proline has been researched along with Cleft Lip in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Oner, DA; Tastan, H | 1 |
Hoshino, A; Kaewkhampa, A; Kantaputra, PN; Lees, M; Masrour, N; McEntagart, M; Moore, GE; Paramee, M; Pauws, E; Stanier, P | 1 |
Ewers, R; Item, CB; Lauer, G; Sinko, K; Turhani, D; Watzinger, E; Watzinger, F | 1 |
Camacho, J; Heymann, WR; Honig, PJ; Ilyas, E; Imaizumi, S; Li, W; Pawel, BR; Payne, AS; Schnur, RE; Seykora, JT; Yan, AC; Young, TL | 1 |
4 other study(ies) available for proline and Cleft Lip
Article | Year |
---|---|
Association Between the Transforming Growth Factor Beta 1 Gene Polymorphisms and Turkish Patients with Nonsyndromic Cleft Lip With/Without Cleft Palate.
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.
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.
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.
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 |