Results 1 to 10 of about 1,493,018 (273)

The Contribution of Tissue Inhibitor of Metalloproteinase-2 Genotypes to Breast Cancer Risk in Taiwan

open access: yesLife, 2023
Tissue inhibitor of metalloproteinase-2 (TIMP-2) is an endogenous inhibitor of matrix metalloproteinase-2 and is highly expressed in breast cancer (BC) cases at diagnosis.
Yun-Chi Wang   +11 more
doaj   +1 more source

Genotype Imputation [PDF]

open access: yesAnnual Review of Genomics and Human Genetics, 2009
Genotype imputation is now an essential tool in the analysis of genome-wide association scans. This technique allows geneticists to accurately evaluate the evidence for association at genetic markers that are not directly genotyped. Genotype imputation is particularly useful for combining results across studies that rely on different genotyping ...
Yun Li   +3 more
openaire   +3 more sources

Study on Some Quality and Morpho-Physiological Traits of Durum Wheat (Triticum durum L. Desf.) Genotypes

open access: yesISPEC Journal of Agricultural Sciences, 2023
The study was carried out in the experimental field of the Department of Field Crops, Faculty of Agriculture, Tekirdağ Namık Kemal University in 2020-2021.
Alpay BALKAN   +4 more
doaj   +1 more source

Compressed Genotyping [PDF]

open access: yesIEEE Transactions on Information Theory, 2010
Significant volumes of knowledge have been accumulated in recent years linking subtle genetic variations to a wide variety of medical disorders from Cystic Fibrosis to mental retardation. Nevertheless, there are still great challenges in applying this knowledge routinely in the clinic, largely due to the relatively tedious and expensive process of DNA ...
Erlich, Yaniv   +4 more
openaire   +3 more sources

Ayurveda and Epigenetics

open access: yesMedicina, 2020
Ayurveda is a comprehensive, natural health care system that originated in the ancient Vedic times of India. Epigenetics refers to the external modification of DNA that turns genes on and off, affecting gene expression. This occurs without changes in the
Hari Sharma, Robert Keith Wallace
doaj   +1 more source

Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia [PDF]

open access: yesVojnosanitetski Pregled, 2013
Background/Aim. Wilson’s disease (WD) is an autosomal-recessive disorder which is characterized with a marked clinical heterogeneity. The gene responsible for WD is located in 13q14.3 chromosome, contains 21 exons and codes for copper specific ...
Tomić Aleksandra   +7 more
doaj   +1 more source

Histopathology of chronic hepatitis C in relation to virus genotype [PDF]

open access: yesVojnosanitetski Pregled, 2006
Background/aim: The natural history of hepatitis C virus (HCV) infection is variable and the factors determining the course of the illness are unclear. There are geographical variations in the distribution of different HCV genotypes, and some of them are
Simonović Jasmina   +8 more
doaj   +1 more source

Association of mutations in the Plasmodium falciparum Kelch13 gene (Pf3D7_1343700) with parasite clearance rates after artemisinin-based treatments—a WWARN individual patient data meta-analysis

open access: yesBMC Medicine, 2019
Background Plasmodium falciparum infections with slow parasite clearance following artemisinin-based therapies are widespread in the Greater Mekong Subregion.
WWARN K13 Genotype-Phenotype Study Group
doaj   +1 more source

CRISPR editing validation, immunostaining and DNA sequencing of individual fixed bovine embryos

open access: yesBioTechniques, 2018
CRISPR technologies used for mammalian embryology have wide implications from basic research to applications in agriculture and biomedicine. Confirmation of successful gene editing following CRISPR/Cas9 delivery is often limited to either protein ...
Bradford W Daigneault   +5 more
doaj   +1 more source

Genetic factors in the development of pulmonary embolism

open access: yesРоссийский кардиологический журнал, 2022
The article presents a literature review on the study of the relationship of FGA, FGB, F2, F5, PAI, ITGA2 gene polymorphisms with the development of pulmonary embolism (PE).
N. M. Kryuchkova   +3 more
doaj   +1 more source

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