Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Runmin, Guo"'
Autor:
Gyan Watson Ray, Qiaoli Zeng, Phidelia Kusi, Hengli Zhang, Taotao Shao, Taili Yang, Yue Wei, Mianqin Li, Xiaoqun Che, Runmin Guo
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Gestational diabetes mellitus (GDM) poses a significant global health concern, impacting both maternal and fetal well-being. Early detection and treatment are imperative to mitigate adverse outcomes during pregnancy. This review delves into the pivot
Externí odkaz:
https://doaj.org/article/eaeac92341384518b3ce99f04058b16d
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Background: There is a growing body of evidence indicating a possible association between genetic variations and attention-deficit hyperactivity disorder (ADHD), although the results have been inconsistent. The objective of this study was to evaluate
Externí odkaz:
https://doaj.org/article/7050ebdf6e6d4f5084080293982c9b98
Autor:
Qiaoli Zeng, Taili Yang, Wenfeng Wei, Dehua Zou, Yue Wei, Fengqiong Han, Jieyun He, Jinzhi Huang, Runmin Guo
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundGlyoxalase 1 (GLO1) plays a crucial role in defending against glycation. Single nucleotide polymorphism (SNP) variants in the GLO1 gene may affect gene expression and alter enzyme activity. However, there have been limited studies evaluatin
Externí odkaz:
https://doaj.org/article/7b78c40c6c1741cbb2672b3ca1845646
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundThe solute carrier family 30 A8 zinc transporter (SLC30A8) plays a crucial role in insulin secretion. This study aimed to investigate the impact of SLC30A8 gene polymorphisms on gestational diabetes mellitus (GDM).MethodsThe research object
Externí odkaz:
https://doaj.org/article/ec1e055cf58e49f0aec5aeee9c3eab84
Publikováno v:
European Journal of Medical Research, Vol 27, Iss 1, Pp 1-12 (2022)
Abstract Background Increasing evidence shows that genetic variants of genes in the diabetes mellitus (DM) metabolic pathway, such as the vitamin D receptor (VDR) gene rs739837 polymorphism, increase the risk of DM susceptibility. However, the findin
Externí odkaz:
https://doaj.org/article/1822cc1b55414ca69a14972ab147ab4a
Autor:
Qiaoli Zeng, Dehua Zou, Na Liu, Yue Wei, Jing Yang, Weibiao Wu, Fengqiong Han, Rongrong He, Runmin Guo
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionMiR-196a2 and miR-27a play a key role in the regulation of the insulin signaling pathway. Previous studies have indicated that miR-27a rs895819 and miR-196a2 rs11614913 have a strong association with type 2 diabetes (T2DM), but very few s
Externí odkaz:
https://doaj.org/article/3c8a63d31dbb4d6d9b4a301f3380b8e7
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
The coronavirus disease 2019 (COVID-19) pandemic has so far damaged the health of millions and has made the treatment of cancer patients more complicated, and so did acute myeloid leukemia (AML). The current problem is the lack of understanding of th
Externí odkaz:
https://doaj.org/article/4a1b05c2f02d43a0910f46fe5912856a
Autor:
Ray, Gyan Watson, Qiaoli Zeng, Phidelia Kusi, Hengli Zhang, Taotao Shao, Taili Yang, Yue Wei, Mianqin Li, Xiaoqun Che, Runmin Guo
Publikováno v:
Frontiers in Endocrinology; 2024, p1-16, 16p
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 21, Iss , Pp 614-622 (2020)
MicroRNA (miR)-137 is highly expressed in the brain and plays a crucial role in the development and prognosis of glioma. In this review, we aim to summarize the latest findings regarding miR-137 in glioma cell apoptosis, proliferation, migration, inv
Externí odkaz:
https://doaj.org/article/4a9fd22677b7490fb071ef33d8229f53
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Background:CDK5 regulatory subunit associated protein 1 like 1 (CDKAL1) is a major pathogenesis-related protein for type 2 diabetes mellitus (T2DM). Recently, some studies have investigated the association of CDKAL1 susceptibility variants, including
Externí odkaz:
https://doaj.org/article/03250b8b6ae048d1ab957b9219dd4883