Page last updated: 2024-11-08

serine and Progeria

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.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Moiseeva, O1
Lopes-Paciencia, S1
Huot, G1
Lessard, F1
Ferbeyre, G1
Kirschner, J1
Brune, T1
Wehnert, M1
Denecke, J1
Wasner, C1
Feuer, A1
Marquardt, T1
Ketelsen, UP1
Wieacker, P1
Bönnemann, CG1
Korinthenberg, R1

Other Studies

2 other studies available for serine and Progeria

ArticleYear
Permanent farnesylation of lamin A mutants linked to progeria impairs its phosphorylation at serine 22 during interphase.
    Aging, 2016, Volume: 8, Issue:2

    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.
    Annals of neurology, 2005, Volume: 57, Issue:1

    Topics: Blotting, Western; Child; DNA Mutational Analysis; Female; Humans; Lamin Type A; Muscles; Muscular D

2005