serine has been researched along with Metabolic Diseases 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.
Metabolic Diseases: Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed)
| 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 Metabolic Diseases
| 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 Metabolic Diseases
| 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 |