M Bessler|P Mason|P Hillmen|L Luzzatto - JoVE Visualize

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Lancet (London, England)|April 16, 1994

Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.

Somatic Cell and Molecular Genetics|March 1, 1993

Paroxysmal nocturnal hemoglobinuria: correction of abnormal phenotype by somatic cell hybridizationP Hillmen, M Bessler, J Bungey, et al.

Haematologica|November 1, 1996

Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosisK Nafa, M Bessler, P Mason, et al.

British Journal of Haematology|August 1, 1994

Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuriaM Bessler, P J Mason, P Hillmen, et al.

Blood|January 1, 1993

Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotypeP Hillmen, M Bessler, D H Crawford, 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.

The New England Journal of Medicine|November 9, 1995

Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993

Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuriaP Hillmen, M Bessler, P J Mason, et al.

Seminars in Hematology|June 13, 1998

Somatic mutation and clonal selection in the pathogenesis and in the control of paroxysmal nocturnal hemoglobinuriaM Bessler, P Hillmen

Pageof 162

Showing results (1-10 of 1,616) with videos related to

Sort By:

Pageof 162

Lancet (London, England)|April 16, 1994

Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.

Somatic Cell and Molecular Genetics|March 1, 1993

Paroxysmal nocturnal hemoglobinuria: correction of abnormal phenotype by somatic cell hybridizationP Hillmen, M Bessler, J Bungey, et al.

Haematologica|November 1, 1996

Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosisK Nafa, M Bessler, P Mason, et al.

British Journal of Haematology|August 1, 1994

Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuriaM Bessler, P J Mason, P Hillmen, et al.

Blood|January 1, 1993

Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotypeP Hillmen, M Bessler, D H Crawford, 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.

The New England Journal of Medicine|November 9, 1995

Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993

Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuriaP Hillmen, M Bessler, P J Mason, et al.

Seminars in Hematology|June 13, 1998

Somatic mutation and clonal selection in the pathogenesis and in the control of paroxysmal nocturnal hemoglobinuriaM Bessler, P Hillmen

Pageof 162