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R J Smith

Showing results (581-590 of 636) with videos related to

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Physical Review Letters|October 10, 2006
Spheromak formation by steady inductive helicity injectionT R Jarboe, W T Hamp, G J Marklin, et al.
American Journal of Medical Genetics|June 1, 1994
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysisL Ni, M J Wagner, W J Kimberling, et al.
Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
Genomics|July 8, 1998
A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C geneP K Jain, A K Lalwani, X C Li, et al.
The Journal of Clinical Endocrinology and Metabolism|April 19, 2000
Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitusS K Rasmussen, C Lautier, L Hansen, et al.
Human Mutation|April 24, 2001
Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.
Journal of Natural Products|January 1, 1994
New bioactive taxoids from cell cultures of Taxus baccataW Ma, G L Park, G A Gomez, et al.
Clinical Genetics|November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1JK T Booth, K Kahrizi, M Babanejad, et al.
Journal of Medicinal Chemistry|January 8, 1993
Pyrazoline bisphosphonate esters as novel antiinflammatory and antiarthritic agentsR A Nugent, M Murphy, S T Schlachter, et al.
Henry Ford Hospital Medical Journal|January 1, 1992
Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2M F Robinson, E J Furst, V Nunziata, et al.
Pageof 64

Showing results (581-590 of 636) with videos related to

Sort By:
Pageof 64
Physical Review Letters|October 10, 2006
Spheromak formation by steady inductive helicity injectionT R Jarboe, W T Hamp, G J Marklin, et al.
American Journal of Medical Genetics|June 1, 1994
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysisL Ni, M J Wagner, W J Kimberling, et al.
Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
Genomics|July 8, 1998
A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C geneP K Jain, A K Lalwani, X C Li, et al.
The Journal of Clinical Endocrinology and Metabolism|April 19, 2000
Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitusS K Rasmussen, C Lautier, L Hansen, et al.
Human Mutation|April 24, 2001
Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.
Journal of Natural Products|January 1, 1994
New bioactive taxoids from cell cultures of Taxus baccataW Ma, G L Park, G A Gomez, et al.
Clinical Genetics|November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1JK T Booth, K Kahrizi, M Babanejad, et al.
Journal of Medicinal Chemistry|January 8, 1993
Pyrazoline bisphosphonate esters as novel antiinflammatory and antiarthritic agentsR A Nugent, M Murphy, S T Schlachter, et al.
Henry Ford Hospital Medical Journal|January 1, 1992
Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2M F Robinson, E J Furst, V Nunziata, et al.
Pageof 64