Zobrazeno 1 - 10
of 105
pro vyhledávání: '"molecular-genetic studies"'
Publikováno v:
Сахарный диабет, Vol 23, Iss 4, Pp 329-339 (2020)
The review focuses on the new WHO classification published in 2019. Unlike the previous classification, this classification does not recognize subtypes of T1DM and T2DM and offers new types of diabetes: “hybrid types of diabetes” and “unclassif
Externí odkaz:
https://doaj.org/article/2ee149cb621347f4a5240cfd954e3a2a
Publikováno v:
Hitit Medical Journal, Vol 2, Iss 2, Pp 49-55 (2020)
Bireylerin mevcut biyolojik cinsiyetlerinden hoşnutsuzlukları ve karşıt cinsiyete ait hissetme durumu cinsiyet disforisi olarak tanımlanır. Bu davranış özelliğinin oluşmasında çevresel birçok faktörün yanı sıra kişilerin kendine ha
Externí odkaz:
https://doaj.org/article/89d8947a9e0f48a2be111769ee8b5073
Publikováno v:
Mìžnarodnij Endokrinologìčnij Žurnal, Vol 16, Iss 4, Pp 355-360 (2020)
The preoperative diagnosis of differentiated thyroid cancer (DTC) remains an urgent problem. During cytological evaluation of thyroid nodes, it is impossible to distinguish clearly benign and malignant pathology in 5–20 % of cases, which is especia
Externí odkaz:
https://doaj.org/article/cf7fd2190e43458eb167315227f4b00b
Publikováno v:
Klinicist, Vol 14, Iss 1-2, Pp 34-41 (2020)
Calcific aortic stenosis is a common heart disease and the most common cause of surgical interventions on heart valves in old age. Eliminated course, nonspecific clinical symptoms, and late patients seeking surgical help, lead to high mortality, reac
Externí odkaz:
https://doaj.org/article/bd3fcd8212334318b6a76e787302d871
Autor:
D. R. Kaydarova, K. K. Smagulova, N. A. Chichua, E. A. Ukolova, A. Z. Kurmankulova, E. I. Ishkinin
Publikováno v:
Сибирский онкологический журнал, Vol 19, Iss 1, Pp 82-89 (2020)
In 2016 3158 patients with colorectal cancer (CRC) were registered in the Republic of Kazakhstan, out of them, 1,484 patients died. Colorectal and colon cancers are the 8th and the 5th leading causes of mortality, respectively. One of the most signif
Externí odkaz:
https://doaj.org/article/d1d56d860aac43259d50f78cf3b004db
Publikováno v:
Эпидемиология и вакцинопрофилактика, Vol 18, Iss 5, Pp 33-41 (2019)
Relevance. Annual elevation of enterovirus infection (EVI) incidence in the Russian Federation as well as in the Sakhalin region determine a necessity of continuous surveillance involving molecular-genetic methods and phylogenetic analysis. Objective
Externí odkaz:
https://doaj.org/article/59dc21d5fae84d6d866a6ee7f5ec779b
Molecular-genetic investigations of sturgeon (Acipenseridae). Thematic English language bibliography
Autor:
M. Simon
Publikováno v:
Ribogospodarsʹka Nauka Ukraïni, Iss 4(46), Pp 102-123 (2018)
Purpose. Forming a thematic bibliographic list of English-language publications on certain issues of molecular genetic and cytogenetic studies of sturgeon (Acipenseridae). Methods. The complete and selective methods were applied in the process of
Externí odkaz:
https://doaj.org/article/2efe84d880ee43828634ab5303972e45
Publikováno v:
Репродуктивная эндокринология, Iss 42, Pp 16-20 (2018)
Phenylketonuria (PKU) is a congenital, genetically determined metabolic disorder of the essential amino acid phenylalanine (PA). PKU is caused by mutation in the phenylalanine hydroxylase gene (PAH). In different populations PKU affects about one in
Externí odkaz:
https://doaj.org/article/15fd6f45a52544cfb3879a133deb57a2
Publikováno v:
Brain Sciences, Vol 12, Iss 1, p 27 (2021)
Dyslexia, a specific reading disability, is a common (up to 10% of children) and highly heritable (~70%) neurodevelopmental disorder. Behavioral and molecular genetic approaches are aimed towards dissecting its significant genetic component. In the p
Externí odkaz:
https://doaj.org/article/2f489852c73e4df69fe581bf2d60e563
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