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A STRAUSS

Showing results (391-400 of 453) with videos related to

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American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 14, 2006
Elective liver transplantation for the treatment of classical maple syrup urine diseaseK A Strauss, G V Mazariegos, R Sindhi, et al.
The Journal of Pediatrics|March 13, 2013
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communitiesThomas W Ferkol, Erik G Puffenberger, Hauw Lie, et al.
Nature Genetics|April 22, 2003
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAATVictoria E H Carlton, Baruch Z Harris, Erik G Puffenberger, et al.
The Journal of Clinical Endocrinology and Metabolism|September 13, 2019
High-Fat Overfeeding Impairs Peripheral Glucose Metabolism and Muscle Microvascular eNOS Ser1177 PhosphorylationSiôn A Parry, Mark C Turner, Rachel M Woods, et al.
Hepatology (Baltimore, Md.)|September 26, 2019
Crigler-Najjar Syndrome Type 1: Pathophysiology, Natural History, and Therapeutic FrontierKevin A Strauss, Charles E Ahlfors, Kyle Soltys, et al.
The Journal of Physiology|January 21, 2020
A 7-day high-fat, high-calorie diet induces fibre-specific increases in intramuscular triglyceride and perilipin protein expression in human skeletal muscleK L Whytock, S A Parry, M C Turner, et al.
Human Molecular Genetics|July 3, 2014
A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorderKevin A Strauss, Sander Markx, Benjamin Georgi, et al.
Brain : a Journal of Neurology|May 25, 2007
Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5Erik G Puffenberger, Kevin A Strauss, Keri E Ramsey, et al.
The Laryngoscope|August 16, 2013
A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humansThierry Morlet, Mindy R Rabinowitz, Liesl R Looney, et al.
Molecular Genetics and Metabolism|June 23, 2015
Liver transplantation for treatment of severe S-adenosylhomocysteine hydrolase deficiencyKevin A Strauss, Carlos Ferreira, Teodoro Bottiglieri, et al.
Pageof 46

Showing results (391-400 of 453) with videos related to

Sort By:
Pageof 46
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 14, 2006
Elective liver transplantation for the treatment of classical maple syrup urine diseaseK A Strauss, G V Mazariegos, R Sindhi, et al.
The Journal of Pediatrics|March 13, 2013
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communitiesThomas W Ferkol, Erik G Puffenberger, Hauw Lie, et al.
Nature Genetics|April 22, 2003
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAATVictoria E H Carlton, Baruch Z Harris, Erik G Puffenberger, et al.
The Journal of Clinical Endocrinology and Metabolism|September 13, 2019
High-Fat Overfeeding Impairs Peripheral Glucose Metabolism and Muscle Microvascular eNOS Ser1177 PhosphorylationSiôn A Parry, Mark C Turner, Rachel M Woods, et al.
Hepatology (Baltimore, Md.)|September 26, 2019
Crigler-Najjar Syndrome Type 1: Pathophysiology, Natural History, and Therapeutic FrontierKevin A Strauss, Charles E Ahlfors, Kyle Soltys, et al.
The Journal of Physiology|January 21, 2020
A 7-day high-fat, high-calorie diet induces fibre-specific increases in intramuscular triglyceride and perilipin protein expression in human skeletal muscleK L Whytock, S A Parry, M C Turner, et al.
Human Molecular Genetics|July 3, 2014
A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorderKevin A Strauss, Sander Markx, Benjamin Georgi, et al.
Brain : a Journal of Neurology|May 25, 2007
Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5Erik G Puffenberger, Kevin A Strauss, Keri E Ramsey, et al.
The Laryngoscope|August 16, 2013
A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humansThierry Morlet, Mindy R Rabinowitz, Liesl R Looney, et al.
Molecular Genetics and Metabolism|June 23, 2015
Liver transplantation for treatment of severe S-adenosylhomocysteine hydrolase deficiencyKevin A Strauss, Carlos Ferreira, Teodoro Bottiglieri, et al.
Pageof 46