tryptophan and Leigh Disease

tryptophan has been researched along with Leigh 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
Gaikwad, SM; Jaokar, TM; Patil, DP; Shouche, YS; Suresh, CG	1

Other Studies

1 other study(ies) available for tryptophan and Leigh Disease

Article	Year
Human mitochondrial NDUFS3 protein bearing Leigh syndrome mutation is more prone to aggregation than its wild-type. Biochimie, 2013, Volume: 95, Issue:12 Topics: Circular Dichroism; Cloning, Molecular; Electron Transport Complex I; Humans; Hydrogen-Ion Concentration; Leigh Disease; Mitochondria; Mutation; NADH Dehydrogenase; Protein Conformation; Protein Denaturation; Protein Stability; Protein Structure, Quaternary; Spectrometry, Fluorescence; Tryptophan	2013

Article

Year

Human mitochondrial NDUFS3 protein bearing Leigh syndrome mutation is more prone to aggregation than its wild-type.

Biochimie, 2013, Volume: 95, Issue:12

Topics: Circular Dichroism; Cloning, Molecular; Electron Transport Complex I; Humans; Hydrogen-Ion Concentration; Leigh Disease; Mitochondria; Mutation; NADH Dehydrogenase; Protein Conformation; Protein Denaturation; Protein Stability; Protein Structure, Quaternary; Spectrometry, Fluorescence; Tryptophan

2013