Compounds > tryptophan

tryptophan and Craniofacial Dysarthrosis

tryptophan has been researched along with Craniofacial Dysarthrosis in 4 studies

Research

Studies (4)

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

Authors

AuthorsStudies
Gong, SG1
Anderson, PJ; Cox, TC; David, DJ; Netherway, DJ; Roscioli, T1
Anderson, C; Can, B; Say, B; Schaefer, F1
Nakakita, N; Sakai, N; Sakata, Y; Shida, H; Susami, T; Takato, T; Tokunaga, K; Uchinuma, E; Yamazaki, Y1

Other Studies

4 other study(ies) available for tryptophan and Craniofacial Dysarthrosis

ArticleYear
The Fgfr2 W290R mouse model of Crouzon syndrome.
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2012, Volume: 28, Issue:9

    Topics: Animals; Arginine; Bone and Bones; Cartilage; Cranial Sutures; Craniofacial Dysostosis; Disease Models, Animal; Humans; Mice; Mutation; Phenotype; Receptor, Fibroblast Growth Factor, Type 2; Tryptophan

2012
Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
    The Journal of craniofacial surgery, 2006, Volume: 17, Issue:1

    Topics: Acrocephalosyndactylia; Adenine; Adolescent; Arginine; Child, Preschool; Craniofacial Dysostosis; Craniosynostoses; Cysteine; Cytosine; DNA Transposable Elements; Female; Follow-Up Studies; Guanine; Humans; Male; Mutation; Receptor, Fibroblast Growth Factor, Type 2; Sequence Deletion; Serine; Syndrome; Thymine; Treatment Outcome; Tryptophan; Twist-Related Protein 1

2006
Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 case.
    American journal of medical genetics, 1998, Jan-23, Volume: 75, Issue:3

    Topics: Acrocephalosyndactylia; Amino Acid Sequence; Codon; Craniofacial Dysostosis; Cysteine; Exons; Female; Humans; Infant, Newborn; Molecular Sequence Data; Mutation; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Tryptophan

1998
Sequence analysis of fibroblast growth factor receptor 2 ( FGFR2 ) in Japanese patients with craniosynostosis.
    The Journal of craniofacial surgery, 2001, Volume: 12, Issue:6

    Topics: Acrocephalosyndactylia; Arginine; Cleft Palate; Codon; Craniofacial Dysostosis; Craniosynostoses; Exons; Female; Heterozygote; Humans; Japan; Male; Mutation; Polymerase Chain Reaction; Proline; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Sequence Analysis, DNA; Serine; Syndactyly; Tryptophan

2001