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Blood
|
May 15, 1989
KU 812: a pluripotent human cell line with spontaneous erythroid terminal maturation
M Nakazawa, M T Mitjavila, N Debili, et al.
Annals of the New York Academy of Sciences
|
July 12, 1995
A new therapeutic approach for sickle cell disease. Blockade of the red cell Ca(2+)-activated K+ channel by clotrimazole
C Brugnara, L De Franceschi, C C Armsby, et al.
Scandinavian Journal of Haematology
|
October 1, 1980
Elevated Hb F associated with beta-thalassaemia trait: haemoglobin synthesis in reticulocytes and in blood BFU-E
A Dubart, U Testa, S Musumeci, et al.
The Journal of Clinical Investigation
|
November 1, 1991
Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease
S Tutois, X Montagutelli, V Da Silva, et al.
La Nouvelle Presse Medicale
|
October 24, 1981
[Detection of haemoglobinopathies at birth, using isoelectric focalization (author's transl)]
N Monplaisir, J C Casius de Linval, M Sellaye, et al.
The New England Journal of Medicine
|
October 17, 1991
Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori
H E Witkowska, B H Lubin, Y Beuzard, et al.
Progress in Clinical and Biological Research
|
January 1, 1981
Isoelectric focusing of human hemoglobins
Y Beuzard, F Galacteros, F Braconnier, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
May 26, 2010
Death switch for gene therapy: application to erythropoietin transgene expression
D S Souza, D M Spencer, T S I Salles, et al.
Science (New York, N.Y.)
|
December 18, 2001
Correction of sickle cell disease in transgenic mouse models by gene therapy
R Pawliuk, K A Westerman, M E Fabry, et al.
Page
of 15
Search research articles
Search
Showing results (141-150 of 149) with videos related to
Sort By:
Page
of 15
You have reached the last page of results.
This site can display upto 149 results.
Blood
|
May 15, 1989
KU 812: a pluripotent human cell line with spontaneous erythroid terminal maturation
M Nakazawa, M T Mitjavila, N Debili, et al.
Annals of the New York Academy of Sciences
|
July 12, 1995
A new therapeutic approach for sickle cell disease. Blockade of the red cell Ca(2+)-activated K+ channel by clotrimazole
C Brugnara, L De Franceschi, C C Armsby, et al.
Scandinavian Journal of Haematology
|
October 1, 1980
Elevated Hb F associated with beta-thalassaemia trait: haemoglobin synthesis in reticulocytes and in blood BFU-E
A Dubart, U Testa, S Musumeci, et al.
The Journal of Clinical Investigation
|
November 1, 1991
Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease
S Tutois, X Montagutelli, V Da Silva, et al.
La Nouvelle Presse Medicale
|
October 24, 1981
[Detection of haemoglobinopathies at birth, using isoelectric focalization (author's transl)]
N Monplaisir, J C Casius de Linval, M Sellaye, et al.
The New England Journal of Medicine
|
October 17, 1991
Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori
H E Witkowska, B H Lubin, Y Beuzard, et al.
Progress in Clinical and Biological Research
|
January 1, 1981
Isoelectric focusing of human hemoglobins
Y Beuzard, F Galacteros, F Braconnier, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
May 26, 2010
Death switch for gene therapy: application to erythropoietin transgene expression
D S Souza, D M Spencer, T S I Salles, et al.
Science (New York, N.Y.)
|
December 18, 2001
Correction of sickle cell disease in transgenic mouse models by gene therapy
R Pawliuk, K A Westerman, M E Fabry, et al.
Page
of 15