Results 61 to 70 of about 1,486,266 (226)

Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human alpha-synuclein in transgenic mouse brain. [PDF]

open access: yes, 2009
Alpha-synuclein (SNCA) gene has been implicated in the development of rare forms of familial Parkinson disease (PD). Recently, it was shown that an increase in SNCA copy numbers leads to elevated levels of wild-type SNCA-mRNA and protein and is ...
Bernard, David J   +10 more
core   +2 more sources

A recessive allele for delayed flowering at the soybean maturity locus E9 is a leaky allele of FT2a, a FLOWERING LOCUS T ortholog

open access: yesBMC Plant Biology, 2016
BackgroundUnderstanding the molecular mechanisms of flowering and maturity is important for improving the adaptability and yield of seed crops in different environments. In soybean, a facultative short-day plant, genetic variation at four maturity genes,
Chen Zhao   +10 more
semanticscholar   +1 more source

Allele mining strategies: principles and utilisation for blast resistance genes in rice (Oryza sativa L.) [PDF]

open access: yes, 2015
Allele mining is a promising way to dissect naturally occurring allelic variants of candidate genes with essential agronomic qualities. With the identification, isolation and characterisation of blast resistance genes in rice, it is now possible to ...
Abdul Latif, Mohammad   +6 more
core  

Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa [PDF]

open access: yes, 2012
Objective: The common single nucleotide polymorphism (SNP) rs9939609 in the fat mass and obesity-associated gene (FTO) is associated with obesity. As genetic variants associated with weight regulation might also be implicated in the etiology of eating ...
André Scherag   +66 more
core   +4 more sources

Inheritance of a sign of apricot color of ray flowers of sunflower (Helianthus annuus L.)

open access: yesPlant Varieties Studying and Protection, 2019
Purpose. To reveal the nature of the inheritance of apricot color of the ray flowers of the sunflower and the type of interaction of genes causing different colors. Methods. Field experiment, genetic analysis. The statistical validity of the results was
К. В. Ведмедєва
doaj   +1 more source

Phenotypic and genotypic characterization of phosphate solubilizing bacteria and their efficiency on the growth of maize

open access: yesJournal of Genetic Engineering and Biotechnology, 2017
Phosphate solubilizing bacteria (PSB) has ability to convert insoluble form of phosphorous to an available form. Applications of PSB as inoculants increase the phosphorus uptake by plant in the agriculture field.
Amit Pande   +4 more
doaj   +1 more source

Spatiotemporal allele organization by allele-specific CRISPR live-cell imaging: SNP-CLING

open access: yesNature Structural & Molecular Biology, 2017
Imaging and chromatin capture techniques have provided important insights into our understanding of nuclear organization. A limitation of these techniques is the inability to resolve allele-specific spatiotemporal properties of genomic loci in living ...
Philipp G. Maass   +5 more
semanticscholar   +1 more source

Genetic variation analysis of superior cotton varieties of Gossypium hirsutum through microsatellite markers

open access: yesInternational Journal of Plant Biology, 2017
This study was conducted in order to obtain information on genetic variation in populations rated as superior cotton (Gossypium hirsutum L.) varieties in Balittas Malang, Indonesia.
Dede Nuraida   +3 more
doaj   +1 more source

Does the catechol-O-methyltransferase (COMT) Val158Met human polymorphism in influence procrastination? [PDF]

open access: yes, 2017
Genetic studies are enlightening how the expression of several genes influences neuronal activity and all facets of human normal and abnormal behaviour. Among these, a growing body of information shows that a few key genes regulating activity of central ...
Abate, Georgia   +3 more
core   +1 more source

TBX6 null variants and a common hypomorphic allele in congenital scoliosis.

open access: yesNew England Journal of Medicine, 2015
BACKGROUND Congenital scoliosis is a common type of vertebral malformation. Genetic susceptibility has been implicated in congenital scoliosis. METHODS We evaluated 161 Han Chinese persons with sporadic congenital scoliosis, 166 Han Chinese controls ...
N. Wu   +56 more
semanticscholar   +1 more source

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