Results 141 to 150 of about 403,028 (282)

mTOR, autophagy, and reprogramming

Frontiers in Cell and Developmental Biology, 2014
Nuclear reprogramming to achieve induced-pluripotency by the Yamanaka factors (Takahashi and Yamanaka, 2006) is largely viewed as a consequence of a cascade of expression profile changes, along with alterations in epigenetic markings, which are primarily nuclear events.
openaire   +5 more sources

Diversity Control in Early Transcribed ROS/RNSbalancing Genes: A Common Mechanism for Healthy Resilience? [PDF]

Innovations in Digital Health, Diagnostics, and Biomarkers, 2022
Birgit Arnholdt-Schmitt, Shahid Aziz, José Hélio Costa   +2 more
doaj   +1 more source

Author Correction: Synthetic Tet-inducible artificial microRNAs targeting β-catenin or HIF-1α inhibit malignant phenotypes of bladder cancer cells T24 and 5637

Scientific Reports, 2023
Yonghao Zhan, Yuchen Liu, Junhao Lin, Xing Fu, Chengle Zhuang, Li Liu, Wen Xu, Jianfa Li, Mingwei Chen, Guoping Zhao, Weiren Huang, Zhiming Cai   +11 more
doaj   +1 more source

Vancomycin resistance in enterococci: reprogramming of the d-Ala–d-Ala ligases in bacterial peptidoglycan biosynthesis [PDF]

, 2000
Vicki L Healy, Ivan A.D. Lessard, David I. Roper, James R. Knox, Christopher T. Walsh   +4 more
openalex   +1 more source

Development and evaluation of siRNA-mediated gene silencing strategies for ADO2 therapy utilizing iPSCs model and DMPC-SPIONs delivery system

Stem Cell Research & Therapy
Background Autosomal dominant osteodystrophy type II (ADO2) is an inherited disease characterized by an abnormal increase in bone mineral density, and CLCN7 (R286W) is its most common causative mutation.
Jiajun Xu, Gengshuo Chen, Chune Mo, Yu Sha, Sha Luo, Minglin Ou   +5 more
doaj   +1 more source

Author Correction: Theophylline controllable RNAi-based genetic switches regulate expression of lncRNA TINCR and malignant phenotypes in bladder cancer cells

Scientific Reports, 2023
Zhicong Chen, Yuchen Liu, Anbang He, Jianfa Li, Mingwei Chen, Yonghao Zhan, Junhao Lin, Chengle Zhuang, Li Liu, Guoping Zhao, Weiren Huang, Zhiming Cai   +11 more
doaj   +1 more source

SUGAR-seq reveals the transcriptome and N-linked glycosylation landscape of mononuclear phagocytes at single-cell resolution in a mouse model of autosomal dominant osteopetrosis type 2

BMC Biology
Background Heterozygous mutation of CLCN7 (R286W) is commonly found in patients with benign autosomal dominant osteopetrosis. However, there is no evidence from animal models to confirm that it is a disease mutation.
Yu Sha, Lingyu Huang, Lei Zhang, Xianliang Hou, Chune Mo, Cuiping Pan, Gengshuo Chen, Sha Luo, Minglin Ou   +8 more
doaj   +1 more source

Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos [PDF]

, 2001
Wendy Dean, Fátima Santos, Miodrag Stojković, Valeri Zakhartchenko, Jörn Walter, Eckhard Wolf, Wolf Reik   +6 more
openalex   +1 more source

Allelic Gene Polymorphisms Suspected to Diversify the Individual Early Metabolic Response Upon Influenza H3N2 and SARS-CoV-2 Infections [PDF]

Innovations in Digital Health, Diagnostics, and Biomarkers, 2022
Birgit Arnholdt-Schmitt, Shahid Aziz, José Hélio Costa   +2 more
doaj   +1 more source

Reprogramming of genome function through epigenetic inheritance [PDF]

, 2001
M. Azim Surani
openalex   +1 more source