proline and Cleft Lip

proline has been researched along with Cleft Lip in 4 studies

Research

Studies (4)

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

Authors

AuthorsStudies
Oner, DA; Tastan, H1
Hoshino, A; Kaewkhampa, A; Kantaputra, PN; Lees, M; Masrour, N; McEntagart, M; Moore, GE; Paramee, M; Pauws, E; Stanier, P1
Ewers, R; Item, CB; Lauer, G; Sinko, K; Turhani, D; Watzinger, E; Watzinger, F1
Camacho, J; Heymann, WR; Honig, PJ; Ilyas, E; Imaizumi, S; Li, W; Pawel, BR; Payne, AS; Schnur, RE; Seykora, JT; Yan, AC; Young, TL1

Other Studies

4 other study(ies) available for proline and Cleft Lip

ArticleYear
Association Between the Transforming Growth Factor Beta 1 Gene Polymorphisms and Turkish Patients with Nonsyndromic Cleft Lip With/Without Cleft Palate.
    Genetic testing and molecular biomarkers, 2016, Volume: 20, Issue:5

    Topics: Amino Acid Substitution; Arginine; Case-Control Studies; Child; Child, Preschool; Cleft Lip; Cleft Palate; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Leucine; Polymorphism, Single Nucleotide; Proline; Transforming Growth Factor beta1; Turkey

2016
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
Mutation analysis of CLPTM 1 and PVRL 1 genes in patients with non-syndromic clefts of lip, alveolus and palate.
    Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery, 2005, Volume: 33, Issue:5

    Topics: Alanine; Alveolar Process; Cell Adhesion Molecules; Child; Child, Preschool; Cleft Lip; Cleft Palate; Exons; Female; Glutamic Acid; Glycine; Humans; Immunoglobulins; Introns; Male; Membrane Proteins; Molecular Sequence Data; Mutation; Nectins; Proline; Receptors, Virus; Sequence Analysis, Protein; Sex Factors

2005
Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype.
    Archives of dermatology, 2005, Volume: 141, Issue:12

    Topics: Abnormalities, Multiple; Arginine; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Genes, Tumor Suppressor; Genotype; Humans; Immunohistochemistry; Infant, Newborn; Male; Mutation, Missense; Phenotype; Phosphoproteins; Proline; Skin; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins

2005