Levi T - Search Results

1

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.

Watkins H, Rosenzweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Watkins H, et al. Among authors: levi t. N Engl J Med. 1992 Apr 23;326(17):1108-14. doi: 10.1056/NEJM199204233261703. N Engl J Med. 1992. PMID: 1552912 Free article.

2

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.

Jarcho JA, McKenna W, Pare JA, Solomon SD, Holcombe RF, Dickie S, Levi T, Donis-Keller H, Seidman JG, Seidman CE. Jarcho JA, et al. Among authors: levi t. N Engl J Med. 1989 Nov 16;321(20):1372-8. doi: 10.1056/NEJM198911163212005. N Engl J Med. 1989. PMID: 2811944

3

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Pollak MR, Brown EM, Chou YH, Hebert SC, Marx SJ, Steinmann B, Levi T, Seidman CE, Seidman JG. Pollak MR, et al. Among authors: levi t. Cell. 1993 Dec 31;75(7):1297-303. doi: 10.1016/0092-8674(93)90617-y. Cell. 1993. PMID: 7916660

4

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE. Basson CT, et al. Among authors: levi t. Nat Genet. 1997 Jan;15(1):30-5. doi: 10.1038/ng0197-30. Nat Genet. 1997. PMID: 8988165

5

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families.

Chou YH, Brown EM, Levi T, Crowe G, Atkinson AB, Arnqvist HJ, Toss G, Fuleihan GE, Seidman JG, Seidman CE. Chou YH, et al. Among authors: levi t. Nat Genet. 1992 Jul;1(4):295-300. doi: 10.1038/ng0792-295. Nat Genet. 1992. PMID: 1302026

6

Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog.

Marigo V, Roberts DJ, Lee SM, Tsukurov O, Levi T, Gastier JM, Epstein DJ, Gilbert DJ, Copeland NG, Seidman CE, et al. Marigo V, et al. Among authors: levi t. Genomics. 1995 Jul 1;28(1):44-51. doi: 10.1006/geno.1995.1104. Genomics. 1995. PMID: 7590746

7

Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome.

Bruneau BG, Logan M, Davis N, Levi T, Tabin CJ, Seidman JG, Seidman CE. Bruneau BG, et al. Among authors: levi t. Dev Biol. 1999 Jul 1;211(1):100-8. doi: 10.1006/dbio.1999.9298. Dev Biol. 1999. PMID: 10373308 Free article.

8

Fine-structure mapping of the hereditary inclusion body myopathy locus.

Eisenberg I, Thiel C, Levi T, Tiram E, Argov Z, Sadeh M, Jackson CL, Thierfelder L, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: levi t. Genomics. 1999 Jan 1;55(1):43-8. doi: 10.1006/geno.1998.5630. Genomics. 1999. PMID: 9888997

9

Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.

Eisenberg I, Hochner H, Shemesh M, Levi T, Potikha T, Sadeh M, Argov Z, Jackson CL, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: levi t. Eur J Hum Genet. 2001 Jul;9(7):501-9. doi: 10.1038/sj.ejhg.5200665. Eur J Hum Genet. 2001. PMID: 11464241

10

Cloning and characterization of a novel human gene RNF38 encoding a conserved putative protein with a RING finger domain.

Eisenberg I, Hochner H, Levi T, Yelin R, Kahan T, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: levi t. Biochem Biophys Res Commun. 2002 Jun 28;294(5):1169-76. doi: 10.1016/S0006-291X(02)00584-3. Biochem Biophys Res Commun. 2002. PMID: 12074600

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