serine has been researched along with Diseases, Metabolic in 12 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 |
|---|---|---|
| "Cystathionine was absent in the cerebrum of a patient with homocystinuria." | 7.64 | HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN. ( GERRITSEN, T; WAISMAN, HA, 1964) |
| "Cystathionine was absent in the cerebrum of a patient with homocystinuria." | 3.64 | HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN. ( GERRITSEN, T; WAISMAN, HA, 1964) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (16.67) | 18.7374 |
| 1990's | 1 (8.33) | 18.2507 |
| 2000's | 1 (8.33) | 29.6817 |
| 2010's | 4 (33.33) | 24.3611 |
| 2020's | 4 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Lone, MA | 1 |
| Bourquin, F | 1 |
| Hornemann, T | 1 |
| Chen, H | 1 |
| Liu, C | 2 |
| Wang, Q | 1 |
| Xiong, M | 1 |
| Zeng, X | 1 |
| Yang, D | 1 |
| Xie, Y | 1 |
| Su, H | 1 |
| Zhang, Y | 2 |
| Huang, Y | 1 |
| Chen, Y | 1 |
| Yue, J | 1 |
| Wang, S | 1 |
| Huang, K | 1 |
| Zheng, L | 1 |
| Wei, X | 1 |
| Jia, X | 1 |
| Liu, R | 1 |
| Zhang, S | 1 |
| Liu, S | 1 |
| An, J | 1 |
| Zhou, L | 1 |
| Mo, Y | 1 |
| Li, X | 1 |
| Sass, JO | 1 |
| Behringer, S | 1 |
| Fernando, M | 1 |
| Cesaroni, E | 1 |
| Cursio, I | 1 |
| Volpini, A | 1 |
| Till, C | 1 |
| Mota de Sá, P | 1 |
| Richard, AJ | 1 |
| Hang, H | 1 |
| Stephens, JM | 1 |
| de Koning, TJ | 1 |
| Vandenbeek, R | 1 |
| Khan, NP | 1 |
| Estall, JL | 1 |
| Becker-Kettern, J | 1 |
| Paczia, N | 1 |
| Conrotte, JF | 1 |
| Zhu, C | 1 |
| Fiehn, O | 1 |
| Jung, PP | 1 |
| Steinmetz, LM | 1 |
| Linster, CL | 1 |
| Kawakami, Y | 1 |
| Yoshida, K | 1 |
| Yang, JH | 1 |
| Suzuki, T | 1 |
| Azuma, N | 1 |
| Sakai, K | 1 |
| Hashikawa, T | 1 |
| Watanabe, M | 1 |
| Yasuda, K | 1 |
| Kuhara, S | 1 |
| Hirabayashi, Y | 1 |
| Furuya, S | 1 |
| GERRITSEN, T | 1 |
| WAISMAN, HA | 1 |
| Miller, WL | 1 |
| Auchus, RJ | 1 |
| Geller, DH | 1 |
| Williams, HE | 1 |
| Smith, LH | 1 |
6 reviews available for serine and Diseases, Metabolic
| Article | Year |
|---|---|
Serine Palmitoyltransferase Subunit 3 and Metabolic Diseases.
Topics: Animals; Coenzyme A; Humans; Mammals; Metabolic Diseases; Serine; Serine C-Palmitoyltransferase; Sph | 2022 |
Transcriptional Regulation of Adipogenesis.
Topics: Adipocytes; Adipogenesis; Animals; CCAAT-Enhancer-Binding Proteins; Gene Expression Regulation; Huma | 2017 |
Amino acid synthesis deficiencies.
Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Asparagine; Bra | 2017 |
Linking Metabolic Disease With the PGC-1α Gly482Ser Polymorphism.
Topics: Amino Acid Substitution; Diabetes Mellitus, Type 2; Genetic Linkage; Genetic Predisposition to Disea | 2018 |
The regulation of 17,20 lyase activity.
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Sequence; Animals; Binding Sites; Cytochrome P-450 Enzym | 1997 |
Disorders of oxalate metabolism.
Topics: Alcohol Oxidoreductases; Glyceric Acids; Glycolates; Humans; Intestinal Absorption; Kidney Calculi; | 1968 |
6 other studies available for serine and Diseases, Metabolic
| Article | Year |
|---|---|
Renal UTX-PHGDH-serine axis regulates metabolic disorders in the kidney and liver.
Topics: Diabetic Nephropathies; Histone Demethylases; Humans; Kidney; Liver; Metabolic Diseases; Obesity; Ph | 2022 |
Metabolic pathway analysis of hyperuricaemia patients with hyperlipidaemia based on high-throughput mass spectrometry: a case‒control study.
Topics: Alanine; Aspartic Acid; Biomarkers; Case-Control Studies; Glycine; Humans; Hyperlipidemias; Hyperuri | 2022 |
d-Glycerate kinase deficiency in a neuropediatric patient.
Topics: Carbohydrate Metabolism, Inborn Errors; Child; Exons; Glyceric Acids; Homozygote; Humans; Male; Meta | 2020 |
NAD(P)HX repair deficiency causes central metabolic perturbations in yeast and human cells.
Topics: Cells, Cultured; Humans; Metabolic Diseases; Metabolome; NAD; NADP; Racemases and Epimerases; Saccha | 2018 |
Impaired neurogenesis in embryonic spinal cord of Phgdh knockout mice, a serine deficiency disorder model.
Topics: Animals; Disease Models, Animal; Embryo, Mammalian; Excitatory Amino Acid Transporter 1; Gene Expres | 2009 |
HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN.
Topics: Amino Acids; Brain; Child; Chromatography; Cystathionine; Cystathionine beta-Synthase; Cystine; Homo | 1964 |