Results 71 to 80 of about 47,618 (305)

Detecção de fatores de virulência de Escherichia coli e análise de Salmonella spp. em psitacídeos Detection of virulence factors in Escherichia coli and analysis of Salmonella spp. in psittacines

open access: yesPesquisa Veterinária Brasileira, 2013
A flora entérica dos psitacídeos é composta principalmente por bactérias Gram positivas. Bactérias Gram negativas, como Escherichia coli e Salmonella spp., apresentam elevado potencial patogênico, sendo consideradas indicativo de problemas de manejo, que
Isadora M. de O. Corrêa   +5 more
doaj  

Sequencing genes in silico using single nucleotide polymorphisms [PDF]

open access: yes, 2012
Background The advent of high throughput sequencing technology has enabled the 1000 Genomes Project Pilot 3 to generate complete sequence data for more than 906 genes and 8,140 exons representing 697 subjects.
Xinyi Zhang   +5 more
core   +2 more sources

Functional and Structural Evidence of Neurofluid Circuit Aberrations in Huntington Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Disrupted neurofluid regulation may contribute to neurodegeneration in Huntington disease (HD). Because neurofluid pathways influence waste clearance, inflammation, and the distribution of central nervous system (CNS)–delivered therapeutics, understanding their dysfunction is increasingly important as targeted treatments emerge.
Kilian Hett   +8 more
wiley   +1 more source

The occurrence of the multidrug resistance (MDR) and the prevalence of virulence genes and QACs resistance genes in E. coli isolated from environmental and avian sources

open access: yesAMB Express, 2019
Colibacillosis is a major disease affecting poultry leads to high morbidity and mortality which causing tremendous economic losses worldwide. These economic disparities are amplified among low and middle-income where sanitation and hygiene are challenged
Mohamed E. Enany   +6 more
doaj   +1 more source

OR03-03 Whole Exome Sequencing (WES) in a Large Prospective Cohort of Idiopathic Short Stature (ISS): New Genes Implicated in the ISS Phenotype

open access: yesJournal of the Endocrine Society
Abstract Disclosure: L.D. Cellin: None. N.L. Andrade: None. A.C. Malaquias: None. R.C. Rezende: None. G.J. Kim: None. P.V. Atique: None. C.C. Luz: None. G.A. Vasques: None. V. Souza: None. E. Quedas: None. P.F. Collett-Solberg: None. S.R. Rauber Antonini: None. C. Longui: None. R.D. Scalco: None. A.A. Jorge: Novo Nordisk.
de Polli Cellin, Laurana   +14 more
openaire   +2 more sources

Gene expression variations during Drosophila metamorphosis in space. The GENE experiment in the Spanish Cervantes mission to the ISS

open access: yesJournal of gravitational physiology, 2005
Manuscript long version, prior to reduction due to the mandatory final 2-pages published version The ISS expedition 8, a 10 days “taxi” flight Soyuz Mission to the International Space Station (ISS) to replace the two-member ISS crew, took place during October 2003.
Herranz, R.   +6 more
openaire   +3 more sources

TBK1‐Associated Primary Lateral Sclerosis Followed by Right Temporal Variant Frontotemporal Dementia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We report a 58‐year‐old woman with a novel splice‐site variant in the TANK‐binding kinase 1 (TBK1:c.993–2A>C p.Ala332TyrfsTer39) who sequentially developed primary lateral sclerosis (PLS) followed by right temporal variant frontotemporal dementia (rtvFTD). Neuroimaging demonstrated right anterior temporal atrophy before cognitive symptoms, and
Tomoyasu Matsubara   +18 more
wiley   +1 more source

Development and Validation of a 9-Gene Prognostic Signature in Patients With Multiple Myeloma

open access: yesFrontiers in Oncology, 2019
Background: Multiple myeloma (MM) is one of the most common types of hematological malignance, and the prognosis of MM patients remains poor.Objective: To identify and validate a genetic prognostic signature in patients with MM.Methods: Co-expression ...
Xiao-Ping Liu   +5 more
doaj   +1 more source

Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce   +72 more
wiley   +1 more source

Studying Planarian Regeneration Aboard The International Space Station Within The Student Space Flight Experimental Program [PDF]

open access: yes, 2018
The growing possibilities of space travel are quickly moving from science fiction to reality. However, to realize the dream of long-term space travel, we must understand how these conditions affect biological and physiological processes.
Bartee, C.   +3 more
core   +2 more sources

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