An experiment was carried out with 231 chickens of the Leghorn breed, 177--of the Cornish breed, and 532--of the White Plymouth Rock breed. In order to check the resistance of the birds to typhoid all of them were infected orally at the age of 2.5 months with an 18-hour broth culture of Salmonella gallinarum. Depending on the clinical course of the disease and the results of the bacteriologic investigations the birds were divided into three groups: A--chickens that did not develop the infection; B--survivors; and C--birds that died. The total protein in the serum was determined by the classical method of Kingsley, the protein spectrum--through electrophoresis in agar by the microexpress method of Wieme, and the antibody production--by the classical serum agglutination test. Differences were established in the level of the total globulins as well as in that of alfa, beta, and gamma globulins and the albumins and total protein in dependence on the resistance of chickens to Salmonella gallinarum. These changes were more slightly expressed in the birds that did not develop the disease, and were more strongly expressed in those that died. There were also breed-associated differences as to the deviations of the protein spectrum indices in relation to the resistance to typhoid. A correlation was also established between the level of globulins and the antibody production.
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Neuropsychopharmacol Rep
March 2025
Department of Psychiatry, School of Medicine, and Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
Background: Contactin-5 (CNTN5), a neural adhesion molecule involved in synaptogenesis and synaptic maturation in the auditory pathway, has been associated with the pathophysiology of autism spectrum disorder (ASD), particularly hyperacusis. To investigate the role of rare CNTN5 variants in ASD susceptibility, we performed resequencing and association analysis in a Japanese population.
Methods: We resequenced the CNTN5 coding regions in 302 patients with ASD and prioritized rare putatively damaging variants.
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Gilead Sciences, Inc., Foster City, California, USA.
Obeldesivir is an oral nucleoside analog prodrug inhibitor of SARS-CoV-2 RNA-dependent RNA polymerase and other viral polymerases. Here, two Phase I studies evaluated potential drug-drug interactions between obeldesivir and substrates or inhibitors of cytochrome P450 and drug transporters in healthy participants. When obeldesivir was tested as a precipitant, pharmacokinetic parameter point estimates for midazolam (CYP3A4 inhibition/induction), caffeine (CYP1A2 inhibition), and metformin (organic cation transporter 1 inhibition) exposures were within 80-125% no-effect bounds representing the interval within which a systemic exposure change does not warrant clinical action based on EMA/FDA guidance.
View Article and Find Full Text PDFVopr Pitan
January 2025
Research Institute for Medical Problems in the North - Division of Federal Research Center "Krasnoyarsk Scientific Center of the Siberian Branch of the Russian Academy of Sciences", 660022, Krasnoyarsk, Russian Federation.
Rosacea is a chronic skin disease in which a violation of its barrier function can lead to the penetration of various allergens that normally do not penetrate, and as a result, the development of sensitization. The study of the spectrum of sensitization to food allergens in patients with rosacea is especially relevant, since it can contribute to the discovery of new disease triggers and determine a personalized approach to therapy. of the research was to study the features of the spectrum of sensitization to food and pollen (cross-reacting) allergens in patients with rosacea.
View Article and Find Full Text PDFNeurol Genet
February 2025
Department of Neurology, Adjunct Medicine, Division Medical Genetics, University of Washington, Seattle.
Alzheimer disease (AD), the most common dementing syndrome in the United States, is currently established by the presence of amyloid-β and tau protein biomarkers in the setting of clinical cognitive impairment. These straightforward diagnostic parameters belie an immense complexity of genetic architecture underlying risk and presentation in AD. In this review, we provide a focused overview of the current state of AD genetics.
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