Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Huayan, Ren"'
Publikováno v:
Technology in Cancer Research & Treatment, Vol 22 (2023)
Purpose: To evaluate the survival benefit of radiation plus chemotherapy in adult females with stage IIIC endometrial cancer and to investigate whether the benefit varies according to histology. Methods: Data from adult females with International Fed
Externí odkaz:
https://doaj.org/article/ae228ed8a13c46319bf9357e1cee31b1
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 2, Pp 287-289 (2019)
A unique case of eyelid metastasis from nasopharyngeal chondroid chordoma in a 63-year-old woman was reported. Chordomas are rare tumors of the bone deriving from remnants of the embryonic notochord. Histologically, the tumor showed lobulated structu
Externí odkaz:
https://doaj.org/article/af895973d5374342b198b6f3f34ef31f
Publikováno v:
Acta Chirurgica Belgica. :1-9
Alveolar soft-part sarcoma (ASPS) is a rare soft tissue sarcoma subtype, occurring mainly in young people, with poor prognosis.We conducted a retrospective analysis of localized or metastatic ASPS patients admitted to the First Affiliated Hospital of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71ff30cebb41ef76b8eadf220c722b89
https://doi.org/10.1080/00015458.2022.2049060
https://doi.org/10.1080/00015458.2022.2049060
Publikováno v:
Virchows Archiv. 480:933-938
A novel molecular subset of epithelioid leiomyosarcomas with rhabdoid features harboring PGR gene rearrangements has recently been documented. Herein, we present a unique case of PGR-rearranged smooth muscle tumor with both PGR-NR4A3 and UBR5-PGR gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ed0533c37be43c4b819f50cc722b02b
https://doi.org/10.1007/s00428-021-03169-4
https://doi.org/10.1007/s00428-021-03169-4
Autor:
Xiangdong Kong, Zhenhua Zhao, Junke Xia, Furong Liu, Huayan Ren, Jing Wu, Yongjiang Zhao, Yanjie Xia
Publikováno v:
Endocrine Practice. 27:137-145
Objective 17 α-hydroxylase/17, 20-lyase deficiency (17-OHD) is a rare recessive hereditary disease that can be attributed to cytochrome P450 17 α-hydroxylase deficiency caused by CYP17A1 gene mutations. Methods A large cohort of 10 Chinese Han pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a6fc934d60a387c2f4ca19a62a7bc49
https://doi.org/10.4158/ep-2020-0478
https://doi.org/10.4158/ep-2020-0478
Autor:
Chenyu He, Mingzhi Zhu, Huifen Huang, Dong Chen, Huayan Ren, Wencai Li, Dongling Gao, Yuanting Gu
Purpose: Several studies discussed different chemotherapy drugs that have influenced the expression of PD-L1 and CD47 in vitro and in vivo experiments. However, in breast cancer, neoadjuvant chemotherapy (NAC) influence on the changes of PD-L1 and CD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89064012bec62a51a73f96dc4276abed
https://doi.org/10.21203/rs.3.rs-1499943/v1
https://doi.org/10.21203/rs.3.rs-1499943/v1
Autor:
Junke, Xia, Luping, Li, Fuhua, Duan, Jingjing, Meng, Shuping, Yan, Shenglei, Li, Huayan, Ren, Xiangdong, Kong
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(8)
To explore the genetic basis for a patient with Leydig cell hypoplasia.Whole exome sequencing was used to detect genetic variants in the patient. Suspect variants were verified by PCR and Sanger sequencing of the family members.The patient was found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::869a0fc5ea9efea87408526c4011ae79
https://pubmed.ncbi.nlm.nih.gov/32761586
https://pubmed.ncbi.nlm.nih.gov/32761586
Autor:
Na Wei, Huayan Ren, Jun-Na Kou, Yuqiong Liu, Xiaoyi Mi, Huang Huifen, Wencai Li, Jianping Yang, Pengyuan Zhao, Meng Zhongqin, Xueyan Zhao, Mingfang Sun, Huixiang Li, Hongyan Zhang
Publikováno v:
Breast cancer research and treatment. 183(2)
TRAF4 plays an important role in the development and progression of breast cancer, but its impact on chemotherapy resistance is as yet, however, poorly understood. Western blotting, immunoprecipitation, and immunofluorescence staining were used to id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7a7f171e485f0281632eec49dde24bd
https://pubmed.ncbi.nlm.nih.gov/32671611
https://pubmed.ncbi.nlm.nih.gov/32671611
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 2, Pp 287-289 (2019)
A unique case of eyelid metastasis from nasopharyngeal chondroid chordoma in a 63-year-old woman was reported. Chordomas are rare tumors of the bone deriving from remnants of the embryonic notochord. Histologically, the tumor showed lobulated structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca685eaec28de0647278f6340e76bf1
http://www.ijpmonline.org/article.asp?issn=0377-4929
http://www.ijpmonline.org/article.asp?issn=0377-4929
Autor:
Shengli Ma, Kui-Sheng Chen, Rui Xue, Huayan Ren, Wei-Wei Wang, Huang Huifen, Na Wei, Kai Zheng, Jingjing Xu
Publikováno v:
Oncotarget
Chronic cerebral hypoperfusion has been associated with cognitive impairment in dementias, such as Alzheimer's disease (AD) and vascular disease (VaD), the two most common neurodegenerative diseases in aged people. However, the effective therapeutic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c0e300669e4c8e0c142c7a7b769a304
https://doi.org/10.18632/oncotarget.22415
https://doi.org/10.18632/oncotarget.22415