Results: 1-13 |
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
Risultati: 1-13 |