Page last updated: 2024-08-21

ethylnitrosourea and Camurati-Engelmann Disease

ethylnitrosourea has been researched along with Camurati-Engelmann Disease 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
Fukumura, R; Furuichi, T; Gondo, Y; Ichimura, S; Ikegawa, S; Murata, T; Sasaki, S	1

Other Studies

1 other study(ies) available for ethylnitrosourea and Camurati-Engelmann Disease

Article	Year
An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes. Experimental animals, 2017, May-03, Volume: 66, Issue:2 Topics: Amino Acid Substitution; Animals; Camurati-Engelmann Syndrome; Cysteine; Ethylnitrosourea; Female; Gene Library; Genetic Association Studies; HEK293 Cells; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Molecular Targeted Therapy; Mutation, Missense; Phenotype; Serine; Signal Transduction; Transforming Growth Factor beta1	2017

Article

Year

An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes.

Experimental animals, 2017, May-03, Volume: 66, Issue:2

Topics: Amino Acid Substitution; Animals; Camurati-Engelmann Syndrome; Cysteine; Ethylnitrosourea; Female; Gene Library; Genetic Association Studies; HEK293 Cells; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Molecular Targeted Therapy; Mutation, Missense; Phenotype; Serine; Signal Transduction; Transforming Growth Factor beta1

2017