Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Huaxia Luo"'
Autor:
Yirong Shi, Yiwei Niu, Peng Zhang, Huaxia Luo, Shuai Liu, Sijia Zhang, Jiajia Wang, Yanyan Li, Xinyue Liu, Tingrui Song, Tao Xu, Shunmin He
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
Abstract Short tandem repeats (STRs) are abundant and highly mutagenic in the human genome. Many STR loci have been associated with a range of human genetic disorders. However, most population-scale studies on STR variation in humans have focused on
Externí odkaz:
https://doaj.org/article/2defb97ff612486cad87b8c16753d8f8
Autor:
Peng Zhang, Huaxia Luo, Yanyan Li, You Wang, Jiajia Wang, Yu Zheng, Yiwei Niu, Yirong Shi, Honghong Zhou, Tingrui Song, Quan Kang, Tao Xu, Shunmin He
Publikováno v:
Cell Reports, Vol 37, Iss 7, Pp 110017- (2021)
Summary: The lack of haplotype reference panels and whole-genome sequencing resources specific to the Chinese population has greatly hindered genetic studies in the world’s largest population. Here, we present the NyuWa genome resource, based on de
Externí odkaz:
https://doaj.org/article/f29a1a206394498f8c982424d66c0e83
Autor:
Tengfei Xiao, Lihui Liu, Hongling Li, Yu Sun, Huaxia Luo, Tangping Li, Shihua Wang, Stephen Dalton, Robert Chunhua Zhao, Runsheng Chen
Publikováno v:
Stem Cell Reports, Vol 5, Iss 5, Pp 856-865 (2015)
C/EBPα is a critical transcriptional regulator of adipogenesis. How C/EBPα transcription is itself regulated is poorly understood, however, and remains a key question that needs to be addressed for a complete understanding of adipogenic development
Externí odkaz:
https://doaj.org/article/f9abc259158a482ca468e6d90cb42e7b
Autor:
Yiwei Niu, Xueyi Teng, Honghong Zhou, Yirong Shi, Yanyan Li, Yiheng Tang, Peng Zhang, Huaxia Luo, Quan Kang, Tao Xu, Shunmin He
Publikováno v:
Nucleic acids research. 50(5)
Mobile element insertions (MEIs) are a major class of structural variants (SVs) and have been linked to many human genetic disorders, including hemophilia, neurofibromatosis, and various cancers. However, human MEI resources from large-scale genome s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cf5b75b5768242ae2a2495493e3066b
https://pubmed.ncbi.nlm.nih.gov/35212372
https://pubmed.ncbi.nlm.nih.gov/35212372
Publikováno v:
Regional Studies in Marine Science. 55:102470
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d82bb864f5767c34c7cda66ce0d0b28a
https://doi.org/10.1016/j.rsma.2022.102470
https://doi.org/10.1016/j.rsma.2022.102470
Autor:
Yunxia Tang, Tao Xu, Xueyi Teng, Quan Kang, Yulong Shi, Y. Li, Shutao He, Huaxia Luo, Yiwei Niu, Peng Zhang
Mobile element insertions (MEIs) are a major class of structural variants (SVs) and have been linked to many human genetic disorders, including hemophilia, neurofibromatosis, and various cancers. However, human MEI resources from large-scale genome s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::333acf6762b4e396ab2a301837fd7bc8
https://doi.org/10.1101/2021.01.22.427873
https://doi.org/10.1101/2021.01.22.427873
Autor:
Di Hao, Honghong Zhou, Tingrui Song, Huaxia Luo, Shunmin He, Peng Zhang, Yajing Hao, Runsheng Chen, Yu Zheng, Quan Kang, Lili Zhang, Yanyan Li, Xiaomin Chen
Publikováno v:
Genomics, proteomicsbioinformatics. 19(4)
Small proteins specifically refer to proteins consisting of less than 100 amino acids translated from small open reading frames (sORFs), which were usually missed in previous genome annotation. The significance of small proteins has been revealed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02abe710ec08ca196d6d57931b789d4a
https://pubmed.ncbi.nlm.nih.gov/34536568
https://pubmed.ncbi.nlm.nih.gov/34536568
Autor:
Yiwei Niu, Yulong Shi, Shutao He, Tao Xu, Tingrui Song, Yuanjie Zheng, Hui-Xia Zhou, Peng Zhang, Huaxia Luo, Wang J, Y. Li, Quan Kang, Y. Wang
The lack of Chinese population specific haplotype reference panel and whole genome sequencing resources has greatly hindered the genetics studies in the world’s largest population. Here we presented the NyuWa genome resource of 71.1M SNPs and 8.2M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5610c33cbe32b934baeffc24bc66298e
https://doi.org/10.1101/2020.11.10.376574
https://doi.org/10.1101/2020.11.10.376574
Publikováno v:
International Journal of Cell Biology, Vol 2012 (2012)
Introduction. Small noncoding RNAs have important regulatory functions in different cell pathways. It is believed that most of them mainly play role in gene post-transcriptional regulation in the cytoplasm. Recent evidence suggests miRNA and siRNA ac
Externí odkaz:
https://doaj.org/article/25df0ace177445b48e153f0a68ac16af
Autor:
Yu Zheng, Yirong Shi, Tao Xu, Wang You, Yiwei Niu, Honghong Zhou, Tingrui Song, Huaxia Luo, Shunmin He, Peng Zhang, Quan Kang, Jiajia Wang, Yanyan Li
Publikováno v:
Cell Reports, Vol 37, Iss 7, Pp 110017-(2021)
Summary The lack of haplotype reference panels and whole-genome sequencing resources specific to the Chinese population has greatly hindered genetic studies in the world’s largest population. Here, we present the NyuWa genome resource, based on dee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88a618a0b4322fe6c7f25bb99325536a
https://doi.org/10.1016/j.celrep.2021.110017
https://doi.org/10.1016/j.celrep.2021.110017