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Results: 1-9 |
Results: 9
Association study on the DUSP6 gene, an affective disorder candidate gene on 12q23, performed by using fluorescence resonance energy transfer-based melting curve analysis on the LightCycler
Authors: Toyota, T Watanabe, A Shibuya, H Nankai, M Hattori, E Yamada, K Kurumaji, A Karkera, JD Detera-Wadleigh, SD Yoshikawa, T
Citation: T. Toyota et al., Association study on the DUSP6 gene, an affective disorder candidate gene on 12q23, performed by using fluorescence resonance energy transfer-based melting curve analysis on the LightCycler, MOL PSYCHI, 5(5), 2000, pp. 489-494
Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2)
Authors: Yoshikawa, T Padigaru, M Karkera, JD Sharma, M Berrettini, WH Esterling, LE Detera-Wadleigh, SD
Citation: T. Yoshikawa et al., Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2), MOL PSYCHI, 5(2), 2000, pp. 165-171
Refinement of regions with allelic loss on chromosome 18p11.2 and 18q12.2 in esophageal squamous cell carcinoma
Authors: Karkera, JD Ayache, S Ransome, RJ Jackson, MA Elsayem, AF Sridhar, R Detera-Wadleigh, SD Wadleigh, RG
Citation: Jd. Karkera et al., Refinement of regions with allelic loss on chromosome 18p11.2 and 18q12.2 in esophageal squamous cell carcinoma, CLIN CANC R, 6(9), 2000, pp. 3565-3569
Missense mutation of the MET gene detected in human glioma
Authors: Moon, YW Weil, RJ Pack, SD Park, WS Pak, E Pham, T Karkera, JD Kim, HK Vortmeyer, AO Fuller, BG Zhuang, ZP
Citation: Yw. Moon et al., Missense mutation of the MET gene detected in human glioma, MOD PATHOL, 13(9), 2000, pp. 973-977
Radiation hybrid mapping of genes in the lithium-sensitive Wnt signaling pathway
Authors: Rhoads, AR Karkera, JD Detera-Wadleigh, SD
Citation: Ar. Rhoads et al., Radiation hybrid mapping of genes in the lithium-sensitive Wnt signaling pathway, MOL PSYCHI, 4(5), 1999, pp. 437-442
Molecular cytogenetic fingerprinting of esophageal squamous cell carcinomaby comparative genomic hybridization reveals a consistent pattern of chromosomal alterations
Authors: Pack, SD Karkera, JD Zhuang, ZP Pak, ED Balan, KV Hwu, P Park, WS Pham, T Ault, DO Glaser, M Liotta, L Detera-Wadleigh, SD Wadleigh, RG
Citation: Sd. Pack et al., Molecular cytogenetic fingerprinting of esophageal squamous cell carcinomaby comparative genomic hybridization reveals a consistent pattern of chromosomal alterations, GENE CHROM, 25(2), 1999, pp. 160-168
Systematic screening of chromosome 18 for loss of heterozygosity in esophageal squamous cell carcinoma
Authors: Karkera, JD Balan, KV Yoshikawa, T Lipman, TO Korman, L Sharma, A Patterson, RH Sani, N Detera-Wadleigh, SD Wadleigh, RG
Citation: Jd. Karkera et al., Systematic screening of chromosome 18 for loss of heterozygosity in esophageal squamous cell carcinoma, CANC GENET, 111(1), 1999, pp. 81-86
A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2
Authors: Detera-Wadleigh, SD Badner, JA Berrettini, WH Yoshikawa, T Goldin, LR Turner, G Rollins, DY Moses, T Sanders, AR Karkera, JD Esterling, LE Zeng, J Ferraro, TN Guroff, JJ Kazuba, D Maxwell, ME Nurnberger, JI Gershon, ES
Citation: Sd. Detera-wadleigh et al., A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2, P NAS US, 96(10), 1999, pp. 5604-5609
Mutation analysis of oculopharyngeal muscular dystrophy in Hispanic American families
Authors: Grewal, RP Karkera, JD Grewal, RK Detera-Wadleigh, SD
Citation: Rp. Grewal et al., Mutation analysis of oculopharyngeal muscular dystrophy in Hispanic American families, ARCH NEUROL, 56(11), 1999, pp. 1378-1381
Risultati: 1-9 |