Page last updated: 2024-08-18

isomethyleugenol and Marfan Syndrome

isomethyleugenol has been researched along with Marfan 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
Hayashi, T; Kato, Y; Nagai, M; Nakamura, M; Sano, A; Sasaki, N; Tomiyasu, A; Tomiyasu, Y; Ueno, SI; Umehara, H; Yokotsuka-Ishida, S	1

Other Studies

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

Article	Year
Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia. Journal of human genetics, 2021, Volume: 66, Issue:6 Topics: Cloning, Molecular; DNA Mutational Analysis; Exome; Exome Sequencing; F-Box Proteins; Female; Genetic Linkage; Genetic Predisposition to Disease; Haplotypes; Histone Demethylases; Histones; Humans; Intellectual Disability; Japan; Jumonji Domain-Containing Histone Demethylases; Male; Marfan Syndrome; Methylation; Mutation; Pedigree; Schizophrenia	2021

Article

Year

Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia.

Journal of human genetics, 2021, Volume: 66, Issue:6

Topics: Cloning, Molecular; DNA Mutational Analysis; Exome; Exome Sequencing; F-Box Proteins; Female; Genetic Linkage; Genetic Predisposition to Disease; Haplotypes; Histone Demethylases; Histones; Humans; Intellectual Disability; Japan; Jumonji Domain-Containing Histone Demethylases; Male; Marfan Syndrome; Methylation; Mutation; Pedigree; Schizophrenia

2021