Results 81 to 90 of about 28,399 (219)

Three-marker window haplotype analysis.

open access: yes, 2018
Three-marker window haplotype analysis.
Hend Hachicha (5410700)   +15 more
core   +1 more source

Genomic Structural Variations Provide Insights Into Litter Size and Teat Number Traits in Hu Sheep

open access: yesAnimal Research and One Health, EarlyView.
Here, we conducted whole genome sequencing on 300 Hu sheep with an average depth of 16.51X. Two candidate genes associated with litter size and teat number traits were identified, namely MAST2 and AFDN. ABSTRACT Litter size and the teat number are important economic indicators in sheep production.
Xin Xiang   +3 more
wiley   +1 more source

Higher Complement C4 Gene Copy Number Constitutes a Shared Genetic Risk Factor for Giant Cell Arteritis and IgA Vasculitis

open access: yesArthritis &Rheumatology, EarlyView.
Objective Low copy number (CN) of complement C4 isoforms and high CN of retroviral HERV‐K elements are known risk factors for many immune‐mediated inflammatory diseases (IMIDs), often showing sex‐biased effects. Here, we assessed whether CN variation within the C4 gene contributes to giant cell arteritis (GCA) and IgA vasculitis (IgAV), two complex ...
Laura Martínez‐Gutiérrez   +295 more
wiley   +1 more source

Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect

open access: yesMolecular Genetics & Genomic Medicine, 2019
Background Dysferlinopathies are a group of autosomal recessive limb‐girdle muscular dystrophies (LGMDs) caused by mutations in DYSF (#603,009). This gene encodes a transmembrane protein called dysferlin.
Marzieh Mojbafan   +5 more
doaj   +1 more source

Haplotype analysis of risk alleles.

open access: yes, 2019
Haplotype analysis of risk alleles.
Gergely Keszler (494131)   +5 more
core   +1 more source

Pharmacogenomic profiling of the efficacy of gemcitabine monotherapy in metastatic pancreatic cancer: Subgroup analysis of the GENESECT study

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Aim In the GENESECT study, no significant gemcitabine (GEM) metabolism‐related germline genetic polymorphisms (GPs) were identified because approximately 70% of patients received combination therapy with nab‐paclitaxel, which has metabolic pathways different from GEM.
Takashi Yokokawa   +21 more
wiley   +1 more source

Genome-wide identification and characterization of soybean GH9 endo-1,4-β-glucanases

open access: yesFrontiers in Plant Science
Cellulases are a crucial class of enzymes involved in cellulose synthesis and metabolism, significantly contributing to plant growth, development, and organ abscission. The role of Glycosyl hydrolase family 9 (GH9), a major gene family encoding cellulase,
Weimin Zhan   +9 more
doaj   +1 more source

Haplotype association analysis.

open access: yes, 2015
a HE2 = Hemorrhagic fever—2 or more symptomsb any3 = Any 3 or more symptomsHaplotype association analysis.
Laura J. Sutherland (209354)   +11 more
core   +1 more source

Haplotype analysis of NOS3 polymorphisms.

open access: yes, 2020
Haplotype analysis of NOS3 polymorphisms.
Faisal A. Almobarak (8269281)   +5 more
core   +1 more source

Risk of venous thromboembolism after SARS‐CoV‐2 vaccination—Evidence from genome‐wide association study and population‐based observational study

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Aim We aimed to investigate whether genetic variation is associated with venous thromboembolism after immunization with SARS‐CoV‐2 vaccines. Methods We conducted a genome‐wide association study (GWAS) on cases of venous thromboembolism within 42 days after SARS‐CoV‐2 vaccination, recruited from reports of adverse drug reactions sent to the Swedish ...
Sofia Attelind   +7 more
wiley   +1 more source

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