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R Greenberg

Showing results (791-800 of 844) with videos related to

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Molecular Genetics and Metabolism|February 17, 2009
The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populationsCheryl R Greenberg, Louise A Dilling, G Robert Thompson, et al.
Gut|October 23, 2014
The relationship between infliximab concentrations, antibodies to infliximab and disease activity in Crohn's diseaseNiels Vande Casteele, Reena Khanna, Barrett G Levesque, et al.
Clinical Therapeutics|September 19, 2024
Differences in Drug Poisonings Among Those Who Identify as Transgender Compared to Cisgender: An Analysis of the Toxicology Investigators Consortium (ToxIC) Core Registry, United States 2017-2021Kristine Magnusson, Emily Glidden, Desiree Mustaquim, et al.
Hormones and Behavior|November 19, 2021
Measuring salivary cortisol in wild carnivoresTracy M Montgomery, Julia R Greenberg, Jessica L Gunson, et al.
Molecular Genetics and Metabolism|May 15, 2001
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening programC Prasad, J P Johnson, J P Bonnefont, et al.
American Journal of Human Genetics|May 26, 2009
Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndromeJoy Armistead, Sunita Khatkar, Britta Meyer, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Reproductive fitness in maternal homocystinuria due to cystathionine beta-synthase deficiencyH L Levy, J E Vargas, S E Waisbren, et al.
American Journal of Human Genetics|September 5, 2001
Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2L S Schmidt, M B Warren, M L Nickerson, et al.
Human Mutation|December 8, 2004
The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populationsPatrick Frosk, Cheryl R Greenberg, Alysa A P Tennese, et al.
Annals of the New York Academy of Sciences|February 11, 2000
Calcium supplements and colorectal adenomas. Polyp Prevention Study GroupJ A Baron, M Beach, J S Mandel, et al.
Pageof 85

Showing results (791-800 of 844) with videos related to

Sort By:
Pageof 85
Molecular Genetics and Metabolism|February 17, 2009
The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populationsCheryl R Greenberg, Louise A Dilling, G Robert Thompson, et al.
Gut|October 23, 2014
The relationship between infliximab concentrations, antibodies to infliximab and disease activity in Crohn's diseaseNiels Vande Casteele, Reena Khanna, Barrett G Levesque, et al.
Clinical Therapeutics|September 19, 2024
Differences in Drug Poisonings Among Those Who Identify as Transgender Compared to Cisgender: An Analysis of the Toxicology Investigators Consortium (ToxIC) Core Registry, United States 2017-2021Kristine Magnusson, Emily Glidden, Desiree Mustaquim, et al.
Hormones and Behavior|November 19, 2021
Measuring salivary cortisol in wild carnivoresTracy M Montgomery, Julia R Greenberg, Jessica L Gunson, et al.
Molecular Genetics and Metabolism|May 15, 2001
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening programC Prasad, J P Johnson, J P Bonnefont, et al.
American Journal of Human Genetics|May 26, 2009
Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndromeJoy Armistead, Sunita Khatkar, Britta Meyer, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Reproductive fitness in maternal homocystinuria due to cystathionine beta-synthase deficiencyH L Levy, J E Vargas, S E Waisbren, et al.
American Journal of Human Genetics|September 5, 2001
Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2L S Schmidt, M B Warren, M L Nickerson, et al.
Human Mutation|December 8, 2004
The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populationsPatrick Frosk, Cheryl R Greenberg, Alysa A P Tennese, et al.
Annals of the New York Academy of Sciences|February 11, 2000
Calcium supplements and colorectal adenomas. Polyp Prevention Study GroupJ A Baron, M Beach, J S Mandel, et al.
Pageof 85