thymine has been researched along with Amelogenesis Imperfecta in 12 studies
Amelogenesis Imperfecta: A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The proven candidate genes for amelogenesis imperfecta (AI) are AMELX, ENAM, MMP20, KLK4, FAM83H, and WDR72." | 1.36 | Novel WDR72 mutation and cytoplasmic localization. ( De La Garza, RJ; Gencay, K; Hu, JC; Hwang, YH; Kang, HY; Kim, JW; Lee, KE; Lee, SK; Nam, KH; Seymen, F; Simmer, JP; Tuna, EB; Yildirim, M, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (58.33) | 29.6817 |
| 2010's | 5 (41.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gasse, B | 1 |
| Karayigit, E | 1 |
| Mathieu, E | 1 |
| Jung, S | 1 |
| Garret, A | 1 |
| Huckert, M | 1 |
| Morkmued, S | 1 |
| Schneider, C | 1 |
| Vidal, L | 1 |
| Hemmerlé, J | 1 |
| Sire, JY | 1 |
| Bloch-Zupan, A | 1 |
| Seymen, F | 3 |
| Lee, KE | 3 |
| Koruyucu, M | 1 |
| Gencay, K | 2 |
| Bayram, M | 1 |
| Tuna, EB | 3 |
| Lee, ZH | 1 |
| Kim, JW | 5 |
| Cherkaoui Jaouad, I | 1 |
| El Alloussi, M | 1 |
| Chafai El Alaoui, S | 1 |
| Laarabi, FZ | 1 |
| Lyahyai, J | 1 |
| Sefiani, A | 1 |
| Kang, HY | 2 |
| Lee, SK | 2 |
| Yildirim, M | 2 |
| Patir, A | 1 |
| Ding, Y | 1 |
| Estrella, MR | 1 |
| Hu, YY | 2 |
| Chan, HL | 2 |
| Zhang, HD | 1 |
| Simmer, JP | 4 |
| Hu, JC | 4 |
| Chan, HC | 1 |
| Mai, L | 1 |
| Oikonomopoulou, A | 1 |
| Richardson, AS | 1 |
| Wang, SK | 1 |
| Hwang, YH | 1 |
| Nam, KH | 1 |
| De La Garza, RJ | 1 |
| Lin, BP | 1 |
| Boyd, C | 1 |
| Wright, JT | 1 |
| Yamada, CJ | 1 |
| Rayes, SK | 1 |
| Feigal, RJ | 1 |
| Ozdemir, D | 1 |
| Hart, PS | 1 |
| Ryu, OH | 1 |
| Choi, SJ | 1 |
| Ozdemir-Karatas, M | 1 |
| Firatli, E | 1 |
| Piesco, N | 1 |
| Hart, TC | 1 |
| Suda, N | 1 |
| Kitahara, Y | 1 |
| Ohyama, K | 1 |
| Gutierrez, SJ | 1 |
| Chaves, M | 1 |
| Torres, DM | 1 |
| Briceño, I | 1 |
| Kindelan, SA | 1 |
| Brook, AH | 1 |
| Gangemi, L | 1 |
| Lench, N | 1 |
| Wong, FS | 1 |
| Fearne, J | 1 |
| Jackson, Z | 1 |
| Foster, G | 1 |
| Stringer, BM | 1 |
12 other studies available for thymine and Amelogenesis Imperfecta
| Article | Year |
|---|---|
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Apatites; Base Sequence; Calcium; Child, Preschool; Codon, Nonsense; Crysta | 2013 |
ENAM mutations with incomplete penetrance.
Topics: Adolescent; Amelogenesis Imperfecta; Child; Chromosome Segregation; Codon, Nonsense; Codon, Terminat | 2014 |
Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
Topics: Alanine; Amelogenesis Imperfecta; Base Sequence; Child; Codon, Nonsense; Cytosine; Dental Enamel Pro | 2015 |
Candidate gene strategy reveals ENAM mutations.
Topics: Adenine; Amelogenesis Imperfecta; Amino Acid Sequence; Codon, Nonsense; Dental Enamel Hypoplasia; De | 2009 |
Fam83h is associated with intracellular vesicles and ADHCAI.
Topics: Aged, 80 and over; Amelogenesis Imperfecta; Animals; Cell Line; Cell Nucleus; Child; Codon, Nonsense | 2009 |
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
Topics: Adenine; Alleles; Amelogenesis Imperfecta; Amino Acid Sequence; Calcium; Casein Kinases; Cytosine; D | 2010 |
Novel WDR72 mutation and cytoplasmic localization.
Topics: Adenine; Alleles; Amelogenesis Imperfecta; Codon, Nonsense; Cytoplasm; Dental Enamel; Exons; Genotyp | 2010 |
Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Amelogenin; Child; Codon; Cytosine; Dental Enamel; Dental Enamel Hypoplasia | 2004 |
MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.
Topics: Adenine; Amelogenesis Imperfecta; Binding Sites; Conserved Sequence; Dental Enamel Proteins; Female; | 2005 |
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 |
Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta.
Topics: Alleles; Amelogenesis Imperfecta; Arginine; Codon; Dental Enamel Proteins; Exons; Female; Genes, Dom | 2007 |
Detection of a novel mutation in X-linked amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Amelogenin; Amino Acid Substitution; Cloning, Molecular; Cytosine; Dental E | 2000 |