Page last updated: 2024-10-21

aminopropionitrile and Progeria

aminopropionitrile has been researched along with Progeria in 1 studies

Aminopropionitrile: Reagent used as an intermediate in the manufacture of beta-alanine and pantothenic acid.

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 (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
von Kleeck, R1
Roberts, E1
Castagnino, P1
Bruun, K1
Brankovic, SA1
Hawthorne, EA1
Xu, T1
Tobias, JW1
Assoian, RK1

Other Studies

1 other study available for aminopropionitrile and Progeria

ArticleYear
Arterial stiffness and cardiac dysfunction in Hutchinson-Gilford Progeria Syndrome corrected by inhibition of lysyl oxidase.
    Life science alliance, 2021, Volume: 4, Issue:5

    Topics: Aging, Premature; Aminopropionitrile; Animals; Disease Models, Animal; Female; Heart Diseases; Lamin

2021