serine has been researched along with Progeria in 2 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Progeria: An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Moiseeva, O | 1 |
Lopes-Paciencia, S | 1 |
Huot, G | 1 |
Lessard, F | 1 |
Ferbeyre, G | 1 |
Kirschner, J | 1 |
Brune, T | 1 |
Wehnert, M | 1 |
Denecke, J | 1 |
Wasner, C | 1 |
Feuer, A | 1 |
Marquardt, T | 1 |
Ketelsen, UP | 1 |
Wieacker, P | 1 |
Bönnemann, CG | 1 |
Korinthenberg, R | 1 |
2 other studies available for serine and Progeria
Article | Year |
---|---|
Permanent farnesylation of lamin A mutants linked to progeria impairs its phosphorylation at serine 22 during interphase.
Topics: Humans; Immunoblotting; Immunoprecipitation; Interphase; Lamin Type A; Microscopy, Fluorescence; Mut | 2016 |
p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeria.
Topics: Blotting, Western; Child; DNA Mutational Analysis; Female; Humans; Lamin Type A; Muscles; Muscular D | 2005 |