tyrosine has been researched along with Erythrocytosis in 11 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (18.18) | 18.7374 |
1990's | 2 (18.18) | 18.2507 |
2000's | 4 (36.36) | 29.6817 |
2010's | 2 (18.18) | 24.3611 |
2020's | 1 (9.09) | 2.80 |
Authors | Studies |
---|---|
Cao, Y; Chen, S; Feng, X; Hao, D; He, Z; Huang, M; Li, S; Li, W; Liao, X; Liu, J; Liu, Z; Long, W; Wang, A; Wang, H; Wang, S; Wu, X; Wu, Y; Xie, M; Xu, Y; Zhao, Q; Zhong, R; Zhong, Y; Zhou, C | 1 |
Cleaver, O; Huang, LJ; Sulahian, R | 1 |
Boissinot, M; Cleyrat, C; Girodon, F; Harousseau, JL; Hermouet, S; Issa, JP; Jelinek, J; Ponge, T | 1 |
Jernigan, NL; Kanagy, NL; Norton, CE; Resta, TC; Walker, BR | 1 |
Ang, S; Guan, Y; Jedlickova, K; Jelinek, J; Krishnamurti, L; Liu, E; Pastore, YD; Prchal, JT | 1 |
Arcasoy, MO; Karayal, AF | 1 |
Gilliland, DG; Tefferi, A | 1 |
Goldberg, A; McColl, KE | 1 |
Brown, K; Greaves, M; Leach, M; Porter, N; Williamson, D | 1 |
Arcasoy, MO; Forget, BG; Harris, KW | 1 |
Dingle, B; Farguharson, H; Huisman, TH; Williams, D; Wilson, JB | 1 |
11 other study(ies) available for tyrosine and Erythrocytosis
Article | Year |
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Tyrosine phosphorylation of band 3 impairs the storage quality of suspended red blood cells in the Tibetan high-altitude polycythemia population.
Topics: Altitude; Altitude Sickness; Erythrocytes; Hemoglobins; Humans; Phosphorylation; Polycythemia; Tibet; Tyrosine | 2023 |
Ligand-induced EpoR internalization is mediated by JAK2 and p85 and is impaired by mutations responsible for primary familial and congenital polycythemia.
Topics: Endocytosis; Humans; Janus Kinase 2; Ligands; Mutation; Phosphatidylinositol 3-Kinases; Polycythemia; Protein Subunits; Receptors, Erythropoietin; Tyrosine | 2009 |
JAK2 mutation and disease phenotype: a double L611V/V617F in cis mutation of JAK2 is associated with isolated erythrocytosis and increased activation of AKT and ERK1/2 rather than STAT5.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Sequence; Animals; B-Lymphocytes; Base Sequence; Blotting, Western; Case-Control Studies; Cell Line; Colony-Forming Units Assay; Female; Genotype; Humans; Janus Kinase 2; Mice; Middle Aged; Mitogen-Activated Protein Kinase 1; Mitogen-Activated Protein Kinase 3; Molecular Sequence Data; Mutation; Myeloproliferative Disorders; Phenotype; Phosphorylation; Polycythemia; Polymerase Chain Reaction; Proto-Oncogene Proteins c-akt; STAT5 Transcription Factor; Thrombosis; Tyrosine; Young Adult | 2010 |
Intermittent hypoxia augments pulmonary vascular smooth muscle reactivity to NO: regulation by reactive oxygen species.
Topics: 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt; Animals; Cyclic GMP; Cyclic GMP-Dependent Protein Kinases; Endothelium-Dependent Relaxing Factors; Free Radical Scavengers; Hypertrophy, Right Ventricular; Hypocapnia; Hypoxia; Ionomycin; Lung; Male; Muscle, Smooth, Vascular; Nitric Oxide; Nitric Oxide Donors; Nitric Oxide Synthase Type III; Polycythemia; Pulmonary Artery; Rats; Rats, Wistar; Reactive Oxygen Species; S-Nitroso-N-Acetylpenicillamine; Superoxides; Tyrosine; Vasodilation | 2011 |
Mutations in the VHL gene in sporadic apparently congenital polycythemia.
Topics: Adolescent; Adult; Arginine; Aspartic Acid; Base Sequence; Child; Child, Preschool; DNA Mutational Analysis; Erythroid Precursor Cells; Erythropoietin; Female; Heterozygote; Homozygote; Humans; Leucine; Ligases; Male; Mutation; Pedigree; Polycythemia; Sequence Analysis, DNA; Tryptophan; Tumor Suppressor Proteins; Tyrosine; Ubiquitin-Protein Ligases; Valine; Von Hippel-Lindau Tumor Suppressor Protein | 2003 |
Erythropoietin hypersensitivity in primary familial and congenital polycythemia: role of tyrosines Y285 and Y344 in erythropoietin receptor cytoplasmic domain.
Topics: Animals; Cell Line; Cell Proliferation; Cytoplasm; DNA-Binding Proteins; Erythropoietin; Humans; Janus Kinase 2; Mice; Milk Proteins; Mutation; Phosphorylation; Polycythemia; Protein Structure, Tertiary; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Receptors, Erythropoietin; STAT1 Transcription Factor; STAT5 Transcription Factor; Trans-Activators; Tyrosine | 2005 |
JAK2 in myeloproliferative disorders is not just another kinase.
Topics: Alleles; Animals; Bone Marrow Cells; Cell Lineage; Cell Proliferation; Cytoplasm; DNA; DNA Mutational Analysis; Erythrocytes; Erythropoietin; Homozygote; Humans; Janus Kinase 2; Mice; Mutation; Myelodysplastic Syndromes; Myeloproliferative Disorders; Phenotype; Phosphorylation; Phosphotransferases; Point Mutation; Polycythemia; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Sequence Analysis, DNA; T-Lymphocytes; Tyrosine; Up-Regulation | 2005 |
Abnormal porphyrin metabolism in diseases other than prophyria.
Topics: Alcohol Drinking; Amino Acid Metabolism, Inborn Errors; Anemia, Hemolytic; Anemia, Hypochromic; Anemia, Megaloblastic; Anemia, Sickle Cell; Anemia, Sideroblastic; Humans; Lead Poisoning; Leukemia; Liver Diseases; Malabsorption Syndromes; Mental Disorders; Polycythemia; Porphyrins; Time Factors; Tyrosine | 1980 |
Haemoglobin Hallamshire (beta146 HIS --> TYR): a new high oxygen affinity haemoglobin responsible for familial erythrocytosis.
Topics: Adult; Blood Protein Electrophoresis; Family Health; Female; Hemoglobins, Abnormal; Heterozygote; Histidine; Humans; Hydrogen-Ion Concentration; Male; Oxyhemoglobins; Point Mutation; Polycythemia; Tyrosine | 1996 |
A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation.
Topics: Animals; Cell Line; Cell Nucleus; DNA-Binding Proteins; Enzyme Activation; Erythropoietin; Family Health; Humans; Janus Kinase 2; Mice; Milk Proteins; Mutation; Phosphorylation; Polycythemia; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Receptors, Erythropoietin; Signal Transduction; STAT5 Transcription Factor; Time Factors; Trans-Activators; Transfection; Tyrosine | 1999 |
Hb Rainier or alpha 2 beta 2 (145 (HC2) Tyr replaced by Cys) observed in members of a Canadian family of Greek origin.
Topics: Canada; Cystine; Greece; Hemoglobins, Abnormal; Heterozygote; Humans; Male; Polycythemia; Tyrosine | 1979 |