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Results: 1-12 |
Results: 12
Cloning, characterization, and genomic structure of the mouse Ikbkap gene
Authors: Cuajungco, MP Leyne, M Mull, J Gill, SP Gusella, JF Slaugenhaupt, SA
Citation: Mp. Cuajungco et al., Cloning, characterization, and genomic structure of the mouse Ikbkap gene, DNA CELL B, 20(9), 2001, pp. 579-586
A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2
Authors: Acierno, JS Kennedy, JC Falardeau, JL Leyne, M Bromley, MC Colman, MW Sun, M Bove, C Ashworth, LK Chadwick, LH Schiripo, T Ma, S Goldin, E Schiffmann, R Slaugenhaupt, SA
Citation: Js. Acierno et al., A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2, GENOMICS, 73(2), 2001, pp. 203-210
Genetic association analysis of behavioral inhibition using candidate locifrom mouse models
Authors: Smoller, JW Rosenbaum, JF Biederman, J Susswein, LS Kennedy, J Kagan, J Snidman, N Laird, N Tsuang, MT Faraone, SV Schwarz, A Slaugenhaupt, SA
Citation: Jw. Smoller et al., Genetic association analysis of behavioral inhibition using candidate locifrom mouse models, AM J MED G, 105(3), 2001, pp. 226-235
Targeted genome screen of panic disorder and anxiety disorder proneness using homology to murine QTL regions
Authors: Smoller, JW Acierno, JS Rosenbaum, JF Biederman, J Pollack, MH Meminger, S Pava, JA Chadwick, LH White, C Bulzacchelli, M Slaugenhaupt, SA
Citation: Jw. Smoller et al., Targeted genome screen of panic disorder and anxiety disorder proneness using homology to murine QTL regions, AM J MED G, 105(2), 2001, pp. 195-206
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia
Authors: Slaugenhaupt, SA Blumenfeld, A Gill, SP Leyne, M Mull, J Cuajungco, MP Liebert, CB Chadwick, B Idelson, M Reznik, L Robbins, CM Makalowska, I Brownstein, MJ Krappmann, D Scheidereit, C Maayan, C Axelrod, FB Gusella, JF
Citation: Sa. Slaugenhaupt et al., Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia, AM J HU GEN, 68(3), 2001, pp. 598-605
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel
Authors: Sun, M Goldin, E Stahl, S Falardeau, JL Kennedy, JC Acierno, JS Bove, C Kaneski, CR Nagle, J Bromley, MC Colman, M Schiffmann, R Slaugenhaupt, SA
Citation: M. Sun et al., Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel, HUM MOL GEN, 9(17), 2000, pp. 2471-2478
Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31
Authors: Chadwick, BP Leyne, M Gill, S Liebert, CB Mull, J Mezey, E Robbins, CM Pinkett, HW Makalowska, I Maayan, C Blumenfeld, A Axelrod, FB Brownstein, M Gusella, JF Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31, MAMM GENOME, 11(1), 2000, pp. 81-83
Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familiar dysautonomia candidate region on 9q31
Authors: Chadwick, BP Mull, J Helbling, LA Gill, S Leyne, M Robbins, CM Pinkett, HW Makalowska, I Maayan, C Blumenfeld, A Axelrod, FB Brownstein, N Gusella, JF Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familiar dysautonomia candidate region on 9q31, GENOMICS, 58(3), 1999, pp. 302-309
Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene
Authors: Chadwick, BP Gill, S Leyne, M Mull, J Liebert, CB Robbins, CM Pinkett, HW Makalowska, I Maayan, C Blumenfeld, A Axelrod, FB Brownstein, M Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene, GENE, 240(1), 1999, pp. 67-73
Mapping of the mucolipidosis type IV gene to chromosome 19p and definitionof founder haplotypes
Authors: Slaugenhaupt, SA Acierno, JS Helbling, LA Bove, C Goldin, E Bach, G Schiffmann, R Gusella, JF
Citation: Sa. Slaugenhaupt et al., Mapping of the mucolipidosis type IV gene to chromosome 19p and definitionof founder haplotypes, AM J HU GEN, 65(3), 1999, pp. 773-778
Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31
Authors: Blumenfeld, A Slaugenhaupt, SA Liebert, CB Temper, V Maayan, C Gill, S Lucente, DE Idelson, M MacCormack, K Monahan, MA Mull, J Leyne, M Mendillo, M Schiripo, T Mishori, E Breakefield, X Axelrod, FB Gusella, JF
Citation: A. Blumenfeld et al., Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31, AM J HU GEN, 64(4), 1999, pp. 1110-1118
Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR
Authors: Chadwick, BP Helbling, LA Angrist, M Chakravarti, A Gusella, JF Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR, CYTOG C GEN, 83(3-4), 1998, pp. 236-237
Risultati: 1-12 |