Results 11 to 20 of about 5,198,783 (315)

A survey of genetic improvement search spaces [PDF]

open access: yes, 2019
Genetic Improvement (GI) uses automated search to improve existing software. Most GI work has focused on empirical studies that successfully apply GI to improve software's running time, fix bugs, add new features, etc. There has been little research into
Alexander, B   +17 more
core   +1 more source

Genetic influences on exercise participation in 37.051 twin pairs from seven countries [PDF]

open access: yes, 2006
Background A sedentary lifestyle remains a major threat to health in contemporary societies. To get more insight in the relative contribution of genetic and environmental influences on individual differences in exercise participation, twin samples from ...
Hunkin, J   +116 more
core   +3 more sources

Molecular Mechanisms in Autoimmune Thyroid Disease

open access: yesCells, 2023
The most common cause of acquired thyroid dysfunction is autoimmune thyroid disease, which is an organ-specific autoimmune disease with two presentation phenotypes: hyperthyroidism (Graves-Basedow disease) and hypothyroidism (Hashimoto’s thyroiditis ...
Hernando Vargas-Uricoechea
doaj   +1 more source

Microsatellite Loci Reveal Heterozygosis and Population Structure in the Critically Endangered Southern River Terrapin (Batagur affinis ssp.) of Peninsular Malaysia

open access: yesChemistry Proceedings, 2022
These freshwater turtles are found across Indochina, mostly in large rivers. There is a lack of genetic research concentrating on Malaysia’s southern river terrapin (Batagur affinis) population.
Mohd Hairul Mohd Salleh, Yuzine Esa
doaj   +1 more source

Genetic ties and genetic mixups [PDF]

open access: yesJournal of Medical Ethics, 2003
In a recent case in Great Britain, a couple described as “white” underwent in vitro fertilisation and gave birth to twins described as “black”. In the sense of a fair adjudication of this particular case, serving justice requires a thick description and a sensitive understanding of the relevant facts.
T H, Murray, G E, Kaebnick
openaire   +2 more sources

Discovery of Sexual Dimorphisms in Metabolic and Genetic Biomarkers [PDF]

open access: yes, 2011
Metabolomic profiling and the integration of whole-genome genetic association data has proven to be a powerful tool to comprehensively explore gene regulatory networks and to investigate the effects of genetic variation at the molecular level.
Polonikov, Alexey   +75 more
core   +1 more source

Congenital solitary kidney in autosomal dominant polycystic kidney disease: Where do known genes end and the unknown begin?

open access: yesClinical Case Reports, 2023
Key Clinical Message We present the case of a 41‐year‐old man patient diagnosed with solitary left kidney with few cysts. He has a family history of unilateral renal agenesis (URA) but no for autosomal dominant polycystic kidney disease (ADPKD).
Romina Bucci   +7 more
doaj   +1 more source

Regional issues on animal genetic resources: trends, policies and networking in Europe [PDF]

open access: yes, 2010
European countries are individually and in collaboration carrying out active work on animal genetic resources (AnGR). The region has a very good starting point for work on AnGR: The breed concept was developed in Europe; current European mainstream ...
A. Mäki-Tanila   +5 more
core   +1 more source

Genetics of melanoma [PDF]

open access: yesFrontiers in Genetics, 2013
Genomic variation is a trend observed in various human diseases including cancer. Genetic studies have set out to understand how and why these variations result in cancer, why some populations are pre-disposed to the disease, and also how genetics affect drug responses. The melanoma incidence has been increasing at an alarming rate worldwide.
Wangari-Talbot, Janet, Chen, Suzie
openaire   +3 more sources

Revisiting genetic artifacts on DNA methylation microarrays exposes novel biological implications [PDF]

open access: yes, 2021
Background: Illumina DNA methylation microarrays enable epigenome-wide analysis vastly used for the discovery of novel DNA methylation variation in health and disease.
Vidaki, Athina   +9 more
core   +2 more sources

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