arginine has been researched along with Cleft Palate in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (63.64) | 29.6817 |
| 2010's | 4 (36.36) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Oner, DA; Tastan, H | 1 |
| Blom, H; Carmichael, SL; Finnell, RH; Shaw, GM; Ueland, PM; Vollset, SE; Yang, W | 1 |
| Ali, A; Raman, R; Singh, SK | 1 |
| Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM | 1 |
| Bailleul-Forestier, I; Bennaceur, S; de Roux, N; Gros, C; Leger, J; Zenaty, D | 1 |
| Hoshino, A; Kaewkhampa, A; Kantaputra, PN; Lees, M; Masrour, N; McEntagart, M; Moore, GE; Paramee, M; Pauws, E; Stanier, P | 1 |
| Adeyemo, WL; Erginel-Unaltuna, N; Ewers, R; Frei, K; Item, CB; Sinko, K; Thurnher, D; Turhani, D; Watzinger, F; Wittwer, G; Yerit, K | 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 |
| Bayet, B; Deggouj, N; Desmyter, L; Ghassibe, M; Gillerot, Y; Revencu, N; Vanwijck, R; Verellen-Dumoulin, C; Vikkula, M | 1 |
| Adès, LC; Gilmour, E; Graf, N; Holme, SA; Maclean, K; Moss, C; Onikul, E; Scheffer, H; Smith, GH; Taylor, M; van Bokhoven, H | 1 |
| Nakakita, N; Sakai, N; Sakata, Y; Shida, H; Susami, T; Takato, T; Tokunaga, K; Uchinuma, E; Yamazaki, Y | 1 |
11 other study(ies) available for arginine and Cleft Palate
| 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 |
Nested case-control study of one-carbon metabolites in mid-pregnancy and risks of cleft lip with and without cleft palate.
Topics: Adult; Arginine; Carbon; Case-Control Studies; Cleft Lip; Cleft Palate; Dietary Supplements; Female; Folic Acid; Humans; Maternal Age; Nutritional Sciences; Odds Ratio; Pregnancy; Vitamins | 2009 |
Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.
Topics: 3' Untranslated Regions; Abnormalities, Multiple; Adenine; Arginine; Cleft Lip; Cleft Palate; Cohort Studies; Cytosine; Exons; Female; Genetic Variation; Genotype; Guanine; Heterozygote; Homozygote; Humans; India; Interferon Regulatory Factors; Introns; Male; Open Reading Frames; Point Mutation; Sequence Analysis, DNA; Serine; Syndrome; Thymine | 2009 |
Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.
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.
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.
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 |
Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
Topics: 5' Untranslated Regions; Abnormalities, Multiple; Anodontia; Arginine; Base Sequence; Cleft Lip; Cleft Palate; DNA; DNA Primers; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Exons; Family Health; Female; Genes, Dominant; Glycine; Heterozygote; Humans; Interferon Regulatory Factors; Male; Molecular Sequence Data; Mouth Abnormalities; Mutation; Pedigree; Penetrance; Phenotype; Promoter Regions, Genetic; Protein Structure, Tertiary; Sequence Analysis, DNA; Syndrome; Transcription Factors; Turkey | 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 |
Orofacial clefting: update on the role of genetics.
Topics: Arginine; Cleft Lip; Cleft Palate; Cohort Studies; Environment; Exons; Genes, Dominant; Genetic Predisposition to Disease; Genotype; Humans; Interferon Regulatory Factors; Leg; Lip; Mutation; Phenotype; Polymorphism, Single Nucleotide; Syndrome | 2006 |
EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation?
Topics: Abnormalities, Multiple; Adult; Arginine; Child, Preschool; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Fingers; Genotype; Glutamine; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins; Urination Disorders | 2007 |
Sequence analysis of fibroblast growth factor receptor 2 ( FGFR2 ) in Japanese patients with craniosynostosis.
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 |