thymine has been researched along with Cleft Lip in 30 studies
Cleft Lip: Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Ectrodactyly-ectodermal dysplasia-clefting syndrome is an uncommon disorder that includes a clinical spectrum of limb, facial, ocular, internal ear, and urogenital malformations." | 1.36 | Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype. ( Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM, 2010) |
| "Cleft palate is found in 4% of individuals with nevoid basal cell carcinoma syndrome." | 1.33 | Contributions of PTCH gene variants to isolated cleft lip and palate. ( Castilla, EE; Cooper, ME; Goldstein, T; Lopez Camelo, JS; Mansilla, MA; Marazita, ML; Murray, JC, 2006) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (3.33) | 18.2507 |
| 2000's | 10 (33.33) | 29.6817 |
| 2010's | 19 (63.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zeng, N | 1 |
| Wu, J | 2 |
| Zhu, WC | 1 |
| Ma, L | 3 |
| Jia, ZL | 1 |
| Shi, B | 2 |
| Estandia-Ortega, B | 1 |
| Velázquez-Aragón, JA | 1 |
| Alcántara-Ortigoza, MA | 1 |
| Reyna-Fabian, ME | 1 |
| Villagómez-Martínez, S | 1 |
| González-Del Angel, A | 1 |
| Han, Y | 1 |
| Zhou, L | 1 |
| Li, D | 1 |
| Xu, M | 1 |
| Yuan, H | 1 |
| Ma, J | 2 |
| Zhang, W | 1 |
| Jiang, H | 1 |
| Wu, Y | 1 |
| Wang, L | 1 |
| Pan, Y | 1 |
| Letra, A | 2 |
| Zhao, M | 1 |
| Silva, RM | 1 |
| Vieira, AR | 2 |
| Hecht, JT | 2 |
| Feng, C | 1 |
| Duan, W | 1 |
| Zhang, D | 1 |
| Zhang, E | 1 |
| Xu, Z | 1 |
| Lu, L | 1 |
| Mi, N | 1 |
| Hao, Y | 1 |
| Jiao, X | 2 |
| Zheng, X | 1 |
| Song, T | 2 |
| Shi, J | 2 |
| Dong, C | 1 |
| Antunes, LS | 1 |
| Tannure, PN | 1 |
| Antunes, LA | 1 |
| Reis, MF | 1 |
| Costa, MC | 1 |
| Gouvêa, CV | 1 |
| Olej, B | 1 |
| Granjeiro, JM | 2 |
| Küchler, EC | 1 |
| Kempa, I | 1 |
| Ambrozaitytė, L | 1 |
| Stavusis, J | 1 |
| Akota, I | 2 |
| Barkane, B | 2 |
| Krumina, A | 2 |
| Matulevičienė, A | 1 |
| Utkus, A | 1 |
| Kučinskas, V | 1 |
| Lace, B | 2 |
| Kerameddin, S | 1 |
| Namipashaki, A | 1 |
| Ebrahimi, S | 1 |
| Ansari-Pour, N | 1 |
| Ehlers Bertoja, A | 1 |
| Sampaio Alho, C | 1 |
| De França, E | 1 |
| Menegotto, B | 1 |
| Miriam Robinson, W | 1 |
| Huang, Y | 1 |
| Beaty, TH | 1 |
| Sull, JW | 1 |
| Zhu, L | 1 |
| Lu, D | 1 |
| Wang, Y | 1 |
| Meng, T | 1 |
| Jianyan, L | 1 |
| Zeqiang, G | 1 |
| Yongjuan, C | 1 |
| Kaihong, D | 1 |
| Bing, D | 1 |
| Rongsheng, L | 1 |
| Ali, A | 1 |
| Singh, SK | 1 |
| Raman, R | 1 |
| Birnbaum, S | 2 |
| Ludwig, KU | 2 |
| Reutter, H | 1 |
| Herms, S | 2 |
| de Assis, NA | 1 |
| Diaz-Lacava, A | 1 |
| Barth, S | 1 |
| Lauster, C | 1 |
| Schmidt, G | 1 |
| Scheer, M | 1 |
| Saffar, M | 1 |
| Martini, M | 1 |
| Reich, RH | 1 |
| Schiefke, F | 1 |
| Hemprich, A | 1 |
| Pötzsch, S | 1 |
| Pötzsch, B | 1 |
| Wienker, TF | 1 |
| Hoffmann, P | 2 |
| Knapp, M | 2 |
| Kramer, FJ | 1 |
| Nöthen, MM | 2 |
| Mangold, E | 2 |
| Paranaíba, LM | 1 |
| Martelli-Júnior, H | 1 |
| de Miranda, RT | 1 |
| Bufalino, A | 1 |
| Abdo Filho, RC | 1 |
| Coletta, RD | 1 |
| Jagomägi, T | 2 |
| Nikopensius, T | 2 |
| Krjutskov, K | 1 |
| Tammekivi, V | 1 |
| Viltrop, T | 1 |
| Saag, M | 2 |
| Metspalu, A | 2 |
| Mostowska, A | 2 |
| Hozyasz, KK | 2 |
| Biedziak, B | 2 |
| Misiak, J | 1 |
| Jagodzinski, PP | 2 |
| Zhang, B | 1 |
| Qin, C | 1 |
| Cao, F | 1 |
| Menezes, R | 1 |
| Cooper, ME | 2 |
| Fonseca, RF | 1 |
| Tropp, S | 1 |
| Govil, M | 1 |
| Imoehl, SR | 1 |
| Mansilla, MA | 2 |
| Murray, JC | 2 |
| Castilla, EE | 2 |
| Orioli, IM | 1 |
| Czeizel, AE | 1 |
| Chiquet, BT | 1 |
| Marazita, ML | 2 |
| Yao, T | 1 |
| Yang, L | 1 |
| Li, PQ | 1 |
| Wu, H | 1 |
| Xie, HB | 1 |
| Shen, X | 1 |
| Xie, XD | 1 |
| Singh, VP | 1 |
| Ramu, D | 1 |
| Wojcicki, P | 1 |
| Lianeri, M | 1 |
| Goldstein, T | 1 |
| Lopez Camelo, JS | 1 |
| Suda, N | 1 |
| Kitahara, Y | 1 |
| Ohyama, K | 1 |
| Vasiljeva, I | 1 |
| Dundure, I | 1 |
| Modesto, A | 1 |
| Moreno, LM | 1 |
| Krahn, K | 1 |
| King, S | 1 |
| Lidral, AC | 1 |
| Matsuzawa, N | 1 |
| Shimozato, K | 1 |
| Natsume, N | 1 |
| Niikawa, N | 1 |
| Yoshiura, K | 1 |
| Shaw, GM | 1 |
| Rozen, R | 1 |
| Finnell, RH | 1 |
| Todoroff, K | 1 |
| Lammer, EJ | 1 |
| Yamachika, E | 1 |
| Tsujigiwa, H | 1 |
| Ishiwari, Y | 1 |
| Mizukawa, N | 1 |
| Nagai, N | 1 |
| Sugahara, T | 1 |
30 other studies available for thymine and Cleft Lip
| Article | Year |
|---|---|
Associations between EYA1 single-nucleotide polymorphisms and non-syndromic orofacial clefts in Western Han Chinese.
Topics: Alleles; China; Cleft Lip; Cleft Palate; Cytosine; Ethnicity; Female; Gene Frequency; Genotype; Hapl | 2013 |
5,10-Methylenetetrahydrofolate reductase single nucleotide polymorphisms and gene-environment interaction analysis in non-syndromic cleft lip/palate.
Topics: Adenine; Adolescent; Case-Control Studies; Child; Child, Preschool; Cleft Lip; Cleft Palate; Cytosin | 2014 |
The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population.
Topics: Adenine; Axin Protein; Case-Control Studies; China; Chromosome Mapping; Cleft Lip; Cleft Palate; Eth | 2014 |
Functional Significance of MMP3 and TIMP2 Polymorphisms in Cleft Lip/Palate.
Topics: Adenine; Alleles; Cell Line, Tumor; Cleft Lip; Cleft Palate; Cytosine; Guanine; Haplotypes; Humans; | 2014 |
C392T polymorphism of the Wnt10a gene in non-syndromic oral cleft in a northeastern Chinese population.
Topics: Case-Control Studies; China; Cleft Lip; Cleft Palate; Cytosine; Ethnicity; Female; Gene Frequency; G | 2014 |
Association study of single nucleotide polymorphisms of MAFB with non-syndromic cleft lip with or without cleft palate in a population in Heilongjiang Province, northern China.
Topics: Adenine; Case-Control Studies; Child; Child, Preschool; China; Cleft Lip; Cleft Palate; Cytosine; Et | 2014 |
Genetic association for caries susceptibility among cleft lip and/or palate individuals.
Topics: Adolescent; Bone Morphogenetic Protein 4; Child; Child, Preschool; Cleft Lip; Cleft Palate; Cohort S | 2014 |
Association of BMP4 polymorphisms with non-syndromic cleft lip with or without cleft palate and isolated cleft palate in Latvian and Lithuanian populations.
Topics: Adenine; Bone Morphogenetic Protein 4; Case-Control Studies; Cleft Lip; Cleft Palate; Cytosine; Exon | 2014 |
IRF6 Is a Marker of Severity in Nonsyndromic Cleft Lip/Palate.
Topics: Adenine; Biomarkers, Tumor; Case-Control Studies; Chromosome Mapping; Cleft Lip; Cleft Palate; Gene | 2015 |
TGFA/TAQ I polymorphism in nonsyndromic cleft lip and palate patients from Rio Grande Do Sul, Brazil.
Topics: Adenine; Adolescent; Adult; Alleles; Case-Control Studies; Child; Child, Preschool; Chromosomes, Hum | 2008 |
Association between IRF6 SNPs and oral clefts in West China.
Topics: Adenine; Alleles; Case-Control Studies; Child; China; Cleft Lip; Cleft Palate; Cytosine; Female; Gen | 2009 |
Analysis of interactions between genetic variants of BMP4 and environmental factors with nonsyndromic cleft lip with or without cleft palate susceptibility.
Topics: Adolescent; Adult; Alcohol Drinking; Biomarkers; Bone Morphogenetic Protein 4; Case-Control Studies; | 2010 |
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 | 2009 |
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.
Topics: Adenine; Alleles; Case-Control Studies; Cleft Lip; Cleft Palate; Cytosine; Europe; Female; Gene Freq | 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; | 2010 |
MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.
Topics: Adenine; B-Cell Lymphoma 3 Protein; Case-Control Studies; Cell Adhesion Molecules; Chromosome Mappin | 2010 |
Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients.
Topics: Adenine; Case-Control Studies; Chromosome Mapping; Chromosomes, Human, Pair 10; Cleft Lip; Cleft Pal | 2010 |
Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Alleles; Betaine-Homocysteine S-Methyltra | 2010 |
CRISPLD2 polymorphisms are associated with non-syndromic cleft lip with or without cleft palate in a northern Chinese population.
Topics: Adolescent; Adult; Case-Control Studies; Cell Adhesion Molecules; Child; Child, Preschool; China; Cl | 2010 |
CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate.
Topics: Adenine; Alternative Splicing; Asian People; Case-Control Studies; Cell Adhesion Molecules; Cleft Li | 2011 |
Association of Wnt3A gene variants with non-syndromic cleft lip with or without cleft palate in Chinese population.
Topics: Adenine; Alleles; Case-Control Studies; China; Cleft Lip; Cleft Palate; Female; Gene Frequency; Gene | 2011 |
Association of MSX1 799 G>T variant with nonsyndromic cleft lip/palate in South Indian adolescent patients.
Topics: Adolescent; Base Pairing; Chromosome Mapping; Cleft Lip; Cleft Palate; Genetic Markers; Genetic Vari | 2012 |
Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate.
Topics: Adenine; Case-Control Studies; Chromosome Mapping; Cleft Lip; Cleft Palate; Cytosine; Epistasis, Gen | 2012 |
Contributions of PTCH gene variants to isolated cleft lip and palate.
Topics: Adenine; Alleles; Basal Cell Nevus Syndrome; Case-Control Studies; Cleft Lip; Cleft Palate; Cytosine | 2006 |
A case of amelogenesis imperfecta, cleft lip and palate and polycystic kidney disease.
Topics: Adult; Alkaline Phosphatase; Amelogenesis Imperfecta; Amelogenin; Calcitonin; Calcium; Cleft Lip; Cl | 2006 |
Mutation analysis of the MSX1 gene exons and intron in patients with nonsyndromic cleft lip and palate.
Topics: Adenine; Cleft Lip; Cleft Palate; Cytosine; Exons; Gene Deletion; Gene Frequency; Guanine; Humans; I | 2006 |
MSX1 and orofacial clefting with and without tooth agenesis.
Topics: Adolescent; Anodontia; Case-Control Studies; Child; Cleft Lip; Cleft Palate; Codon; Cytosine; Female | 2006 |
A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis.
Topics: Adenine; Chromosomes, Human, Pair 1; Cleft Lip; Cleft Palate; DNA; Exons; Female; Genetic Linkage; H | 2006 |
Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip.
Topics: Case-Control Studies; Cleft Lip; Cytosine; Female; Fertilization; Humans; Infant, Newborn; Methylene | 1998 |
Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip.
Topics: Child; Cleft Lip; Cleidocranial Dysplasia; Codon, Terminator; Core Binding Factor Alpha 1 Subunit; C | 2001 |