Search research articles
Contact Us
Filters
Showing results (91-100 of 259) with videos related to
Page
of 26
Sort By:
Early Human Development
|
November 1, 1987
Neonatal jaundice and severity of glucose-6-phosphate dehydrogenase deficiency in Sardinian babies
T Meloni, S Cutillo, U Testa, et al.
The New England Journal of Medicine
|
November 5, 1981
Uracil in DNA in megaloblastic anemia
L Luzzatto, A O Falusi, E A Joju
Blood
|
October 1, 1984
Two populations of erythroid cell progenitors in paroxysmal nocturnal hemoglobinuria
B Rotoli, R Robledo, N Scarpato, et al.
Blood Cells, Molecules & Diseases
|
August 1, 1997
Hematologically important mutations: glucose-6-phosphate dehydrogenase
T Bulliamy, L Luzzatto, A Hirono, et al.
British Journal of Haematology
|
September 1, 1991
Acquired beta thalassaemia trait in MDS
C Hoyle, J Kaeda, J Leslie, et al.
FEBS Letters
|
June 5, 1995
Human glucose-6-phosphate dehydrogenase. Lysine 205 is dispensable for substrate binding but essential for catalysis
J M Bautista, P J Mason, L Luzzatto
Lancet (London, England)
|
April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
M Bessler, P Mason, P Hillmen, et al.
Nature: New Biology
|
February 3, 1971
Synthesis of haemoglobins specified by allelic genes in human heterozygotes
G J Esan, T A Adesina, L Luzzatto
The Journal of Biological Chemistry
|
May 25, 1976
Genetic variants of human erythrocyte glucose-6-phosphate dehydrogenase. Kinetic and thermodynamic parameters of variants A, B, and A- in relation to quaternary structure
A O Babalola, J G Beetlestone, L Luzzatto
Tropical and Geographical Medicine
|
December 1, 1970
Haemophilia in Nigeria
E M Essien, A O Folami, L Luzzatto
Page
of 26
Search research articles
Search
Showing results (91-100 of 259) with videos related to
Sort By:
Page
of 26
Early Human Development
|
November 1, 1987
Neonatal jaundice and severity of glucose-6-phosphate dehydrogenase deficiency in Sardinian babies
T Meloni, S Cutillo, U Testa, et al.
The New England Journal of Medicine
|
November 5, 1981
Uracil in DNA in megaloblastic anemia
L Luzzatto, A O Falusi, E A Joju
Blood
|
October 1, 1984
Two populations of erythroid cell progenitors in paroxysmal nocturnal hemoglobinuria
B Rotoli, R Robledo, N Scarpato, et al.
Blood Cells, Molecules & Diseases
|
August 1, 1997
Hematologically important mutations: glucose-6-phosphate dehydrogenase
T Bulliamy, L Luzzatto, A Hirono, et al.
British Journal of Haematology
|
September 1, 1991
Acquired beta thalassaemia trait in MDS
C Hoyle, J Kaeda, J Leslie, et al.
FEBS Letters
|
June 5, 1995
Human glucose-6-phosphate dehydrogenase. Lysine 205 is dispensable for substrate binding but essential for catalysis
J M Bautista, P J Mason, L Luzzatto
Lancet (London, England)
|
April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
M Bessler, P Mason, P Hillmen, et al.
Nature: New Biology
|
February 3, 1971
Synthesis of haemoglobins specified by allelic genes in human heterozygotes
G J Esan, T A Adesina, L Luzzatto
The Journal of Biological Chemistry
|
May 25, 1976
Genetic variants of human erythrocyte glucose-6-phosphate dehydrogenase. Kinetic and thermodynamic parameters of variants A, B, and A- in relation to quaternary structure
A O Babalola, J G Beetlestone, L Luzzatto
Tropical and Geographical Medicine
|
December 1, 1970
Haemophilia in Nigeria
E M Essien, A O Folami, L Luzzatto
Page
of 26