Page last updated: 2024-08-23

phosphotyrosine and Myeloproliferative Disorders

phosphotyrosine has been researched along with Myeloproliferative Disorders in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Babon, JJ; Ellyard, JI; Kershaw, NJ; Laktyushin, A; Morris, R; Murphy, JM; Vinuesa, CG; Zhang, Y1
Dagger, SA; Duyvestyn, JM; Langdon, WY; Morse, HC; Orandle, M; Taylor, SJ; Thien, CB1
Elabd, M; Freund, P; Gouilleux, F; Groner, B; Hager, M; Han, X; Kerenyi, MA; Krämer, OH; Moriggl, R; Pham, HTT; Sexl, V; Valent, P; Wagner, T; Wingelhofer, B1
Cheng, D; McLaughlin, J; Shokat, KM; Witte, ON; Wong, S; Zhang, C1

Other Studies

4 other study(ies) available for phosphotyrosine and Myeloproliferative Disorders

ArticleYear
Structural and functional analysis of target recognition by the lymphocyte adaptor protein LNK.
    Nature communications, 2021, 10-20, Volume: 12, Issue:1

    Topics: Adaptor Proteins, Signal Transducing; Amino Acid Motifs; Animals; Binding Sites; Crystallography, X-Ray; fms-Like Tyrosine Kinase 3; Humans; Janus Kinase 2; Janus Kinase 3; Mice; Mutation; Myeloproliferative Disorders; Phosphotyrosine; Protein Binding; Proto-Oncogene Proteins c-kit; Receptors, Erythropoietin; Signal Transduction; src Homology Domains

2021
Dasatinib targets B-lineage cells but does not provide an effective therapy for myeloproliferative disease in c-Cbl RING finger mutant mice.
    PloS one, 2014, Volume: 9, Issue:4

    Topics: Animals; B-Lymphocytes; Bone Marrow Cells; Cell Lineage; Dasatinib; Dose-Response Relationship, Drug; Germinal Center; Hematopoietic Stem Cells; Humans; Lymphocyte Count; Male; Mice, Inbred C57BL; Mice, Mutant Strains; Myeloproliferative Disorders; Neutrophils; Phosphorylation; Phosphotyrosine; Precursor Cells, B-Lymphoid; Proto-Oncogene Proteins c-cbl; Pyrimidines; RING Finger Domains; src-Family Kinases; Thiazoles

2014
O-GlcNAcylation of STAT5 controls tyrosine phosphorylation and oncogenic transcription in STAT5-dependent malignancies.
    Leukemia, 2017, Volume: 31, Issue:10

    Topics: Acetylglucosamine; Animals; Cell Line; Cell Transformation, Neoplastic; Female; Gene Expression Regulation, Neoplastic; Genes, Reporter; Glycosylation; Humans; Interleukin-3; Lymphoid Tissue; Male; Mice; Mutagenesis, Site-Directed; Myeloproliferative Disorders; Phosphorylation; Phosphotyrosine; Protein Processing, Post-Translational; Radiation Chimera; Recombinant Fusion Proteins; Signal Transduction; STAT5 Transcription Factor; T-Lymphocytes; Threonine; Transcriptional Activation; Tumor Suppressor Proteins

2017
Sole BCR-ABL inhibition is insufficient to eliminate all myeloproliferative disorder cell populations.
    Proceedings of the National Academy of Sciences of the United States of America, 2004, Dec-14, Volume: 101, Issue:50

    Topics: Apoptosis; B-Lymphocytes; Benzamides; Cell Cycle; Cell Line; Cell Proliferation; Drug Synergism; Enzyme Inhibitors; Fusion Proteins, bcr-abl; Gene Expression Regulation, Enzymologic; Humans; Imatinib Mesylate; Mutation; Myeloproliferative Disorders; Phosphotyrosine; Piperazines; Protein-Tyrosine Kinases; Proto-Oncogene Proteins c-kit; Pyrimidines; Tyrosine

2004