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Tamilla Nechiporuk, Ph.D. - Publications

Affiliations: 
2003 University of Utah, Salt Lake City, UT 
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2001 Nechiporuk T, Urness LD, Keating MT. ETL, a novel seven-transmembrane receptor that is developmentally regulated in the heart. ETL is a member of the secretin family and belongs to the epidermal growth factor-seven-transmembrane subfamily. The Journal of Biological Chemistry. 276: 4150-7. PMID 11050079 DOI: 10.1074/Jbc.M004814200  0.52
1998 Nechiporuk T, Huynh DP, Figueroa K, Sahba S, Nechiporuk A, Pulst SM. The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expression. Human Molecular Genetics. 7: 1301-9. PMID 9668173 DOI: 10.1093/Hmg/7.8.1301  0.6
1998 Sahba S, Nechiporuk A, Figueroa KP, Nechiporuk T, Pulst SM. Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1. Genomics. 47: 359-64. PMID 9480749 DOI: 10.1006/Geno.1997.5131  0.646
1997 Nechiporuk T, Nechiporuk A, Sahba S, Figueroa K, Shibata H, Chen XN, Korenberg JR, de Jong P, Pulst SM. A high-resolution PAC and BAC map of the SCA2 region. Genomics. 44: 321-9. PMID 9325053 DOI: 10.1006/Geno.1997.4886  0.674
1996 Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genetics. 14: 269-76. PMID 8896555 DOI: 10.1038/Ng1196-269  0.665
1996 Nechiporuk T, Nechiporuk A, Guan X, Frederick R, Figueroa K, Chumakov I, Korenberg JR, de Jong PJ, Pulst SM. Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map. Human Genetics. 97: 462-7. PMID 8834243 DOI: 10.1007/Bf02267067  0.642
1996 Nechiporuk A, Lopes-Cendes I, Nechiporuk T, Starkman S, Andermann E, Rouleau GA, Weissenbach JS, Kort E, Pulst SM. Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12. Neurology. 46: 1731-5. PMID 8649579 DOI: 10.1212/Wnl.46.6.1731  0.638
1994 Huynh DP, Nechiporuk T, Pulst SM. Alternative transcripts in the mouse neurofibromatosis type 2 (NF2) gene are conserved and code for schwannomins with distinct C-terminal domains. Human Molecular Genetics. 3: 1075-9. PMID 7981675 DOI: 10.1093/Hmg/3.7.1075  0.324
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