serine has been researched along with Antibody Deficiency Syndrome in 4 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "He does not display features of ectodermal dysplasia and did not suffer from serious infections with the exception of a relapsing Salmonella typhimurium infection." | 1.32 | The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes. ( Bredius, R; Hoeve, MA; Janssen, R; Lankester, A; Ottenhoff, TH; ten Dam, M; van de Vosse, E; van der Burg, M; van Dissel, JT; van Dongen, J; van Tol, M; van Wengen, A; Weemaes, C, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mueller, W | 1 |
| Schütz, D | 1 |
| Nagel, F | 1 |
| Schulz, S | 1 |
| Stumm, R | 1 |
| Bellacchio, E | 1 |
| Palma, A | 1 |
| Corrente, S | 1 |
| Di Girolamo, F | 1 |
| Helen Kemp, E | 1 |
| Di Matteo, G | 1 |
| Comelli, L | 1 |
| Carsetti, R | 1 |
| Cascioli, S | 1 |
| Cancrini, C | 1 |
| Fierabracci, A | 1 |
| Janssen, R | 1 |
| van Wengen, A | 1 |
| Hoeve, MA | 1 |
| ten Dam, M | 1 |
| van der Burg, M | 1 |
| van Dongen, J | 1 |
| van de Vosse, E | 1 |
| van Tol, M | 1 |
| Bredius, R | 1 |
| Ottenhoff, TH | 1 |
| Weemaes, C | 1 |
| van Dissel, JT | 1 |
| Lankester, A | 1 |
| Mancebo, E | 1 |
| Moreno-Pelayo, MA | 1 |
| Mencía, A | 1 |
| de la Calle-Martín, O | 1 |
| Allende, LM | 1 |
| Sivadorai, P | 1 |
| Kalaydjieva, L | 1 |
| Bertranpetit, J | 1 |
| Coto, E | 1 |
| Calleja-Antolín, S | 1 |
| Ruiz-Contreras, J | 1 |
| Paz-Artal, E | 1 |
4 other studies available for serine and Antibody Deficiency Syndrome
| Article | Year |
|---|---|
Hierarchical organization of multi-site phosphorylation at the CXCR4 C terminus.
Topics: Binding Sites; Calcium; Chemokine CXCL12; G-Protein-Coupled Receptor Kinase 2; G-Protein-Coupled Rec | 2013 |
The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant.
Topics: Adolescent; AIRE Protein; Amino Acid Sequence; Amino Acid Substitution; Autoimmunity; Cysteine; Huma | 2014 |
The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes.
Topics: Active Transport, Cell Nucleus; Adult; Alleles; B-Lymphocytes; Cell Division; Cell Nucleus; Child, P | 2004 |
Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies.
Topics: Adolescent; CD8 Antigens; DNA Mutational Analysis; Female; Glycine; Haplotypes; Humans; Immunologic | 2008 |