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Annals of Human Genetics|May 1, 1981

New genetic variants of glucose 6-phosphate dehydrogenase (G6PD) in ItalyG Sansone, L Perroni, U Testa, et al.

Experimental Hematology|January 1, 1994

Retroviral-mediated gene transfer of a mutant H-ras gene into normal human bone marrow alters myeloid cell proliferation and differentiationJ Maher, F Colonna, D Baker, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985

Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the geneG Battistuzzi, M D'Urso, D Toniolo, et al.

Cancer|October 1, 1991

Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndromeS J Whittaker, N P Smith, R R Jones, et al.

Annals of Human Genetics|October 1, 1989

A new genetic polymorphism in the 16S ribosomal RNA gene of human mitochondrial DNAA B Mehta, T Vulliamy, E C Gordon-Smith, et al.

British Journal of Haematology|November 13, 2001

Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuriaD J Araten, D Swirsky, A Karadimitris, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979

Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphismG Modiano, G Battistuzzi, G J Esan, et al.

Journal of Internal Medicine|January 1, 1994

Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuriaM F McMullin, P Hillmen, J Jackson, et al.

Blood|December 15, 1995

Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift typeK Nafa, P J Mason, P Hillmen, et al.

Human Molecular Genetics|May 1, 1994

Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21M Bessler, P Hillmen, L Longo, et al.

Pageof 21

Showing results (71-80 of 207) with videos related to

Sort By:

Pageof 21

Annals of Human Genetics|May 1, 1981

New genetic variants of glucose 6-phosphate dehydrogenase (G6PD) in ItalyG Sansone, L Perroni, U Testa, et al.

Experimental Hematology|January 1, 1994

Retroviral-mediated gene transfer of a mutant H-ras gene into normal human bone marrow alters myeloid cell proliferation and differentiationJ Maher, F Colonna, D Baker, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985

Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the geneG Battistuzzi, M D'Urso, D Toniolo, et al.

Cancer|October 1, 1991

Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndromeS J Whittaker, N P Smith, R R Jones, et al.

Annals of Human Genetics|October 1, 1989

A new genetic polymorphism in the 16S ribosomal RNA gene of human mitochondrial DNAA B Mehta, T Vulliamy, E C Gordon-Smith, et al.

British Journal of Haematology|November 13, 2001

Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuriaD J Araten, D Swirsky, A Karadimitris, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979

Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphismG Modiano, G Battistuzzi, G J Esan, et al.

Journal of Internal Medicine|January 1, 1994

Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuriaM F McMullin, P Hillmen, J Jackson, et al.

Blood|December 15, 1995

Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift typeK Nafa, P J Mason, P Hillmen, et al.

Human Molecular Genetics|May 1, 1994

Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21M Bessler, P Hillmen, L Longo, et al.

Pageof 21