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Results: 1-24 |
Results: 24
Evolutionary breakpoints on human chromosome 21
Authors: Davisson, MT Bechtel, LJ Akeson, EC Fortna, A Slavov, D Gardiner, K
Citation: Mt. Davisson et al., Evolutionary breakpoints on human chromosome 21, GENOMICS, 78(1-2), 2001, pp. 99-106
Ts65Dn - localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome
Authors: Akeson, EC Lambert, JP Narayanswami, S Gardiner, K Bechtel, LJ Davisson, MT
Citation: Ec. Akeson et al., Ts65Dn - localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome, CYTOG C GEN, 93(3-4), 2001, pp. 270-276
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
Report of the Ninth International Workshop on the Molecular Biology of Human Chromosome 21 and Down syndrome
Authors: Davisson, MT Gardiner, K Costa, ACS
Citation: Mt. Davisson et al., Report of the Ninth International Workshop on the Molecular Biology of Human Chromosome 21 and Down syndrome, CYTOG C GEN, 92(1-2), 2001, pp. 2-2
Availability and characterization of transgenic and knockout mice with behavioral manifestations: where to look and what to search for
Authors: Anagnostopoulos, AV Sharp, JJ Mobraaten, LE Eppig, JT Davisson, MT
Citation: Av. Anagnostopoulos et al., Availability and characterization of transgenic and knockout mice with behavioral manifestations: where to look and what to search for, BEH BRA RES, 125(1-2), 2001, pp. 33-37
Transgenic and knockout databases: Behavioral profiles of mouse mutants
Authors: Anagnostopoulos, AV Mobraaten, LE Sharp, JJ Davisson, MT
Citation: Av. Anagnostopoulos et al., Transgenic and knockout databases: Behavioral profiles of mouse mutants, PHYSL BEHAV, 73(5), 2001, pp. 675-689
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4
Authors: Newton, JM Cohen-Barak, O Hagiwara, N Gardner, JM Davisson, MT King, RA Brilliant, MH
Citation: Jm. Newton et al., Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4, AM J HU GEN, 69(5), 2001, pp. 981-988
The mouse brain transcriptome by SAGE: Differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals
Authors: Chrast, R Scott, HS Papasavvas, MP Rossier, C Antonarakis, ES Barras, C Davisson, MT Schmidt, C Estivill, X Dierssen, M Pritchard, M Antonarakis, SE
Citation: R. Chrast et al., The mouse brain transcriptome by SAGE: Differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals, GENOME RES, 10(12), 2000, pp. 2006-2021
Grey intense: a new mouse mutation affecting pigmentation
Authors: Davisson, MT Johnson, KR Bronson, RT Ward-Bailey, PF Cook, SA Harris, BS Donahue, LR
Citation: Mt. Davisson et al., Grey intense: a new mouse mutation affecting pigmentation, MAMM GENOME, 11(12), 2000, pp. 1139-1141
Neuromuscular ataxia: a new spontaneous mutation in the mouse
Authors: Ward-Bailey, PF Wood, B Johnson, KR Bronson, RT Donahue, LR Davisson, MT
Citation: Pf. Ward-bailey et al., Neuromuscular ataxia: a new spontaneous mutation in the mouse, MAMM GENOME, 11(10), 2000, pp. 820-823
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
The Mouse Genome Database (MGD): expanding genetic and genomic resources for the laboratory mouse
Authors: Blake, JA Eppig, JT Richardson, JE Davisson, MT
Citation: Ja. Blake et al., The Mouse Genome Database (MGD): expanding genetic and genomic resources for the laboratory mouse, NUCL ACID R, 28(1), 2000, pp. 108-111
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
Repositories of mouse mutations and inbred, congenic, and recombinant inbred strains
Authors: Davisson, MT Sharp, JJ
Citation: Mt. Davisson et Jj. Sharp, Repositories of mouse mutations and inbred, congenic, and recombinant inbred strains, SYSTEMATIC APPROACH TO EVALUATION OF MOUSE MUTATIONS, 2000, pp. 177-190
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
Revised nomenclature for strain 129 mice
Authors: Festing, MFW Simpson, EM Davisson, MT Mobraaten, LE
Citation: Mfw. Festing et al., Revised nomenclature for strain 129 mice, MAMM GENOME, 10(8), 1999, pp. 836-836
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
The mouse genome database (MGD): genetic and genomic information about thelaboratory mouse
Authors: Blake, JA Richardson, JE Davisson, MT Eppig, JT
Citation: Ja. Blake et al., The mouse genome database (MGD): genetic and genomic information about thelaboratory mouse, NUCL ACID R, 27(1), 1999, pp. 95-98
Motor dysfunction in a mouse model for Down syndrome
Authors: Costa, ACS Walsh, K Davisson, MT
Citation: Acs. Costa et al., Motor dysfunction in a mouse model for Down syndrome, PHYSL BEHAV, 68(1-2), 1999, pp. 211-220
Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, mapsto the pseudoautosomal boundary region
Authors: Korobova, O Lane, PW Perry, J Palmer, S Ashworth, A Davisson, MT Arnheim, N
Citation: O. Korobova et al., Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, mapsto the pseudoautosomal boundary region, GENOMICS, 54(3), 1998, pp. 556-559
A new allelic series for the underwhite gene on mouse chromosome 15
Authors: Sweet, HO Brilliant, MH Cook, SA Johnson, KR Davisson, MT
Citation: Ho. Sweet et al., A new allelic series for the underwhite gene on mouse chromosome 15, J HEREDITY, 89(6), 1998, pp. 546-551
Risultati: 1-24 |