Page last updated: 2024-08-23

colforsin and Chondrodystrophic Myotonia

colforsin has been researched along with Chondrodystrophic Myotonia 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
Abdel Khalek, W; Auzan, C; Bertherat, J; Clauser, E; Couvineau, A; Le Stunff, C; Linglart, A; Rhayem, Y; Silve, C	1
Bichara, M; Escoubet, B; Ferrary, E; Friedlander, G; Grayeli, AB; Julien, N; Silve, C; Sterkers, O	1

Other Studies

2 other study(ies) available for colforsin and Chondrodystrophic Myotonia

Article	Year
Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney Complex. The Journal of biological chemistry, 2015, Nov-13, Volume: 290, Issue:46 Topics: Amino Acid Substitution; Bioluminescence Resonance Energy Transfer Techniques; Carney Complex; Codon, Nonsense; Colforsin; Cyclic AMP; Cyclic AMP-Dependent Protein Kinase RIalpha Subunit; Dysostoses; Enzyme Activation; HEK293 Cells; Humans; Intellectual Disability; Mutation, Missense; Osteochondrodysplasias; Parathyroid Hormone; Protein Structure, Tertiary; Thyrotropin; Transcription, Genetic	2015
Increased activity of the diastrophic dysplasia sulfate transporter in otosclerosis and its inhibition by sodium fluoride. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 2003, Volume: 24, Issue:6 Topics: Adult; Alkaline Phosphatase; Analysis of Variance; Anion Transport Proteins; Biological Transport; Carrier Proteins; Case-Control Studies; Cells, Cultured; Colforsin; Ear Canal; Female; Hearing Loss; Humans; Male; Membrane Transport Proteins; Middle Aged; Osteochondrodysplasias; Otosclerosis; Phenotype; Sodium Fluoride; Stapes; Sulfate Transporters; Verapamil	2003

Article

Year

Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney Complex.

The Journal of biological chemistry, 2015, Nov-13, Volume: 290, Issue:46

Topics: Amino Acid Substitution; Bioluminescence Resonance Energy Transfer Techniques; Carney Complex; Codon, Nonsense; Colforsin; Cyclic AMP; Cyclic AMP-Dependent Protein Kinase RIalpha Subunit; Dysostoses; Enzyme Activation; HEK293 Cells; Humans; Intellectual Disability; Mutation, Missense; Osteochondrodysplasias; Parathyroid Hormone; Protein Structure, Tertiary; Thyrotropin; Transcription, Genetic

2015

Increased activity of the diastrophic dysplasia sulfate transporter in otosclerosis and its inhibition by sodium fluoride.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 2003, Volume: 24, Issue:6

Topics: Adult; Alkaline Phosphatase; Analysis of Variance; Anion Transport Proteins; Biological Transport; Carrier Proteins; Case-Control Studies; Cells, Cultured; Colforsin; Ear Canal; Female; Hearing Loss; Humans; Male; Membrane Transport Proteins; Middle Aged; Osteochondrodysplasias; Otosclerosis; Phenotype; Sodium Fluoride; Stapes; Sulfate Transporters; Verapamil

2003