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Results: 1-25 | 26-32
Results: 1-25/32
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
Authors: Mykytyn, K Braun, T Carmi, R Haider, NB Searby, CC Shastri, M Beck, G Wright, AF Iannaccone, A Elbedour, K Riise, R Baldi, A Raas-Rothschild, A Gorman, SW Duhl, DM Jacobson, SG Casavant, T Stone, EM Sheffield, VC
Citation: K. Mykytyn et al., Identification of the gene that, when mutated, causes the human obesity syndrome BBS4, NAT GENET, 28(2), 2001, pp. 188-191
Strategies for mapping susceptibility genes in age-related maculopathy
Authors: Wright, AF
Citation: Af. Wright, Strategies for mapping susceptibility genes in age-related maculopathy, EYE, 15, 2001, pp. 401-406
Determination of solid-state sulfidation mechanisms in ion-implanted copper
Authors: Barbour, JC Braithwaite, JW Wright, AF
Citation: Jc. Barbour et al., Determination of solid-state sulfidation mechanisms in ion-implanted copper, NUCL INST B, 175, 2001, pp. 382-387
Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa
Authors: Yokoyama, A Maruiwa, F Hayakawa, M Kanai, A Vervoort, R Wright, AF Yamada, K Niikawa, N Naoi, N
Citation: A. Yokoyama et al., Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa, AM J MED G, 104(3), 2001, pp. 232-238
Phenotypic marker for early disease detection in dominant late-onset retinal degeneration
Authors: Jacobson, SG Cideciyan, AV Wright, E Wright, AF
Citation: Sg. Jacobson et al., Phenotypic marker for early disease detection in dominant late-onset retinal degeneration, INV OPHTH V, 42(8), 2001, pp. 1882-1890
Medicine - Short cut to disease genes
Authors: Wright, AF Van Heyningen, V
Citation: Af. Wright et V. Van Heyningen, Medicine - Short cut to disease genes, NATURE, 414(6865), 2001, pp. 705-706
Interaction of hydrogen with gallium vacancies in wurtzite GaN
Authors: Wright, AF
Citation: Af. Wright, Interaction of hydrogen with gallium vacancies in wurtzite GaN, J APPL PHYS, 90(3), 2001, pp. 1164-1169
Interaction of hydrogen with nitrogen interstitials in wurtzite GaN
Authors: Wright, AF
Citation: Af. Wright, Interaction of hydrogen with nitrogen interstitials in wurtzite GaN, J APPL PHYS, 90(12), 2001, pp. 6526-6532
Theoretical description of H behavior in GaN p-n junctions
Authors: Myers, SM Wright, AF
Citation: Sm. Myers et Af. Wright, Theoretical description of H behavior in GaN p-n junctions, J APPL PHYS, 90(11), 2001, pp. 5612-5622
Lattice location of hydrogen in Mg doped GaN
Authors: Wampler, WR Myers, SM Wright, AF Barbour, JC Seager, CH Han, J
Citation: Wr. Wampler et al., Lattice location of hydrogen in Mg doped GaN, J APPL PHYS, 90(1), 2001, pp. 108-117
Diffusion, release, and uptake of hydrogen in magnesium-doped gallium nitride: Theory and experiment
Authors: Myers, SM Wright, AF Petersen, GA Wampler, WR Seager, CH Crawford, MH Han, J
Citation: Sm. Myers et al., Diffusion, release, and uptake of hydrogen in magnesium-doped gallium nitride: Theory and experiment, J APPL PHYS, 89(6), 2001, pp. 3195-3202
Effects of biaxial strain and chemical ordering on the band gap of InGaN
Authors: Wright, AF Leung, K van Schilfgaarde, M
Citation: Af. Wright et al., Effects of biaxial strain and chemical ordering on the band gap of InGaN, APPL PHYS L, 78(2), 2001, pp. 189-191
Simulation of H behavior in p-GaN(Mg) at elevated temperatures
Authors: Myers, SM Wright, AF Petersen, GA Seager, CH Crawford, MH Wampler, WR Han, J
Citation: Sm. Myers et al., Simulation of H behavior in p-GaN(Mg) at elevated temperatures, MRS I J N S, 5, 2000, pp. NIL_424-NIL_429
Lattice location of deuterium in plasma and gas charged Mg doped GaN
Authors: Wampler, WR Barbour, JC Seager, CH Myers, SM Wright, AF Han, J
Citation: Wr. Wampler et al., Lattice location of deuterium in plasma and gas charged Mg doped GaN, MRS I J N S, 5, 2000, pp. NIL_475-NIL_480
A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophy
Authors: Poehner, WJ Fossarello, M Rapoport, AL Aleman, TS Cideciyan, AV Jacobson, SG Wright, AF Danciger, M Farber, DB
Citation: Wj. Poehner et al., A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophy, MOL VIS, 6(24), 2000, pp. 192-198
For want of a disc, the cell was lost....
Authors: Wright, AF
Citation: Af. Wright, For want of a disc, the cell was lost...., NAT MED, 6(5), 2000, pp. 508-510
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa
Authors: Vervoort, R Lennon, A Bird, AC Tulloch, B Axton, R Miano, MG Meindl, A Meitinger, T Ciccodicola, A Wright, AF
Citation: R. Vervoort et al., Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa, NAT GENET, 25(4), 2000, pp. 462-466
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
Authors: Haider, NB Jacobson, SG Cideciyan, AV Swiderski, R Streb, LM Searby, C Beck, G Hockey, R Hanna, DB Gorman, S Duhl, D Carmi, R Bennett, J Weleber, RG Fishman, GA Wright, AF Stone, EM Sheffield, VC
Citation: Nb. Haider et al., Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate, NAT GENET, 24(2), 2000, pp. 127-131
Identification of a novel protein interacting with RPGR
Authors: Boylan, JP Wright, AF
Citation: Jp. Boylan et Af. Wright, Identification of a novel protein interacting with RPGR, HUM MOL GEN, 9(14), 2000, pp. 2085-2093
Clinical and genetic analysis of a large north European Caucasian family affected by early-onset periodontitis
Authors: Hodge, PJ Teague, PW Wright, AF Kinane, DF
Citation: Pj. Hodge et al., Clinical and genetic analysis of a large north European Caucasian family affected by early-onset periodontitis, J DENT RES, 79(3), 2000, pp. 857-863
Equilibrium state of hydrogen in gallium nitride: Theory and experiment
Authors: Myers, SM Wright, AF Petersen, GA Seager, CH Wampler, WR Crawford, MH Han, J
Citation: Sm. Myers et al., Equilibrium state of hydrogen in gallium nitride: Theory and experiment, J APPL PHYS, 88(8), 2000, pp. 4676-4687
Pitfalls in homozygosity mapping
Authors: Miano, MG Jacobson, SG Carothers, A Hanson, I Teague, P Lovell, J Cideciyan, AV Haider, N Stone, EM Sheffield, VC Wright, AF
Citation: Mg. Miano et al., Pitfalls in homozygosity mapping, AM J HU GEN, 67(5), 2000, pp. 1348-1351
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15
Authors: Mears, AJ Hiriyanna, S Vervoort, R Yashar, B Gieser, L Fahrner, S Daiger, SP Heckenlively, JR Sieving, PA Wright, AF Swaroop, A
Citation: Aj. Mears et al., Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15, AM J HU GEN, 67(4), 2000, pp. 1000-1003
Population choice in mapping genes for complex diseases
Authors: Wright, AF Carothers, AD Pirastu, M
Citation: Af. Wright et al., Population choice in mapping genes for complex diseases, NAT GENET, 23(4), 1999, pp. 397-404
Identification of a 5 ' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3)
Authors: Dry, KL Manson, FDC Lennon, A Bergen, AA Van Dorp, DB Wright, AF
Citation: Kl. Dry et al., Identification of a 5 ' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3), HUM MUTAT, 13(2), 1999, pp. 141-145
Risultati: 1-25 | 26-32