Page last updated: 2024-08-17

methionine and Antibody Deficiency Syndrome

methionine has been researched along with Antibody Deficiency Syndrome 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
Abinun, M; Bozzi, F; Cortes, P; Gomez, CA; Pasic, S; Santagata, S; Sobacchi, C; Vezzoni, P; Villa, A	1

Other Studies

1 other study(ies) available for methionine and Antibody Deficiency Syndrome

Article	Year
N-terminal RAG1 frameshift mutations in Omenn's syndrome: internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domains. Proceedings of the National Academy of Sciences of the United States of America, 2000, Dec-19, Volume: 97, Issue:26 Topics: Alleles; Cell Line, Transformed; DNA Nucleotidyltransferases; DNA-Binding Proteins; Frameshift Mutation; Homeodomain Proteins; Humans; Immunologic Deficiency Syndromes; Methionine; Nuclear Proteins; Protein Structure, Tertiary; Recombination, Genetic; VDJ Recombinases	2000

Article

Year

N-terminal RAG1 frameshift mutations in Omenn's syndrome: internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domains.

Proceedings of the National Academy of Sciences of the United States of America, 2000, Dec-19, Volume: 97, Issue:26

Topics: Alleles; Cell Line, Transformed; DNA Nucleotidyltransferases; DNA-Binding Proteins; Frameshift Mutation; Homeodomain Proteins; Humans; Immunologic Deficiency Syndromes; Methionine; Nuclear Proteins; Protein Structure, Tertiary; Recombination, Genetic; VDJ Recombinases

2000