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A Kutlar

Showing results (1-10 of 141) with videos related to

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Hemoglobin|January 1, 1987
The thalassemia repositoryA Kutlar, K D Lanclos
American Journal of Hematology|July 14, 1998
Are sickle cell disease patients with stroke genetically predisposed to the event by inheriting a tendency to high tumor necrosis factor levels?J E Carroll, V McKie, A Kutlar
Journal of Chromatography|April 23, 1986
Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatographyF Kutlar, A Kutlar, T H Huisman
Biochemical Genetics|February 1, 1986
Differences between the levels of G gamma chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequenceI Bakioglu, A Kutlar, T H Huisman
Hemoglobin|January 1, 1979
Further data on one of the first examples of sickle cell alpha-thalassemia diseaseE Bermek, M Aksoy, G Almis, et al.
Bone Marrow Transplantation|November 18, 2000
Autoimmune thrombocytopenia following autologous hematopoietic cell transplantation: review of literature and treatment optionsA P Jillella, A M Kallab, A Kutlar
Hemoglobin|August 2, 2001
The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell diseaseA Kutlar, F Kutlar, I Turker, et al.
Acta Haematologica|January 1, 1982
beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four familiesM Aksoy, E Bermek, G Almiş, et al.
Hemoglobin|January 1, 1992
Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencingM A Cürük, A Kutlar, T H Huisman
American Journal of Human Genetics|June 1, 1986
Haplotypes among Vietnamese hemoglobin E homozygotes including one with a gamma-globin gene triplicationT Nakatsuji, A Kutlar, F Kutlar, et al.
Pageof 15

Showing results (1-10 of 141) with videos related to

Sort By:
Pageof 15
Hemoglobin|January 1, 1987
The thalassemia repositoryA Kutlar, K D Lanclos
American Journal of Hematology|July 14, 1998
Are sickle cell disease patients with stroke genetically predisposed to the event by inheriting a tendency to high tumor necrosis factor levels?J E Carroll, V McKie, A Kutlar
Journal of Chromatography|April 23, 1986
Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatographyF Kutlar, A Kutlar, T H Huisman
Biochemical Genetics|February 1, 1986
Differences between the levels of G gamma chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequenceI Bakioglu, A Kutlar, T H Huisman
Hemoglobin|January 1, 1979
Further data on one of the first examples of sickle cell alpha-thalassemia diseaseE Bermek, M Aksoy, G Almis, et al.
Bone Marrow Transplantation|November 18, 2000
Autoimmune thrombocytopenia following autologous hematopoietic cell transplantation: review of literature and treatment optionsA P Jillella, A M Kallab, A Kutlar
Hemoglobin|August 2, 2001
The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell diseaseA Kutlar, F Kutlar, I Turker, et al.
Acta Haematologica|January 1, 1982
beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four familiesM Aksoy, E Bermek, G Almiş, et al.
Hemoglobin|January 1, 1992
Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencingM A Cürük, A Kutlar, T H Huisman
American Journal of Human Genetics|June 1, 1986
Haplotypes among Vietnamese hemoglobin E homozygotes including one with a gamma-globin gene triplicationT Nakatsuji, A Kutlar, F Kutlar, et al.
Pageof 15