Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shuai-Hong Li"'
Autor:
Feng-Min Liu, Yu-fei Gao, Yanyan Kong, Yihui Guan, Jinsen Zhang, Shuai-Hong Li, Dan Ye, Wenyu Wen, Chuantao Zuo, Wei Hua
Publikováno v:
BMC Cancer, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Non-invasive diagnosis of IDH1 mutation for gliomas has great clinical significance, and PET has natural advantage to detect metabolism, as IDH mutated gliomas share lower glucose consumption. Methods Clinical data of patients wit
Externí odkaz:
https://doaj.org/article/729bec0131124d6285692998711433fe
Autor:
Liu, Feng-Min, Gao, Yu-Fei, Yanyan Kong, Yihui Guan, Jinsen Zhang, Shuai-Hong Li, Ye, Dan, Wenyu Wen, Chuantao Zuo, Hua, Wei
Additional file 1 Supplementary Table 1: Characteristic of patient population subjected to pathological evaluation, related to Fig. 1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c771c851176d41a086aa0c3c11f99c7
Autor:
Liu, Feng-Min, Gao, Yu-Fei, Yanyan Kong, Yihui Guan, Jinsen Zhang, Shuai-Hong Li, Ye, Dan, Wenyu Wen, Chuantao Zuo, Hua, Wei
Additional file 4.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470e05712c3526b773d1478f931389e6
Autor:
Liu, Feng-Min, Gao, Yu-Fei, Yanyan Kong, Yihui Guan, Jinsen Zhang, Shuai-Hong Li, Ye, Dan, Wenyu Wen, Chuantao Zuo, Hua, Wei
Additional file 6.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13e134656cbc6f15b2d9359a7cb3ec82
Autor:
Liu, Feng-Min, Gao, Yu-Fei, Yanyan Kong, Yihui Guan, Jinsen Zhang, Shuai-Hong Li, Ye, Dan, Wenyu Wen, Chuantao Zuo, Hua, Wei
Additional file 2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166a85ebdc844781964277888c4f93c7
Autor:
Liu, Feng-Min, Gao, Yu-Fei, Yanyan Kong, Yihui Guan, Jinsen Zhang, Shuai-Hong Li, Ye, Dan, Wenyu Wen, Chuantao Zuo, Hua, Wei
Additional file 3.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6210a562aa0ae51993b25c6741dc5e1a
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary vascular disease caused by mutations in NOTCH3 , that are primarily localized in exons 4, 3, and 11. The Arg332Cys mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f084dda6912eb7df20159d25d1eb041e
https://europepmc.org/articles/PMC6995735/
https://europepmc.org/articles/PMC6995735/