tryptophan and At-V1

tryptophan has been researched along with At-V1 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
Antoccia, A; Ascenzi, P; di Masi, A; Polticelli, F; Tanzarella, C; Viganotti, M	1

Other Studies

1 other study(ies) available for tryptophan and At-V1

Article	Year
The R215W mutation in NBS1 impairs gamma-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients. Biochemical and biophysical research communications, 2008, May-09, Volume: 369, Issue:3 Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Cell Cycle Proteins; DNA Breaks, Double-Stranded; DNA Repair; Histones; Humans; Molecular Sequence Data; Mutation, Missense; Nijmegen Breakage Syndrome; Nuclear Proteins; Phenotype; Protein Binding; Protein Structure, Tertiary; Sequence Deletion; Severity of Illness Index; Transfection; Tryptophan	2008

Article

Year

The R215W mutation in NBS1 impairs gamma-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients.

Biochemical and biophysical research communications, 2008, May-09, Volume: 369, Issue:3

Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Cell Cycle Proteins; DNA Breaks, Double-Stranded; DNA Repair; Histones; Humans; Molecular Sequence Data; Mutation, Missense; Nijmegen Breakage Syndrome; Nuclear Proteins; Phenotype; Protein Binding; Protein Structure, Tertiary; Sequence Deletion; Severity of Illness Index; Transfection; Tryptophan

2008