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Molecular Pharmacology
|
July 1, 1999
DNA interactions of new antitumor aminophosphine platinum(II) complexes
K Neplechová, J Kaspárková, O Vrána, et al.
Vnitrni Lekarstvi
|
January 1, 1995
[Structural variants in hemoglobin occurring in the Czech Republic]
K Indrák, V Brabec, V Divoký, et al.
Vnitrni Lekarstvi
|
June 8, 1999
[Haplotypes of the beta-globulin locus in Czechs and Slovaks with beta-thalassemia and structurally variant hemoglobins]
E Kynclová, L Kovaríková, P Fajkosová, et al.
Annals of Hematology
|
August 1, 1994
Hb Nottingham or alpha 2 beta 2 98 (FG5) Val-->Gly in a Czech child
V Brabec, K Indrák, H Fortová, et al.
Annals of Hematology
|
July 1, 1991
A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplication
K Indrak, Y J Fei, H W Li, et al.
Vnitrni Lekarstvi
|
April 1, 1994
[Dominant beta-thalassemia alleles in the Czech and Slovak population (beta-thalassemia mutations in 112(T-A) and 121(G-T) codons and the unstable Hradec Králové hemoglobin or alpha 2 beta 2 115 (G17) Ala-Asp)]
K Indrák, V Divoký, V Brabec, et al.
Blood
|
February 1, 1995
Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis
P Jarolim, H L Rubin, V Brabec, et al.
Dalton Transactions (Cambridge, England : 2003)
|
April 28, 2023
Triplex metallohelices have enantiomer-dependent mechanisms of action in colon cancer cells
J P C Coverdale, H Kostrhunova, L Markova, et al.
Human Genetics
|
February 1, 1992
Molecular characterization of beta-thalassemia in Czechoslovakia
K Indrak, V Brabec, J Indrakova, et al.
Blood
|
July 1, 1997
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency
H Hassoun, J N Vassiliadis, J Murray, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 182) with videos related to
Sort By:
Page
of 19
Molecular Pharmacology
|
July 1, 1999
DNA interactions of new antitumor aminophosphine platinum(II) complexes
K Neplechová, J Kaspárková, O Vrána, et al.
Vnitrni Lekarstvi
|
January 1, 1995
[Structural variants in hemoglobin occurring in the Czech Republic]
K Indrák, V Brabec, V Divoký, et al.
Vnitrni Lekarstvi
|
June 8, 1999
[Haplotypes of the beta-globulin locus in Czechs and Slovaks with beta-thalassemia and structurally variant hemoglobins]
E Kynclová, L Kovaríková, P Fajkosová, et al.
Annals of Hematology
|
August 1, 1994
Hb Nottingham or alpha 2 beta 2 98 (FG5) Val-->Gly in a Czech child
V Brabec, K Indrák, H Fortová, et al.
Annals of Hematology
|
July 1, 1991
A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplication
K Indrak, Y J Fei, H W Li, et al.
Vnitrni Lekarstvi
|
April 1, 1994
[Dominant beta-thalassemia alleles in the Czech and Slovak population (beta-thalassemia mutations in 112(T-A) and 121(G-T) codons and the unstable Hradec Králové hemoglobin or alpha 2 beta 2 115 (G17) Ala-Asp)]
K Indrák, V Divoký, V Brabec, et al.
Blood
|
February 1, 1995
Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis
P Jarolim, H L Rubin, V Brabec, et al.
Dalton Transactions (Cambridge, England : 2003)
|
April 28, 2023
Triplex metallohelices have enantiomer-dependent mechanisms of action in colon cancer cells
J P C Coverdale, H Kostrhunova, L Markova, et al.
Human Genetics
|
February 1, 1992
Molecular characterization of beta-thalassemia in Czechoslovakia
K Indrak, V Brabec, J Indrakova, et al.
Blood
|
July 1, 1997
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency
H Hassoun, J N Vassiliadis, J Murray, et al.
Page
of 19