Zobrazeno 1 - 10
of 254
pro vyhledávání: '"Yong Hui Jiang"'
Autor:
Zhenchun Yang, Jiawen Liao, Yi Zhang, Yan Lin, Yihui Ge, Wu Chen, Chenyu Qiu, Kiros Berhane, Zhipeng Bai, Bin Han, Jia Xu, Yong Hui Jiang, Frank Gilliland, Weili Yan, Zhanghua Chen, Guoying Huang, Junfeng (Jim) Zhang
Publikováno v:
Environmental Research: Health, Vol 2, Iss 1, p 015001 (2023)
Few studies have examined the association between greenness exposure and birth outcomes. This study aims to identify critical exposure time windows during preconception and pregnancy for the association between greenness exposure and birth weight. A
Externí odkaz:
https://doaj.org/article/b41c2c4e2a794c4c9b75582da2d8960b
Autor:
Roman Thaler, Farzaneh Khani, Ines Sturmlechner, Sharareh S. Dehghani, Janet M. Denbeigh, Xianhu Zhou, Oksana Pichurin, Amel Dudakovic, Sofia S. Jerez, Jian Zhong, Jeong-Heon Lee, Ramesh Natarajan, Ivo Kalajzic, Yong-hui Jiang, David R. Deyle, Eleftherios P. Paschalis, Barbara M. Misof, Tamas Ordog, Andre J. van Wijnen
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-18 (2022)
For decades vitamin C’s primary function in bone has been attributed to its involvement in collagen synthesis. Here, the authors uncover that vitamin C’s central role in bone is to globally orchestrate osteogenesis via epigenetic mechanisms.
Externí odkaz:
https://doaj.org/article/03ddd7fcf25c4309b04599c7af2fbd14
Autor:
Sarah Moyon, Rebecca Frawley, Damien Marechal, Dennis Huang, Katy L. H. Marshall-Phelps, Linde Kegel, Sunniva M. K. Bøstrand, Boguslawa Sadowski, Yong-Hui Jiang, David A. Lyons, Wiebke Möbius, Patrizia Casaccia
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-18 (2021)
Myelin formation is regulated by epigenetic mechanisms and ensures proper neuronal function during development and after demyelination. Here, the authors show that TET1, a DNA hydroxymethylase, regulates myelin repair in adult mice, but is defective
Externí odkaz:
https://doaj.org/article/0cc9b5962f0a40eabbf4462ab04b7567
Autor:
Liansheng Zhang, Yun Qian, Jie Li, Xuan Zhou, He Xu, Jie Yan, Jialing Xiang, Xiang Yuan, Beicheng Sun, Sangram S. Sisodia, Yong-Hui Jiang, Xiaohua Cao, Naihe Jing, Anning Lin
Publikováno v:
iScience, Vol 24, Iss 9, Pp 102942- (2021)
Summary: Alzheimer’s disease (AD) is the most common progressive neurodegenerative disease. However, the underlying molecular mechanism is incompletely understood. Here we report that the pro-apoptotic protein BAD as a key regulator for neuronal ap
Externí odkaz:
https://doaj.org/article/4f8639ed15974668b2c7dbbdfeb33c90
Autor:
Su‐Yan Wang, Daniela D. Herrera‐Balandrano, Yong‐Hui Jiang, Xin‐Chi Shi, Xin Chen, Feng‐Quan Liu, Pedro Laborda
Publikováno v:
Comprehensive Reviews in Food Science and Food Safety. 22:1722-1762
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a1fd1a6bd2232efc302860468732536
https://doi.org/10.1111/1541-4337.13128
https://doi.org/10.1111/1541-4337.13128
Autor:
Qiong Xu, Yuan-yuan Liu, Xiaoming Wang, Guo-he Tan, Hui-ping Li, Samuel W. Hulbert, Chun-yang Li, Chun-chun Hu, Zhi-qi Xiong, Xiu Xu, Yong-hui Jiang
Publikováno v:
Molecular Autism, Vol 9, Iss 1, Pp 1-17 (2018)
Abstract Background Mutations in CHD8, chromodomain helicase DNA-binding protein 8, are among the most replicated and common findings in genetic studies of autism spectrum disorder (ASD). The CHD8 protein is believed to act as a transcriptional regul
Externí odkaz:
https://doaj.org/article/f5e82f90f69d4bb7af33c882d69be995
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-5 (2018)
Abstract Background Verheij syndrome is a rare microdeletion syndrome of chromosome 8q24.3 that harbors PUF60, SCRIB, and NRBP2 genes. Subsequently, loss of function mutations in PUF60 have been found in children with clinical features significantly
Externí odkaz:
https://doaj.org/article/9d910014222e4651af6a5c3dafbef518
Autor:
Nicole M. Walley, Loren D. M. Pena, Stephen R. Hooper, Heidi Cope, Yong-Hui Jiang, Allyn McConkie-Rosell, Camilla Sanders, Kelly Schoch, Rebecca C. Spillmann, Kimberly Strong, Alexa T. McCray, Paul Mazur, Cecilia Esteves, Kimberly LeBlanc, Undiagnosed Diseases Network, Anastasia L. Wise, Vandana Shashi
Publikováno v:
BMC Health Services Research, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background The majority of undiagnosed diseases manifest with objective findings that warrant further investigation. The Undiagnosed Diseases Network (UDN) receives applications from patients whose symptoms and signs have been intractable to
Externí odkaz:
https://doaj.org/article/41a86d65a9524c2abee5f89c183cb163
Publikováno v:
Molecular Autism, Vol 9, Iss 1, Pp 1-13 (2018)
Abstract Background Human genetic and genomic studies have supported a strong causal role of SHANK3 deficiency in autism spectrum disorder (ASD). However, the molecular mechanism underlying SHANK3 deficiency resulting in ASD is not fully understood.
Externí odkaz:
https://doaj.org/article/76d8d4748b244b049725f5167964fe4a
Publikováno v:
Neurobiology of Disease, Vol 110, Iss , Pp 12-19 (2018)
Epilepsy is prevalent and often medically intractable in Angelman syndrome (AS). AS mouse model (Ube3am−/p+) shows reduced excitatory neurotransmission but lower seizure threshold. The neural mechanism linking the synaptic dysfunction to the seizur
Externí odkaz:
https://doaj.org/article/0082dc84acac421492c82f07cf46503c