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Journal of Molecular Biology
|
August 28, 1971
Nuclear magnetic resonance studies of hemoglobins. VI. Heme proton spectra of human deoxyhemoglobins and their relevance to the nature of co-operative oxygenation of hemoglobin
D G Davis, T R Lindstrom, N H Mock, et al.
American Journal of Clinical Pathology
|
September 1, 1987
Noninvasive assessment of tissue iron stores
S Charache, A M Gittlelsohn, H Allen, et al.
Blood
|
February 1, 1978
Hb Potomac (101 Glu replaced by Asp): speculations on placental oxygen transport in carriers of high-affinity hemoglobins
S Charache, R Jacobson, B Brimhall, et al.
American Journal of Human Genetics
|
January 1, 1981
The molecular basis of hemoglobin Grady
A F Scott, J A Phillips, K E Young, et al.
Blood
|
March 1, 1986
Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell production
G J Dover, R K Humphries, J G Moore, et al.
The New England Journal of Medicine
|
September 23, 1971
Hereditary persistence of fetal hemoglobin. Heterogeneity of fetal hemoglobin in homozygotes and in conjunction with -thalassemia
T H Huisman, W A Schroeder, S Charache, et al.
Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology
|
December 1, 1981
Variability of oxygen affinity of blood: human subjects native to high altitude
R M Winslow, C C Monge, N J Statham, et al.
Controlled Clinical Trials
|
December 1, 1995
Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea
S Charache, M L Terrin, R D Moore, et al.
The New England Journal of Medicine
|
May 18, 1995
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia
S Charache, M L Terrin, R D Moore, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1984
beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site
S E Antonarakis, S H Irkin, T C Cheng, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 133) with videos related to
Sort By:
Page
of 14
Journal of Molecular Biology
|
August 28, 1971
Nuclear magnetic resonance studies of hemoglobins. VI. Heme proton spectra of human deoxyhemoglobins and their relevance to the nature of co-operative oxygenation of hemoglobin
D G Davis, T R Lindstrom, N H Mock, et al.
American Journal of Clinical Pathology
|
September 1, 1987
Noninvasive assessment of tissue iron stores
S Charache, A M Gittlelsohn, H Allen, et al.
Blood
|
February 1, 1978
Hb Potomac (101 Glu replaced by Asp): speculations on placental oxygen transport in carriers of high-affinity hemoglobins
S Charache, R Jacobson, B Brimhall, et al.
American Journal of Human Genetics
|
January 1, 1981
The molecular basis of hemoglobin Grady
A F Scott, J A Phillips, K E Young, et al.
Blood
|
March 1, 1986
Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell production
G J Dover, R K Humphries, J G Moore, et al.
The New England Journal of Medicine
|
September 23, 1971
Hereditary persistence of fetal hemoglobin. Heterogeneity of fetal hemoglobin in homozygotes and in conjunction with -thalassemia
T H Huisman, W A Schroeder, S Charache, et al.
Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology
|
December 1, 1981
Variability of oxygen affinity of blood: human subjects native to high altitude
R M Winslow, C C Monge, N J Statham, et al.
Controlled Clinical Trials
|
December 1, 1995
Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea
S Charache, M L Terrin, R D Moore, et al.
The New England Journal of Medicine
|
May 18, 1995
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia
S Charache, M L Terrin, R D Moore, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1984
beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site
S E Antonarakis, S H Irkin, T C Cheng, et al.
Page
of 14