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Results: 1-9 |
Results: 9
Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aorticlipid deposition
Authors: Chen, ZT Karaplis, AC Ackerman, SL Pogribny, IP Melnyk, S Lussier-Cacan, S Chen, MF Pai, A John, SWM Smith, RS Bottiglieri, T Bagley, P Selhub, J Rudnicki, MA James, SJ Rozen, R
Citation: Zt. Chen et al., Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aorticlipid deposition, HUM MOL GEN, 10(5), 2001, pp. 433-443
Targeted disruption of the myocilin gene (Myoc) suggests that human glaucoma-causing mutations are gain of function
Authors: Kim, BS Savinova, OV Reedy, MV Martin, J Lun, Y Gan, L Smith, RS Tomarev, SI John, SWM Johnson, RL
Citation: Bs. Kim et al., Targeted disruption of the myocilin gene (Myoc) suggests that human glaucoma-causing mutations are gain of function, MOL CELL B, 21(22), 2001, pp. 7707-7713
Mouse mutants from chemically mutagenized embryonic stem cells
Authors: Munroe, RJ Bergstrom, RA Zheng, QY Libby, B Smith, R John, SWM Schimenti, KJ Browning, VL Schimenti, JC
Citation: Rj. Munroe et al., Mouse mutants from chemically mutagenized embryonic stem cells, NAT GENET, 24(3), 2000, pp. 318-321
Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results inaberrant ocular development
Authors: Smith, RS Zabaleta, A Kume, T Savinova, OV Kidson, SH Martin, JE Nishimura, DY Alward, WLM Hogan, BLM John, SWM
Citation: Rs. Smith et al., Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results inaberrant ocular development, HUM MOL GEN, 9(7), 2000, pp. 1021-1032
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
Altered expression of natriuretic peptide receptors in proANP gene disrupted mice
Authors: Vera, N Tse, MY Watson, JD Sarda, S Steinhelper, ME John, SWM Flynn, TG Pang, SC
Citation: N. Vera et al., Altered expression of natriuretic peptide receptors in proANP gene disrupted mice, CARDIO RES, 46(3), 2000, pp. 595-603
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
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
Mouse genetics: A tool to help unlock the mechanisms of glaucoma
Authors: John, SWM Anderson, MG Smith, RS
Citation: Swm. John et al., Mouse genetics: A tool to help unlock the mechanisms of glaucoma, J GLAUCOMA, 8(6), 1999, pp. 400-412
Risultati: 1-9 |