Page last updated: 2024-08-17

methionine and Severe Combined Immunodeficiency

methionine has been researched along with Severe Combined Immunodeficiency in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hirose, K; Ikeda, K; Iwamoto, I; Kagami, S; Kanari, H; Nakajima, H; Owada, T; Saito, Y; Suto, A; Watanabe, N	1
Arrendondo-Vega, FX; Buckley, R; Conley, ME; El Dahr, J; Hershfield, MS; Notarangelo, LD; Roifman, C; Santisteban, I	1

Other Studies

2 other study(ies) available for methionine and Severe Combined Immunodeficiency

Article	Year
Protein geranylgeranylation regulates the balance between Th17 cells and Foxp3+ regulatory T cells. International immunology, 2009, Volume: 21, Issue:6 Topics: Animals; Benzamides; Cell Differentiation; Forkhead Transcription Factors; Gene Expression Regulation; Interleukin-17; Interleukin-6; Methionine; Mice; Mice, Inbred BALB C; Mice, Transgenic; Ovalbumin; Peptide Fragments; Prenylation; Receptors, Antigen, T-Cell, alpha-beta; Severe Combined Immunodeficiency; Simvastatin; STAT3 Transcription Factor; Suppressor of Cytokine Signaling 3 Protein; Suppressor of Cytokine Signaling Proteins; T-Lymphocyte Subsets; T-Lymphocytes, Regulatory	2009
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online. Human mutation, 1998, Volume: 11, Issue:6 Topics: Adenosine Deaminase; Adolescent; Adult; Age of Onset; Arginine; Cysteine; Glutamic Acid; Glutamine; Glycine; Humans; Methionine; Mutation; Proline; Sequence Deletion; Severe Combined Immunodeficiency; Tryptophan; Valine	1998

Article

Year

Protein geranylgeranylation regulates the balance between Th17 cells and Foxp3+ regulatory T cells.

International immunology, 2009, Volume: 21, Issue:6

Topics: Animals; Benzamides; Cell Differentiation; Forkhead Transcription Factors; Gene Expression Regulation; Interleukin-17; Interleukin-6; Methionine; Mice; Mice, Inbred BALB C; Mice, Transgenic; Ovalbumin; Peptide Fragments; Prenylation; Receptors, Antigen, T-Cell, alpha-beta; Severe Combined Immunodeficiency; Simvastatin; STAT3 Transcription Factor; Suppressor of Cytokine Signaling 3 Protein; Suppressor of Cytokine Signaling Proteins; T-Lymphocyte Subsets; T-Lymphocytes, Regulatory

2009

Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online.

Human mutation, 1998, Volume: 11, Issue:6

Topics: Adenosine Deaminase; Adolescent; Adult; Age of Onset; Arginine; Cysteine; Glutamic Acid; Glutamine; Glycine; Humans; Methionine; Mutation; Proline; Sequence Deletion; Severe Combined Immunodeficiency; Tryptophan; Valine

1998