Genetics of the relB locus in Escherichia coli [PDF]
Journal of Bacteriology, 1977 A mutant of Escherichia coli with a delayed relaxed phenotype very similar to that of a previously described relB mutant has been obtained using a new selection procedure. The mutation giving rise to this phenotype has been shown to map at 34.5 min and to be 12% cotransducible with man. It is recessive, revertible, and most likely an allele of the relB
B Diderichsen, Niels P. Fiil, R Lavallé
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Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy
Journal of Human Genetics, 2022 Amyotrophic lateral sclerosis (ALS) is an intractable disease that causes respiratory failure leading to mortality. The main locus of ALS is motor neurons.
N. Suzuki +3 more
semanticscholar +1 more source
BMC Plant Biology, 2020 Background Angelica dahurica (Apiaceae) is an important herb in traditional Chinese medicine. Because of its important medicinal and economic values, its wild resources were over-exploited and increasingly reduced.
Qianqian Liu +7 more
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An X-STRs analysis of the Iraqi Sorani Kurds.
PLoS ONE, 2023 A database for the Iraqi Sorani Kurds, specifically focused on the 12 X-short tandem repeat (STR) loci, has been developed to fascilitate forensic and population genetics investigations.
Balnd M Albarzinji +5 more
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A molecular quantitative trait locus map for osteoarthritis
Nature Communications, 2021 Osteoarthritis causes pain and functional disability for over 500 million people worldwide. To develop disease-stratifying tools and modifying therapies, we need a better understanding of the molecular basis of the disease in relevant tissue and cell ...
J. Steinberg +15 more
semanticscholar +1 more source
Increasing power for voxel-wise genome-wide association studies : the random field theory, least square kernel machines and fast permutation procedures [PDF]
, 2012 Imaging traits are thought to have more direct links to genetic variation than diagnostic measures based on cognitive or clinical assessments and provide a powerful substrate to examine the influence of genetics on human brains. Although imaging genetics
Feng, Jianfeng +4 more
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Allelic heterogeneity and trade-off shape natural variation for response to soil micronutrient [PDF]
, 2012 Peer reviewedPublisher ...
Andreatta, Matthew +6 more
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Frontiers in Aging Neuroscience, 2022 Alzheimer’s disease (AD) genetics studies have identified a coding variant within ABI3 gene that increases the risk of developing AD. Recently, we demonstrated that deletion of the Abi3 gene locus dramatically exacerbates AD neuropathology in a ...
Daniel C. Smith +16 more
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Towards precision medicine for hypertension: a review of genomic, epigenomic, and microbiomic effects on blood pressure in experimental rat models and humans [PDF]
, 2017 Compelling evidence for the inherited nature of essential hypertension has led to extensive research in rats and humans. Rats have served as the primary model for research on the genetics of hypertension resulting in identification of genomic regions ...
Allbutt TC +34 more
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The effect of recurrent mutations on genetic diversity in a large population of varying size [PDF]
, 2016 Recurrent mutations are a common phenomenon in population genetics. They may be at the origin of the fixation of a new genotype, if they give a phenotypic advantage to the carriers of the new mutation.
Smadi, Charline
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