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1.
Physiol Res ; 72(S3): S225-S232, 2023 10 27.
Artigo em Inglês | MEDLINE | ID: mdl-37888966

RESUMO

The aim of this narrative review is to summarize recent knowledge about the diagnostic significance of immunobiological detection of C3d with a focus on renal and skin tissue biopsies. We completed the present narrative review with our own experiences with preparation and practical use of monoclonal C3d antibodies at a small national level.


Assuntos
Transplante de Rim , Rim , Rim/patologia , Pele , Anticorpos Monoclonais
2.
J Appl Genet ; 50(4): 371-4, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19875887

RESUMO

Variation of the PrP gene was examined in healthy and BSE-affected Slovak cattle. According to previous studies, the 23-bp indel polymorphism is supposed to be associated with higher susceptibility to BSE. We investigated 301 samples from healthy cattle of various Slovak breeds and 24 samples obtained from tissues of BSE-affected cattle in Slovakia. We examined the PrP gene for the 23-bp indel polymorphism in the putative promoter region, 12-bp indel polymorphism in the first intron of the PrP gene, variations in number of octapeptide repeat units, and presence of the silent AAC>AAT transition in codon 192 within the protein-coding region of the PrP gene. Altogether we found 23 different genotypes in the group of healthy cattle and only 6 genotypes in the group of BSE-affected cattle. Comparison of homozygotes for the 23-bp insertion and heterozygotes showed significant differences (P < 0.05) in genotype distribution between the examined groups. Thereby the homozygous insertion genotype at the 23-bp indel polymorphism site in the promoter region of the prion protein gene seems to have a protective effect against BSE.


Assuntos
Encefalopatia Espongiforme Bovina/genética , Polimorfismo Genético , Príons/genética , Alelos , Animais , Sequência de Bases , Bovinos , Primers do DNA/genética , Encefalopatia Espongiforme Bovina/prevenção & controle , Feminino , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Heterozigoto , Homozigoto , Mutação INDEL , Íntrons , Masculino , Sequências Repetitivas de Aminoácidos , Eslováquia , Especificidade da Espécie
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