valine has been researched along with Bare Lymphocyte Syndrome in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Arvin, A; Che, X; Gu, H; Qiao, Y; Reichelt, M; Zerboni, L | 1 |
Arrendondo-Vega, FX; Buckley, R; Conley, ME; El Dahr, J; Hershfield, MS; Notarangelo, LD; Roifman, C; Santisteban, I | 1 |
2 other study(ies) available for valine and Bare Lymphocyte Syndrome
Article | Year |
---|---|
Herpes simplex virus 1 tropism for human sensory ganglion neurons in the severe combined immunodeficiency mouse model of neuropathogenesis.
Topics: Acyclovir; Animals; Ganglia, Spinal; Gene Expression; Herpes Simplex; Herpesvirus 1, Human; Herpesvirus 3, Human; Humans; Luciferases; Mice; Mice, SCID; Satellite Cells, Perineuronal; Severe Combined Immunodeficiency; Transplantation, Heterologous; Valacyclovir; Valine; Viral Proteins; Viral Tropism; Virus Latency; Virus Replication | 2013 |
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.
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 |