Zobrazeno 1 - 10
of 89
pro vyhledávání: '"FPRP"'
Publikováno v:
Pharmacogenomics and Personalized Medicine, Vol Volume 15, Pp 827-842 (2022)
Shuyong Yu,1,* Guihong Yuan,2,* Feixiang Hu,1,* Yongyu Li,2 Zhuang Chen,2 Ronglin Zhang,3 Ping Li,3 Zhaowei Chen,2 Jian Song4 1Department of Gastrointestinal Surgery, Hainan Cancer Hospital, Haikou, 570100, People’s Republic of China; 2
Externí odkaz:
https://doaj.org/article/cac7c02584de4de98177ad072a28244d
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Background: Studies have shown that glutathione S-transferase M1 (GSTM1) and. glutathione S-transferase T1 (GSTT1) null genotype may increase the risk of cervical cancer (CC) or ovarian cancer (OC), however, the results of published original studies
Externí odkaz:
https://doaj.org/article/dad6a0cd90b04ce384820d389361e38c
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Numerous studies have demonstrated an association between osteoprotegerin (OPG) polymorphisms (A163G (rs3102735), T245G (rs3134069), T950C (rs2073617), G1181C (rs2073618)) and osteoporosis risk. However, their conclusions are inconsistent
Externí odkaz:
https://doaj.org/article/7a6b29ef449f4cd39f37e82e54cab1cf
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Fourteen meta-analyses reported the individual effects of the GSTM1 and GSTT1 polymorphisms on leukemia risk. However, over 40 studies were not included in previously published meta-analyses. Moreover, one key aspect was that previous met
Externí odkaz:
https://doaj.org/article/bf3f32b2af364ecabad8590232afa2d2
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Numerous studies reported the associations between endothelial nitric oxide synthase (eNOS) polymorphisms (4b/a VNTR (rs869109213), G894T (rs1799983) and T786C (rs2070744)) and type 2 diabetes mellitus (T2DM) risk. However, the conclusion
Externí odkaz:
https://doaj.org/article/bb3dfc4115e84b09b3a27a74f59476a3
Publikováno v:
The Journal of Headache and Pain, Vol 21, Iss 1, Pp 1-15 (2020)
Abstract Objective Numerous genetic variants from meta-analyses of observational studies and GWAS were reported to be associated with migraine susceptibility. However, due to the random errors in meta-analyses, the noteworthiness of the results showi
Externí odkaz:
https://doaj.org/article/c77aaf0b683b49538a37d69de2c468c1
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Since the 1990s, there have been a lot of research on single-nucleotide polymorphism (SNP) and different diseases, including many studies on 5,10-methylenetetrahydrofolate reductase (MTHFR) polymorphism and essential hypertension (EH). Ne
Externí odkaz:
https://doaj.org/article/513beca431f74be897195683ae9ea0d6
Autor:
Jinhee Lee, Min Ji Son, Chei Yun Son, Gwang Hun Jeong, Keum Hwa Lee, Kwang Seob Lee, Younhee Ko, Jong Yeob Kim, Jun Young Lee, Joaquim Radua, Michael Eisenhut, Florence Gressier, Ai Koyanagi, Brendon Stubbs, Marco Solmi, Theodor B. Rais, Andreas Kronbichler, Elena Dragioti, Daniel Fernando Pereira Vasconcelos, Felipe Rodolfo Pereira da Silva, Kalthoum Tizaoui, André Russowsky Brunoni, Andre F. Carvalho, Sarah Cargnin, Salvatore Terrazzino, Andrew Stickley, Lee Smith, Trevor Thompson, Jae Il Shin, Paolo Fusar-Poli
Publikováno v:
Brain Sciences, Vol 10, Iss 10, p 692 (2020)
This study aimed to verify noteworthy findings between genetic risk factors and autism spectrum disorder (ASD) by employing the false positive report probability (FPRP) and the Bayesian false-discovery probability (BFDP). PubMed and the Genome-Wide A
Externí odkaz:
https://doaj.org/article/bc5b13cc1a8941d9bebcd3e2e34557a8
Autor:
Gross, Thomas
The project establishes the strength of evidence present in a systematically drawn sample of cyber security user studies, in terms of simulated posterior probabilities (PPV/FPRP), likelihood ratios (LRs) and reverse Bayesian priors (RBPs). It invetig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81de17957b9b06fc95277ee336aceab4
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