Page last updated: 2024-08-18

isomethyleugenol and Noonan Syndrome

isomethyleugenol has been researched along with Noonan 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	0 (0.00)	24.3611
2020's	1 (100.00)	2.80

Authors

Authors	Studies
Billia, F; Brown, KR; Burston, HE; Chen, S; Cowen, J; Coyaud, E; Dadson, K; De Carvalho, DD; He, HH; Ishak, C; Kannu, P; Kent, OA; Laurent, EM; Law, N; Matsumoto, Y; Montgomery-Song, A; Raught, B; Rose, J; Rottapel, R; Saha, M; St-Germain, J; Sun, RX	1

Other Studies

1 other study(ies) available for isomethyleugenol and Noonan Syndrome

Article	Year
Haploinsufficiency of RREB1 causes a Noonan-like RASopathy via epigenetic reprogramming of RAS-MAPK pathway genes. Nature communications, 2020, 09-16, Volume: 11, Issue:1 Topics: Abnormalities, Multiple; Animals; Chromosome Deletion; Chromosomes, Human, Pair 6; DNA-Binding Proteins; Epigenesis, Genetic; Female; Fibroblast Growth Factors; Haploinsufficiency; Histone Demethylases; Histones; Humans; Male; MAP Kinase Signaling System; Methylation; Mice, Inbred C57BL; Mice, Knockout; Noonan Syndrome; ras Proteins; Sin3 Histone Deacetylase and Corepressor Complex; Transcription Factors	2020

Article

Year

Haploinsufficiency of RREB1 causes a Noonan-like RASopathy via epigenetic reprogramming of RAS-MAPK pathway genes.

Nature communications, 2020, 09-16, Volume: 11, Issue:1

Topics: Abnormalities, Multiple; Animals; Chromosome Deletion; Chromosomes, Human, Pair 6; DNA-Binding Proteins; Epigenesis, Genetic; Female; Fibroblast Growth Factors; Haploinsufficiency; Histone Demethylases; Histones; Humans; Male; MAP Kinase Signaling System; Methylation; Mice, Inbred C57BL; Mice, Knockout; Noonan Syndrome; ras Proteins; Sin3 Histone Deacetylase and Corepressor Complex; Transcription Factors

2020