Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Xiao-dong Teng"'
Autor:
Jie Zhou, Wei-Ran Wang, Hui-Fang Zhang, Qi-Qi Gao, Wei-Bin Wang, Jian-Hua Zhu, Yu-Shuai Han, Jing Chen, Tong-Hui Ma, Xiao-Yan Zhang, Xiao-Dong Teng
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
PurposeGenotyping is fundamental in papillary thyroid cancer (PTC) and helps to enhance diagnosis and prognosis and determine appropriate treatments. The phenotype-genotype association in PTC was previously studied, with BRAF V600E characterizing cla
Externí odkaz:
https://doaj.org/article/d4ed934bf3a3406cb0787301145af2c1
Autor:
Ling Peng, Qi-Qi Mao, Bo Jiang, Jin Zhang, Yi-Lei Zhao, Xiao-Dong Teng, Jin-Song Yang, Yang Xia, Shi-Qing Chen, Justin Stebbing, Hai Jiang
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Immune checkpoint inhibitors (ICIs) cause fewer toxicities than conventional chemotherapy. Although most of the immune-related adverse events (irAEs) are mild, reversible, and manageable, potentially severe and rare irAEs remain relevant. We present
Externí odkaz:
https://doaj.org/article/1d3d6e17982949a2a9d96a8816c17f39
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
Systemic amyloidosis is a rare disease and patients with hepatic amyloidosis often present with hepatomegaly. Hepatomegaly can also be a feature of hepatic veno-occlusive disease (HVOD). We report here a case of systemic amyloidosis in a patient who
Externí odkaz:
https://doaj.org/article/7db25a1919604bf7b58bd442adbe2254
Autor:
Xiao-tong Wang, Ru Fang, Hui-ying He, Wei Zhang, Qing Li, Su-an Sun, Xuan Wang, Ru-song Zhang, Xiao-dong Teng, Xiao-jun Zhou, Qiu-yuan Xia, Ming Zhao, Qiu Rao
Publikováno v:
American Journal of Surgical Pathology; Jul2024, Vol. 48 Issue 7, p874-882, 9p
Background Large B-cell lymphoma (LBCL) with interferon regulatory factor 4 (IRF4) rearrangement (LBCL-IRF4) is a rare entity of LBCL with a specific clinical presentation. Notably, it is defined by the presence of an IRF4 rearrangement. Case present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6cba5cc8ebb765a64065f8fc670bcb3
https://doi.org/10.21203/rs.3.rs-1860645/v1
https://doi.org/10.21203/rs.3.rs-1860645/v1
Autor:
Hong Chen, Qiu-Yuan Xia, Ni Chen, Ye Shengbing, Rui Li, Heng-hui Ma, Xuan Wang, Xiao-Dong Teng, Qiu Rao, Zhe Wang, Ru Fang, Xiaotong Wang, Zhen-feng Lu, Xiao-jun Zhou, Ming Zhao, Xue Wei
Publikováno v:
American Journal of Surgical Pathology. 44:477-489
Xp11 renal cell carcinoma (RCC) with different gene fusions may have different clinicopathologic features. We sought to identify variant fusions in TFEB translocation RCC. A total of 31 cases of TFEB RCCs were selected for the current study; MALAT1-T
Autor:
Shuang-Xi Xiong, Xiao Dong Teng, Wenzhe Yin, Zhong-Nan Yang, Jun Zhu, Cheng Zhang, Jie Yang Lu, Yue Lou, Jing Nan Gu, Zoe A. Wilson
Publikováno v:
Journal of Experimental Botany
MS188 and MS1 are essential anther tapetum transcription factors; MS188 directly regulates MS1, which controls the expression of pollen coat protein genes, which are key components of the pollen wall.
Sporophytic pollen coat proteins (sPCPs) der
Sporophytic pollen coat proteins (sPCPs) der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::053c42815c96ca2d8bdbba5e64148d8c
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
The Journal of International Medical Research
The Journal of International Medical Research
Systemic amyloidosis is a rare disease and patients with hepatic amyloidosis often present with hepatomegaly. Hepatomegaly can also be a feature of hepatic veno-occlusive disease (HVOD). We report here a case of systemic amyloidosis in a patient who
Autor:
Ru-song Zhang, Ye Shengbing, Zhen-feng Lu, Qiu-Yuan Xia, Ru Fang, Xiao-jun Zhou, Heng-hui Ma, Xuan Wang, Xiao Tan, Qiu Rao, Xiaotong Wang, Jie-Yu Chen, Xiao-Dong Teng, Shanshan Shi, Rui Li, Ke Sun
Publikováno v:
Modern Pathology. 31:1346-1360
Both Xp11 translocation renal cell carcinomas and the corresponding mesenchymal neoplasms are characterized by a variety of gene fusions involving TFE3. It has been known that tumors with different gene fusions may have different clinicopathologic fe
Autor:
Qiu Rao, Heng-hui Ma, Ye Shengbing, Xuan Wang, Ru-song Zhang, Wenjuan Yu, Xiao-Dong Teng, Qi‐chang Yang, Ru Fang, Jie-Yu Chen, Yujun Li, Xiaotong Wang, Chong Liu, Feng‐hua Wang, Jian‐guo Zhang, Rui Li, Zhen-feng Lu, Xiao-jun Zhou, Rui Pan, Ming Zhao, Yong‐sheng Zhang, Qiu-Yuan Xia
Publikováno v:
The Journal of pathologyReferences. 251(4)
The classification of the distinct group of mesenchymal neoplasms, first described as 'Xp11 translocation perivascular epithelioid cell tumor (PEComa)' and for which the term 'melanotic Xp11 neoplasm' or 'Xp11 neoplasm with melanocytic differentiatio