Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Zhengke Zhi"'
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Extracellular vesicles (EV) are vesicular vesicles with phospholipid bilayer, which are present in biological fluids and extracellular microenvironment. Extracellular vesicles serve as pivotal mediators in intercellular communication by delivering li
Externí odkaz:
https://doaj.org/article/1aeb2c7de784410e92bb958de328e672
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundSkin cutaneous melanoma (SKCM) is the most frequently encountered tumor of the skin. Immunotherapy has opened a new horizon in melanoma treatment. We aimed to construct a CD8+ T cell-associated immune gene prognostic model (CDIGPM) for SKCM
Externí odkaz:
https://doaj.org/article/b60098f74c9b40f5aba7bbea5b0c246c
Autor:
Lingling Zhou, Zhengke Zhi, Pingfa Chen, Chunxia Du, Binyu Wang, Xiang Fang, Weibing Tang, Hongxing Li
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Hirschsprung's disease (HSCR) is a congenital disorder characterized by the absence of enteric neural crest cells (ENCCs). LncRNA rhabdomyosarcoma 2-associated transcript (RMST) is essential for the growth and development of neuron. This study aimed
Externí odkaz:
https://doaj.org/article/24259eed46814e02b3e6fdc90a089329
Publikováno v:
Frontiers in immunology. 13
Skin cutaneous melanoma (SKCM) is the most frequently encountered tumor of the skin. Immunotherapy has opened a new horizon in melanoma treatment. We aimed to construct a CD8Single-cell SKCM transcriptomes were utilized in conjunction with immune gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db45deaea4c1f654650411ff95630fd3
https://pubmed.ncbi.nlm.nih.gov/36341357
https://pubmed.ncbi.nlm.nih.gov/36341357
Autor:
Weibing Tang, Zhonghong Wei, Hongxing Li, Zhengke Zhi, Huan Chen, Yuhan Li, Lingling Zhou, Binyu Wang, Xiurui Lv
Publikováno v:
Journal of Proteome Research. 20:2308-2318
Hirschsprung's disease (HSCR) is characterized by the lack of ganglion cells in the distal part of the digestive tract. It occurs due to migration disorders of enteric neural crest cells (ENCCs) from 5 to 12 weeks of embryonic development. More and m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9fc38c337df0a33a05bd9c2882b1407
https://doi.org/10.1021/acs.jproteome.0c00811
https://doi.org/10.1021/acs.jproteome.0c00811
Autor:
Hongxing Li, Xiurui Lv, Zhengke Zhi, Weibing Tang, Xin Zhang, Meiling Tong, Zhonghong Wei, Lingling Zhou
Publikováno v:
Aging (Albany NY)
Hirschsprung disease (HSCR) is a congenital disorder attributed to the failure of the neural crest derivatives migrating and/or differentiating along the hindgut. The most frequent complication in Hirschsprung disease patients is Hirschsprung-associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e12dced69c5230fa4d378f85f417986
https://doi.org/10.18632/aging.103852
https://doi.org/10.18632/aging.103852
Autor:
Xiaoqun Xu, Weibing Tang, Hongxing Li, Feng Wu, Zhengke Zhi, Yang Li, Lingling Zhou, Zechao Wen
Publikováno v:
Journal of Pediatric Surgery. 54:2032-2037
Background We previously studied the metabolomics, transcriptomics and proteomics of intestinal tissue of Hirschsprung disease (HSCR) patients; the results suggested that the expression of prostaglandin E2(PGE2), prostaglandin E receptor 2(PTGER2) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::374f5161b00dd1fb1db297c6ee4ed1f2
https://doi.org/10.1016/j.jpedsurg.2019.01.001
https://doi.org/10.1016/j.jpedsurg.2019.01.001
Publikováno v:
Frontiers in Immunology; 10/20/2022, Vol. 13, p1-11, 11p
Autor:
Hongxing Li, Zhengke Zhi, Lingling Zhou, Xiang Fang, Weibing Tang, Chunxia Du, Pingfa Chen, Binyu Wang
Background：Hirschsprung’s disease (HSCR) is a congenital colon disease characterized by the lack of ganglion cells which is closely related to impaired migration and proliferation of enteric neural crest cells (ENCCs). Long non-coding RNAs (lncRN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a6e35629bb712500b0c9b2acd854d87
https://doi.org/10.21203/rs.3.rs-147665/v1
https://doi.org/10.21203/rs.3.rs-147665/v1
Autor:
Lingling Zhou, Zhengke Zhi, Pingfa Chen, Zhonghong Wei, Chunxia Du, Binyu Wang, Xiang Fang, Weibing Tang, Hongxing Li
Hirschsprung’s disease (HSCR) is a congenital disorder characterized by the absence of enteric neural crest cells (ENCCs). Non-coding RNAs including long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) have been authenticated as important regulato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::661d680cd0e5d2bf4faf7d282b77d8f5
https://doi.org/10.1101/2020.09.23.309930
https://doi.org/10.1101/2020.09.23.309930