Page last updated: 2024-08-21

quinazolines and Neurodevelopmental Disorders

quinazolines has been researched along with Neurodevelopmental Disorders 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
Abe, K; Ishitani, S; Ishitani, T; Kosaki, K; Oginuma, M; Okamoto, N; Takenouchi, T; Uehara, T; Yoshihashi, H	1

Other Studies

1 other study(ies) available for quinazolines and Neurodevelopmental Disorders

Article	Year
Pathogenesis of CDK8-associated disorder: two patients with novel CDK8 variants and in vitro and in vivo functional analyses of the variants. Scientific reports, 2020, 10-16, Volume: 10, Issue:1 Topics: Abnormalities, Multiple; Animals; Child; Craniofacial Abnormalities; Cyclin-Dependent Kinase 8; Cyclin-Dependent Kinases; Embryo, Nonmammalian; Female; Heart Defects, Congenital; Heterozygote; High-Throughput Nucleotide Sequencing; Humans; Infant; Intellectual Disability; Loss of Function Mutation; Male; Mutation, Missense; Neurodevelopmental Disorders; Point Mutation; Protein Domains; Protein Kinase Inhibitors; Quinazolines; RNA, Messenger; Zebrafish; Zebrafish Proteins	2020

Article

Year

Pathogenesis of CDK8-associated disorder: two patients with novel CDK8 variants and in vitro and in vivo functional analyses of the variants.

Scientific reports, 2020, 10-16, Volume: 10, Issue:1

Topics: Abnormalities, Multiple; Animals; Child; Craniofacial Abnormalities; Cyclin-Dependent Kinase 8; Cyclin-Dependent Kinases; Embryo, Nonmammalian; Female; Heart Defects, Congenital; Heterozygote; High-Throughput Nucleotide Sequencing; Humans; Infant; Intellectual Disability; Loss of Function Mutation; Male; Mutation, Missense; Neurodevelopmental Disorders; Point Mutation; Protein Domains; Protein Kinase Inhibitors; Quinazolines; RNA, Messenger; Zebrafish; Zebrafish Proteins

2020