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G A Diaz

Showing results (11-20 of 31) with videos related to

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Biochemistry|August 20, 1996
The stability of abortively cycling T7 RNA polymerase complexes depends upon template conformationG A Diaz, M Rong, W T McAllister, et al.
Molecular Psychiatry|September 24, 2004
Effects of dopamine D2 receptor (DRD2) and transporter (SLC6A3) polymorphisms on smoking cue-induced cigarette craving among African-American smokersJ Erblich, C Lerman, D W Self, et al.
The Pharmacogenomics Journal|January 21, 2004
Stress-induced cigarette craving: effects of the DRD2 TaqI RFLP and SLC6A3 VNTR polymorphismsJ Erblich, C Lerman, D W Self, et al.
Nature Genetics|July 3, 1999
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndromeG A Diaz, M Banikazemi, K Oishi, et al.
Circulation|June 15, 1999
Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21M Satoda, M E Pierpont, G A Diaz, et al.
Molecular Genetics and Metabolism|March 6, 1999
Localization of the thiamine-responsive megaloblastic anemia syndrome locus to a 1.4-cM region of 1q23M Banikazemi, G A Diaz, P Vossough, et al.
American Journal of Human Genetics|August 18, 2001
Maple syrup urine disease: identification and carrier-frequency determination of a novel founder mutation in the Ashkenazi Jewish populationL Edelmann, M P Wasserstein, R Kornreich, et al.
The Journal of Biological Chemistry|October 20, 2000
Impact of the reduced folate carrier on the accumulation of active thiamin metabolites in murine leukemia cellsR Zhao, F Gao, Y Wang, et al.
American Journal of Medical Genetics|April 15, 2000
WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studiesR J Gorlin, B Gelb, G A Diaz, et al.
American Journal of Medical Genetics|June 22, 1999
Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinementG A Diaz, B D Gelb, F Ali, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Biochemistry|August 20, 1996
The stability of abortively cycling T7 RNA polymerase complexes depends upon template conformationG A Diaz, M Rong, W T McAllister, et al.
Molecular Psychiatry|September 24, 2004
Effects of dopamine D2 receptor (DRD2) and transporter (SLC6A3) polymorphisms on smoking cue-induced cigarette craving among African-American smokersJ Erblich, C Lerman, D W Self, et al.
The Pharmacogenomics Journal|January 21, 2004
Stress-induced cigarette craving: effects of the DRD2 TaqI RFLP and SLC6A3 VNTR polymorphismsJ Erblich, C Lerman, D W Self, et al.
Nature Genetics|July 3, 1999
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndromeG A Diaz, M Banikazemi, K Oishi, et al.
Circulation|June 15, 1999
Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21M Satoda, M E Pierpont, G A Diaz, et al.
Molecular Genetics and Metabolism|March 6, 1999
Localization of the thiamine-responsive megaloblastic anemia syndrome locus to a 1.4-cM region of 1q23M Banikazemi, G A Diaz, P Vossough, et al.
American Journal of Human Genetics|August 18, 2001
Maple syrup urine disease: identification and carrier-frequency determination of a novel founder mutation in the Ashkenazi Jewish populationL Edelmann, M P Wasserstein, R Kornreich, et al.
The Journal of Biological Chemistry|October 20, 2000
Impact of the reduced folate carrier on the accumulation of active thiamin metabolites in murine leukemia cellsR Zhao, F Gao, Y Wang, et al.
American Journal of Medical Genetics|April 15, 2000
WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studiesR J Gorlin, B Gelb, G A Diaz, et al.
American Journal of Medical Genetics|June 22, 1999
Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinementG A Diaz, B D Gelb, F Ali, et al.
Pageof 4