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Experientia
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February 15, 1994
The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes
A J Dimovski, A D Adekile, T H Huisman
Die Pharmazie
|
January 2, 2014
Characterization of the most common CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Macedonia
K Jakovski, A Kapedanovska Nestorovska, N Labacevski, et al.
Hemoglobin
|
January 1, 1991
Detection of beta-thalassemia mutations by ASO hybridization of PCR amplified DNA with digoxigenin ddUTP labeled oligonucleotides
D G Efremov, A J Dimovski, G D Efremov
Blood
|
June 1, 1994
The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin
D G Efremov, A J Dimovski, T H Huisman
Acta Haematologica
|
January 1, 1991
Mutant oligonucleotide extension amplification: a nonlabeling polymerase-chain-reaction-based assay for the detection of point mutations
D G Efremov, A J Dimovski, L Janković, et al.
British Journal of Haematology
|
June 1, 1994
The relative levels of beta A and beta S mRNAs in Hb S heterozygotes and in patients with Hb S-beta(+)-thalassaemia or Hb S-beta(+)-HPFH combinations
A J Dimovski, D G Efremov, L H Gu, et al.
Haematologica
|
March 1, 1992
A new mutation in the beta-globin gene (IVS II-850 G-C) found in a Yugoslavian beta-thalassemia heterozygote
L Jankovic, A J Dimovski, E Sukarova, et al.
American Journal of Hematology
|
January 1, 1994
Polymorphic pattern of the (AT)X(T)Y motif at -530 5' to the beta-globin gene in over 40 patients homozygous for various beta-thalassemia mutations
A J Dimovski, A D Adekile, V Divoky, et al.
Acta Haematologica
|
November 20, 2001
An Alu insert as the cause of a severe form of hemophilia A
E Sukarova, A J Dimovski, P Tchacarova, et al.
International Journal of Hematology
|
August 1, 1991
A C----G mutation at nt position 6 3' to the terminating codon may be the cause of a silent beta-thalassemia
L Jankovic, A J Dimovski, P Kollia, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Experientia
|
February 15, 1994
The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes
A J Dimovski, A D Adekile, T H Huisman
Die Pharmazie
|
January 2, 2014
Characterization of the most common CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Macedonia
K Jakovski, A Kapedanovska Nestorovska, N Labacevski, et al.
Hemoglobin
|
January 1, 1991
Detection of beta-thalassemia mutations by ASO hybridization of PCR amplified DNA with digoxigenin ddUTP labeled oligonucleotides
D G Efremov, A J Dimovski, G D Efremov
Blood
|
June 1, 1994
The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin
D G Efremov, A J Dimovski, T H Huisman
Acta Haematologica
|
January 1, 1991
Mutant oligonucleotide extension amplification: a nonlabeling polymerase-chain-reaction-based assay for the detection of point mutations
D G Efremov, A J Dimovski, L Janković, et al.
British Journal of Haematology
|
June 1, 1994
The relative levels of beta A and beta S mRNAs in Hb S heterozygotes and in patients with Hb S-beta(+)-thalassaemia or Hb S-beta(+)-HPFH combinations
A J Dimovski, D G Efremov, L H Gu, et al.
Haematologica
|
March 1, 1992
A new mutation in the beta-globin gene (IVS II-850 G-C) found in a Yugoslavian beta-thalassemia heterozygote
L Jankovic, A J Dimovski, E Sukarova, et al.
American Journal of Hematology
|
January 1, 1994
Polymorphic pattern of the (AT)X(T)Y motif at -530 5' to the beta-globin gene in over 40 patients homozygous for various beta-thalassemia mutations
A J Dimovski, A D Adekile, V Divoky, et al.
Acta Haematologica
|
November 20, 2001
An Alu insert as the cause of a severe form of hemophilia A
E Sukarova, A J Dimovski, P Tchacarova, et al.
International Journal of Hematology
|
August 1, 1991
A C----G mutation at nt position 6 3' to the terminating codon may be the cause of a silent beta-thalassemia
L Jankovic, A J Dimovski, P Kollia, et al.
Page
of 4