Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jiansuo LIN"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-23 (2024)
Abstract The prognosis for patients with colorectal cancer (CRC) remains worse than expected due to metastasis, recurrence, and resistance to chemotherapy. Colorectal cancer stem cells (CRCSCs) play a vital role in tumor metastasis, recurrence, and c
Externí odkaz:
https://doaj.org/article/3d146d6c1a54454abf0546f0ed6f51ed
Autor:
Yan-Lian Liang, Yu Shi, Yu-Qing Su, Fan Wu, Yanwen Liang, Xiuchu Fan, Jiansuo Lin, Yi Liu, Long Peng, Jianwei Ren, Shuang Liang
Publikováno v:
Iranian Journal of Immunology, Vol 20, Iss 1, Pp 129-134 (2023)
Several cases of the hemolytic disease of the fetus and newborn (HDFN) caused by immunoglobulin G (IgG) anti-M antibodies have been reported, in which almost all the HDFN-associated anti-M were warmly reacting. Here we report two cases of severe HDFN
Externí odkaz:
https://doaj.org/article/8e6b826f790c405b93cecd364f99a10d
Publikováno v:
Zhongguo shuxue zazhi, Vol 35, Iss 9, Pp 887-891 (2022)
Objective To analyze the polymorphisms of GYPA and GYPB mRNA spliceosomes associated with MNS blood group, and to explore the mechanism of subcellular localization of GPA and GPB protein isomerism encoded by various spliceosomes as well as the expres
Externí odkaz:
https://doaj.org/article/a993c7c2fae44767b67beb9b6e369de1
Autor:
Yanlian Liang, Jianwei Ren, Fuling Zhong, Wenxu Hong, Yuqing Su, Fan Wu, Shuang Liang, Jun Liu, Shuanghua Fang, Yanwen Liang, Xiuchu Fan, Jiansuo Lin, Yi Liu, Bo Feng, Yunping Xu
Publikováno v:
Vox sanguinisREFERENCES. 117(5)
The molecular basis of MNS blood group variants is not fully clear yet. In this study, we have characterized mRNA variants of GYPA and GYPB genes to reveal whether alternative RNA splicing may cause antigenic diversity of the MNS system.Total RNA was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b3f2ba6b19829281e81a74f8f11efd3
https://pubmed.ncbi.nlm.nih.gov/35138639
https://pubmed.ncbi.nlm.nih.gov/35138639
Autor:
Xiujie Zheng, Chengbo Fang, Jian Li, Jiansuo Lin, Bing Luan, Haijiang Zeng, Zhen-Ning Zhang, Jianjun Chen, Sihan Lv, Zehua Wu, Delong Meng, Zilin Zhong
Publikováno v:
Molecular Medicine Reports
The present study aimed to identify the disease‑causing gene of a four‑generation Chinese family affected with congenital posterior subcapsular cataracts (CPSC), to additionally investigate the frequency of paired like homeodomain 3 (PITX3) mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34010307ba9a804002562533379ff68a
https://doi.org/10.3892/mmr.2019.9989
https://doi.org/10.3892/mmr.2019.9989
Autor:
Lin Liu, Jiansuo Lin, Jian Liao, J. Duan, Zilin Zhong, A. Lu, M. Li, Nengjun Ma, M. Zhong, Zehua Wu, F. Xu, H. Huang, K. Guo, Jianjun Chen
Publikováno v:
Current molecular medicine. 18(5)
Background To screen variants in pre-mRNA Splicing genes in 95 Chinese autosomal dominant retinitis pigmentosa (adRP) families. Methods Clinical examination and pedigree analysis were performed. Targeted exome sequencing (TES) and / or Sanger sequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5621e5f16e12c87e98f25d952ee2332
https://pubmed.ncbi.nlm.nih.gov/30360737
https://pubmed.ncbi.nlm.nih.gov/30360737