Page last updated: 2024-08-22

isopentenyladenosine and Hutchinson Gilford Progeria Syndrome

isopentenyladenosine has been researched along with Hutchinson Gilford Progeria Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bifulco, M; Caruso, MG; D'Alessandro, A; Laezza, C; Malfitano, AM; Notarnicola, M; Paladino, S	1

Other Studies

1 other study(ies) available for isopentenyladenosine and Hutchinson Gilford Progeria Syndrome

Article	Year
N6-isopentenyladenosine improves nuclear shape in fibroblasts from humans with progeroid syndromes by inhibiting the farnesylation of prelamin A. The FEBS journal, 2013, Volume: 280, Issue:23 Topics: Adolescent; Adult; Blotting, Western; Cell Nucleus; Cells, Cultured; Child; Fibroblasts; Geranyltranstransferase; Humans; Immunoprecipitation; Isopentenyladenosine; Lamin Type A; Male; Microscopy, Fluorescence; Nuclear Proteins; Plant Growth Regulators; Progeria; Protein Precursors; Protein Prenylation; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger	2013

Article

Year

N6-isopentenyladenosine improves nuclear shape in fibroblasts from humans with progeroid syndromes by inhibiting the farnesylation of prelamin A.

The FEBS journal, 2013, Volume: 280, Issue:23

Topics: Adolescent; Adult; Blotting, Western; Cell Nucleus; Cells, Cultured; Child; Fibroblasts; Geranyltranstransferase; Humans; Immunoprecipitation; Isopentenyladenosine; Lamin Type A; Male; Microscopy, Fluorescence; Nuclear Proteins; Plant Growth Regulators; Progeria; Protein Precursors; Protein Prenylation; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger

2013