Page last updated: 2024-10-16

adenine and Amelogenesis Imperfecta

adenine has been researched along with Amelogenesis Imperfecta in 9 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.

Research Excerpts

ExcerptRelevanceReference
"The proven candidate genes for amelogenesis imperfecta (AI) are AMELX, ENAM, MMP20, KLK4, FAM83H, and WDR72."1.36Novel 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)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (11.11)18.2507
2000's5 (55.56)29.6817
2010's3 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dashash, M1
Bazrafshani, MR1
Poulton, K1
Jaber, S1
Naeem, E1
Blinkhorn, AS1
Kang, HY2
Seymen, F2
Lee, SK2
Yildirim, M2
Tuna, EB2
Patir, A1
Lee, KE2
Kim, JW2
Chan, HC1
Mai, L1
Oikonomopoulou, A1
Chan, HL1
Richardson, AS1
Wang, SK1
Simmer, JP3
Hu, JC3
Gencay, K1
Hwang, YH1
Nam, KH1
De La Garza, RJ1
Ozdemir, D2
Hart, PS2
Ryu, OH2
Choi, SJ1
Ozdemir-Karatas, M1
Firatli, E2
Piesco, N1
Hart, TC3
Aren, G1
Wright, JT1
Daly, B1
Simmons, D1
Hong, S1
Hart, SP1
Atsawasuwan, P1
Yamauchi, M1
Papagerakis, P1
Lin, HK1
Lee, KY1
Hu, Y1
Bartlett, JD1
Collier, PM1
Sauk, JJ1
Rosenbloom, SJ1
Yuan, ZA1
Gibson, CW1

Other Studies

9 other studies available for adenine and Amelogenesis Imperfecta

ArticleYear
Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
    Journal of investigative and clinical dentistry, 2011, Volume: 2, Issue:1

    Topics: Adenine; Amelogenesis Imperfecta; Amino Acid Sequence; Case-Control Studies; Child; Child, Preschool

2011
Candidate gene strategy reveals ENAM mutations.
    Journal of dental research, 2009, Volume: 88, Issue:3

    Topics: Adenine; Amelogenesis Imperfecta; Amino Acid Sequence; Codon, Nonsense; Dental Enamel Hypoplasia; De

2009
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
    Journal of dental research, 2010, Volume: 89, Issue:7

    Topics: Adenine; Alleles; Amelogenesis Imperfecta; Amino Acid Sequence; Calcium; Casein Kinases; Cytosine; D

2010
Novel WDR72 mutation and cytoplasmic localization.
    Journal of dental research, 2010, Volume: 89, Issue:12

    Topics: Adenine; Alleles; Amelogenesis Imperfecta; Codon, Nonsense; Cytoplasm; Dental Enamel; Exons; Genotyp

2010
MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.
    Journal of dental research, 2005, Volume: 84, Issue:11

    Topics: Adenine; Amelogenesis Imperfecta; Binding Sites; Conserved Sequence; Dental Enamel Proteins; Female;

2005
Phenotype of ENAM mutations is dosage-dependent.
    Journal of dental research, 2005, Volume: 84, Issue:11

    Topics: Adenine; Adolescent; Amelogenesis Imperfecta; Child; Codon, Nonsense; Cytosine; Dental Enamel Protei

2005
Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation.
    European journal of oral sciences, 2006, Volume: 114 Suppl 1

    Topics: Adenine; Amelogenesis Imperfecta; Crystallization; Crystallography; Dental Enamel; Dental Enamel Pro

2006
Premature stop codon in MMP20 causing amelogenesis imperfecta.
    Journal of dental research, 2008, Volume: 87, Issue:1

    Topics: Adenine; Amelogenesis Imperfecta; Child; Codon, Nonsense; Dental Enamel; Exons; Female; Guanine; Hum

2008
An amelogenin gene defect associated with human X-linked amelogenesis imperfecta.
    Archives of oral biology, 1997, Volume: 42, Issue:3

    Topics: Adenine; Ameloblasts; Amelogenesis Imperfecta; Amelogenin; Base Sequence; Cytosine; Dental Enamel; D

1997