phenylalanine and Ataxia

phenylalanine has been researched along with Ataxia 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
Bove, C; D'Adamo, MC; Hasan, S; Hunter, G; Hunter, T; Macchioni, L; Mantuano, E; Modoni, A; Pessia, M; Silvestri, G; Veneziano, L	1
Cudia, P; D'Adamo, MC; De Grandis, D; Ferlini, A; Gualandi, F; Imbrici, P; Mannucci, R; Masieri, MT; Nicoletti, I; Pessia, M; Tucker, SJ	1

Other Studies

2 other study(ies) available for phenylalanine and Ataxia

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
A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1. Neuroscience, 2008, Dec-02, Volume: 157, Issue:3 Topics: Adult; Animals; Ataxia; Biophysical Phenomena; Chromosomes, Human, Pair 12; Cysteine; DNA Mutational Analysis; Electric Stimulation; Family Health; Green Fluorescent Proteins; Humans; Italy; Kv1.1 Potassium Channel; Kv1.2 Potassium Channel; Male; Membrane Potentials; Microinjections; Models, Molecular; Mutation, Missense; Myokymia; Oocytes; Patch-Clamp Techniques; Phenylalanine; Xenopus laevis; Xenopus Proteins; Young Adult	2008

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

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1.

Neuroscience, 2008, Dec-02, Volume: 157, Issue:3

Topics: Adult; Animals; Ataxia; Biophysical Phenomena; Chromosomes, Human, Pair 12; Cysteine; DNA Mutational Analysis; Electric Stimulation; Family Health; Green Fluorescent Proteins; Humans; Italy; Kv1.1 Potassium Channel; Kv1.2 Potassium Channel; Male; Membrane Potentials; Microinjections; Models, Molecular; Mutation, Missense; Myokymia; Oocytes; Patch-Clamp Techniques; Phenylalanine; Xenopus laevis; Xenopus Proteins; Young Adult

2008