Compounds > tyrosine

tyrosine and Dwarfism, Thanatophoric

tyrosine has been researched along with Dwarfism, Thanatophoric in 4 studies

Research

Studies (4)

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

Authors

AuthorsStudies
Baruzzi, A; Ferrarini, F; Liboi, E; Lievens, PM; Montone, R; Romanelli, MG1
Blais, S; Chen, H; Huang, Z; Li, X; Mohammadi, M; Neubert, TA1
Bonaventure, J; Freisinger, P; Nerlich, AG1
Brodie, SG; Kitoh, H; Lipson, M; Sifry-Platt, M; Wilcox, WR1

Other Studies

4 other study(ies) available for tyrosine and Dwarfism, Thanatophoric

ArticleYear
Mutant FGFR3 associated with SADDAN disease causes cytoskeleton disorganization through PLCĪ³1/Src-mediated paxillin hyperphosphorylation.
    The international journal of biochemistry & cell biology, 2018, Volume: 95

    Topics: Achondroplasia; Amino Acid Substitution; Animals; Cell Line, Transformed; Cell Line, Tumor; Chondrocytes; Cytoskeleton; Humans; Mice; Mutation; Paxillin; Phospholipase C gamma; Phosphorylation; Protein Kinase Inhibitors; Protein Processing, Post-Translational; Protein Transport; Receptor, Fibroblast Growth Factor, Type 3; Recombinant Fusion Proteins; Signal Transduction; src-Family Kinases; Thanatophoric Dysplasia; Tyrosine

2018
Structural mimicry of a-loop tyrosine phosphorylation by a pathogenic FGF receptor 3 mutation.
    Structure (London, England : 1993), 2013, Oct-08, Volume: 21, Issue:10

    Topics: Catalytic Domain; Crystallography, X-Ray; Enzyme Activation; Enzyme Stability; Humans; Hydrogen Bonding; Models, Molecular; Molecular Mimicry; Mutation, Missense; Phosphoproteins; Phosphorylation; Protein Processing, Post-Translational; Protein Structure, Secondary; Receptor, Fibroblast Growth Factor, Type 3; Skull; Thanatophoric Dysplasia; Tyrosine

2013
Radiological and histological variants of thanatophoric dysplasia are associated with common mutations in FGFR-3.
    American journal of medical genetics, 1996, May-03, Volume: 63, Issue:1

    Topics: Adult; Arginine; Bone and Bones; Cartilage; Cysteine; Diagnosis, Differential; Female; Fetus; Genetic Variation; Gestational Age; Humans; Infant, Newborn; Phenotype; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Pregnancy; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Thanatophoric Dysplasia; Tyrosine

1996
Thanatophoric dysplasia type I with syndactyly.
    American journal of medical genetics, 1998, Nov-16, Volume: 80, Issue:3

    Topics: Cysteine; Fetal Diseases; Humans; Male; Point Mutation; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndactyly; Thanatophoric Dysplasia; Tyrosine

1998