Zobrazeno 1 - 10
of 85
pro vyhledávání: '"MAD1L1"'
Autor:
Aleksandr V. Sokolov, Diana-Maria Manu, Didi O. T. Nordberg, Adrian D. E. Boström, Jussi Jokinen, Helgi B. Schiöth
Publikováno v:
Clinical Epigenetics, Vol 15, Iss 1, Pp 1-23 (2023)
Abstract Depression is a multifactorial disorder representing a significant public health burden. Previous studies have linked multiple single nucleotide polymorphisms with depressive phenotypes and suicidal behavior. MAD1L1 is a mitosis metaphase ch
Externí odkaz:
https://doaj.org/article/995d929cbfba46debdb1c441217cf1c7
Autor:
Ying Chan, Yize Liu, Yamin Kong, Weiming Xu, Xiaohong Zeng, Haichun Li, Yan Guo, Xinhua Tang, Jinman Zhang, Baosheng Zhu
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: The genetic etiology of fetal chromosome abnormalities remains unknown, which brings about an enormous burden for patients, families, and society. The spindle assembly checkpoint (SAC) controls the normal procedure of chromosome disjuncti
Externí odkaz:
https://doaj.org/article/e2e63da7608444ba884310f4dc1de4ae
Autor:
Xianglai Liu, Hailing Xie, Zejuan Fu, Qiankun Yao, Tianming Han, Dafei Zhan, Zhan Lin, Hong Zhu
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-10 (2021)
Abstract Background Schizophrenia (SCZ) is a severe mental illness with high heritability. This study aimed to explore the correlation between MAD1L1, TSNARE polymorphisms and SCZ susceptibility. Methods A total of 493 SCZ patients and 493 healthy co
Externí odkaz:
https://doaj.org/article/444721e32754453aa259a45832889d15
Akademický článek
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Autor:
Sokolov, Aleksandr V., Manu, Diana-Maria, Nordberg, Didi O. T., Boström, Adrian D. E., Jokinen, Jussi, Schiöth, Helgi B.
Depression is a multifactorial disorder representing a significant public health burden. Previous studies have linked multiple single nucleotide polymorphisms with depressive phenotypes and suicidal behavior. MAD1L1 is a mitosis metaphase checkpoint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a1fd02af12230410c9c45af5ef1ea80
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-202575
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-202575
Autor:
Bradley J. Kemp, Anil N. Kurup, Sean P. Cleary, Danielle E. Jondal, Julie K. Heimbach, Mark Jacobson, Garima Suman, Jun Yin, Tyler Zemla, James C. Andrews, Lewis R. Roberts, Brian T. Welch, Anurima Patra, Scott M. Thompson, Eric C. Ehman, Sudhakar K. Venkatesh, Amit Mahipal, Mark J. Truty, Zongming E. Chen, Geoffrey B. Johnson, Chen Wang, Rory L. Smoot, Chad J. Fleming, Kymberly D. Watt, Michael Torbenson, Nguyen H Tran, David A. Woodrum, Zachary C. Fogarty, Ajit H. Goenka
Publikováno v:
Hepatology Communications. 6:1172-1185
Prostate-specific membrane antigen (PSMA) is a validated target for molecular diagnostics and targeted radionuclide therapy. Our purpose was to evaluate PSMA expression in hepatocellular carcinoma (HCC), cholangiocarcinoma (CCA), and hepatic adenoma
Akademický článek
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Akademický článek
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Autor:
Xiaoge Zhang, Zhengwen Liu, Na Li, Huan Deng, Kun Zhang, Shan He, Qunying Han, Lu Zeng, Xiude Fan, Xiaoyun Wang
Publikováno v:
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-14 (2020)
BMC Medical Genomics
BMC Medical Genomics
Background NEK2 has an established involvement in hepatocellular carcinoma (HCC) but the roles of NEK2 and its interacting proteins in HCC have not been systematically explored. Methods This study examined NEK2 and its interacting proteins in HCC bas
Publikováno v:
Translational Cancer Research
Background: Pancreatic cancer is common in elderly persons, and less than 20% of patients present with localized, potentially curable tumors. Methods: We compared the methylated sites and genes in pericarcinous tissues compared to cancer tissue, and