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Results: 1-12 |
Results: 12

Authors: Maqbool, SB Riazuddin, S Loc, NT Gatehouse, AMR Gatehouse, JA Christou, P
Citation: Sb. Maqbool et al., Expression of multiple insecticidal genes confers broad resistance againsta range of different rice pests, MOL BREED, 7(1), 2001, pp. 85-93

Authors: Liburd, N Ghosh, M Riazuddin, S Naz, S Khan, S Ahmed, Z Riazuddin, S Liang, Y Menon, PSN Smith, T Smith, ACM Chen, KS Lupski, JR Wilcox, ER Potocki, L Friedman, TB
Citation: N. Liburd et al., Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome, HUM GENET, 109(5), 2001, pp. 535-541

Authors: Wilcox, ER Burton, QL Naz, S Riazuddin, S Smith, TN Ploplis, B Belyantseva, I Ben-Yosef, T Liburd, NA Morell, RJ Kachar, B Wu, DK Griffith, AJ Riazuddin, S Friedman, TB
Citation: Er. Wilcox et al., Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29, CELL, 104(1), 2001, pp. 165-172

Authors: Ben-Yosef, T Wattenhofer, M Riazuddin, S Ahmed, ZM Scot, HS Kudoh, J Shibuya, K Antonarakis, SE Bonne-Tamir, B Radhakrishna, U Naz, S Ahmed, Z Riazuddin, S Pandya, A Nance, WE Wilcox, ER Friedman, TB Morell, RJ
Citation: T. Ben-yosef et al., Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness, J MED GENET, 38(6), 2001, pp. 396-400

Authors: Ahmed, ZM Riazuddin, S Bernstein, SL Ahmed, Z Khan, S Griffith, AJ Morell, RJ Friedman, TB Riazuddin, S Wilcox, ER
Citation: Zm. Ahmed et al., Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F, AM J HU GEN, 69(1), 2001, pp. 25-34

Authors: Bork, JM Peters, LM Riazuddin, S Bernstein, SL Ahmed, ZM Ness, SL Polomeno, R Ramesh, A Schloss, M Srisailpathy, CRS Wayne, S Bellman, S Desmukh, D Ahmed, Z Khan, SN Kaloustian, VMD Li, XC Lalwani, A Riazuddin, S Bitner-Glindzicz, M Nance, WE Liu, XZ Wistow, G Smith, RJH Griffith, AJ Wilcox, ER Friedman, TB Morell, RJ
Citation: Jm. Bork et al., Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 arecaused by allelic mutations of the novel cadherin-like gene CDH23, AM J HU GEN, 68(1), 2001, pp. 26-37

Authors: Riazuddin, S Castelein, CM Ahmed, ZM Lalwani, AK Mastroianni, MA Naz, S Smith, TN Liburd, NA Friedman, TB Griffith, AJ Riazuddin, S Wilcox, ER
Citation: S. Riazuddin et al., Dominant modifier DFNM1 suppresses recessive deafness DFNB26, NAT GENET, 26(4), 2000, pp. 431-434

Authors: Friedman, T Battey, J Kachar, B Riazuddin, S Noben-Trauth, K Griffith, A Wilcox, E
Citation: T. Friedman et al., Modifier genes of hereditary hearing loss, CUR OP NEUR, 10(4), 2000, pp. 487-493

Authors: Khan, SN Riazuddin, S Galanello, R
Citation: Sn. Khan et al., Identification of three rare beta-thalassemia mutations in the Pakistani population, HEMOGLOBIN, 24(1), 2000, pp. 15-22

Authors: Khan, SN Butt, FI Riazuddin, S Galanello, R
Citation: Sn. Khan et al., Hb Sallanches [alpha 104(G11)Cys -> Tyr]: a rare alpha 2-globin chain variant found in the homozygous state in three members of a Pakistani family, HEMOGLOBIN, 24(1), 2000, pp. 31-35

Authors: Karim, S Riazuddin, S Gould, F Dean, DH
Citation: S. Karim et al., Determination of receptor binding properties of Bacillus thuringiensis delta-endotoxins to cotton bollworm (Helicoverpa zea) and pink bollworm (Pectinophora gossypiella) midgut brush border membrane vesicles, PEST BIOCH, 67(3), 2000, pp. 198-216

Authors: Maqbool, SB Husnain, T Riazuddin, S Masson, L Christou, P
Citation: Sb. Maqbool et al., Effective control of yellow stem borer and rice leaf folder in transgenic rice indica varieties Basmati 370 and M 7 using the novel delta-endotoxin cry2A Bacillus thuringiensis gene, MOL BREED, 4(6), 1998, pp. 501-507
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