Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Frontiers in Gastroenterology (Lausanne, Switzerland)|March 13, 2026
An association study on PSCA rs2294008 polymorphism and gastric cancer: A meta-analysisHangLong Li, Qiang Zhao, ShuHan Si, et al.Journal of Nanobiotechnology|February 1, 2026
Research progress of nanoparticles in the diagnosis and treatment of renal ischemia-reperfusion injuryShuhan Si, Kunzhe Wu, Xiaoyu Zhang, et al.International Journal of Nanomedicine|February 26, 2026
Nanotechnology-Driven Precision Modulation of Transplant Immunity: From Mechanistic Insights to Clinical ToleranceLong Zhang, Kunzhe Wu, Shuhan Si, et al.International Journal of Nanomedicine|July 20, 2026
Nanomedicine-Driven Precision Therapy for Renal Fibrosis: From Mechanistic Insights to Kidney-Targeted InterventionsXiaoyu Zhang, Kunzhe Wu, Long Zhang, et al.Science Advances|January 17, 2025
LEDGF/p75 promotes transcriptional pausing through preventing SPT5 phosphorylationChenghao Guo, Shuhan Si, Haitong Fang, et al.Genome Biology|June 12, 2026
DNA-contact mutant p53 displaces BRCA2 from chromatin and drives R-loop-associated genome instabilityFanfan Li, Ke Fang, Shuhan Si, et al.Bioscience Reports|May 21, 2020
Combinatorial approach of in silico and in vitro evaluation of MLH1 variant associated with Lynch syndrome like metastatic colorectal cancerKomal Saleem, Tahir Zaib, Wei Ji, et al.Pigment Cell & Melanoma Research|July 5, 2023
Identification and characterization of the compound heterozygous variants of TYR gene in a northern Chinese family with Oculocutaneous albinism type 1Shuhan Si, Xueyuan Jia, Lidan Xu, et al.BMC Medical Genetics|December 25, 2019
A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese familyTahir Zaib, Wei Ji, Komal Saleem, et al.Nature Structural & Molecular Biology|January 17, 2025
Maternal ELL3 loss-of-function leads to oocyte aneuploidy and early miscarriageShiqi Zhu, Peng Xie, Yi Yang, et al.Pageof 1