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O Levran

Showing results (1-10 of 19) with videos related to

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Blood|October 15, 1992
Identification and expression of a common missense mutation (L302P) in the acid sphingomyelinase gene of Ashkenazi Jewish type A Niemann-Pick disease patientsO Levran, R J Desnick, E H Schuchman
Human Mutation|August 26, 1998
Identification of Alu-mediated deletions in the Fanconi anemia gene FAAO Levran, N A Doggett, A D Auerbach
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1991
Niemann-Pick disease: a frequent missense mutation in the acid sphingomyelinase gene of Ashkenazi Jewish type A and B patientsO Levran, R J Desnick, E H Schuchman
The Journal of Clinical Investigation|September 1, 1991
Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patientsO Levran, R J Desnick, E H Schuchman
Genomics|February 1, 1992
Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1)E H Schuchman, O Levran, L V Pereira, et al.
Pharmacology, Biochemistry, and Behavior|August 3, 2011
Regional mRNA expression of the endogenous opioid and dopaminergic systems in brains of C57BL/6J and 129P3/J mice: strain and heroin effectsS D Schlussman, J Cassin, Y Zhang, et al.
The New England Journal of Medicine|July 21, 1994
A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndromeL Pereira, O Levran, F Ramirez, et al.
The Pharmacogenomics Journal|March 2, 2011
Nerve growth factor β polypeptide (NGFB) genetic variability: association with the methadone dose required for effective maintenance treatmentO Levran, E Peles, S Hamon, et al.
Psychoneuroendocrinology|May 22, 2014
Stress-related genes and heroin addiction: a role for a functional FKBP5 haplotypeO Levran, E Peles, M Randesi, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 16, 1997
Sequence variation in the Fanconi anemia gene FAAO Levran, T Erlich, N Magdalena, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Blood|October 15, 1992
Identification and expression of a common missense mutation (L302P) in the acid sphingomyelinase gene of Ashkenazi Jewish type A Niemann-Pick disease patientsO Levran, R J Desnick, E H Schuchman
Human Mutation|August 26, 1998
Identification of Alu-mediated deletions in the Fanconi anemia gene FAAO Levran, N A Doggett, A D Auerbach
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1991
Niemann-Pick disease: a frequent missense mutation in the acid sphingomyelinase gene of Ashkenazi Jewish type A and B patientsO Levran, R J Desnick, E H Schuchman
The Journal of Clinical Investigation|September 1, 1991
Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patientsO Levran, R J Desnick, E H Schuchman
Genomics|February 1, 1992
Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1)E H Schuchman, O Levran, L V Pereira, et al.
Pharmacology, Biochemistry, and Behavior|August 3, 2011
Regional mRNA expression of the endogenous opioid and dopaminergic systems in brains of C57BL/6J and 129P3/J mice: strain and heroin effectsS D Schlussman, J Cassin, Y Zhang, et al.
The New England Journal of Medicine|July 21, 1994
A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndromeL Pereira, O Levran, F Ramirez, et al.
The Pharmacogenomics Journal|March 2, 2011
Nerve growth factor β polypeptide (NGFB) genetic variability: association with the methadone dose required for effective maintenance treatmentO Levran, E Peles, S Hamon, et al.
Psychoneuroendocrinology|May 22, 2014
Stress-related genes and heroin addiction: a role for a functional FKBP5 haplotypeO Levran, E Peles, M Randesi, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 16, 1997
Sequence variation in the Fanconi anemia gene FAAO Levran, T Erlich, N Magdalena, et al.
Pageof 2