Zobrazeno 1 - 10
of 198
pro vyhledávání: '"Genetic Examination"'
Autor:
Sylvia Cherninkova, Boryana Zaharova, Kunka Kamenarova, Kalina Mihova, Slavena Atemin, Tihomir Todorov, Vasil Haykin, Alexander Oscar, Ivailo Tournev, Radka Kaneva, Albena Todorova
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 37, Iss 1 (2023)
AbstractLeber’s hereditary optic neuropathy (LHON) is a rare maternally inherited disease caused by mutations in mitochondrial DNA (mtDNA) genes encoding subunits of complex I in the mitochondrial respiratory chain. The most common mutations causin
Externí odkaz:
https://doaj.org/article/4ca00a1855a9411e9a9c632f17e2074f
Autor:
Taira Hada, Morikazu Miyamoto, Yuka Ohtsuka, Jin Suminokura, Tsubasa Ito, Naohisa Kishimoto, Soko Nishitani, Minori Takada, Akari Imauji, Risa Tanabe, Masashi Takano
Publikováno v:
Diagnostic Pathology, Vol 18, Iss 1, Pp 1-6 (2023)
Abstract Background Mucinous carcinoma (MC) is a histological subtype of ovarian cancer that has a worse prognosis at advanced stages than the most prevalent histological subtype, high-grade serous carcinomas. Invasive patterns have been recognized a
Externí odkaz:
https://doaj.org/article/7859204bcddb4f4dbbb376c93858a7a7
Autor:
R. L. Stepaniuk, V. V. Kikinchuk
Publikováno v:
Вісник Харківського національного університету внутрішніх справ, Vol 97, Iss 2, Pp 234-249 (2022)
An analysis of European standards and main trends in the field of legal regulation of forensic DNA analysis has been carried out. It has been established that the general European legislation defines recommendations on the general principles of using
Externí odkaz:
https://doaj.org/article/d52341e46ded49418af3c7c61966f74e
Autor:
Fidan A. Aghayeva, Alexander K. Schuster, Heidi Diel, Panagiotis Chronopoulos, Felix M. Wagner, Franz Grehn, Nina Pirlich, Susann Schweiger, Norbert Pfeiffer, Esther M. Hoffmann
Publikováno v:
BMC Research Notes, Vol 15, Iss 1, Pp 1-10 (2022)
Abstract Objective The aim of this prospective pilot study is to establish an initial database to register patients diagnosed with different types of childhood glaucoma and the set-up of a national registry for childhood glaucoma (ReCG) in Germany. 2
Externí odkaz:
https://doaj.org/article/836cfc6dbb7948f5b75ce3aa8ffeb8e3
Autor:
Ya. O. Sinitsyna
Publikováno v:
Вісник Харківського національного університету внутрішніх справ, Vol 93, Iss 2, Pp 303-312 (2021)
The article is focused on the problem of studying mixed biological traces during the research of the growing number and severity of sexual crimes. The presence of blood and epithelial cells with a small amount of sperm on things removed at the crime
Externí odkaz:
https://doaj.org/article/4368b84bdb894374a450d0437bc6a119
Autor:
S. O. Ziubrii
Publikováno v:
Вісник Харківського національного університету внутрішніх справ, Vol 93, Iss 2, Pp 276-287 (2021)
The article is focused on the procedure of sampling as a criminal procedural action necessary for the commissioning and carrying out molecular genetic expert examination in the divisions of the Expert Service of the Ministry of Internal Affairs, name
Externí odkaz:
https://doaj.org/article/c144ba5af2e94b11b2b9fabf07a53378
Publikováno v:
European Psychiatry, Vol 65, Pp S387-S388 (2022)
Introduction Histamine intolerance (HI) is a disorder associated with an impairment of ability to metabolize ingested histamine. The incidence of HI in general population is 1-3%. Clinical manifestation of HI contains nonspecific predominantly gastro
Externí odkaz:
https://doaj.org/article/f236adc4de5e469db8f56913e878ad13
Autor:
I. V. Kornienko, K. V. Stepanov, T. G. Faleeva, V. S. Rakuts, I. N. Ivanov, E. S. Mishin, N. V. Kononov, N. E. Levchenko, Y. S. Sidorenko
Publikováno v:
Теория и практика судебной экспертизы, Vol 14, Iss 2, Pp 107-114 (2019)
The question of whether it is appropriate to classify genetic examinations of kinship as a medical service is considered in the article. Establishment of identity of an unknown individual (alive or dead) with a specific person is a classic example of
Externí odkaz:
https://doaj.org/article/22c0e2d801994cce98e1a6281f4fc54c
Autor:
A.N. Volkov, E.V. Tsurkan
Publikováno v:
Analiz Riska Zdorovʹû, Iss 2, Pp 123-129 (2019)
Gilbert's syndrome is a widely spread multi-factor pathology which is to a great extent genetically determined. Its basic etiological factor is lower activity of a liver enzyme, UDP-glucuronosyltransferase A1, caused by mutations in UGT1A1 gene. Func
Externí odkaz:
https://doaj.org/article/25755d6e500b4688a194c1b9d20e3c1d
Autor:
Yasuhiro Murata, Katsuhiko Ando, Masanobu Usui, Hiromu Sugiyama, Akinobu Hayashi, Akihiro Tanemura, Hiroyuki Kato, Naohisa Kuriyama, Masashi Kishiwada, Shugo Mizuno, Hiroyuki Sakurai, Shuji Isaji
Publikováno v:
BMC Infectious Diseases, Vol 18, Iss 1, Pp 1-7 (2018)
Abstract Background Anisakid nematodes (Anisakis spp. or Pseudoterranova spp.) usually infect gastric or intestinal walls, while they rarely infect in extra-gastrointestinal sites of human body. Generally, Anisakis spp. larvae are highly infected in
Externí odkaz:
https://doaj.org/article/9c780f50ec5742788ced66681ffa21ab