Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Xue-min Gao"'
Autor:
Jian-xin Wang, Rui Sun, Dong-xu Si, Man-ping Guo, Lijing Zhang, Yuan-yuan Sun, Xue-min Gao, Rui Gao
Publikováno v:
Complementary Therapies in Medicine, Vol 85, Iss , Pp 103077- (2024)
Objectives: To analyze the methodology, evidence, recommendations, quality, and implementation of traditional Chinese patent medicine (CPM) guidelines. Methods: We retrieved clinical application guidelines of CPM published from 2019 to 2022. Independ
Externí odkaz:
https://doaj.org/article/5c7475accaa645cbb81240e4b027cecd
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/5b5b4276d2504ff9a6020cb53af26aef
Autor:
Ya-Qian Li, Xu-Liang An, Fu-Yu Jin, Yi-Fei Bai, Tian Li, Xin-Yu Yang, Shu-Peng Liu, Xue-Min Gao, Na Mao, Hong Xu, Wen-Chen Cai, Fang Yang
Publikováno v:
Ecotoxicology and Environmental Safety, Vol 264, Iss , Pp 115410- (2023)
The role and mechanisms of integrated stress response inhibitor (ISRIB) on silicosis are still not well defined. In the present study, the effects of ISRIB on cellular senescence and pulmonary fibrosis in silicosis were evaluated by RNA sequencing, m
Externí odkaz:
https://doaj.org/article/727326a2b92f4d5d826f3911b4ea8fb6
Publikováno v:
Cell Communication and Signaling, Vol 20, Iss 1, Pp 1-16 (2022)
Abstract Langerhans cell histiocytosis (LCH) is an inflammatory myeloid malignancy in the “L-group” histiocytosis. Mitogen-activated protein kinase (MAPK) pathway activating mutations are detectable in nearly all LCH lesions. However, the pathoge
Externí odkaz:
https://doaj.org/article/d759bc25800e4ddda8a73ad15c73084b
Autor:
Yan-ying Yu, Xue-min Gao, Hao Zhao, Hao Cai, Jun Feng, Lu Zhang, Xin-xin Cao, Daobin Zhou, Jian Li
Publikováno v:
Blood Cancer Journal, Vol 11, Iss 8, Pp 1-5 (2021)
Externí odkaz:
https://doaj.org/article/30452f3c1c85418898d5a5985efba0f5
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes (POEMS) syndrome is a rare paraneoplastic syndrome involving multisystem. Optic disc edema (ODE) is the most common ocular manifestation in patie
Externí odkaz:
https://doaj.org/article/6a276458b27b44b892955af6cfce8b82
Autor:
Ai-lin Zhao, Jian Sun, Xue-min Gao, Xinxin Cao, Daobin Zhou, Jia Chen, Ting Liu, Minghui Duan, Hao Cai, Jian Li, Zhiyong Liang
Publikováno v:
Leukemia. 36:573-576
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fe2037b3daf2eef12a361e9717009ff
https://doi.org/10.1038/s41375-021-01439-3
https://doi.org/10.1038/s41375-021-01439-3
Autor:
Xinxin Cao, Jun Feng, Lu Zhang, Yan-ying Yu, Hao Zhao, Xue-min Gao, Daobin Zhou, Hao Cai, Jian Li
Publikováno v:
Blood Cancer Journal, Vol 11, Iss 8, Pp 1-5 (2021)
Blood Cancer Journal
Blood Cancer Journal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc8102feef2ff8b811dc815d9885d211
https://doaj.org/article/30452f3c1c85418898d5a5985efba0f5
https://doaj.org/article/30452f3c1c85418898d5a5985efba0f5
Publikováno v:
Journal of Cellular and Molecular Medicine
POEMS syndrome is a rare plasma cell dyscrasia with distinct lipid metabolism abnormalities at disease onset. However, the serum lipidomic characteristics in patients with POEMS syndrome were not investigated. The study performed an untargeted lipido
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf95a8d340de0ee99f29a26ddea0a4b
http://europepmc.org/articles/PMC8093959
http://europepmc.org/articles/PMC8093959
Publikováno v:
Leukemia. 35:1100-1107
Background: POEMS syndrome is a rare plasma cell dyscrasia. Despite the presence of monoclonal protein, POEMS syndrome patients commonly have less than 5% monoclonal plasma cells in the bone marrow. Only one study has reported the genetic and transcr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::697a29971f2992e43a81eb85c56ba8a1
https://doi.org/10.1038/s41375-020-01101-4
https://doi.org/10.1038/s41375-020-01101-4