Zobrazeno 1 - 10
of 1 052
pro vyhledávání: '"9p21"'
Autor:
Tammy Anderson, Sharon Hartman, William Dunn, Harvey Bellin, Thomas W. Ehlers, Sarah Groen, Jason A. Ramos
Publikováno v:
Cancer Cell International, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background This study aims to compare the technical performance of Abbott’s UroVysion and Biocare’s CytoFISH urine cytology probe panel and position the CytoFISH probe panel as an alternative to UroVysion. The CytoFISH probe panel was de
Externí odkaz:
https://doaj.org/article/970b64c1cdf54f55b31f94f320fcf9d1
Akademický článek
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Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Single nucleotide polymorphisms in the 9p21 region have been associated with cardiovascular disease and to a lesser extent insulin sensitivity. Previous studies have focused on older populations, and few have examined the impact of gene-d
Externí odkaz:
https://doaj.org/article/3be213c742d14a06a16476746a701f07
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/61bc229d6c2a4d5c9c05217185e61e07
Autor:
Umer Farooq, Dimple Notani
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
9p21 locus is one of the most reproducible regions in genome-wide association studies (GWAS). The region harbors CDKN2A/B genes that code for p16INK4a, p15INK4b, and p14ARF proteins, and it also harbors a long gene desert adjacent to these genes. The
Externí odkaz:
https://doaj.org/article/4dbb5a24a5c4423c97722a48394f609a
Publikováno v:
International Journal of General Medicine, Vol Volume 14, Pp 1699-1707 (2021)
Neda Bogari,1 Anas Dannoun,1 Mohammad Athar,1,2 Osama Elkhateeb,3,4 Massimo Porqueddu,5,6 Reem Allam,7 Francesco Alamanni6 1Department of Medical Genetics, Faculty of Medicine, Umm Al-Qura University, Makkah, Kingdom of Saudi Arabia; 2Science and Tec
Externí odkaz:
https://doaj.org/article/67d06cdd777341809c47887576c98c04
Autor:
Anja Trillhaase, Beatrice Schmidt, Marlon Märtens, Undine Haferkamp, Jeanette Erdmann, Zouhair Aherrahrou
Publikováno v:
Stem Cell Research & Therapy, Vol 12, Iss 1, Pp 1-12 (2021)
Abstract Background Coronary artery disease (CAD) is the leading cause of death worldwide. Chromosome locus 9p21 was the first to be associated with increased risk of CAD and coronary artery calcification (CAC). Vascular calcification increases the r
Externí odkaz:
https://doaj.org/article/f24270848db44a4c81e8b4b3bfb582b0
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Several studies have reported that chromosome 9p21 is significantly associated with ischemic stroke (IS) risk, with the G allele associated with increased risk. However, controversial results have been reported in the literature. We systematically as
Externí odkaz:
https://doaj.org/article/737c15f87e044a059f1357b918fc3241
Autor:
Lei Hua, Jin-Xia Yuan, Shu He, Chen-Hui Zhao, Qiao-Wei Jia, Jing Zhang, Feng-Hui An, Zhao-Hong Chen, Li-Hua Li, Lian-Sheng Wang, Wen-Zhu Ma, Guang-Xu Xu, En-Zhi Jia
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Rs4977574 (A > G) and Rs1333045 (C > T) are both single nucleotide polymorphisms (SNPs) related with coronary artery disease, locating on chromosome 9p21.3. The study aimed to identify the correlation between rs4977574 and rs13330
Externí odkaz:
https://doaj.org/article/a319e958888e42f8815bef436c6ecf9e
Akademický článek
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