AAAAAA

   
Results: 1-10 |
Results: 10
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene ismutated in recessive hereditary inclusion body myopathy
Authors: Eisenberg, I Avidan, N Potikha, T Hochner, H Chen, M Olender, T Barash, M Shemesh, M Sadeh, M Grabov-Nardini, G Shmilevich, I Friedmann, A Karpati, G Bradley, WG Baumbach, L Lancet, D Ben Asher, E Beckmann, JS Argov, Z Mitrani-Rosenbaum, S
Citation: I. Eisenberg et al., The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene ismutated in recessive hereditary inclusion body myopathy, NAT GENET, 29(1), 2001, pp. 83-87
Mucolipidosis type IV: Novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population
Authors: Bargal, R Avidan, N Olender, T Ben Asher, E Zeigler, M Raas-Rothschild, A Frumkin, A Ben-Yoseph, O Friedlender, Y Lancet, D Bach, G
Citation: R. Bargal et al., Mucolipidosis type IV: Novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population, HUM MUTAT, 17(5), 2001, pp. 397-402
Mechanisms for evolving hypervariability: The case of conopeptides
Authors: Conticello, SG Gilad, Y Avidan, N Ben-Asher, E Levy, Z Fainzilber, M
Citation: Sg. Conticello et al., Mechanisms for evolving hypervariability: The case of conopeptides, MOL BIOL EV, 18(2), 2001, pp. 120-131
Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1
Authors: Levanon, D Glusman, C Bangsow, T Ben-Asher, E Male, DA Avidan, N Bangsow, C Hattori, M Taylor, TD Taudien, S Blechschmidt, K Shimizu, N Rosenthal, A Sakaki, Y Lancet, D Groner, Y
Citation: D. Levanon et al., Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1, GENE, 262(1-2), 2001, pp. 23-33
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
Authors: Lahat, H Pras, E Olender, T Avidan, N Ben-Asher, E Man, O Levy-Nissenbaum, E Khoury, A Lorber, A Goldman, B Lancet, D Eldar, M
Citation: H. Lahat et al., A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel, AM J HU GEN, 69(6), 2001, pp. 1378-1384
Harvesting the human genome: the Israeli perspective
Authors: Ben-Asher, E Chalifa-Caspi, V Horn-Saban, S Avidan, N Olender, Z Adato, A Glusman, G Safran, M Rubinstein, M Lancet, D
Citation: E. Ben-asher et al., Harvesting the human genome: the Israeli perspective, ISR MED ASS, 2(9), 2000, pp. 657-664
Identification of the gene causing mucolipidosis type IV
Authors: Bargal, R Avidan, N Ben-Asher, E Olender, Z Zeigler, M Frumkin, A Raas-Rothschild, A Glusman, G Lancet, D Bach, G
Citation: R. Bargal et al., Identification of the gene causing mucolipidosis type IV, NAT GENET, 26(1), 2000, pp. 118-121
Sequence, structure, and evolution of a complete human olfactory receptor gene cluster
Authors: Glusman, G Sosinsky, A Ben-Asher, E Avidan, N Sonkin, D Bahar, A Rosenthal, A Clifton, S Roe, B Ferraz, C Demaille, J Lancet, D
Citation: G. Glusman et al., Sequence, structure, and evolution of a complete human olfactory receptor gene cluster, GENOMICS, 63(2), 2000, pp. 227-245
Possible juvenile-related proteins in olive tree tissues
Authors: Garcia, JL Avidan, N Troncoso, A Sarmiento, R Lavee, S
Citation: Jl. Garcia et al., Possible juvenile-related proteins in olive tree tissues, SCI HORT A, 85(4), 2000, pp. 271-284
High-resolution linkage analysis and physical characterization of the EIX-responding locus in tomato
Authors: Ron, M Kantety, R Martin, GB Avidan, N Eshed, Y Zamir, D Avni, A
Citation: M. Ron et al., High-resolution linkage analysis and physical characterization of the EIX-responding locus in tomato, THEOR A GEN, 100(2), 2000, pp. 184-189
Risultati: 1-10 |