scholarly article | Q13442814 |
P50 | author | Thomas A. Rando | Q79331501 |
P2093 | author name string | Howard Y Chang | |
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SIRT6 is a histone H3 lysine 9 deacetylase that modulates telomeric chromatin | Q24310658 | ||
SIRT6 links histone H3 lysine 9 deacetylation to NF-kappaB-dependent gene expression and organismal life span | Q24315083 | ||
Transplantation of Living Nuclei From Blastula Cells into Enucleated Frogs' Eggs | Q24519327 | ||
Sir2 mediates longevity in the fly through a pathway related to calorie restriction | Q24560016 | ||
SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging | Q24595900 | ||
Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients | Q24595997 | ||
The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms | Q24597989 | ||
Telomerase reactivation reverses tissue degeneration in aged telomerase-deficient mice | Q24598687 | ||
Extending healthy life span--from yeast to humans | Q24599191 | ||
The ageing systemic milieu negatively regulates neurogenesis and cognitive function. | Q24599219 | ||
Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cells | Q24617599 | ||
Long noncoding RNA in genome regulation: prospects and mechanisms | Q24621946 | ||
Histone H3K27ac separates active from poised enhancers and predicts developmental state | Q24628758 | ||
Chromatin regulation and genome maintenance by mammalian SIRT6 | Q24634557 | ||
Regulation of lifespan in Drosophila by modulation of genes in the TOR signaling pathway | Q24643816 | ||
Combinatorial patterns of histone acetylations and methylations in the human genome | Q24647290 | ||
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice | Q24647805 | ||
Calorie restriction and the exercise of chromatin | Q24652611 | ||
Protein homeostasis and aging in neurodegeneration | Q37785711 | ||
The DNA damage response: Balancing the scale between cancer and ageing | Q37824549 | ||
The Janus face of DNA methylation in aging | Q39914567 | ||
Chromatin signature of embryonic pluripotency is established during genome activation | Q40694812 | ||
The AMP-activated protein kinase AAK-2 links energy levels and insulin-like signals to lifespan in C. elegans | Q41711470 | ||
Stem cells: The promises and perils of p53. | Q42380567 | ||
Change of the hepatic cells in parabiosis between old and young rats | Q44185928 | ||
Nuclear reprogramming of somatic cells by in vitro hybridization with ES cells. | Q48876988 | ||
Epigenetic gambling and epigenetic drift as an antagonistic pleiotropic mechanism of aging. | Q51650811 | ||
Recreating Pluripotency? | Q51902675 | ||
Parabiosis in physiological studies | Q73969149 | ||
Parabiosis between old and young rats | Q74418620 | ||
Increase in activity during calorie restriction requires Sirt1 | Q81598148 | ||
Acquisition and extinction of gene expression programs are separable events in heterokaryon reprogramming | Q83201737 | ||
Does damage to DNA and other macromolecules play a role in aging? If so, how? | Q37126672 | ||
Bmi-1 regulates the Ink4a/Arf locus to control pancreatic beta-cell proliferation | Q37175990 | ||
Chromatin analysis of occluded genes | Q37239866 | ||
C. elegans dauer formation and the molecular basis of plasticity | Q37245616 | ||
Fat metabolism links germline stem cells and longevity in C. elegans | Q37383382 | ||
The connections between general and reproductive senescence and the evolutionary basis of menopause | Q37782376 | ||
Histone demethylase JMJD3 contributes to epigenetic control of INK4a/ARF by oncogenic RAS | Q24657459 | ||
Histone H4 lysine 16 acetylation regulates cellular lifespan | Q24657553 | ||
Motif module map reveals enforcement of aging by continual NF-kappaB activity | Q24680880 | ||
Insulin signaling and dietary restriction differentially influence the decline of learning and memory with age | Q27324536 | ||
Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors | Q27860937 | ||
Requirement of NAD and SIR2 for life-span extension by calorie restriction in Saccharomyces cerevisiae | Q27933365 | ||
The histone H3 lysine-27 demethylase Jmjd3 links inflammation to inhibition of polycomb-mediated gene silencing | Q28116655 | ||
Generation of germline-competent induced pluripotent stem cells | Q28131699 | ||
Increased dosage of a sir-2 gene extends lifespan in Caenorhabditis elegans | Q28131824 | ||
The H3K27me3 demethylase JMJD3 contributes to the activation of the INK4A-ARF locus in response to oncogene- and stress-induced senescence | Q28245403 | ||
Nuclear reprogramming of somatic cells after fusion with human embryonic stem cells | Q28269087 | ||
Sheep cloned by nuclear transfer from a cultured cell line | Q28275874 | ||
Genomic instability and aging-like phenotype in the absence of mammalian SIRT6 | Q28509079 | ||
Ink4a/Arf expression is a biomarker of aging | Q28570483 | ||
Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors | Q28589872 | ||
daf-2, an insulin receptor-like gene that regulates longevity and diapause in Caenorhabditis elegans | Q28611331 | ||
The Polycomb complex PRC2 and its mark in life | Q29547358 | ||
The genetics of ageing | Q29547430 | ||
Dissecting direct reprogramming through integrative genomic analysis | Q29614211 | ||
A unique chromatin signature uncovers early developmental enhancers in humans | Q29614327 | ||
Methylation of lysine 4 on histone H3: intricacy of writing and reading a single epigenetic mark | Q29614516 | ||
Control of the embryonic stem cell state | Q29614793 | ||
Rejuvenation of aged progenitor cells by exposure to a young systemic environment | Q29615250 | ||
Understanding the odd science of aging | Q29617341 | ||
Extrachromosomal rDNA circles--a cause of aging in yeast | Q29618308 | ||
Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis | Q29619965 | ||
Accumulation of mitochondrial DNA deletion mutations in aged muscle fibers: evidence for a causal role in muscle fiber loss | Q33280200 | ||
mTOR regulation and therapeutic rejuvenation of aging hematopoietic stem cells | Q33609242 | ||
Genome-wide views of chromatin structure | Q33611702 | ||
Widespread and tissue specific age-related DNA methylation changes in mice. | Q33736551 | ||
Protein homeostasis and aging: The importance of exquisite quality control | Q33925901 | ||
Molecular coupling of Xist regulation and pluripotency. | Q34013837 | ||
Epigenetic reprogramming in plant and animal development | Q34024503 | ||
Nuclear cloning and epigenetic reprogramming of the genome | Q34086441 | ||
Telomere rejuvenation during nuclear reprogramming | Q34100113 | ||
Epigenetic modifications in pluripotent and differentiated cells | Q34143430 | ||
The aging stress response | Q34144973 | ||
Molecular signals of epigenetic states | Q34146698 | ||
TGF-β and insulin signaling regulate reproductive aging via oocyte and germline quality maintenance | Q34204996 | ||
Induced pluripotency: history, mechanisms, and applications | Q34206028 | ||
Adult frogs derived from the nuclei of single somatic cells | Q34252349 | ||
The essence of senescence | Q34288983 | ||
Stem cell ageing and non-random chromosome segregation. | Q34402704 | ||
Stem cells from the Mammalian blastocyst | Q34442507 | ||
Suppression of Polycomb group proteins by JNK signalling induces transdetermination in Drosophila imaginal discs | Q34466613 | ||
Noncoding RNA landmarks of pluripotency and reprogramming | Q34523201 | ||
Increased cell-to-cell variation in gene expression in ageing mouse heart | Q34540791 | ||
Pluripotency and cellular reprogramming: facts, hypotheses, unresolved issues | Q34545153 | ||
Timescales of genetic and epigenetic inheritance | Q34576261 | ||
Theoretical analysis of epigenetic cell memory by nucleosome modification. | Q34629739 | ||
DNMT1 maintains progenitor function in self-renewing somatic tissue | Q34632106 | ||
Absence of effects of Sir2 overexpression on lifespan in C. elegans and Drosophila | Q34632518 | ||
How stem cells age and why this makes us grow old. | Q34667132 | ||
The pluripotency factor Oct4 interacts with Ctcf and also controls X-chromosome pairing and counting | Q34675046 | ||
Sirtuins in aging and disease | Q34770789 | ||
Members of the H3K4 trimethylation complex regulate lifespan in a germline-dependent manner in C. elegans | Q34784199 | ||
Imbalance between pSmad3 and Notch induces CDK inhibitors in old muscle stem cells. | Q34786450 | ||
Germination, genetics, and growth of an ancient date seed. | Q34786697 | ||
Manifestations and mechanisms of stem cell aging. | Q34825281 | ||
DNA methyltransferase 1 is essential for and uniquely regulates hematopoietic stem and progenitor cells | Q35005985 | ||
Using heterokaryons to understand pluripotency and reprogramming | Q35088507 | ||
DNA damage and ageing: new-age ideas for an age-old problem | Q35153827 | ||
Emerging models and paradigms for stem cell ageing | Q35671770 | ||
Transgenerational epigenetic inheritance of longevity in Caenorhabditis elegans | Q36010849 | ||
Aging and genome maintenance | Q36357846 | ||
Stem cells, ageing and the quest for immortality. | Q36523915 | ||
Biological aging is no longer an unsolved problem | Q36802089 | ||
The role of nuclear architecture in genomic instability and ageing | Q36911164 | ||
Human embryonic stem cells: mechanisms to escape replicative senescence? | Q37008502 | ||
Chromatin structure and the regulation of gene expression: the lessons of PEV in Drosophila | Q37087566 | ||
Systematic identification of cis-silenced genes by trans complementation | Q37092437 | ||
P433 | issue | 1-2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | epigenetic rejuvenation | Q107569137 |
P304 | page(s) | 46-57 | |
P577 | publication date | 2012-01-01 | |
P1433 | published in | Cell | Q655814 |
P1476 | title | Aging, rejuvenation, and epigenetic reprogramming: resetting the aging clock | |
P478 | volume | 148 |
Q33714246 | A Fine-Tune Role of Mir-125a-5p on Foxn1 During Age-Associated Changes in the Thymus |
Q26781342 | A Tale from TGF-β Superfamily for Thymus Ontogeny and Function |
Q33719048 | A paternal environmental legacy: evidence for epigenetic inheritance through the male germ line. |
Q94521923 | A β-galactosidase kiss of death for senescent cells |
Q90640124 | Age-Associated DNA Methylation Patterns Are Shared Between the Hippocampus and Peripheral Blood Cells |
Q37195037 | Age-associated epigenetic drift: implications, and a case of epigenetic thrift? |
Q46320656 | Age-related epigenetic drift and phenotypic plasticity loss: implications in prevention of age-related human diseases |
Q90469129 | Age-related trends in lipid levels: a large-scale cross-sectional study of the general Chinese population |
Q35096716 | Age-specific functional epigenetic changes in p21 and p16 in injury-activated satellite cells |
Q38886086 | Ageing and ocular surface immunity. |
Q55025189 | Aging Hallmarks: The Benefits of Physical Exercise. |
Q36518127 | Aging and reprogramming: a two-way street |
Q21183983 | Aging of blood can be tracked by DNA methylation changes at just three CpG sites |
Q38259859 | Aging with ING: a comparative study of different forms of stress induced premature senescence |
Q38018293 | An aging program at the systems level? |
Q48098265 | An epigenetic clock controls aging |
Q52691452 | Analysis of long non-coding RNA (lncRNA) expression in hepatitis B patients. |
Q41475139 | Axonal Degeneration during Aging and Its Functional Role in Neurodegenerative Disorders |
Q38642565 | Back and forth in time: Directing age in iPSC-derived lineages. |
Q41422353 | Biogenesis of Pro-senescent Microparticles by Endothelial Colony Forming Cells from Premature Neonates is driven by SIRT1-Dependent Epigenetic Regulation of MKK6. |
Q41468737 | Blockade of PD-1 or p38 MAP kinase signaling enhances senescent human CD8(+) T-cell proliferation by distinct pathways |
Q35153456 | Blue journal conference. Aging and susceptibility to lung disease |
Q48911542 | Caenorhabditis elegans: an old genetic model can learn new epigenetic tricks. |
Q36638131 | Causes, consequences, and reversal of immune system aging |
Q35947877 | Cdc42 activity regulates hematopoietic stem cell aging and rejuvenation |
Q26767454 | Cellular Senescence as the Causal Nexus of Aging |
Q98939376 | Cellular quality control during gametogenesis |
Q34496408 | Cellular reprogramming for understanding and treating human disease |
Q55346896 | Chromatin changes trigger laminin genes dysregulation in aging kidneys. |
Q33918478 | Chromatin modifications as determinants of muscle stem cell quiescence and chronological aging. |
Q92257276 | Clonal Hematopoiesis in Aging |
Q36861673 | Concise review: hematopoietic stem cell aging, life span, and transplantation |
Q56001204 | DNA methylation-based biomarkers and the epigenetic clock theory of ageing |
Q43098018 | Direct Lineage Reprogramming Reveals Disease-Specific Phenotypes of Motor Neurons from Human ALS Patients |
Q38411818 | Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects. |
Q49552882 | Dynamic and Diverse Changes in the Functional Properties of Vascular Smooth Muscle Cells in Pulmonary Hypertension. |
Q36912509 | Early events in lymphopoiesis: an update |
Q50187342 | Elixir of Life: Thwarting Aging With Regenerative Reprogramming. |
Q37611719 | Emerging Molecular Pathways Governing Dietary Regulation of Neural Stem Cells during Aging. |
Q35674189 | Epigenetic Aging Signatures Are Coherently Modified in Cancer |
Q64071921 | Epigenetic Analysis in Human Neurons: Considerations for Disease Modeling in PD |
Q92042145 | Epigenetic changes during aging and their reprogramming potential |
Q34514496 | Epigenetic clock analyses of cellular senescence and ageing |
Q38814870 | Epigenetic drift, epigenetic clocks and cancer risk. |
Q38216619 | Epigenetic resolution of the 'curse of complexity' in adaptive evolution of complex traits |
Q33616185 | Epigenetics of aging and aging-related disease. |
Q50422460 | Epigenome comparisons reveal linkage between gene expression and postnatal remodeling of chromatin domain topology. |
Q38838046 | Evaluating cell reprogramming, differentiation and conversion technologies in neuroscience |
Q50541796 | Experimental manipulation of telomere length: does it reveal a corner-stone role for telomerase in the natural variability of individual fitness? |
Q88755179 | Extracellular vesicles extracted from young donor serum attenuate inflammaging via partially rejuvenating aged T-cell immunotolerance |
Q59090300 | Facing up to the global challenges of ageing |
Q46314960 | Fleeting factors, turning back time. |
Q37001419 | Functional annotation of noncoding variants and prioritization of cancer-associated lncRNAs in lung cancer |
Q60951267 | GRK5 - A Functional Bridge Between Cardiovascular and Neurodegenerative Disorders |
Q98289675 | Ganoderic Acid D Protects Human Amniotic Mesenchymal Stem Cells against Oxidative Stress-Induced Senescence through the PERK/NRF2 Signaling Pathway |
Q94465937 | Genetic predispositions of Parkinson's disease revealed in patient-derived brain cells |
Q26853420 | Genetic regulation of thymocyte progenitor aging |
Q34511671 | Genetic variants near MLST8 and DHX57 affect the epigenetic age of the cerebellum |
Q26828858 | Genomic imprinting in mammals |
Q38622592 | Germline and Pluripotent Stem Cells |
Q38914376 | Global reorganization of the nuclear landscape in senescent cells |
Q26740026 | Hallmarks of progeroid syndromes: lessons from mice and reprogrammed cells |
Q33811539 | Heterochronic parabiosis: historical perspective and methodological considerations for studies of aging and longevity |
Q58765738 | Horizons in the evolution of aging |
Q47813385 | How regularities of mortality statistics explain why we age despite having potentially ageless somatic stem cells |
Q55005606 | Implications of Cellular Aging in Cardiac Reprogramming. |
Q48201443 | In Vivo Transient and Partial Cell Reprogramming to Pluripotency as a Therapeutic Tool for Neurodegenerative Diseases |
Q51823732 | Influence of anaerobic and aerobic exercise on age-related pathways in skeletal muscle. |
Q39106739 | Interaction between epigenetic and metabolism in aging stem cells |
Q38738844 | Interindividual epigenetic variability: Sound or noise? |
Q90422160 | Investigating the role of Sirtuins in cell reprogramming |
Q34547502 | In Vivo Amelioration of Age-Associated Hallmarks by Partial Reprogramming |
Q36692844 | Lifespan of neurons is uncoupled from organismal lifespan |
Q37514776 | Long non-coding RNA H19 enhances cell proliferation and anchorage-independent growth of cervical cancer cell lines |
Q37553716 | Long non-coding RNA LOC283070 mediates the transition of LNCaP cells into androgen-independent cells possibly via CAMK1D |
Q64898040 | Long-term every-other-day administration of DMAMCL has little effect on aging and age-associated physiological decline in mice. |
Q55002845 | MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells. |
Q37366137 | Mechanistic links between aging and lung fibrosis |
Q39085780 | Metabolism and Skeletal Muscle Homeostasis in Lung Disease. |
Q39334309 | MicroRNA-191 triggers keratinocytes senescence by SATB1 and CDK6 downregulation |
Q64272061 | Mitochondria: multifaceted regulators of aging |
Q33563545 | Mitochondrial protein Fus1/Tusc2 in premature aging and age-related pathologies: critical roles of calcium and energy homeostasis |
Q39363647 | Mitotic Dysfunction Associated with Aging Hallmarks |
Q28076026 | Modeling ALS with motor neurons derived from human induced pluripotent stem cells |
Q38574034 | Molecular biomarkers for chronological age in animal ecology |
Q27021113 | Molecular mechanism of extrinsic factors affecting anti-aging of stem cells |
Q41358122 | Molecular mechanisms involved in the aging of the T-cell immune response. |
Q51765832 | Molecular profiling of aged neural progenitors identifies Dbx2 as a candidate regulator of age-associated neurogenic decline. |
Q35262077 | Muscle dysfunction in patients with lung diseases: a growing epidemic |
Q27025990 | NF-kB in premature aging |
Q38848975 | NF-κB activation impairs somatic cell reprogramming in ageing |
Q42220488 | NF-κB inhibition delays DNA damage-induced senescence and aging in mice |
Q36964401 | NF-κB pathway activators as potential ageing biomarkers: targets for new therapeutic strategies. |
Q37040356 | Negative reciprocal regulation between Sirt1 and Per2 modulates the circadian clock and aging |
Q38213553 | New insights into skin stem cell aging and cancer. |
Q37409450 | Nfatc1 orchestrates aging in hair follicle stem cells |
Q39270104 | Nuclear lamina defects cause ATM-dependent NF-κB activation and link accelerated aging to a systemic inflammatory response |
Q97527575 | Optimized method for extraction of exosomes from human primary muscle cells |
Q64900318 | Perspective: Why Exercise Is Good and Its Lack Bad for Everything. |
Q28533351 | Phenethylisothiocyanate alters site- and promoter-specific histone tail modifications in cancer cells |
Q90952568 | Pluripotent Stem Cells to Model Degenerative Retinal Diseases: The RPE Perspective |
Q39256627 | Pluripotent stem cells escape from senescence-associated DNA methylation changes |
Q33915908 | Prolonged fasting reduces IGF-1/PKA to promote hematopoietic-stem-cell-based regeneration and reverse immunosuppression. |
Q37402142 | Promoting longevity by maintaining metabolic and proliferative homeostasis |
Q90634541 | Quantitative iTRAQ-based proteomic analysis of differentially expressed proteins in aging in human and monkey |
Q34737490 | Regenerative capacity of old muscle stem cells declines without significant accumulation of DNA damage |
Q34023658 | Regulation of the mRNA half-life in breast cancer |
Q92493414 | Rehmannia glutinosa exhibits anti-aging effect through maintaining the quiescence and decreasing the senescence of hematopoietic stem cells |
Q38981139 | Rejuvenating Strategies for Stem Cell-Based Therapies in Aging |
Q60044565 | Rejuvenation by cell reprogramming: a new horizon in gerontology |
Q38763576 | Renal Aging: Causes and Consequences |
Q35684586 | Replication stress is a potent driver of functional decline in ageing haematopoietic stem cells |
Q44955740 | Reversal of aging and lifespan elongation. Current biomedical key publications and the implications for geriatrics |
Q38761159 | Roles for long non-coding RNAs in physiology and disease. |
Q35782076 | SIRT1 affects DNA methylation of polycomb group protein target genes, a hotspot of the epigenetic shift observed in ageing |
Q35093088 | SIRT1-mediated epigenetic downregulation of plasminogen activator inhibitor-1 prevents vascular endothelial replicative senescence |
Q33802446 | SOX17 Regulates Conversion of Human Fibroblasts Into Endothelial Cells and Erythroblasts by Dedifferentiation Into CD34+ Progenitor Cells |
Q93067806 | Sarcopenia: Aging-Related Loss of Muscle Mass and Function |
Q26777962 | Satellite cells in human skeletal muscle plasticity |
Q92599529 | Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1 |
Q97883660 | Searching for the Mechanisms of Mammalian Cellular Aging Through Underlying Gene Regulatory Networks |
Q83230352 | Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
Q37150507 | Sirtuins, tissue maintenance, and tumorigenesis |
Q41848436 | Solar-simulated ultraviolet radiation induces histone 3 methylation changes in the gene promoters of matrix metalloproteinases 1 and 3 in primary human dermal fibroblasts |
Q36118417 | Stem cell aging in adult progeria. |
Q38702921 | Stem cells and healthy aging |
Q33616166 | Stem cells as vehicles for youthful regeneration of aged tissues. |
Q48377058 | Stress-associated H3K4 methylation accumulates during postnatal development and aging of rhesus macaque brain |
Q36756829 | Suppression of EZH2 Prevents the Shift of Osteoporotic MSC Fate to Adipocyte and Enhances Bone Formation During Osteoporosis |
Q55426070 | TGF-β signaling alters H4K20me3 status via miR-29 and contributes to cellular senescence and cardiac aging. |
Q93047344 | Ten Years of BrainAGE as a Neuroimaging Biomarker of Brain Aging: What Insights Have We Gained? |
Q37029584 | The Aging Epigenome |
Q47105441 | The Potential of iPSCs for the Treatment of Premature Aging Disorders |
Q89532840 | The ageing epigenome and its rejuvenation |
Q38098875 | The ageing haematopoietic stem cell compartment |
Q39089125 | The aging hematopoietic stem cell niche: Phenotypic and functional changes and mechanisms that contribute to hematopoietic aging |
Q34386434 | The aging signature: a hallmark of induced pluripotent stem cells? |
Q30819335 | The anti-aging effects of LW-AFC via correcting immune dysfunctions in senescence accelerated mouse resistant 1 (SAMR1) strain |
Q38180970 | The biochemistry and cell biology of aging: metabolic regulation through mitochondrial signaling. |
Q28648405 | The cerebellum ages slowly according to the epigenetic clock |
Q47806831 | The chromatin accessibility signature of human immune aging stems from CD8+ T cells. |
Q38239897 | The decalog of long non-coding RNA involvement in cancer diagnosis and monitoring. |
Q94103502 | The effect of age on stem cell function and utility for therapy |
Q34864525 | The expanding epigenetic landscape of non-model organisms |
Q28131641 | The hallmarks of aging |
Q39157599 | The mystery of puberty initiation: genetics and epigenetics of idiopathic central precocious puberty (ICPP). |
Q34379834 | The nexus of chromatin regulation and intermediary metabolism. |
Q43937697 | The place of genetics in ageing research. |
Q38967406 | The role of hydrogen sulfide in aging and age-related pathologies |
Q57034268 | The rs2147578 C > G polymorphism in the Inc-LAMC2-1:1 gene is associated with increased neuroblastoma risk in the Henan children |
Q34371037 | The scientific quest for lasting youth: prospects for curing aging |
Q35578950 | Three-dimensional human facial morphologies as robust aging markers |
Q34385068 | Topical hypochlorite ameliorates NF-κB-mediated skin diseases in mice |
Q89018656 | Transient non-integrative expression of nuclear reprogramming factors promotes multifaceted amelioration of aging in human cells |
Q48590196 | Treadmill exercise alters histone acetyltransferases and histone deacetylases activities in frontal cortices from wistar rats. |
Q90854384 | Turning back time with emerging rejuvenation strategies |
Q36956854 | Two Conserved Histone Demethylases Regulate Mitochondrial Stress-Induced Longevity |
Q47191098 | UNC-120/SRF independently controls muscle aging and lifespan in Caenorhabditis elegans. |
Q51768235 | Ultraviolet A irradiation induces senescence in human dermal fibroblasts by down-regulating DNMT1 via ZEB1. |
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Q38163265 | Using zebrafish models to explore genetic and epigenetic impacts on evolutionary developmental origins of aging |
Q89752915 | When function follows form: Nuclear compartment structure and the epigenetic landscape of the aging neuron |
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