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P J Mason

Showing results (61-70 of 80) with videos related to

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American Journal of Human Genetics|December 1, 1990
Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle EastB Kurdi-Haidar, P J Mason, A Berrebi, et al.
Blood|August 10, 1999
Dyskeratosis congenita caused by a 3' deletion: germline and somatic mosaicism in a female carrierT J Vulliamy, S W Knight, N S Heiss, et al.
Human Genetics|March 1, 1992
Molecular heterogeneity underlying the G6PD Mediterranean phenotypeC M Corcoran, V Calabrò, G Tamagnini, et al.
American Journal of Human Genetics|March 1, 1993
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysisV Calabrò, P J Mason, S Filosa, et al.
Molecular and Biochemical Parasitology|April 1, 1994
Cloning of the glucose 6-phosphate dehydrogenase gene from Plasmodium falciparumE O'Brien, B Kurdi-Haidar, W Wanachiwanawin, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 31, 2001
Asthma severity, atopic status, allergen exposure and quality of life in elderly personsK Huss, P L Naumann, P J Mason, et al.
Brain Research. Molecular Brain Research|August 1, 1995
Apoptotic DNA fragmentation in the rat cerebral cortex induced by permanent middle cerebral artery occlusionM D Linnik, J A Miller, J Sprinkle-Cavallo, et al.
Nature Genetics|May 20, 1998
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functionsN S Heiss, S W Knight, T J Vulliamy, et al.
Human Molecular Genetics|June 1, 1992
G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutationA Ahluwalia, C M Corcoran, T J Vulliamy, et al.
Blood|April 1, 1996
Glucose 6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzymeC E Naylor, P Rowland, A K Basak, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|December 1, 1990
Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle EastB Kurdi-Haidar, P J Mason, A Berrebi, et al.
Blood|August 10, 1999
Dyskeratosis congenita caused by a 3' deletion: germline and somatic mosaicism in a female carrierT J Vulliamy, S W Knight, N S Heiss, et al.
Human Genetics|March 1, 1992
Molecular heterogeneity underlying the G6PD Mediterranean phenotypeC M Corcoran, V Calabrò, G Tamagnini, et al.
American Journal of Human Genetics|March 1, 1993
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysisV Calabrò, P J Mason, S Filosa, et al.
Molecular and Biochemical Parasitology|April 1, 1994
Cloning of the glucose 6-phosphate dehydrogenase gene from Plasmodium falciparumE O'Brien, B Kurdi-Haidar, W Wanachiwanawin, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 31, 2001
Asthma severity, atopic status, allergen exposure and quality of life in elderly personsK Huss, P L Naumann, P J Mason, et al.
Brain Research. Molecular Brain Research|August 1, 1995
Apoptotic DNA fragmentation in the rat cerebral cortex induced by permanent middle cerebral artery occlusionM D Linnik, J A Miller, J Sprinkle-Cavallo, et al.
Nature Genetics|May 20, 1998
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functionsN S Heiss, S W Knight, T J Vulliamy, et al.
Human Molecular Genetics|June 1, 1992
G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutationA Ahluwalia, C M Corcoran, T J Vulliamy, et al.
Blood|April 1, 1996
Glucose 6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzymeC E Naylor, P Rowland, A K Basak, et al.
Pageof 8