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M E Fabry

Showing results (81-90 of 92) with videos related to

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Blood|April 1, 1987
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF levelR L Nagel, S K Rao, O Dunda-Belkhodja, et al.
Blood|January 12, 2001
Second generation knockout sickle mice: the effect of HbFM E Fabry, S M Suzuka, R S Weinberg, et al.
Microvascular Research|November 18, 2000
Velocity measurements of normal and sickle red blood cells in the rat retinal and choroidal vasculaturesS D Wajer, M Taomoto, D S McLeod, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.
Blood|December 3, 1998
HbS-oman heterozygote: a new dominant sickle syndromeR L Nagel, S Daar, J R Romero, et al.
Blood Cells, Molecules & Diseases|July 2, 1999
Anti-beta s-ribozyme reduces beta s mRNA levels in transgenic mice: potential application to the gene therapy of sickle cell anemiaR Alami, J G Gilman, Y Q Feng, et al.
Blood|March 15, 1991
The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patientsR L Nagel, S Erlingsson, M E Fabry, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|February 1, 1996
Pulmonary entrapment of sickle cells: the role of regional alveolar hypoxiaT K Aldrich, S K Dhuper, N S Patwa, et al.
Journal of Molecular Biology|November 1, 1996
Roles of alpha 114 and beta 87 amino acid residues in the polymerization of hemoglobin S: implications for gene therapyC Ho, B F Willis, T J Shen, et al.
Blood|September 15, 1995
A second generation transgenic mouse model expressing both hemoglobin S (HbS) and HbS-Antilles results in increased phenotypic severityM E Fabry, A Sengupta, S M Suzuka, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Blood|April 1, 1987
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF levelR L Nagel, S K Rao, O Dunda-Belkhodja, et al.
Blood|January 12, 2001
Second generation knockout sickle mice: the effect of HbFM E Fabry, S M Suzuka, R S Weinberg, et al.
Microvascular Research|November 18, 2000
Velocity measurements of normal and sickle red blood cells in the rat retinal and choroidal vasculaturesS D Wajer, M Taomoto, D S McLeod, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.
Blood|December 3, 1998
HbS-oman heterozygote: a new dominant sickle syndromeR L Nagel, S Daar, J R Romero, et al.
Blood Cells, Molecules & Diseases|July 2, 1999
Anti-beta s-ribozyme reduces beta s mRNA levels in transgenic mice: potential application to the gene therapy of sickle cell anemiaR Alami, J G Gilman, Y Q Feng, et al.
Blood|March 15, 1991
The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patientsR L Nagel, S Erlingsson, M E Fabry, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|February 1, 1996
Pulmonary entrapment of sickle cells: the role of regional alveolar hypoxiaT K Aldrich, S K Dhuper, N S Patwa, et al.
Journal of Molecular Biology|November 1, 1996
Roles of alpha 114 and beta 87 amino acid residues in the polymerization of hemoglobin S: implications for gene therapyC Ho, B F Willis, T J Shen, et al.
Blood|September 15, 1995
A second generation transgenic mouse model expressing both hemoglobin S (HbS) and HbS-Antilles results in increased phenotypic severityM E Fabry, A Sengupta, S M Suzuka, et al.
Pageof 10