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J Gitschier

Showing results (61-70 of 84) with videos related to

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American Journal of Human Genetics|April 16, 1998
Absolute pitch: an approach for identification of genetic and nongenetic componentsS Baharloo, P A Johnston, S K Service, et al.
Nature Genetics|April 1, 1994
The mottled gene is the mouse homologue of the Menkes disease geneB Levinson, C Vulpe, B Elder, et al.
Neurology|June 12, 2002
HARP syndrome is allelic with pantothenate kinase-associated neurodegenerationK H L Ching, S K Westaway, J Gitschier, et al.
Annals of the New York Academy of Sciences|January 1, 1986
On the mechanism by which saxitoxin binds to and blocks sodium channelsG Strichartz, T Rando, S Hall, et al.
Nature Genetics|August 2, 2001
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndromeB Zhou, S K Westaway, B Levinson, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Prenatal diagnosis of Menkes disease by mutation analysisS Das, S Whitney, J Taylor, et al.
Pediatric Research|October 6, 1997
Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes diseaseY Murata, H Kodama, T Abe, et al.
Advances in Experimental Medicine and Biology|January 1, 1995
Molecular etiology of factor VIII deficiency in hemophilia AS E Antonarakis, H H Kazazian, J Gitschier, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Cloned factor VIII and the molecular genetics of hemophiliaR M Lawn, W I Wood, J Gitschier, et al.
Nature|May 5, 1985
Detection and sequence of mutations in the factor VIII gene of haemophiliacsJ Gitschier, W I Wood, E G Tuddenham, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|April 16, 1998
Absolute pitch: an approach for identification of genetic and nongenetic componentsS Baharloo, P A Johnston, S K Service, et al.
Nature Genetics|April 1, 1994
The mottled gene is the mouse homologue of the Menkes disease geneB Levinson, C Vulpe, B Elder, et al.
Neurology|June 12, 2002
HARP syndrome is allelic with pantothenate kinase-associated neurodegenerationK H L Ching, S K Westaway, J Gitschier, et al.
Annals of the New York Academy of Sciences|January 1, 1986
On the mechanism by which saxitoxin binds to and blocks sodium channelsG Strichartz, T Rando, S Hall, et al.
Nature Genetics|August 2, 2001
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndromeB Zhou, S K Westaway, B Levinson, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Prenatal diagnosis of Menkes disease by mutation analysisS Das, S Whitney, J Taylor, et al.
Pediatric Research|October 6, 1997
Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes diseaseY Murata, H Kodama, T Abe, et al.
Advances in Experimental Medicine and Biology|January 1, 1995
Molecular etiology of factor VIII deficiency in hemophilia AS E Antonarakis, H H Kazazian, J Gitschier, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Cloned factor VIII and the molecular genetics of hemophiliaR M Lawn, W I Wood, J Gitschier, et al.
Nature|May 5, 1985
Detection and sequence of mutations in the factor VIII gene of haemophiliacsJ Gitschier, W I Wood, E G Tuddenham, et al.
Pageof 9