Compounds > valine

valine and Chromosomal Translocation

valine has been researched along with Chromosomal Translocation in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cheong, JW; Choi, JR; Kim, SJ; Lee, KA; Lee, KW; Park, TS; Song, J; Song, S; Suh, B1
Dal Cin, P; Hernandez, JM; Kuo, FC; Leon, A; Longtine, JA; Staropoli, JF1
Baxter, EJ; Campbell, PJ; Culligan, DA; Fourouclas, N; Green, AR; Huntly, BJ; Li, J; Munro, LR; Roberts, I; Scott, LM; Swanton, S; Vassiliou, GS1
Hasselbalch, HC; Kerndrup, GB; Larsen, TS; Pallisgaard, N1

Other Studies

4 other study(ies) available for valine and Chromosomal Translocation

ArticleYear
Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia.
    Cancer genetics and cytogenetics, 2009, Apr-01, Volume: 190, Issue:1

    Topics: Amino Acid Substitution; Antineoplastic Agents; Base Sequence; Benzamides; Chromosomes, Human, Pair 19; Chromosomes, Human, Pair 3; Drug Resistance, Neoplasm; Female; Glutamic Acid; Humans; Imatinib Mesylate; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Middle Aged; Mutation, Missense; Piperazines; Prognosis; Pyrimidines; Translocation, Genetic; Trisomy; Valine

2009
Translocation t(1;9) is a recurrent cytogenetic abnormality associated with progression of essential thrombocythemia patients displaying the JAK2 V617F mutation.
    Leukemia research, 2011, Volume: 35, Issue:9

    Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Chromosome Aberrations; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 9; Cohort Studies; Disease Progression; Female; Humans; Janus Kinase 2; Male; Middle Aged; Mutation, Missense; Phenylalanine; Recurrence; Thrombocythemia, Essential; Translocation, Genetic; Valine

2011
An acquired translocation in JAK2 Val617Phe-negative essential thrombocythemia associated with autosomal spread of X-inactivation.
    Haematologica, 2006, Volume: 91, Issue:8

    Topics: Amino Acid Substitution; Base Sequence; Blotting, Southern; Bone Marrow; Breast Neoplasms; Chromosome Disorders; Chromosome Mapping; Chromosome Walking; Chromosomes, Human, Pair 5; Chromosomes, Human, X; DNA Methylation; DNA Primers; Female; Humans; Janus Kinase 2; Middle Aged; Phenylalanine; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Reverse Transcriptase Polymerase Chain Reaction; Sex Chromosome Disorders; Thrombocythemia, Essential; Translocation, Genetic; Valine

2006
A der(18)t(9;18)(p13;p11) and a der(9;18)(p10;q10) in polycythemia vera associated with a hyperproliferative phenotype in transformation to postpolycythemic myelofibrosis.
    Cancer genetics and cytogenetics, 2007, Jan-15, Volume: 172, Issue:2

    Topics: Aged; Cell Proliferation; Cell Transformation, Neoplastic; Chromosomes, Human, Pair 18; Chromosomes, Human, Pair 9; Female; Humans; Janus Kinase 2; Male; Middle Aged; Phenotype; Phenylalanine; Polycythemia Vera; Primary Myelofibrosis; Translocation, Genetic; Valine

2007