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L Nagel

Showing results (361-370 of 401) with videos related to

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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.
The Journal of Biological Chemistry|September 20, 1996
Hb Montefiore (126(H9)Asp-->Tyr). High oxygen affinity and loss of cooperativity secondary to C-terminal disruptionH Wajcman, J Kister, F Galactéros, et al.
The Journal of Biological Chemistry|December 19, 2002
Conformational changes in hemoglobin S (betaE6V) imposed by mutation of the beta Glu7-beta Lys132 salt bridge and detected by UV resonance Raman spectroscopyLaura J Juszczak, Christophe Fablet, Veronique Baudin-Creuza, et al.
The Journal of Trauma|December 1, 1992
Noninvasive assessment of metabolism in wounded skin by 31P-NMR in vivoM P Schweizer, J I Olsen, J Shelby, 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.
JACEP|August 1, 1976
Prehospital use of the military anti-shock trouser (MAST)J M Civetta, S R Nussenfeld, T R Rowe, et al.
American Journal of Hematology|March 1, 1995
Gender and haplotype effects upon hematological manifestations of adult sickle cell anemiaM H Steinberg, H Hsu, R L Nagel, et al.
American Journal of Hematology|June 1, 1997
Effect of alpha-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in IndiaM B Mukherjee, C Y Lu, R Ducrocq, et al.
The Protein Journal|November 30, 2006
Pair-wise interactions of polymerization inhibitory contact site mutations of hemoglobin-SSonati Srinivasulu, Krishnaveni Perumalsamy, Rajendra Upadhya, et al.
Pageof 41

Showing results (361-370 of 401) with videos related to

Sort By:
Pageof 41
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.
The Journal of Biological Chemistry|September 20, 1996
Hb Montefiore (126(H9)Asp-->Tyr). High oxygen affinity and loss of cooperativity secondary to C-terminal disruptionH Wajcman, J Kister, F Galactéros, et al.
The Journal of Biological Chemistry|December 19, 2002
Conformational changes in hemoglobin S (betaE6V) imposed by mutation of the beta Glu7-beta Lys132 salt bridge and detected by UV resonance Raman spectroscopyLaura J Juszczak, Christophe Fablet, Veronique Baudin-Creuza, et al.
The Journal of Trauma|December 1, 1992
Noninvasive assessment of metabolism in wounded skin by 31P-NMR in vivoM P Schweizer, J I Olsen, J Shelby, 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.
JACEP|August 1, 1976
Prehospital use of the military anti-shock trouser (MAST)J M Civetta, S R Nussenfeld, T R Rowe, et al.
American Journal of Hematology|March 1, 1995
Gender and haplotype effects upon hematological manifestations of adult sickle cell anemiaM H Steinberg, H Hsu, R L Nagel, et al.
American Journal of Hematology|June 1, 1997
Effect of alpha-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in IndiaM B Mukherjee, C Y Lu, R Ducrocq, et al.
The Protein Journal|November 30, 2006
Pair-wise interactions of polymerization inhibitory contact site mutations of hemoglobin-SSonati Srinivasulu, Krishnaveni Perumalsamy, Rajendra Upadhya, et al.
Pageof 41