MT Hawes, NL Chang, B
Citation: Rs. Smith et al., The Bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization, P NAS US, 97(5), 2000, pp. 2191-2195
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
Authors: Akhmedov, NB Piriev, NI Chang, B Rapoport, AL Hawes, NL Nishina, PM Nusinowitz, S Heckenlively, JR Roderick, TH Kozak, CA Danciger, M Davisson, MT Farber, DB
Citation: Nb. Akhmedov et al., A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse, P NAS US, 97(10), 2000, pp. 5551-5556
Mouse fundus photography and angiography: A catalogue of normal and mutantphenotypes
Authors: Hawes, NL Smith, RS Chang, B Davisson, M Heckenlively, JR John, SWM
Citation: Nl. Hawes et al., Mouse fundus photography and angiography: A catalogue of normal and mutantphenotypes, MOL VIS, 5(22), 1999, pp. NIL_1-NIL_8
Identification of a missense mutation in the alpha A-crystallin gene of the lop18 mouse
Authors: Chang, B Hawes, NL Roderick, TH Smith, RS Heckenlively, JR Horwitz, J Davisson, MT
Citation: B. Chang et al., Identification of a missense mutation in the alpha A-crystallin gene of the lop18 mouse, MOL VIS, 5(21), 1999, pp. NIL_1-NIL_5
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice
Authors: Chang, B Smith, RS Hawes, NL Anderson, MG Zabaleta, A Savinova, O Roderick, TH Heckenlively, JR Davisson, MT John, SWM
Citation: B. Chang et al., Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice, NAT GENET, 21(4), 1999, pp. 405-409
Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17
Authors: Smith, RS Johnson, KR Hawes, NL Harris, BS Sundberg, JP Davisson, MT
Citation: Rs. Smith et al., Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17, MAMM GENOME, 10(2), 1999, pp. 102-106
Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient mice
Authors: Ikeda, S Hawes, NL Chang, B Avery, CS Smith, RS Nishina, PM
Citation: S. Ikeda et al., Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient mice, INV OPHTH V, 40(8), 1999, pp. 1874-1878
Risultati: 1-10 |