methionine has been researched along with Progeria in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 5 (71.43) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bárcena, C; Caravia, XM; Durand, S; Fernández-García, MT; Freije, JMP; Garabaya, C; Kroemer, G; López-Otín, C; Mariño, G; Mayoral, P; Quirós, PM; Rodríguez, F | 1 |
Bárcena, C; Kroemer, G; López-Otín, C | 1 |
Acín-Perez, R; Andrés, V; Cabezas-Sánchez, P; Cámara, C; Enríquez, JA; Gonzalez-Gómez, C; López-Otín, C; Luque-García, JL; Megias, D; Osorio, FG; Rivera-Torres, J | 1 |
Bhargava, S; Tyagi, SC | 1 |
Bridger, JM; Kill, IR; Mehta, IS | 1 |
Broers, JL; Hennekam, RC; Kamps, M; Kuijpers, HJ; Marcelis, CL; Merckx, D; Ramaekers, FC; Smeets, HJ; Steijlen, PM; van den Wijngaard, A; van Steensel, MA; Verstraeten, VL; Zinn-Justin, S | 1 |
Cummings, KS; Ji, JY; Lammerding, J; Lee, RT; Verstraeten, VL | 1 |
1 review(s) available for methionine and Progeria
Article | Year |
---|---|
Nutriepigenetic regulation by folate-homocysteine-methionine axis: a review.
Topics: Animals; Epigenesis, Genetic; Fatigue Syndrome, Chronic; Folic Acid; Folic Acid Deficiency; Gene-Environment Interaction; Homocysteine; Humans; Methionine; Neural Tube Defects; Progeria | 2014 |
6 other study(ies) available for methionine and Progeria
Article | Year |
---|---|
Methionine Restriction Extends Lifespan in Progeroid Mice and Alters Lipid and Bile Acid Metabolism.
Topics: Animals; Bile Acids and Salts; Disease Models, Animal; Humans; Lipid Metabolism; Methionine; Mice; Progeria | 2018 |
Methionine restriction for improving progeria: another autophagy-inducing anti-aging strategy?
Topics: Aging; Animals; Autophagy; Autophagy-Related Protein 5; Autophagy-Related Protein 7; Caloric Restriction; Disease Models, Animal; Longevity; Methionine; Mice; Progeria; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins | 2019 |
Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture.
Topics: Adenosine Triphosphate; Adolescent; Amino Acids; Animals; Child; Diphosphonates; Female; Fibroblasts; Galactose; Gene Expression Regulation; Glucose; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Imidazoles; Lamin Type A; Male; Methionine; Mice; Mitochondria; Mutation; Nuclear Proteins; Oxygen Consumption; Pravastatin; Progeria; Protein Precursors; Proteomics; Skin; Zoledronic Acid | 2013 |
Progeria, the nucleolus and farnesyltransferase inhibitors.
Topics: Cell Nucleolus; Child; Chromosomal Proteins, Non-Histone; Clinical Trials as Topic; Enzyme Inhibitors; Farnesyltranstransferase; Humans; Lamin Type A; Methionine; Progeria | 2010 |
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation.
Topics: Adult; Bone and Bones; Cell Survival; Cells, Cultured; Child, Preschool; Female; Fibroblasts; Heterozygote; Humans; Imaging, Three-Dimensional; Immunohistochemistry; Lamin Type A; Lovastatin; Male; Methionine; Models, Molecular; Mutation; Nuclear Proteins; Progeria; Protein Precursors; Protein Prenylation; Radiography | 2006 |
Increased mechanosensitivity and nuclear stiffness in Hutchinson-Gilford progeria cells: effects of farnesyltransferase inhibitors.
Topics: Adolescent; Aged, 80 and over; Apoptosis; Cell Movement; Cell Nucleus; Cell Survival; Cells, Cultured; Child; Child, Preschool; Dose-Response Relationship, Drug; Farnesyltranstransferase; Female; Fibroblasts; Humans; Male; Methionine; Nuclear Proteins; Progeria; Sensitivity and Specificity; Skin; Wound Healing | 2008 |