Compounds > valine

valine and Autosomal Chromosome Disorders

valine has been researched along with Autosomal Chromosome Disorders in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boespflug, A; Bringuier, PP; Couraud, S; Durieu, I; Edery, P; Gérinière, L; Isaac, S; Perrot, E; Souquet, PJ1
Baxter, EJ; Campbell, PJ; Culligan, DA; Fourouclas, N; Green, AR; Huntly, BJ; Li, J; Munro, LR; Roberts, I; Scott, LM; Swanton, S; Vassiliou, GS1
van der Horst, JL; Wadman, SK1

Other Studies

3 other study(ies) available for valine and Autosomal Chromosome Disorders

ArticleYear
Primary lung adenocarcinoma occurring in a PTEN related syndrome (Cowden's disease): routine EGFR sequencing also highlights two rare somatic mutations S768I and V769L.
    Lung cancer (Amsterdam, Netherlands), 2013, Volume: 79, Issue:3

    Topics: Adenocarcinoma; Adult; Chromosome Disorders; Diagnosis, Differential; DNA Mutational Analysis; ErbB Receptors; Female; Germ-Line Mutation; Hamartoma Syndrome, Multiple; Humans; Lung Neoplasms; Phosphatidylinositol 3-Kinases; Proto-Oncogene Proteins c-akt; PTEN Phosphohydrolase; Serine; Signal Transduction; Valine

2013
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 variant form of branched-chain keto aciduria.
    Acta paediatrica Scandinavica, 1971, Volume: 60, Issue:5

    Topics: Amino Acids; Child Behavior Disorders; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diet Therapy; Dietary Proteins; Female; Heterozygote; Humans; Infant; Intellectual Disability; Isoleucine; Keto Acids; Leucine; Male; Maple Syrup Urine Disease; Methionine; Motor Skills; Pedigree; Phenylketonurias; Tyrosine; Valine

1971