Zobrazeno 1 - 10
of 123
pro vyhledávání: '"MingWei Huang"'
Autor:
Mingwei Huang, Pawares Funoi
Publikováno v:
Cogent Arts & Humanities, Vol 11, Iss 1 (2024)
Many Chinese have chosen to invest in Southeast Asian real estate in recent years. The term ‘rigid demander’ is used to refer to a subset of these enormous overseas real estate investment organizations. These three types of individuals consist of
Externí odkaz:
https://doaj.org/article/cb3d1149237a4fbb89ea697396b7e627
Publikováno v:
Brain and Behavior, Vol 14, Iss 5, Pp n/a-n/a (2024)
Abstract Background Several biallelic truncating and missense variants of the gem nuclear organelle–associated protein 5 (GEMIN5) gene have been reported to cause neurodevelopmental disorders characterized by cerebellar atrophy, intellectual disabi
Externí odkaz:
https://doaj.org/article/5c14682b5e004721b44781e419b2c3bb
Publikováno v:
BMJ Open, Vol 14, Iss 2 (2024)
Introduction Curing locally advanced gastric cancer (GC) or gastro-oesophageal junction adenocarcinoma (GEJ) with surgery alone is challenging. Neoadjuvant chemotherapy (NCT) has become the standard treatment for patients with locally advanced GC/GEJ
Externí odkaz:
https://doaj.org/article/157ed14a96304c34831dff655483dadb
Publikováno v:
Acta Cirúrgica Brasileira, Vol 38 (2023)
ABSTRACT Purpose: Interstitial cystitis/bladder pain syndrome (IC/BPS) is a devastating urological chronic pelvic pain condition. In search of a potential treatment, we investigated the effect of emodin on IC/BPS inflammation and fibrosis, and explor
Externí odkaz:
https://doaj.org/article/3ab9d129ef6e47fd8ab0b4ed3f2e79c8
Autor:
Yan Hu, Mingwei Huang, Jialun Wen, Jian Gao, Weiwei Long, Yansheng Shen, Qi Zeng, Yan Chen, Tian Zhang, Jianxiang Liao, Qiuli Liu, Nannan Li, Sufang Lin
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
NUS1 is responsible for encoding of the Nogo-B receptor (NgBR), which is a subunit of cis-prenyltransferase. Over 25 variants in NUS1 have been reported, and these variants have been found to be associated with various phenotypes, such as congenital
Externí odkaz:
https://doaj.org/article/54b7dc4f7e45485d98a488b615892961
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
STXBP1 variants are one of the most common genetic causes of neurodevelopmental disorders and epilepsy, wherein STXBP1-related disorders are characterized by neurodevelopmental abnormalities in 95% and seizures in 89% of affected patients. However, t
Externí odkaz:
https://doaj.org/article/8d5cc2fded604bf9b8d8c367a3e5fba6
Autor:
Linyan Zhang, Xinyu Liu, Mingwei Huang, Ping Xu, Yanting Lai, Yafen Liu, Xiufeng Zhong, Songshan Li, Xiaoyan Ding
Publikováno v:
Stem Cell Research, Vol 65, Iss , Pp 102937- (2022)
X-linked juvenile retinoschisis (XLRS), caused by the mutation of RS1 gene, is one of the most common causes of macular degeneration for male adolescents. The mutations and clinical manifestations of the disease are diverse. Neither the relationship
Externí odkaz:
https://doaj.org/article/304ea977cf3a45bb8edb10c4d84868db
Publikováno v:
Entropy, Vol 25, Iss 3, p 522 (2023)
Photon-counting LiDAR encounters interference from background noise in remote target detection, and the statistical detection of the accumulation of multiple pulses is necessary to eliminate the uncertainty of responses from the Geiger-mode avalanche
Externí odkaz:
https://doaj.org/article/40133915d6fe4fb59305b23f68d1d7da
Publikováno v:
Stem Cell Research, Vol 57, Iss , Pp 102595- (2021)
X-linked juvenile retinoschisis (XLRS) is an inherited disease characterized by splitting within inner retinal layers and impaired vision, which begins in childhood and occurs mostly in males. Peripheral blood mononuclear cells (PBMCs) were isolated
Externí odkaz:
https://doaj.org/article/f36574e60f02466288246bd7ddb93651
Autor:
Dejian Yuan, Tizhen Yan, Shiqiang Luo, Jun Huang, Jianqiang Tan, Jianping Zhang, Victor Wei Zhang, Yueyuan Lan, Taobo Hu, Jing Guo, Mingwei Huang, Dingyuan Zeng
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
ARR3 has been associated with X-linked, female-limited, high myopia. However, using exome sequencing (ES), we identified the first high myopia case with hemizygous ARR3-related mutation in a male patient in a Southern Chinese family. This novel trunc
Externí odkaz:
https://doaj.org/article/23c904e13f4e46448a4b1e2fb757cabd