Results 1 to 10 of about 519,404 (274)

Allele interaction--single locus genetics meets regulatory biology. [PDF]

open access: goldPLoS ONE, 2010
BACKGROUND: Since the dawn of genetics, additive and dominant gene action in diploids have been defined by comparison of heterozygote and homozygote phenotypes.
Arne B Gjuvsland   +3 more
doaj   +8 more sources

Genetics of the Rh-Hr Locus in Humans [PDF]

open access: bronzeActa geneticae medicae et gemellologiae, 1975
An analysis is attempted to throw more light on the inheritance of rhesus factor in humans and the Fisher-Race and Wiener's concepts are respectively evaluated.It is claimed that the Rh-Hr locus is not comprised of the recombination of C, D, E, c and e genes, much less the help of the auxiliary (d) which merely appears to be a conventional approach ...
Syed Shane Raza Zaidi   +2 more
openalex   +4 more sources

Genetics of the relB locus in Escherichia coli [PDF]

open access: bronzeJournal 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
openalex   +4 more sources

A genetic locus for paranoia [PDF]

open access: yesBiology Letters, 2018
The psychological effects of brain-expressed imprinted genes in humans are virtually unknown. Prader–Willi syndrome (PWS) is a neurogenetic condition mediated by genomic imprinting, which involves high rates of psychosis characterized by hallucinations and paranoia, as well as autism.
Bernard Crespi   +3 more
openaire   +2 more sources

Lack of variation at phosphoglucose isomerase (pgi) in bumblebees: implications for conservation genetics studies. [PDF]

open access: yesPLoS ONE, 2013
Assessing genetic variation underlying ecologically important traits is increasingly of interest and importance in population and conservation genetics. For some groups generally useful markers exist for examining the relative role of selection and drift
Jonathan S Ellis   +2 more
doaj   +1 more source

Genetic Elements at the Alpha-Synuclein Locus

open access: yesFrontiers in Neuroscience, 2022
Genome-wide association studies have consistently shown that the alpha-synuclein locus is significantly associated with Parkinson’s disease. The mechanism by which this locus modulates the disease pathology and etiology remains largely under-investigated.
Jordan Prahl, Gerhard A. Coetzee
openaire   +3 more sources

Genetic variability at the PARK16 locus [PDF]

open access: yesEuropean Journal of Human Genetics, 2010
Parkinson's disease (PD) is a complex neurodegenerative disease which is clinically heterogeneous and pathologically consists of loss of dopaminergic neurons in the substantia nigra and intracytoplasmic neuronal inclusions containing alpha-synuclein aggregations known as Lewy bodies.
Tamas Revesz   +7 more
openaire   +3 more sources

Genetic Imprinting: Conflict at the Callipyge Locus [PDF]

open access: yesCurrent Biology, 2005
The imprinted Dlk1-Gtl2 region of the mammalian genome - which in sheep encompasses the Callipyge locus, known for its unusual mode of inheritance - encodes a number of maternally expressed miRNAs. Five of these miRNAs, hosted by the antisense transcript antiPeg11, have now been shown to target degradation of the paternally expressed Peg11 mRNA by an ...
Annabelle Lewis, Lisa Redrup
openaire   +3 more sources

The Gene Encoding Dihydroflavonol 4-Reductase Is a Candidate for the anthocyaninless Locus of Rapid Cycling Brassica rapa (Fast Plants Type). [PDF]

open access: yesPLoS ONE, 2016
Rapid cycling Brassica rapa, also known as Wisconsin Fast Plants, are a widely used organism in both K-12 and college science education. They are an excellent system for genetics laboratory instruction because it is very easy to conduct genetic crosses ...
Douglas L Wendell   +2 more
doaj   +1 more source

A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk

open access: yesScientific Reports, 2022
Genome-wide association studies (GWAS) have identified many common variant loci associated with asthma susceptibility, but few studies investigate the genetics underlying moderate-to-severe asthma risk.
Diana Chang   +23 more
doaj   +1 more source

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