glycine has been researched along with Bare Lymphocyte Syndrome in 4 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Patients with severe combined immune deficiency (SCID) suffer from defective T-cell Ca2+ signaling." | 1.35 | Increased hydrophobicity at the N terminus/membrane interface impairs gating of the severe combined immunodeficiency-related ORAI1 mutant. ( Bergsmann, J; Carugo, O; Derler, I; Eshaghi, S; Fahrner, M; Frischauf, I; Muik, M; Romanin, C; Schindl, R, 2009) |
| "Most patients are infants with severe combined immunodeficiency (SCID), but in about 20 percent immune dysfunction becomes manifest later in childhood ("delayed-onset"); several patients with "late" or "adult" onset of immune dysfunction have been diagnosed at 15-39 years." | 1.30 | 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. ( Arrendondo-Vega, FX; Buckley, R; Conley, ME; El Dahr, J; Hershfield, MS; Notarangelo, LD; Roifman, C; Santisteban, I, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Derler, I | 1 |
| Fahrner, M | 1 |
| Carugo, O | 1 |
| Muik, M | 1 |
| Bergsmann, J | 1 |
| Schindl, R | 1 |
| Frischauf, I | 1 |
| Eshaghi, S | 1 |
| Romanin, C | 1 |
| KOZINETS, GI | 1 |
| OSECHENSKAIA, GV | 1 |
| Sasaki, Y | 1 |
| Iseki, M | 1 |
| Yamaguchi, S | 1 |
| Kurosawa, Y | 1 |
| Yamamoto, T | 1 |
| Moriwaki, Y | 1 |
| Kenri, T | 1 |
| Sasaki, T | 1 |
| Yamashita, R | 1 |
| Arrendondo-Vega, FX | 1 |
| Santisteban, I | 1 |
| Notarangelo, LD | 1 |
| El Dahr, J | 1 |
| Buckley, R | 1 |
| Roifman, C | 1 |
| Conley, ME | 1 |
| Hershfield, MS | 1 |
4 other studies available for glycine and Bare Lymphocyte Syndrome
| Article | Year |
|---|---|
Increased hydrophobicity at the N terminus/membrane interface impairs gating of the severe combined immunodeficiency-related ORAI1 mutant.
Topics: Amino Acid Substitution; Calcium Channels; Cell Line; Cell Membrane; Cloning, Molecular; Computation | 2009 |
[Uptake of C14-labelled glycine into the hematopoietic cells of patients with leukoses].
Topics: Autoradiography; Blood Platelets; Bone Marrow; Erythrocytes; Genetic Diseases, X-Linked; Glycine; Hu | 1962 |
Direct evidence of autosomal recessive inheritance of Arg24 to termination codon in purine nucleoside phosphorylase gene in a family with a severe combined immunodeficiency patient.
Topics: Amino Acid Sequence; Arginine; Base Sequence; Child, Preschool; Chromosome Mapping; Chromosomes, Hum | 1998 |
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; | 1998 |