Results 31 to 40 of about 17,814 (205)

HindIII-based restriction fragment length polymorphism in hemophilic and nonhemophilic patients

open access: yesJournal of Natural Science, Biology and Medicine, 2010
Hemophilia A is most common recessively inherited bleeding disorder, which affect one in five thousand male births throughout the world. In most of the hemophilic A patients, no common mutation is easily identifiable. This limitation has been overcome by the use of polymorphic DNA marker, i.e., restriction fragment length polymorphism (RFLP).
Dubey, Alok Kumar   +2 more
openaire   +3 more sources

MOLEKULYaRNO-GENETIChESKIE MARKERY OSTEOPOROZA U ZhITELEY BLOKADNOGO LENINGRADA

open access: yesОстеопороз и остеопатии, 2011
The aim of our study is researching influence of vitamin D and osteocalcin polymorphic gene markers in people, who lived in Blockaded Leningrad in 1941-1944 and detecting “critical age” of peak bone mass formation in these people.
O N Semenova   +7 more
doaj   +1 more source

Biosynthesis of fucoxanthin and diadinoxanthin and function of initial pathway genes in Phaeodactylum tricornutum [PDF]

open access: yes, 2012
The biosynthesis pathway to diadinoxanthin and fucoxanthin was elucidated in Phaeodactylum tricornutum by a combined approach involving metabolite analysis identification of gene function.
Breitenbach, Jürgen   +5 more
core   +1 more source

Relationship of metabolic syndrome and its components with -844 G/A and HindIII C/G PAI-1 gene polymorphisms in Mexican children

open access: yesBMC Pediatrics, 2012
Background Several association studies have shown that -844 G/A and HindIII C/G PAI-1 polymorphisms are related with increase of PAI-1 levels, obesity, insulin resistance, glucose intolerance, hypertension and dyslipidemia, which are components of ...
De la Cruz-Mosso Ulises   +6 more
doaj   +1 more source

ASSOCIATION OF LPL-HINDIII POLYMORPHISM WITH CORONARY ARTERY DISEASE IN MACEDONIAN POPULATION [PDF]

open access: yesSanamed, 2013
Objective: Coronary artery disease (CAD) is a leading cause of high mortality and morbidity in worldwide. The HindIII polymorphism of the LPL gene (LPL-HindIII) is a common variant and has been associated with plasma lipid and lipoprotein variability in ...
Georgiev Antonio
doaj  

Genome sequencing analysis of Streptomyces coelicolor mutants that overcome the phosphate-depending vancomycin lethal effect [PDF]

open access: yes, 2018
Background Glycopeptide antibiotics inhibit bacterial cell-wall synthesis, and are important for the treatment of infections caused by multi drug-resistant strains of enterococci, streptococci and staphylococci.
Santos Beneit, Fernando
core   +1 more source

The Lipoprotein Lipase HindIII Polymorphism And The Susceptibility To Hypertension

open access: yesEgyptian Journal of Biochemistry and Molecular Biology, 2009
Lipoprotein lipase (LPL) enzyme plays a central role in lipidmetabolism. The primary function of LPL enzyme is the hydrolysis ofthe core triglycerides of circulating chylomicron and very low densitylipoprotein (VLDL). It releases monoglycerides and free fatty acids,which are taken up by skeletal muscle or adipose tissue.
El Din Hemimi, NS   +2 more
openaire   +2 more sources

Impact of lipoprotein lipase gene polymorphism, S447X, on postprandial triacylglycerol and glucose response to sequential meal ingestion [PDF]

open access: yes, 2016
Lipoprotein lipase (LPL) is a key rate-limiting enzyme for the hydrolysis of triacylglycerol (TAG) in chylomicrons and very low-density lipoprotein. Given that postprandial assessment of lipoprotein metabolism may provide a more physiological perspective
Anne-Marie Minihane   +7 more
core   +2 more sources

Gene-environment interactions due to quantile-specific heritability of triglyceride and VLDL concentrations. [PDF]

open access: yes, 2020
"Quantile-dependent expressivity" is a dependence of genetic effects on whether the phenotype (e.g., triglycerides) is high or low relative to its distribution in the population.
Williams, Paul T
core   +1 more source

An additional Hindlll polymorphism at the coagulation factor XlllA locus

open access: yesNucleic Acids Research, 1990
[No abstract available]
IODICE, CARLA   +3 more
openaire   +4 more sources

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