DNA damage—how and why we age?

M Yousefzadeh, C Henpita, R Vyas, C Soto-Palma… - Elife, 2021 - elifesciences.org
Aging is a complex process that results in loss of the ability to reattain homeostasis following
stress, leading, thereby, to increased risk of morbidity and mortality. Many factors contribute …

Fanconi anaemia and cancer: an intricate relationship

G Nalepa, DW Clapp - Nature Reviews Cancer, 2018 - nature.com
Fanconi anaemia (FA) is a genetic disorder that is characterized by bone marrow failure
(BMF), developmental abnormalities and predisposition to cancer. Together with other …

Nuclear genomic instability and aging

LJ Niedernhofer, AU Gurkar, Y Wang… - Annual review of …, 2018 - annualreviews.org
The nuclear genome decays as organisms age. Numerous studies demonstrate that the
burden of several classes of DNA lesions is greater in older mammals than in young …

Human RecQ helicases in DNA repair, recombination, and replication

DL Croteau, V Popuri, PL Opresko… - Annual review of …, 2014 - annualreviews.org
RecQ helicases are an important family of genome surveillance proteins conserved from
bacteria to humans. Each of the five human RecQ helicases plays critical roles in genome …

Vegetables and their bioactive compounds as anti-aging drugs

H Mechchate, A El Allam, N El Omari, N El Hachlafi… - Molecules, 2022 - mdpi.com
Aging is a continuous process over time that is mainly related to natural alterations in
mechanical–biological processes. This phenomenon is due to several factors, including the …

Human RecQ helicases in DNA double-strand break repair

H Lu, AJ Davis - Frontiers in Cell and Developmental Biology, 2021 - frontiersin.org
RecQ DNA helicases are a conserved protein family found in bacteria, fungus, plants, and
animals. These helicases play important roles in multiple cellular functions, including DNA …

Cell cycle-dependent phosphorylation regulates RECQL4 pathway choice and ubiquitination in DNA double-strand break repair

H Lu, RA Shamanna, JK de Freitas, M Okur… - Nature …, 2017 - nature.com
Pathway choice within DNA double-strand break (DSB) repair is a tightly regulated process
to maintain genome integrity. RECQL4, deficient in Rothmund-Thomson Syndrome …

Prevalent intron retention fine‐tunes gene expression and contributes to cellular senescence

J Yao, D Ding, X Li, T Shen, H Fu, H Zhong, G Wei… - Aging cell, 2020 - Wiley Online Library
Intron retention (IR) is the least well‐understood alternative splicing type in animals, and its
prevalence and function in physiological and pathological processes have long been …

Mutations in ANAPC1, encoding a scaffold subunit of the anaphase-promoting complex, cause Rothmund-Thomson syndrome type 1

NF Ajeawung, TTM Nguyen, L Lu, TJ Kucharski… - The American Journal of …, 2019 - cell.com
Rothmund-Thomson syndrome (RTS) is an autosomal-recessive disorder characterized by
poikiloderma, sparse hair, short stature, and skeletal anomalies. Type 2 RTS, which is …

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective

P Cau, C Navarro, K Harhouri, P Roll, S Sigaudy… - Seminars in cell & …, 2014 - Elsevier
Lamin A-related progeroid syndromes are genetically determined, extremely rare and
severe. In the past ten years, our knowledge and perspectives for these diseases has widely …