Page last updated: 2024-08-18

2-naphthol and Chondrodystrophic Myotonia

2-naphthol has been researched along with Chondrodystrophic Myotonia 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	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Beddington, RS; Clements, M; Conlon, RA; Dunwoodie, SL; Sa, X; Sparrow, DB	1

Other Studies

1 other study(ies) available for 2-naphthol and Chondrodystrophic Myotonia

Article	Year
Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development (Cambridge, England), 2002, Volume: 129, Issue:7 Topics: Alleles; Animals; Gene Expression Regulation, Developmental; Gene Targeting; Humans; In Situ Hybridization; Intracellular Signaling Peptides and Proteins; Membrane Proteins; Mice; Mice, Knockout; Mice, Mutant Strains; Mutation; Naphthols; Osteochondrodysplasias; Receptors, Notch; Signal Transduction; Somites; Triazines	2002

Article

Year

Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm.

Development (Cambridge, England), 2002, Volume: 129, Issue:7

Topics: Alleles; Animals; Gene Expression Regulation, Developmental; Gene Targeting; Humans; In Situ Hybridization; Intracellular Signaling Peptides and Proteins; Membrane Proteins; Mice; Mice, Knockout; Mice, Mutant Strains; Mutation; Naphthols; Osteochondrodysplasias; Receptors, Notch; Signal Transduction; Somites; Triazines

2002