phenylalanine and Channelopathies

phenylalanine has been researched along with Channelopathies 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
Bove, C; D'Adamo, MC; Hasan, S; Hunter, G; Hunter, T; Macchioni, L; Mantuano, E; Modoni, A; Pessia, M; Silvestri, G; Veneziano, L	1

Other Studies

1 other study(ies) available for phenylalanine and Channelopathies

Article	Year
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia. Scientific reports, 2017, 07-04, Volume: 7, Issue:1 Topics: Alleles; Amino Acid Sequence; Ataxia; Channelopathies; Conserved Sequence; Female; Genotype; Humans; Ion Channel Gating; Kv1.1 Potassium Channel; Male; Models, Molecular; Mutation; Pedigree; Phenylalanine; Protein Conformation; Symptom Assessment	2017

Article

Year

A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia.

Scientific reports, 2017, 07-04, Volume: 7, Issue:1

Topics: Alleles; Amino Acid Sequence; Ataxia; Channelopathies; Conserved Sequence; Female; Genotype; Humans; Ion Channel Gating; Kv1.1 Potassium Channel; Male; Models, Molecular; Mutation; Pedigree; Phenylalanine; Protein Conformation; Symptom Assessment

2017