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Nature Genetics
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October 1, 1996
Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton
C D Southgate, A H Chishti, B Mitchell, et al.
American Journal of Hematology
|
July 11, 1991
Spinal cord compression secondary to extramedullary hematopoiesis: a noninvasive management based on MRI
H Hassoun, L Lawn-Tsao, E R Langevin, et al.
British Journal of Haematology
|
October 1, 1995
Beta spectrin PRAGUE: a truncated beta spectrin producing spectrin deficiency, defective spectrin heterodimer self-association and a phenotype of spherocytic elliptocytosis
P Jarolim, H Wichterle, M Hanspal, et al.
Blood
|
January 1, 1981
Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis
J Palek, S C Liu, P Y Liu, et al.
Blood
|
September 1, 1993
Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis
M Hanspal, J S Hanspal, K E Sahr, et al.
Molecular and Biochemical Parasitology
|
June 1, 1992
Isolation of skeleton-associated knobs from human red blood cells infected with malaria parasite Plasmodium falciparum
A H Chishti, K I Andrabi, L H Derick, et al.
Blood
|
July 15, 1992
Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2
P Jarolim, J Palek, H L Rubin, et al.
The Journal of Laboratory and Clinical Medicine
|
January 1, 1977
Effect of propranolol on normal human erythrocytes
N L Fortier, L M Snyder, J Palek, et al.
Blood
|
October 1, 1988
Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis
J Lawler, T L Coetzer, V N Mankad, et al.
Blood
|
April 16, 1998
Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene
H Hassoun, T Hanada, M Lutchman, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 118) with videos related to
Sort By:
Page
of 12
Nature Genetics
|
October 1, 1996
Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton
C D Southgate, A H Chishti, B Mitchell, et al.
American Journal of Hematology
|
July 11, 1991
Spinal cord compression secondary to extramedullary hematopoiesis: a noninvasive management based on MRI
H Hassoun, L Lawn-Tsao, E R Langevin, et al.
British Journal of Haematology
|
October 1, 1995
Beta spectrin PRAGUE: a truncated beta spectrin producing spectrin deficiency, defective spectrin heterodimer self-association and a phenotype of spherocytic elliptocytosis
P Jarolim, H Wichterle, M Hanspal, et al.
Blood
|
January 1, 1981
Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis
J Palek, S C Liu, P Y Liu, et al.
Blood
|
September 1, 1993
Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis
M Hanspal, J S Hanspal, K E Sahr, et al.
Molecular and Biochemical Parasitology
|
June 1, 1992
Isolation of skeleton-associated knobs from human red blood cells infected with malaria parasite Plasmodium falciparum
A H Chishti, K I Andrabi, L H Derick, et al.
Blood
|
July 15, 1992
Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2
P Jarolim, J Palek, H L Rubin, et al.
The Journal of Laboratory and Clinical Medicine
|
January 1, 1977
Effect of propranolol on normal human erythrocytes
N L Fortier, L M Snyder, J Palek, et al.
Blood
|
October 1, 1988
Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis
J Lawler, T L Coetzer, V N Mankad, et al.
Blood
|
April 16, 1998
Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene
H Hassoun, T Hanada, M Lutchman, et al.
Page
of 12