Compounds > arginine

arginine and Facies

arginine has been researched along with Facies 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
Blumenthal, RM; Cheng, X; Horton, JR; Huang, Y; Li, J; Yang, J; Zhang, X1
Caldarelli, M; Di Rocco, C; Di Rocco, F; Sabatino, G; Tamburrini, G; Zampino, G1
Ariga, T; Fujioka, H; Horiuchi, K; Igawa, H; Kawashima, K; Sakiyama, Y; Sugihara, T; Yamamoto, Y1
Fleming, J; Gerritsen, J; Graham, GE; Jabs, EW; Lowry, RB1

Other Studies

4 other study(ies) available for arginine and Facies

ArticleYear
Structural basis for preferential binding of human TCF4 to DNA containing 5-carboxylcytosine.
    Nucleic acids research, 2019, 09-19, Volume: 47, Issue:16

    Topics: Amino Acid Sequence; Arginine; Binding Sites; Cloning, Molecular; Cytosine; DNA; Electrophoretic Mobility Shift Assay; Escherichia coli; Facies; Gene Expression; Humans; Hyperventilation; Intellectual Disability; Models, Molecular; Mutation; Nucleotide Motifs; Protein Binding; Protein Conformation, alpha-Helical; Protein Interaction Domains and Motifs; Recombinant Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Thymine; Transcription Factor 4

2019
Muenke syndrome.
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2004, Volume: 20, Issue:5

    Topics: Arginine; Bone and Bones; Craniosynostoses; Facies; Female; Genes, Dominant; History, 20th Century; Humans; Infant, Newborn; Mutation; Penetrance; Proline; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndrome; Tomography, X-Ray Computed

2004
Treacher Collins syndrome with craniosynostosis, choanal atresia, and esophageal regurgitation caused by a novel nonsense mutation in TCOF1.
    American journal of medical genetics. Part A, 2004, Jul-15, Volume: 128A, Issue:2

    Topics: Arginine; Child, Preschool; Codon, Nonsense; Codon, Terminator; Craniosynostoses; DNA Mutational Analysis; Exons; Facies; Female; Gastroesophageal Reflux; Gene Deletion; Humans; Mandibulofacial Dysostosis; Mutation; Nuclear Proteins; Phosphoproteins; Polymorphism, Single-Stranded Conformational; Tomography, X-Ray Computed

2004
Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.
    American journal of medical genetics, 2001, Nov-22, Volume: 104, Issue:2

    Topics: Adult; Arginine; Child, Preschool; Craniosynostoses; Facies; Family Health; Female; Humans; Klippel-Feil Syndrome; Male; Mutation; Pedigree; Point Mutation; Proline; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Shoulder; Syndrome

2001