Редактирование: Aging genes 30-59 (раздел)

==FGF21==

* {{medline-title
|title=Differential effects of sulfur amino acid-restricted and low-calorie diets on gut microbiome profile and bile acid composition in male C57BL6/J mice.
|date=27.10.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/33106871
|full-text-url=https://sci-hub.do/10.1093/gerona/glaa270
}}
* {{medline-title
|title=Relationship between physical activity and circulating fibroblast growth factor 21 in middle-aged and older adults.
|date=11.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32911033
|full-text-url=https://sci-hub.do/10.1016/j.exger.2020.111081
}}
* {{medline-title
|title=Exercise and dietary intervention ameliorate high-fat diet-induced NAFLD and liver aging by inducing lipophagy.
|date=09.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32863214
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365984
}}
* {{medline-title
|title=Mitochondria, immunosenescence and inflammaging: a role for mitokines?
|date=10.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32757036
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666292
}}
* {{medline-title
|title=Age-at-onset-dependent effects of sulfur amino acid restriction on markers of growth and stress in male F344 rats.
|date=07.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32573078
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426777
}}
* {{medline-title
|title=Fibroblast growth factor 21 prolongs lifespan and improves stress tolerance in the silkworm, [i]Bombyx mori[/i].
|date=03.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32309367
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154471
}}
* {{medline-title
|title=Neurogenesis and prolongevity signaling in young germ-free mice transplanted with the gut microbiota of old mice.
|date=13.11.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31723038
|full-text-url=https://sci-hub.do/10.1126/scitranslmed.aau4760
}}
* {{medline-title
|title=Fibroblast Growth Factor 21 Mediates the Associations between Exercise, Aging, and Glucose Regulation.
|date=02.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31490857
|full-text-url=https://sci-hub.do/10.1249/MSS.0000000000002150
}}
* {{medline-title
|title=Effects of Moderate Chronic Food Restriction on the Development of Postprandial Dyslipidemia with Ageing.
|date=10.08.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31405194
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723802
}}
* {{medline-title
|title=Inhibition of the Fission Machinery Mitigates [[OPA1]] Impairment in Adult Skeletal Muscles.
|date=15.06.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31208084
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627087
}}
* {{medline-title
|title=Higher serum levels of fibroblast growth factor 21 in old patients with cachexia.
|date=07-08.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30933730
|full-text-url=https://sci-hub.do/10.1016/j.nut.2018.11.004
}}
* {{medline-title
|title=Impact of aging and caloric restriction on fibroblast growth factor 21 signaling in rat white adipose tissue.
|date=04.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30620889
|full-text-url=https://sci-hub.do/10.1016/j.exger.2019.01.001
}}
* {{medline-title
|title=Kotho and aging.
|date=09.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30557478

}}
* {{medline-title
|title=The Klotho proteins in health and disease.
|date=01.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30455427
|full-text-url=https://sci-hub.do/10.1038/s41581-018-0078-3
}}
* {{medline-title
|title=Towards frailty biomarkers: Candidates from genes and pathways regulated in aging and age-related diseases.
|date=11.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30071357
|full-text-url=https://sci-hub.do/10.1016/j.arr.2018.07.004
}}
* {{medline-title
|title=Aging is associated with increased [[FGF21]] levels but unaltered [[FGF21]] responsiveness in adipose tissue.
|date=10.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30043445
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156525
}}
* {{medline-title
|title=Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium.
|date=12.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29988085
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326896
}}
* {{medline-title
|title=Human Aging and Longevity Are Characterized by High Levels of Mitokines.
|date=23.04.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29955888
|full-text-url=https://sci-hub.do/10.1093/gerona/gly153
}}
* {{medline-title
|title=[Fibroblast growth factor-21 as a marker of premature aging in young and middled-aged men with type 2 diabetes].
|date=03.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29634140

}}
* {{medline-title
|title=Fibroblast growth factor 21 delayed endothelial replicative senescence and protected cells from H O -induced premature senescence through [[SIRT1]].
|date=2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29118911
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666058
}}
* {{medline-title
|title=Integrated stress response stimulates [[FGF21]] expression: Systemic enhancer of longevity.
|date=12.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28844867
|full-text-url=https://sci-hub.do/10.1016/j.cellsig.2017.08.009
}}
* {{medline-title
|title=Fibroblast growth factor 21: a regulator of metabolic disease and health span.
|date=01.09.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28559437
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625087
}}
* {{medline-title
|title=Age-Associated Loss of [[OPA1]] in Muscle Impacts Muscle Mass, Metabolic Homeostasis, Systemic Inflammation, and Epithelial Senescence.
|date=06.06.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28552492
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462533
}}
* {{medline-title
|title=Regulation of longevity by [[FGF21]]: Interaction between energy metabolism and stress responses.
|date=08.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28552719
|full-text-url=https://sci-hub.do/10.1016/j.arr.2017.05.004
}}
* {{medline-title
|title=[[FGF21]] activates AMPK signaling: impact on metabolic regulation and the aging process.
|date=02.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27678528
|full-text-url=https://sci-hub.do/10.1007/s00109-016-1477-1
}}
* {{medline-title
|title=Methionine restriction improves renal insulin signalling in aged kidneys.
|date=07.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27453066
|full-text-url=https://sci-hub.do/10.1016/j.mad.2016.07.003
}}
* {{medline-title
|title=[[FGF21]] represses cerebrovascular aging via improving mitochondrial biogenesis and inhibiting p53 signaling pathway in an AMPK-dependent manner.
|date=15.08.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27364911
|full-text-url=https://sci-hub.do/10.1016/j.yexcr.2016.06.020
}}
* {{medline-title
|title=Role of mitochondrial function in cell death and body metabolism.
|date=01.06.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27100503
|full-text-url=https://sci-hub.do/10.2741/4453
}}
* {{medline-title
|title=Prolongevity hormone [[FGF21]] protects against immune senescence by delaying age-related thymic involution.
|date=26.01.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26755598
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743827
}}
* {{medline-title
|title=Differentiated embryo chondrocyte 1 (DEC1) is a novel negative regulator of hepatic fibroblast growth factor 21 ([[FGF21]]) in aging mice.
|date=15.01.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26697751
|full-text-url=https://sci-hub.do/10.1016/j.bbrc.2015.12.045
}}
* {{medline-title
|title=Effect of mitochondrial stress on systemic metabolism.
|date=09.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26100439
|full-text-url=https://sci-hub.do/10.1111/nyas.12822
}}
* {{medline-title
|title=Muscle-specific 4E-BP1 signaling activation improves metabolic parameters during aging and obesity.
|date=03.08.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26121750
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563739
}}
* {{medline-title
|title=Circulating levels of fibroblast growth factor-21 increase with age independently of body composition indices among healthy individuals.
|date=01.06.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26042208
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450097
}}
* {{medline-title
|title=A preliminary candidate approach identifies the combination of chemerin, fetuin-A, and fibroblast growth factors 19 and 21 as a potential biomarker panel of successful aging.
|date=06.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25911468
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409588
}}
* {{medline-title
|title=Fibroblast growth factor 21 protects mouse brain against D-galactose induced aging via suppression of oxidative stress response and advanced glycation end products formation.
|date=06.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25871519
|full-text-url=https://sci-hub.do/10.1016/j.pbb.2015.03.020
}}
* {{medline-title
|title=Cardiorespiratory fitness and visceral fat are key determinants of serum fibroblast growth factor 21 concentration in Japanese men.
|date=10.2014
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25013999
|full-text-url=https://sci-hub.do/10.1210/jc.2014-1877
}}
* {{medline-title
|title=Methionine restriction restores a younger metabolic phenotype in adult mice with alterations in fibroblast growth factor 21.
|date=10.2014
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24935677
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331744
}}