Results 181 to 190 of about 17,814 (205)
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The Journal of Immunology, 1991
Abstract An RFLP was found in the DNA of 25 unrelated persons, two families, and five cell lines that correlated with their membrane cofactor protein phenotype. If restricted with HindIII, DNA derived from upper band predominant protein (U) phenotypes had a band at 2 kb, whereas DNA of lower band predominant (L) phenotypes had a 4-kb ...
N S, Bora, T W, Post, J P, Atkinson
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Abstract An RFLP was found in the DNA of 25 unrelated persons, two families, and five cell lines that correlated with their membrane cofactor protein phenotype. If restricted with HindIII, DNA derived from upper band predominant protein (U) phenotypes had a band at 2 kb, whereas DNA of lower band predominant (L) phenotypes had a 4-kb ...
N S, Bora, T W, Post, J P, Atkinson
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Association of the HindIII Polymorphism of the Lipoprotein Lipase Gene with Myocardial Infarction
Molecular Biology, 2001The success in complete sequencing of "small" genomes and development of new technologies which sharply accelerate processes of cloning and sequencing made real an intensive development of plant genomics and complete sequencing of DNA of some species. It is assumed that the success in plant genomics will result in revolutionary changes in biotechnology
O. E. Mustafina +3 more
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Human Genetics, 1995
The gene encoding human phenol-preferring phenol sulfotransferase (STP) has been cloned and mapped to chromosome 16p. A HindIII RFLP in this gene is described.
R D, Henkel, L V, Galindo, T P, Dooley
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The gene encoding human phenol-preferring phenol sulfotransferase (STP) has been cloned and mapped to chromosome 16p. A HindIII RFLP in this gene is described.
R D, Henkel, L V, Galindo, T P, Dooley
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Clinica Chimica Acta, 2011
We aimed to investigate the polymorphism HindIII of the lipoprotein lipase (LPL) gene to explore whether it had a potential role in susceptibility to type 2 diabetes mellitus (T2DM) among Han Chinese, and whether this effect was influenced by regulating LPL or other risk factors.Overall, 654 Han Chinese adults were selected from a community-based cross-
Yue, Qi +8 more
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We aimed to investigate the polymorphism HindIII of the lipoprotein lipase (LPL) gene to explore whether it had a potential role in susceptibility to type 2 diabetes mellitus (T2DM) among Han Chinese, and whether this effect was influenced by regulating LPL or other risk factors.Overall, 654 Han Chinese adults were selected from a community-based cross-
Yue, Qi +8 more
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[HindIII polymorphism of lipoprotein lipase gene and risk of myocardial infarction].
Molekuliarnaia genetika, mikrobiologiia i virusologiia, 2001The purpose of this study was to determine whether HindIII restriction polymorphism found in intron 8 of lipoprotein lipase gene is associated with the onset of myocardial infarction (MI) in Russians and Tartars living in Bashkortostan. HindIII polymorphism was investigated by the polymerase chain reaction in myocardial infarction survivors (males aged
E I, Shagisultanova +3 more
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Wiener klinische Wochenschrift, 2007
HDL-cholesterol (HDL-C) is a recognized athero-protective factor and low levels of HDL-C occur frequently in patients with coronary artery disease. Regulation of HDL-C level most probably results from the interaction of genes involved in lipoprotein metabolism and also from non-genetic factors.
Martin, Javorský +9 more
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HDL-cholesterol (HDL-C) is a recognized athero-protective factor and low levels of HDL-C occur frequently in patients with coronary artery disease. Regulation of HDL-C level most probably results from the interaction of genes involved in lipoprotein metabolism and also from non-genetic factors.
Martin, Javorský +9 more
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[The HindIII polymorphism of the ribosomal DNA in the German cockroach (Blattella germanica L.)].
TSitologiia i genetika, 1998Structural polymorphism of rDNA from Blattella germanica was analyzed in six colonies of Moscow city different regions. Two electrophoretic variants of HindIII fragments of rDNA were detected by using 28S-like rDNA probe.
D V, Mukha +2 more
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Zhongguo shi yan xue ye xue za zhi, 2012
This study was aimed to investigate the suitability of FVIII gene BclI (intron 18)and HindIII (intron 19) site polymorphism for genetic diagnosis of patients with hemophilia A (HA) and their families, and for detection of carriers. The FVIII gene bclI (intron 18) and HindIII (intron 19) site polymorphism on the X chromosome of 8 patients with HA and 45
Xiu-Qiang, Qiao +4 more
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This study was aimed to investigate the suitability of FVIII gene BclI (intron 18)and HindIII (intron 19) site polymorphism for genetic diagnosis of patients with hemophilia A (HA) and their families, and for detection of carriers. The FVIII gene bclI (intron 18) and HindIII (intron 19) site polymorphism on the X chromosome of 8 patients with HA and 45
Xiu-Qiang, Qiao +4 more
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HindIII polymorphism in the BCL6 gene
Human Molecular Genetics, 1993B W, Baron +3 more
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