Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Lianbao, Cao"'
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-14 (2024)
Abstract Centromere pairing is crucial for synapsis in meiosis. This study delves into the Skp1-Cullin1-F-box protein (SCF) E3 ubiquitin ligase complex, specifically focusing on F-box protein 47 (FBXO47), in mouse meiosis. Here, we revealed that FBXO
Externí odkaz:
https://doaj.org/article/05a4b34e7b6e474bacc178380da3e36f
Autor:
Xiaojuan, Wang, Tingting, Zhang, Hao, Li, Deze, Kong, Jianqiang, Zhou, Jianlin, Liu, Lianbao, Cao, Wei, Li, Bigui, Wei
Publikováno v:
In Journal of Water Process Engineering July 2024 64
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Multiple morphological changes in two or more sites of concurrent multifocal mucinous lesions in the female genital tract are indicative of SMMN-FGT, which is unrelated to high-risk HPV infection. MUC6 and HIK-1083 showed positive characteristic immu
Externí odkaz:
https://doaj.org/article/164be8775e7a486c93ed37a58e9b87aa
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 28, Iss 10, p 253 (2023)
Background: Ovarian cancer (OC) is one of the most lethal gynecological malignant neoplasms. The aim of this study was to use high-throughput sequencing data to investigate the molecular and clinical characteristics of OC subtypes related to lipid me
Externí odkaz:
https://doaj.org/article/f5cde65519dc48ca9a41f8e81e38b2b1
Publikováno v:
Gynecology and Minimally Invasive Therapy, Vol 6, Iss 3, Pp 103-107 (2017)
Objective: To evaluate the effects of different treatment methods for previous ectopic pregnancies (EP) on cryopreserved embryo transfer (CET) outcomes. Materials and Methods: This was a retrospective cohort study. Patients with EP histories were div
Externí odkaz:
https://doaj.org/article/00516cfaebce4ee3bf9a0822045ee8ab
Autor:
Jiajie Tu, Chao Wan, Fengjie Zhang, Lianbao Cao, Patrick Wai Nok Law, Yuyao Tian, Gang Lu, Owen M. Rennert, Wai‐Yee Chan, Hoi‐Hung Cheung
Publikováno v:
Aging Cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::589ccee7fd3a0398bf04957053c48c63
https://doi.org/10.1111/acel.13227
https://doi.org/10.1111/acel.13227
Autor:
Hoi-Hung Cheung, Fengjie Zhang, Patrick Wai Nok Law, Chao Wan, Lianbao Cao, Owen M. Rennert, Jiajie Tu, Yuyao Tian, Wai-Yee Chan, Gang Lu
Publikováno v:
Aging Cell
WRN mutation causes a premature aging disease called Werner syndrome (WS). However, the mechanism by which WRN loss leads to progeroid features evident with impaired tissue repair and regeneration remains unclear. To determine this mechanism, we perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3187aa73e3b53e9dd6687299c1e1089
http://europepmc.org/articles/PMC7253065
http://europepmc.org/articles/PMC7253065