Zobrazeno 1 - 10
of 158
pro vyhledávání: '"candidate gene studies"'
Publikováno v:
Eating and Weight Disorders, Vol 29, Iss 1, Pp 1-16 (2024)
Abstract Purpose Several studies have investigated the association between anorexia nervosa and polymorphisms of genes regulating serotonin neurotransmission, with a focus on the rs6311 polymorphism of 5-HTR2A. However, inconsistent results of these
Externí odkaz:
https://doaj.org/article/b8356f15e7854492a105cb67a24d060b
Publikováno v:
Journal of Education, Health and Sport, Vol 59 (2024)
Introduction and objective: The purpose of this paper is a systematic review of articles and research in the context of the relationship between genetic determinants of migraine and thyroid dysfunction. Materials and methods: A non-systematic revie
Externí odkaz:
https://doaj.org/article/8b6f6ea0f5f744ed964f9480066bf4f0
Publikováno v:
Pharmacogenomics and Personalized Medicine, Vol Volume 13, Pp 89-103 (2020)
Javier Perez-Garcia,1 Antonio Espuela-Ortiz,1 Fabian Lorenzo-Diaz,1,2 Maria Pino-Yanes1,3,4 1Genomics and Health Group, Department of Biochemistry, Microbiology, Cell Biology and Genetics, Universidad de La Laguna, San Cristóbal de La Laguna, Santa
Externí odkaz:
https://doaj.org/article/413eaf96b5ed46b9a6c08d2763426452
Autor:
Zukić Branka, Anđelković Marina, Gašić Vladimir, Grubin Jasmina, Pavlović Sonja, Đerić Dragoslava
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 148, Iss 9-10, Pp 621-625 (2020)
Introduction. Otosclerosis is a disorder of the bone labyrinth and stapes resulting in conductive hearing loss. The genetic basis of otosclerosis still remains unknown. We aimed at reporting a comprehensive review of up-to-date knowledge on genetic b
Externí odkaz:
https://doaj.org/article/8ba6a2b82b1a427bad233d257fd773d6
Publikováno v:
Lipids in Health and Disease, Vol 16, Iss 1, Pp 1-22 (2017)
Abstract Hypercholesterolemia is a strong determinant of mortality and morbidity associated with cardiovascular diseases and a major contributor to the global disease burden. Mutations in four genes (LDLR, APOB, PCSK9 and LDLRAP1) account for the maj
Externí odkaz:
https://doaj.org/article/8236b2976aa94432b277ae03c06fb277
Autor:
Cuch Barbara, Polaczek Anna, Idziak Magdalena, Kotuła Lidia, Maciejewski Ryszard, Madej-Czerwonka Barbara, Kocki Janusz
Publikováno v:
Current Issues in Pharmacy and Medical Sciences, Vol 28, Iss 2, Pp 115-119 (2015)
Attention Deficit Hyperactivity Disorder is the full name of the disease commonly deemed ADHD. This disease is most frequently diagnosed in childhood, and it affects up to 12 % of all children world-wide. The current clinical criteria (the base for d
Externí odkaz:
https://doaj.org/article/1606913b2cb4473292aecc80725c6996
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Branka Zukic, Jasmina Grubin, Marina Andjelkovic, Vladimir Gasic, Dragoslava Djeric, Sonja Pavlovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 148, Iss 9-10, Pp 621-625 (2020)
Introduction. Otosclerosis is a disorder of the bone labyrinth and stapes resulting in conductive hearing loss. The genetic basis of otosclerosis still remains unknown. We aimed at reporting a comprehensive review of up-to-date knowledge on genetic b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c4fd86dd62f8767fcc709c928b06a3c
http://www.doiserbia.nb.rs/img/doi/0370-8179/2020/0370-81792000026Z.pdf
http://www.doiserbia.nb.rs/img/doi/0370-8179/2020/0370-81792000026Z.pdf
Autor:
Marie Udnesseter Lie, Linda Margareth Pedersen, Ingrid Heuch, Bendik Winsvold, Johannes Gjerstad, Eivind Hasvik, Øystein Petter Nygaard, Margreth Grotle, Dagfinn Matre, John-Anker Zwart, Kristian Bernhard Nilsen
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2022)
Frontiers in Genetics, Vol 12 (2022)
In a recently published genome-wide association study (GWAS) chronic back pain was associated with three loci; SOX5, CCDC26/GSDMC and DCC. This GWAS was based on a heterogeneous sample of back pain disorders, and it is unknown whether these loci are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84b0f6243ef03fc6c3048f455b853e56
http://hdl.handle.net/10852/94886
http://hdl.handle.net/10852/94886
