Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M R Hayden

Showing results (211-220 of 292) with videos related to

Pageof 30
Sort By:
Clinical Genetics|February 21, 2007
Managing genetic discrimination: strategies used by individuals found to have the Huntington disease mutationY Bombard, E Penziner, J Decolongon, et al.
Human Gene Therapy|January 20, 1997
Efficient adenovirus-mediated ectopic gene expression of human lipoprotein lipase in human hepatic (HepG2) cellsG Liu, K J Excoffon, P Benoit, et al.
Clinical Genetics|December 1, 1992
Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and CanadaJ C Defesche, M A van de Ree, J J Kastelein, et al.
Neurology|August 29, 2001
Clinical markers of early disease in persons near onset of Huntington's diseaseJ S Paulsen, H Zhao, J C Stout, et al.
The Netherlands Journal of Medicine|November 1, 1996
Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiencyS M Bijvoet, H Wiebusch, Y Ma, et al.
The Journal of Clinical Investigation|June 1, 1991
Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric originH E Henderson, Y Ma, M F Hassan, et al.
Clinical Pharmacology and Therapeutics|April 17, 2013
Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in childrenK Pussegoda, C J Ross, H Visscher, et al.
Human Gene Therapy|January 26, 2000
Phenotypic correction of feline lipoprotein lipase deficiency by adenoviral gene transferG Liu, K J Ashbourne Excoffon, J E Wilson, et al.
Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Journal of Lipid Research|June 1, 1994
High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoformY Ma, T C Ooi, M S Liu, et al.
Pageof 30

Showing results (211-220 of 292) with videos related to

Sort By:
Pageof 30
Clinical Genetics|February 21, 2007
Managing genetic discrimination: strategies used by individuals found to have the Huntington disease mutationY Bombard, E Penziner, J Decolongon, et al.
Human Gene Therapy|January 20, 1997
Efficient adenovirus-mediated ectopic gene expression of human lipoprotein lipase in human hepatic (HepG2) cellsG Liu, K J Excoffon, P Benoit, et al.
Clinical Genetics|December 1, 1992
Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and CanadaJ C Defesche, M A van de Ree, J J Kastelein, et al.
Neurology|August 29, 2001
Clinical markers of early disease in persons near onset of Huntington's diseaseJ S Paulsen, H Zhao, J C Stout, et al.
The Netherlands Journal of Medicine|November 1, 1996
Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiencyS M Bijvoet, H Wiebusch, Y Ma, et al.
The Journal of Clinical Investigation|June 1, 1991
Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric originH E Henderson, Y Ma, M F Hassan, et al.
Clinical Pharmacology and Therapeutics|April 17, 2013
Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in childrenK Pussegoda, C J Ross, H Visscher, et al.
Human Gene Therapy|January 26, 2000
Phenotypic correction of feline lipoprotein lipase deficiency by adenoviral gene transferG Liu, K J Ashbourne Excoffon, J E Wilson, et al.
Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Journal of Lipid Research|June 1, 1994
High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoformY Ma, T C Ooi, M S Liu, et al.
Pageof 30