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Results:
1-13
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Results: 13
Authors:
Mears, AJ
Kondo, M
Swain, PK
Takada, Y
Bush, RA
Saunders, TL
Sieving, PA
Swaroop, A
Citation: Aj. Mears et al., Nrl is required for rod photoreceptor development, NAT GENET, 29(4), 2001, pp. 447-452
Authors:
Swain, PK
Hicks, D
Mears, AJ
Apel, IJ
Smith, JE
John, SK
Hendrickson, A
Milam, AH
Swaroop, A
Citation: Pk. Swain et al., Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptors, J BIOL CHEM, 276(39), 2001, pp. 36824-36830
Authors:
Bessant, DAR
Payne, AM
Plant, C
Bird, AC
Swaroop, A
Bhattacharya, SS
Citation: Dar. Bessant et al., NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies, EUR J HUM G, 8(10), 2000, pp. 783-787
Authors:
Hughes, BA
Kumar, G
Yuan, Y
Swaminathan, A
Yan, D
Sharma, A
Plumley, L
Yang-Feng, TL
Swaroop, A
Citation: Ba. Hughes et al., Cloning and functional expression of human retinal Kir2.4, a pH-sensitive inwardly rectifying K+ channel, AM J P-CELL, 279(3), 2000, pp. C771-C784
Authors:
Sinha, S
Sharma, A
Agarwal, N
Swaroop, A
Yang-Feng, TL
Citation: S. Sinha et al., Expression profile and chromosomal location of cDNA clones, identified from an enriched adult human retina library, INV OPHTH V, 41(1), 2000, pp. 24-28
Authors:
Mitton, KP
Swain, PK
Chen, SM
Xu, SQ
Zack, DJ
Swaroop, A
Citation: Kp. Mitton et al., The leucine zipper of NRL interacts with the CRX homeodomain - A possible mechanism of transcriptional synergy in rhodopsin regulation, J BIOL CHEM, 275(38), 2000, pp. 29794-29799
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
Authors:
Zack, DJ
Dean, M
Molday, RS
Nathans, J
Redmond, TM
Stone, EM
Swaroop, A
Valle, D
Weber, BHF
Citation: Dj. Zack et al., What can we learn about age-related macular degeneration from other retinal diseases?, MOL VIS, 5(24-35), 1999, pp. NIL_37-NIL_43
Authors:
Bessant, DAR
Payne, AM
Mitton, KP
Wang, QL
Swain, PK
Plant, C
Bird, AC
Zack, DJ
Swaroop, A
Bhattacharya, SS
Citation: Dar. Bessant et al., A mutation in NRL is associated with autosomal dominant retinitis pigmentosa, NAT GENET, 21(4), 1999, pp. 355-356
Authors:
Swaroop, A
Wang, QL
Wu, WP
Cook, J
Coats, C
Xu, SQ
Chen, SM
Zack, DJ
Sieving, PA
Citation: A. Swaroop et al., Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for theinvolvement of CRX in the development of photoreceptor function, HUM MOL GEN, 8(2), 1999, pp. 299-305
Authors:
Nirmala,"Kumar, A
Kapoor, AK
Lal, B
Dutta, GP
Swaroop, A
Citation: A. Nirmala,"kumar et al., Plasmodium falciparum: Drug-resistant malaria complicating leukemias and lymphomas in children, EXP PARASIT, 93(1), 1999, pp. 33-37
Authors:
Mears, AJ
Gieser, L
Yan, D
Chen, C
Fahrner, S
Hiriyanna, S
Fujita, R
Jacobson, SG
Sieving, PA
Swaroop, A
Citation: Aj. Mears et al., Protein-truncation mutations in the RP2 gene in a North American cohort offamilies with X-linked retinitis pigmentosa, AM J HU GEN, 64(3), 1999, pp. 897-900
Authors:
Fishman, GA
Grover, S
Jacobson, SG
Alexander, KR
Derlacki, DJ
Wu, WP
Buraczynska, M
Swaroop, A
Citation: Ga. Fishman et al., X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60, OPHTHALMOL, 105(12), 1998, pp. 2286-2296
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1-13
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