Zobrazeno 1 - 10
of 220
pro vyhledávání: '"new generation sequencing"'
Autor:
László Baráti, Anita Maász, Alexandra Mikó, Éva Bércesi, Sultan Al Kalbani, Judit Bene, Sebestyén Kovács, László Mangel, Kinga Hadzsiev
Publikováno v:
Pathology and Oncology Research, Vol 30 (2024)
Hereditary breast and ovarian cancer is a well-known genetic condition, inherited mainly in an autosomal dominant way, which elevates the risk of developing malignancies at a young age in heterozygous carriers. Advances in new generation sequencing h
Externí odkaz:
https://doaj.org/article/fb767625ea7a4894a3b07f00cc6af71e
Autor:
George L. Mendz
Publikováno v:
Applied Microbiology, Vol 3, Iss 4, Pp 1302-1338 (2023)
This study appraises the progress in the understanding of the composition of the vaginal microflora with a focus on the microbiome during pregnancy. This knowledge is presented with the background of the global health contribution, along with the imp
Externí odkaz:
https://doaj.org/article/4055885aa0e54aeda2a823e2453b636b
Autor:
Nathália Cristina Cirone Silva, Yongqiang Yang, Marjory Xavier Rodrigues, Tiago Tomazi, Rodrigo Carvalho Bicalho
Publikováno v:
BMC Veterinary Research, Vol 17, Iss 1, Pp 1-15 (2021)
Abstract Background Bovine mastitis is an important cause of economic loss in dairy farms. Streptococcus uberis is among the most frequently isolated bacterial species isolated from cows with mastitis. The aim of this study was to perform an in-depth
Externí odkaz:
https://doaj.org/article/3968972beb13448cae768ed76d526f52
Autor:
Iara Sant’ Ana, Renato Torrini, Maria Caroline Alves Coelho, Joyce Cantoni, Miguel Madeira, Márcia Ribeiro
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Background X‐linked hypophosphatemic rickets (XLHR) is a rare genetic disease, often delayed in diagnosis due to the low degree of suspicion and limited access to sophisticated diagnostic tools that confirm the diagnosis, such as genetic t
Externí odkaz:
https://doaj.org/article/d8339027b4b145c495240e49135b5c23
Autor:
T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 12, Iss 1, Pp 59-66 (2020)
Autism spectrum disorders (ASDs) are a group of complex disintegrative disorders of mental development, characterized by a lack of ability to social interaction, communication, stereotyped behavior, leading to social maladaptation. We present a rare
Externí odkaz:
https://doaj.org/article/05c85c96985147bc90352ef32e394e61
Akademický článek
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Akademický článek
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Autor:
Angelika V. Timofeeva, Aleksandra V. Asaturova, Maya V. Sannikova, Grigory N. Khabas, Vitaliy V. Chagovets, Ivan S. Fedorov, Vladimir E. Frankevich, Gennady T. Sukhikh
Publikováno v:
Life, Vol 12, Iss 12, p 2017 (2022)
Recent studies have attempted to develop molecular signatures of epithelial ovarian cancer (EOC) based on the quantitation of protein-coding and non-coding RNAs to predict disease prognosis. Due to the heterogeneity of EOC, none of the developed prog
Externí odkaz:
https://doaj.org/article/c68c76559e4a4eff8686fe342678f9c2
Autor:
M. Jauvain, E. Bessède
Publikováno v:
Microbiota in Health and Disease, Vol 3 (2021)
This past year, only a few articles concerning Helicobacter pylori endoscopic diagnosis were published but one aimed to develop a computer-aided diagnosis system based on linked color imaging. A meta-analysis also allowed to generate an algorithm use
Externí odkaz:
https://doaj.org/article/ef17b496ac544d488e2a1f2a2355af1c
Autor:
Buyuksimsek M, Togun M, Oguz Kara I, Bisgin A, Boga I, Tohumcuoglu M, Ogul A, Evren Yetisir A, Sahin B, Sumbul HE, Mirili C
Publikováno v:
Balkan Journal of Medical Genetics, Vol 22, Iss 2, Pp 17-24 (2019)
Several studies demonstrated the utility of plasma-based cell-free circulating tumor DNA (ccfDNA) in determination of mutations in non-small cell lung cancer (NSCLC). We aimed to report our results of next generation sequencing (NGS) using liquid bio
Externí odkaz:
https://doaj.org/article/b8150cdb158a48dabd74479f1fe9f638