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P J Mason

Showing results (71-80 of 80) with videos related to

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Acta Crystallographica. Section D, Biological Crystallography|March 25, 1999
Solution of the structure of tetrameric human glucose 6-phosphate dehydrogenase by molecular replacementS W Au, C E Naylor, S Gover, et al.
Journal of Medical Genetics|December 24, 1998
1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysisS W Knight, T J Vulliamy, N S Heiss, et al.
Blood|March 1, 1995
New glucose-6-phosphate dehydrogenase mutations associated with chronic anemiaP J Mason, M F Sonati, D MacDonald, et al.
British Journal of Haematology|July 23, 1998
Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemiaT J Vulliamy, J S Kaeda, D Ait-Chafa, et al.
Circulation|November 1, 1982
Radionuclide angiographic assessment of global and segmental left ventricular function at rest and during exercise after coronary artery bypass graft surgeryY L Lim, V Kalff, M J Kelly, et al.
American Journal of Human Genetics|June 12, 1999
X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 geneS W Knight, N S Heiss, T J Vulliamy, et al.
British Journal of Haematology|December 3, 1999
Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1S W Knight, N S Heiss, T J Vulliamy, et al.
Blood|February 15, 1996
Quantification of residual disease in chronic myelogenous leukemia patients on interferon-alpha therapy by competitive polymerase chain reactionA Hochhaus, F Lin, A Reiter, et al.
British Journal of Haematology|April 7, 1999
Three major G6PD-deficient polymorphic variants identified among the Mauritian populationR Kotea, J S Kaeda, S L Yan, et al.
Blood|November 11, 1999
Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infectionsD Roos, R van Zwieten, J T Wijnen, et al.
Pageof 8

Showing results (71-80 of 80) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Acta Crystallographica. Section D, Biological Crystallography|March 25, 1999
Solution of the structure of tetrameric human glucose 6-phosphate dehydrogenase by molecular replacementS W Au, C E Naylor, S Gover, et al.
Journal of Medical Genetics|December 24, 1998
1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysisS W Knight, T J Vulliamy, N S Heiss, et al.
Blood|March 1, 1995
New glucose-6-phosphate dehydrogenase mutations associated with chronic anemiaP J Mason, M F Sonati, D MacDonald, et al.
British Journal of Haematology|July 23, 1998
Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemiaT J Vulliamy, J S Kaeda, D Ait-Chafa, et al.
Circulation|November 1, 1982
Radionuclide angiographic assessment of global and segmental left ventricular function at rest and during exercise after coronary artery bypass graft surgeryY L Lim, V Kalff, M J Kelly, et al.
American Journal of Human Genetics|June 12, 1999
X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 geneS W Knight, N S Heiss, T J Vulliamy, et al.
British Journal of Haematology|December 3, 1999
Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1S W Knight, N S Heiss, T J Vulliamy, et al.
Blood|February 15, 1996
Quantification of residual disease in chronic myelogenous leukemia patients on interferon-alpha therapy by competitive polymerase chain reactionA Hochhaus, F Lin, A Reiter, et al.
British Journal of Haematology|April 7, 1999
Three major G6PD-deficient polymorphic variants identified among the Mauritian populationR Kotea, J S Kaeda, S L Yan, et al.
Blood|November 11, 1999
Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infectionsD Roos, R van Zwieten, J T Wijnen, et al.
Pageof 8