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Results: 1-7 |
Results: 7
Genomic organization and promoter analysis of human KCNN3 gene
Authors: Sun, GF Tomita, H Shakkottai, VG Gargus, JJ
Citation: Gf. Sun et al., Genomic organization and promoter analysis of human KCNN3 gene, J HUM GENET, 46(8), 2001, pp. 463-470
Phenotype and genotype variation in primary carnitine deficiency
Authors: Wang, YH Korman, SH Ye, J Gargus, JJ Gutman, A Taroni, F Garavaglia, B Longo, N
Citation: Yh. Wang et al., Phenotype and genotype variation in primary carnitine deficiency, GENET MED, 3(6), 2001, pp. 387-392
Design and characterization of a highly selective peptide inhibitor of thesmall conductance calcium-activated K+ channel, SkCa2
Authors: Shakkottai, VG Regaya, I Wulff, H Fajloun, Z Tomita, H Fathallah, M Cahalan, MD Gargus, JJ Sabatier, JM Chandy, KG
Citation: Vg. Shakkottai et al., Design and characterization of a highly selective peptide inhibitor of thesmall conductance calcium-activated K+ channel, SkCa2, J BIOL CHEM, 276(46), 2001, pp. 43145-43151
Nuclear localization and dominant-negative suppression by a mutant SKCa3N-terminal channel fragment identified in a patient with schizophrenia
Authors: Miller, MJ Rauer, H Tomita, H Rauer, H Gargus, JJ Gutman, GA Cahalan, MD Chandy, KG
Citation: Mj. Miller et al., Nuclear localization and dominant-negative suppression by a mutant SKCa3N-terminal channel fragment identified in a patient with schizophrenia, J BIOL CHEM, 276(30), 2001, pp. 27753-27756
hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats withschizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21
Authors: Dror, V Shamir, E Ghanshani, S Kimhi, R Swartz, M Barak, Y Weizman, R Avivi, L Litmanovitch, T Fantino, E Kalman, K Jones, EG Chandy, KG Gargus, JJ Gutman, GA Navon, R
Citation: V. Dror et al., hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats withschizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21, MOL PSYCHI, 4(3), 1999, pp. 254-260
Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21
Authors: Antonarakis, SE Blouin, JL Lasseter, VK Gehrig, C Radhakrishna, U Nestadt, G Housman, DE Kazazian, HH Kalman, K Gutman, G Fantino, E Chandy, KG Gargus, JJ Arm, E
Citation: Se. Antonarakis et al., Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21, AM J MED G, 88(4), 1999, pp. 348-351
A piece in the puzzle: an ion channel candidate gene for schizophrenia
Authors: Gargus, JJ Fantino, E Gutman, GA
Citation: Jj. Gargus et al., A piece in the puzzle: an ion channel candidate gene for schizophrenia, MOL MED TOD, 4(12), 1998, pp. 518-524
Risultati: 1-7 |