Page last updated: 2024-08-23

colforsin and Autosomal Chromosome Disorders

colforsin has been researched along with Autosomal Chromosome Disorders in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Iwase, S; Kim, HG; Murata-Nakamura, Y; Nagasu, H; Porter, RS	1
Clayton, PE; Dattani, MT; Eblé, A; Flück, CE; Lochmatter, D; Mullis, PE; Petkovic, V; Robinson, IC; Trainer, PJ; Turton, J	1

Other Studies

2 other study(ies) available for colforsin and Autosomal Chromosome Disorders

Article	Year
Transcriptome Analysis Revealed Impaired cAMP Responsiveness in PHF21A-Deficient Human Cells. Neuroscience, 2018, 02-01, Volume: 370 Topics: Cell Line; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 11; Colforsin; Cyclic AMP; Exostoses, Multiple Hereditary; Gene Expression Profiling; Gene Expression Regulation; Gene Knockdown Techniques; Histone Deacetylases; Humans; Lymphocytes; RNA, Small Interfering; Transcription, Genetic	2018
Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency. The Journal of clinical endocrinology and metabolism, 2007, Volume: 92, Issue:11 Topics: Adolescent; Adult; Blotting, Western; Body Height; Cell Proliferation; Cell Survival; Cells, Cultured; Chromosome Disorders; Colforsin; Endoplasmic Reticulum; Exons; Female; Genes, Dominant; Genetic Vectors; Golgi Apparatus; Human Growth Hormone; Humans; Male; Microscopy, Confocal; Mutation; Pedigree; Protein Isoforms; RNA, Messenger; Secretory Vesicles	2007

Article

Year

Transcriptome Analysis Revealed Impaired cAMP Responsiveness in PHF21A-Deficient Human Cells.

Neuroscience, 2018, 02-01, Volume: 370

Topics: Cell Line; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 11; Colforsin; Cyclic AMP; Exostoses, Multiple Hereditary; Gene Expression Profiling; Gene Expression Regulation; Gene Knockdown Techniques; Histone Deacetylases; Humans; Lymphocytes; RNA, Small Interfering; Transcription, Genetic

2018

Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.

The Journal of clinical endocrinology and metabolism, 2007, Volume: 92, Issue:11

Topics: Adolescent; Adult; Blotting, Western; Body Height; Cell Proliferation; Cell Survival; Cells, Cultured; Chromosome Disorders; Colforsin; Endoplasmic Reticulum; Exons; Female; Genes, Dominant; Genetic Vectors; Golgi Apparatus; Human Growth Hormone; Humans; Male; Microscopy, Confocal; Mutation; Pedigree; Protein Isoforms; RNA, Messenger; Secretory Vesicles

2007