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Mostrando ítems 61-70 de 1960
Imputation of microsatellite alleles from dense SNP genotypes for parentage verification across multiple Bos taurus and Bos indicus breeds
(2013)
To assist cattle producers transition from microsatellite (MS) to single nucleotide polymorphism (SNP) genotyping for parental verification we previously devised an effective and inexpensive method to impute MS alleles ...
Estimation of the Allele Frequency of Type 1 Polysaccharide Storage Myopathy and Malignant Hyperthermia in Quarter Horses in Brazil
(Elsevier B.V., 2018-11-01)
Type 1 polysaccharide storage myopathy (PSSM1) and malignant hyperthermia (MH) are autosomal dominant genetic diseases caused by a point mutation in equine GYS1 and RYR1, respectively. Although the prevalence of PSSM1 and ...
Whole Genome Shotgun Sequencing Shows Selection on Leptospira Regulatory Proteins During in vitro Culture Attenuation
(American Society of Tropical Medicine and Hygiene, 2016)
Leptospirosis is the most common zoonotic disease worldwide with an estimated 500,000 severe cases reported annually, and case fatality rates of 12-25%, due primarily to acute kidney and lung injuries. Despite its prevalence, ...
New Findings in the Amino Acid Profile and Gene Expression in Contrasting Durum Wheat Gluten Strength Genotypes during Grain Filling
(AMER CHEMICAL SOC, 2020)
Grain protein composition is important in wheat quality and may influence the amino acidic sequence of bioactive peptides obtained from this feedstock. However, the genetic basis modulating the amino acid profile in durum ...
Accurate and rapid species typing from cutaneous and mucocutaneous leishmaniasis lesions of the New World
(Elsevier, 2012)
The heat-shock protein 70 gene (hsp70) has been exploited for Leishmania species identification in the Old and New World, using polymerase chain reaction (PCR) followed by restriction fragment length polymorphism analysis. ...
Weak D antigen expression caused by a novel RHD allele in Argentineans
(Wiley Blackwell Publishing, Inc, 2016-11)
RHD polymorphism shows substantial ethnic variability. In this study, we report the novel RHD exon 3 c.359C>A mutation responsible for the amino acid change p.Ala120Asp found in 28 individuals from Argentina with weak D ...