Compounds > tryptophan

tryptophan and Cleft Palate

tryptophan has been researched along with Cleft Palate in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's0 (0.00)18.2507
2000's2 (33.33)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM1
Bailleul-Forestier, I; Bennaceur, S; de Roux, N; Gros, C; Leger, J; Zenaty, D1
Hoshino, A; Kaewkhampa, A; Kantaputra, PN; Lees, M; Masrour, N; McEntagart, M; Moore, GE; Paramee, M; Pauws, E; Stanier, P1
Nakakita, N; Sakai, N; Sakata, Y; Shida, H; Susami, T; Takato, T; Tokunaga, K; Uchinuma, E; Yamazaki, Y1
Britto, JA; Evans, RD; Hayward, RD; Jones, BM1
Freire-Maia, N1

Other Studies

6 other study(ies) available for tryptophan and Cleft Palate

ArticleYear
Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.
    The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5

    Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female; Foot Deformities, Congenital; Genotype; Hand Deformities, Congenital; Heterozygote; Humans; Melanosis; Mutation, Missense; Phenotype; Sequence Analysis, Protein; Thymine; Transcription Factors; Tryptophan; Tumor Suppressor Proteins

2010
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.
    International journal of paediatric dentistry, 2010, Volume: 20, Issue:4

    Topics: Adenine; Adolescent; Adult; Anodontia; Arginine; Bicuspid; Child, Preschool; Cleft Palate; Cysteine; Cytosine; Female; Glutamine; Glycine; Guanine; Humans; Incisor; Kallmann Syndrome; Male; Middle Aged; Molar; Mutation; Receptor, Fibroblast Growth Factor, Type 1; Sequence Deletion; Tooth Abnormalities; Tooth Root; Tooth, Deciduous; Tryptophan; Young Adult

2010
Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.
    Journal of dental research, 2011, Volume: 90, Issue:4

    Topics: Adolescent; Anodontia; Arginine; Child; Child, Preschool; Cleft Lip; Cleft Palate; Cohort Studies; Conserved Sequence; DNA-Binding Proteins; Exons; Female; Genetic Variation; Glutamine; Humans; Labial Frenum; Leucine; Male; Mutation, Missense; Phenotype; Polymorphism, Genetic; Proline; Promoter Regions, Genetic; Serine; T-Box Domain Proteins; Tongue Diseases; Transcription, Genetic; Tryptophan; Tyrosine

2011
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
Toward pathogenesis of Apert cleft palate: FGF, FGFR, and TGF beta genes are differentially expressed in sequential stages of human palatal shelf fusion.
    The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2002, Volume: 39, Issue:3

    Topics: Acrocephalosyndactylia; Apoptosis; Cleft Palate; DNA-Binding Proteins; Epithelium; Exons; Fibroblast Growth Factor 2; Fibroblast Growth Factor 7; Fibroblast Growth Factors; Gene Expression Regulation, Developmental; Humans; Image Processing, Computer-Assisted; Immunohistochemistry; In Situ Hybridization; Keratinocytes; Mesoderm; Mutation; Palate; Protein Isoforms; Receptors, Fibroblast Growth Factor; Serine; Signal Transduction; STAT1 Transcription Factor; Trans-Activators; Transcription, Genetic; Transforming Growth Factor beta; Transforming Growth Factor beta3; Tryptophan; Up-Regulation

2002
A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities.
    American journal of human genetics, 1970, Volume: 22, Issue:4

    Topics: Abnormalities, Multiple; Adolescent; Adult; Alopecia; Animals; Brazil; Breast; Child; Cleft Lip; Cleft Palate; Ear Deformities, Acquired; Ectodermal Dysplasia; Ectromelia; Electrocardiography; Electroencephalography; Growth Disorders; Heart Function Tests; Humans; Hypogonadism; Infant, Newborn; Intellectual Disability; Limb Deformities, Congenital; Male; Pedigree; Sibling Relations; Skin Abnormalities; Thyroid Gland; Tooth Abnormalities; Tryptophan

1970