glycine has been researched along with Lupus Erythematosus, Systemic in 7 studies
Lupus Erythematosus, Systemic: A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow.
| Excerpt | Relevance | Reference |
|---|---|---|
| "They developed systemic lupus erythematosus-like symptoms during adolescence." | 2.41 | Molecular analysis of hereditary deficiency of the third component of complement (C3) in two sisters. ( Matsuyama, W; Muranaga, F; Nakagawa, M; Osame, M; Sano, Y; Takashima, H, 2001) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (28.57) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, X | 1 |
| Sun, X | 1 |
| Yang, W | 1 |
| Yang, B | 1 |
| Zhao, X | 1 |
| Chen, S | 1 |
| He, L | 1 |
| Chen, H | 1 |
| Yang, C | 1 |
| Xiao, L | 1 |
| Chang, Z | 1 |
| Guo, J | 1 |
| He, J | 1 |
| Zhang, F | 1 |
| Zheng, F | 1 |
| Hu, Z | 1 |
| Yang, Z | 1 |
| Lou, J | 1 |
| Zheng, W | 1 |
| Qi, H | 1 |
| Xu, C | 1 |
| Zhang, H | 1 |
| Shan, H | 1 |
| Zhou, XJ | 1 |
| Wang, Q | 1 |
| Shi, Y | 1 |
| Lai, L | 1 |
| Li, Z | 1 |
| Liu, W | 1 |
| Racz, Z | 1 |
| Nagy, E | 1 |
| Rosivall, L | 1 |
| Szebeni, J | 1 |
| Hamar, P | 1 |
| VOLKOV, VP | 1 |
| Weiss, G | 1 |
| Madsen, HO | 1 |
| Garred, P | 2 |
| Marquart, HV | 1 |
| Schejbel, L | 1 |
| Sjoholm, A | 1 |
| Martensson, U | 1 |
| Nielsen, S | 1 |
| Koch, A | 1 |
| Svejgaard, A | 1 |
| Matsuyama, W | 1 |
| Nakagawa, M | 1 |
| Takashima, H | 1 |
| Muranaga, F | 1 |
| Sano, Y | 1 |
| Osame, M | 1 |
| Saito, A | 1 |
| Ogawa, H | 1 |
| Takagi, T | 1 |
| Matsumoto, M | 1 |
| Yoshimasu, S | 1 |
1 review available for glycine and Lupus Erythematosus, Systemic
| Article | Year |
|---|---|
Molecular analysis of hereditary deficiency of the third component of complement (C3) in two sisters.
Topics: Adolescent; Adult; Blotting, Western; Codon, Terminator; Complement C3; Cysteine; Female; Glycine; H | 2001 |
6 other studies available for glycine and Lupus Erythematosus, Systemic
| Article | Year |
|---|---|
An autoimmune disease variant of IgG1 modulates B cell activation and differentiation.
Topics: Amino Acid Substitution; Animals; Arginine; Autoantibodies; Autoimmunity; B-Lymphocytes; Cell Differ | 2018 |
Sugar-free, glycine-stabilized intravenous immunoglobulin prevents skin but not renal disease in the MRL/lpr mouse model of systemic lupus.
Topics: Animals; Disease Models, Animal; Glycine; Immunoglobulins, Intravenous; Kidney Diseases; Lupus Eryth | 2010 |
[FREE AMINO ACIDS IN THE BLOOD AND URINE OF PATIENTS WITH SOME FORMS OF DERMATOSIS].
Topics: Alanine; Amino Acids; Arginine; Aspartic Acid; Blood; Cystine; Dermatitis; Eczema; Erythema Multifor | 1964 |
A novel mannose-binding lectin-associated serine protease 1/3 gene variant.
Topics: Amino Acid Substitution; Genetic Variation; Glutamic Acid; Glycine; Humans; Inflammation; Lupus Eryt | 2007 |
C1q deficiency in an Inuit family: identification of a new class of C1q disease-causing mutations.
Topics: Adolescent; Arginine; Child; Child, Preschool; Complement C1q; Complement Hemolytic Activity Assay; | 2007 |
A new autologous plasma exchange system with salt-amino acid coprecipitation (SAC) method.
Topics: Ammonium Sulfate; Animals; Arthritis, Rheumatoid; Blood Proteins; Cattle; Chemical Precipitation; Et | 1985 |