Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Aixiang Luo"'
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4593 (2023)
M2-like polarized tumor-associated macrophages (TAMs) are the major component of infiltrating immune cells in hepatocellular carcinoma (HCC), which have been proved to exhibit significant immunosuppressive and pro-tumoral effects. However, the underl
Externí odkaz:
https://doaj.org/article/5054659361e04019b76e8a36ba19296c
Autor:
Aixiang Luo, Dehua Cheng, Shimin Yuan, Haiyu Li, Juan Du, Yang Zhang, Chuanchun Yang, Ge Lin, Wenyong Zhang, Yue-Qiu Tan
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Abstract Background 1q43-q44 deletion syndrome is a well-defined chromosomal disorder which is characterized by moderate to severe mental retardation, and variable but characteristic facial features determined by the size of the segment and the numbe
Externí odkaz:
https://doaj.org/article/286d938fad5f47fc954147c054fb3c7f
Autor:
Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, Shimin Yuan, Chaofeng Tu, Lanlan Meng, Aixiang Luo, Ge Lin, Guangxiu Lu, Yue-Qiu Tan
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Abstract Background Small supernumerary marker chromosomes (sSMCs) are common structurally abnormal chromosomes that occur in 0.288% of cases of mental retardation. Isodicentric 15 (idic(15)) is common in sSMCs and usually leads to a rare chromosome
Externí odkaz:
https://doaj.org/article/d2def8e0d8bb425cbe52590e2dd2c7ce
Autor:
Dama Faniriantsoa Henrio Marcellin, Limin Guo, Haiyang Yu, Shuchao Wang, Paul Pielnaa, Adonira Saro, Ismail Bilal Masokano, Malik Muhammad Adil, Ling Yuan, Yanxia Huang, Deyang Cai, Ruping Zheng, Zhongjun Huang, Aixiang Luo, Cyrollah Disoma, Pinjia Liu, Zanxian Xia, Jufang Huang
Publikováno v:
Advances in Microbiology. 12:198-217
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e083ed076baeacb29f4a80b5e518eea5
https://doi.org/10.4236/aim.2022.124016
https://doi.org/10.4236/aim.2022.124016
Autor:
Juan Du, Chuanchun Yang, Shimin Yuan, Wenyong Zhang, Haiyu Li, Aixiang Luo, Dehua Cheng, Ge Lin, Yue-Qiu Tan, Yang Zhang
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Molecular Cytogenetics
Molecular Cytogenetics
Background 1q43-q44 deletion syndrome is a well-defined chromosomal disorder which is characterized by moderate to severe mental retardation, and variable but characteristic facial features determined by the size of the segment and the number of gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573c31415d658032c83dd7ac2a88741b
http://link.springer.com/article/10.1186/s13039-018-0371-7
http://link.springer.com/article/10.1186/s13039-018-0371-7
Autor:
Dehua Cheng, Wen Li, Bo Xiong, Chaofeng Tu, Aixiang Luo, Juan Du, Wen-Bin He, Ge Lin, Duo Yi, Shimin Yuan, Haiyu Li, Guangxiu Lu, Yue-Qiu Tan, Lanlan Meng
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Molecular Cytogenetics
Molecular Cytogenetics
Background Small supernumerary marker chromosomes (sSMCs) are common structurally abnormal chromosomes that occur in 0.288% of cases of mental retardation. Isodicentric 15 (idic(15)) is common in sSMCs and usually leads to a rare chromosome disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a42f83e7037f0d3a2a7201112ba8a3e
http://link.springer.com/article/10.1186/s13039-018-0365-5
http://link.springer.com/article/10.1186/s13039-018-0365-5
Autor:
Chang-Gao Zhong, Chaofeng Tu, Wen-Bin He, Fu-Sheng He, Juan Shen, Liqing Fan, Yue-Qiu Tan, Guangxiu Lu, Qiang Liu, Juan Du, Ge Lin, Wen Li, Lanlan Meng, Aixiang Luo, Shimin Yuan
Publikováno v:
Journal of Medical Genetics. 55:198-204
BackgroundThe genetic causes of the majority of male and female infertility caused by human non-obstructive azoospermia (NOA) and premature ovarian insufficiency (POI) with meiotic arrest are unknown.ObjectiveTo identify the genetic cause of NOA and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5009cdae729b49f782d2593ff1ae3565
https://doi.org/10.1136/jmedgenet-2017-104992
https://doi.org/10.1136/jmedgenet-2017-104992
Autor:
Chaofeng Tu, Wen-Bin He, Guangxiu Lu, Ge Lin, Wen Li, Shimin Yuan, Haiyu Li, Juan Du, Aixiang Luo, Lanlan Meng, Hongchuan Nie, Yue-Qiu Tan
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Male infertility due to spermatogenesis defects affects millions of men worldwide. However, the genetic etiology of the vast majority remains unclear. Here we describe three men with primary infertility due to multiple morphological abnormalities of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4225d09dcfac92038908dfe24c165bf7
https://pubmed.ncbi.nlm.nih.gov/31676830
https://pubmed.ncbi.nlm.nih.gov/31676830
Autor:
Aixiang Luo, Dehua Cheng, Shimin Yuan, Haiyu Li, Du, Juan, Zhang, Yang, Chuanchun Yang, Lin, Ge, Wenyong Zhang, Yue-Qiu Tan
Table S2. The list of primers for PCR amplification of chromosomal breakpoint regions. (DOCX 16Â kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96f38ea62697be8bbefced96037984ce
Autor:
Aixiang Luo, Dehua Cheng, Shimin Yuan, Haiyu Li, Du, Juan, Zhang, Yang, Chuanchun Yang, Lin, Ge, Wenyong Zhang, Yue-Qiu Tan
Table S1. The Gesell Development Scale results of the patients. (DOCX 16Â kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a101daf3fdcc7b038e5b397bc6208a2