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T R Prezant

Showing results (11-20 of 22) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
Long-acting peptidomimergic control of gigantism caused by pituitary acidophilic stem cell adenomaH G Maheshwari, T R Prezant, V Herman-Bonert, et al.
American Journal of Medical Genetics|May 8, 1995
Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literatureC A Bacino, R Schreck, N Fischel-Ghodsian, et al.
Molecular Endocrinology (Baltimore, Md.)|January 19, 1999
Structure, expression, and function of human pituitary tumor-transforming gene (PTTG)X Zhang, G A Horwitz, T R Prezant, et al.
American Journal of Medical Genetics|March 27, 1995
Screening for mtDNA diabetes mutations in Pima Indians with NIDDMB Sepehrnia, T R Prezant, J I Rotter, et al.
Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Pituitary tumor transforming gene (PTTG) expression in pituitary adenomasX Zhang, G A Horwitz, A P Heaney, et al.
The Journal of Pediatrics|October 1, 1993
Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndromeS M Bernes, C Bacino, T R Prezant, et al.
American Journal of Medical Genetics|July 1, 1993
Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13N Fischel-Ghodsian, X Bu, T R Prezant, et al.
American Journal of Otolaryngology|May 1, 1997
Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicityN Fischel-Ghodsian, T R Prezant, W E Chaltraw, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Loss of heterozygosity on chromosome 11q13 in two families with acromegaly/gigantism is independent of mutations of the multiple endocrine neoplasia type I geneM R Gadelha, T R Prezant, K N Une, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

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Pageof 3
The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
Long-acting peptidomimergic control of gigantism caused by pituitary acidophilic stem cell adenomaH G Maheshwari, T R Prezant, V Herman-Bonert, et al.
American Journal of Medical Genetics|May 8, 1995
Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literatureC A Bacino, R Schreck, N Fischel-Ghodsian, et al.
Molecular Endocrinology (Baltimore, Md.)|January 19, 1999
Structure, expression, and function of human pituitary tumor-transforming gene (PTTG)X Zhang, G A Horwitz, T R Prezant, et al.
American Journal of Medical Genetics|March 27, 1995
Screening for mtDNA diabetes mutations in Pima Indians with NIDDMB Sepehrnia, T R Prezant, J I Rotter, et al.
Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Pituitary tumor transforming gene (PTTG) expression in pituitary adenomasX Zhang, G A Horwitz, A P Heaney, et al.
The Journal of Pediatrics|October 1, 1993
Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndromeS M Bernes, C Bacino, T R Prezant, et al.
American Journal of Medical Genetics|July 1, 1993
Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13N Fischel-Ghodsian, X Bu, T R Prezant, et al.
American Journal of Otolaryngology|May 1, 1997
Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicityN Fischel-Ghodsian, T R Prezant, W E Chaltraw, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Loss of heterozygosity on chromosome 11q13 in two families with acromegaly/gigantism is independent of mutations of the multiple endocrine neoplasia type I geneM R Gadelha, T R Prezant, K N Une, et al.
Pageof 3