Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Dehua MA"'
Autor:
Yongshuai XIE, Ying PENG, Youmei WANG, Dehua MA, Yuan CHENG, Luyi ZHU, Jiecai HAN, Xinghong ZHANG
Publikováno v:
Journal of Advanced Ceramics, Vol 12, Iss 1, Pp 24-35 (2023)
The difficulty of reducing the diameter of lutetium oxide (Lu2O3) continuous fibers below 50 μm not only limits the flexibility of the sample but also seriously affects their application and development in high-energy lasers. In this work, a Lu-cont
Externí odkaz:
https://doaj.org/article/545c5548dfd74c55ac3879dfb85c30d5
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Lung adenocarcinoma (LUAD) is the main pathological subtype of Non-small cell lung cancer. We downloaded the gene expression profile and immune-related gene set from the TCGA and ImmPort database, respectively, to establish immune-related ge
Externí odkaz:
https://doaj.org/article/489ea5a767a440d3bcc42c4ea085936d
Publikováno v:
Frontiers in Surgery, Vol 9 (2022)
BackgroundCrigler-Najjar syndrome type 2 (CNS-II) is a rare genetic disease that is associated with a lack of uridine diphosphate-glucuronosyltransferase. Esophageal carcinoma is the sixth most common cause of cancer-related death worldwide, for whic
Externí odkaz:
https://doaj.org/article/5987680877b049fba9b839b97ae37d03
Publikováno v:
PeerJ, Vol 9, p e11319 (2021)
Background Lung adenocarcinoma (LUAD) is the leading histological subtype of non-small cell lung cancer (NSCLC). Methods In the present study, the gene matrixes of LUAD were downloaded from The Cancer Genome Atlas to infer immune and stromal scores w
Externí odkaz:
https://doaj.org/article/c583b48406ec46fc9e7e8d1d56969b92
Autor:
Minghui Cai, Xinxin Zhang, Lizhen Fan, Shuwen Cheng, Abdukahar Kiram, Shaoqin Cen, Baofu Chen, Minhua Ye, Qian Gao, Chengchu Zhu, Long Yi, Dehua Ma
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Birt–Hogg–Dubé syndrome (BHDS, MIM #135150), caused by germline mutations of FLCN gene, is a rare autosomal dominant inherited disorder characterized by skin fibrofolliculomas, renal cancer, pulmonary cysts and spontaneous pneumothorax. The synd
Externí odkaz:
https://doaj.org/article/1209bfcba77e4f409a939750924b9756
Publikováno v:
PeerJ, Vol 9, p e11233 (2021)
Background Lung adenocarcinoma (LUAD) is the most common pathological subtype of lung cancer. Ferroptosis, an oxidative, iron-dependent form of necrotic cell death, is highly associated with tumorigenesis and cancer progression. However, the prognost
Externí odkaz:
https://doaj.org/article/099b4f05c5634bdf82df8c82e6710048
Publikováno v:
Case Reports in Surgery, Vol 2017 (2017)
Mediastinal glomus tumors are rarely recognized, and only seven cases have been reported in the literature. Here, we describe a rare mediastinal glomus tumor and review the characteristics of this rare clinical case. The patient was a 50-year-old fem
Externí odkaz:
https://doaj.org/article/c0b4f2840e2e4a95a52d4ad4ddb1a69a
Autor:
Baofu Chen, Bo Zhang, Chengchu Zhu, Zhongrui Ye, Chunguo Wang, Dehua Ma, Minhua Ye, Min Kong, Jiang Jin, Jiang Lin, Chunlei Wu, Zheng Wang, Jiahong Ye, Jian Zhang, Quanteng Hu
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e82428 (2013)
BACKGROUND: To achieve decreased invasiveness and lower morbidity, minimally invasive esophagectomy (MIE) was introduced in 1997 for localized esophageal cancer. The combined thoracoscopic-laparoscopic esophagectomy (left neck anastomosis, defined as
Externí odkaz:
https://doaj.org/article/974a254abb1c42a69dac9c03510d506f
Publikováno v:
Tsinghua Science and Technology. 28:786-798
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f24d9f1c473700567192bd611f1c067e
https://doi.org/10.26599/tst.2022.9010050
https://doi.org/10.26599/tst.2022.9010050
Autor:
Xinxin Zhang, Minghui Cai, Yuanchun Ma, Jie Chen, Shaoping Huang, Mengru Cai, Yibing Ding, Dehua Ma, Qian Gao, Xiaowen Hu, Chengchu Zhu, Long Yi
Publikováno v:
The Journal of Molecular Diagnostics. 25:110-120
Primary spontaneous pneumothorax (PSP) or pulmonary cyst is one of the manifestations of Birt-Hogg-Dubé syndrome, which is caused by pathogenic variants in FLCN gene. Genetic testing in patients with PSP identifies a certain number of missense or in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c00432f5550b36edab0529ea379f201
https://doi.org/10.1016/j.jmoldx.2022.10.005
https://doi.org/10.1016/j.jmoldx.2022.10.005