Compounds > tridemorph

Page last updated: 2024-08-23

tridemorph and Amelogenesis Imperfecta

tridemorph has been researched along with Amelogenesis Imperfecta in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	7 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bayrak, S; Hu, J; Hyun, HK; Kang, J; Kim, JW; Kim, YJ; Koruyucu, M; Lee, SH; Lee, ZH; Seymen, F; Shin, TJ; Simmer, J; Tuloglu, N; Tuna, EB	1
Brookes, SJ; Brown, CJ; Hussain, H; Inglehearn, CF; Kirkham, J; Mighell, AJ; Murillo, G; Patel, A; Poulter, JA; Silva, S; Smith, CEL	1
El-Sayed, W; Inglehearn, CF; Kirkham, J; Mighell, AJ; Poulter, JA; Shore, RC	1
Gencay, K; Hu, JC; Kim, JW; Ko, J; Kyun, HK; Lee, KE; Seymen, F; Shin, TJ; Simmer, JP; Tuna, EB; Yildirim, M	1
Hyun, HK; Kim, JW; Ko, J; Le, CG; Lee, KE; Lee, SH; Shin, TJ	1
Qin, M; Wang, X; Yang, Y; Zhao, Y	1
Hyun, HK; Kim, JW; Kim, YJ; Lee, SH; Lee, ZH; Shin, TJ	1

Other Studies

7 other study(ies) available for tridemorph and Amelogenesis Imperfecta

Article	Year
Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta. Clinical oral investigations, 2019, Volume: 23, Issue:3 Topics: Amelogenesis Imperfecta; Cell Adhesion Molecules; Codon, Nonsense; Dental Enamel Proteins; DNA Mutational Analysis; Homozygote; Humans; INDEL Mutation; Kalinin; Pedigree; Sequence Deletion; Turkey	2019
Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis Imperfecta. Journal of dental research, 2019, Volume: 98, Issue:6 Topics: Amelogenesis Imperfecta; Cell Adhesion Molecules; Codon, Nonsense; Female; Frameshift Mutation; Heterozygote; Humans; Kalinin; Male; Pedigree; Phenotype	2019
Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. European journal of human genetics : EJHG, 2014, Volume: 22, Issue:1 Topics: Amelogenesis Imperfecta; Cell Adhesion Molecules; Epidermolysis Bullosa, Junctional; Exome; Female; Frameshift Mutation; Genetic Linkage; High-Throughput Nucleotide Sequencing; Humans; Kalinin; Male; Pedigree	2014
LAMB3 mutations causing autosomal-dominant amelogenesis imperfecta. Journal of dental research, 2013, Volume: 92, Issue:10 Topics: Amelogenesis Imperfecta; Cell Adhesion Molecules; Child; Codon, Nonsense; DNA Mutational Analysis; Female; Frameshift Mutation; Genes, Dominant; Humans; Kalinin	2013
Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity. Clinical genetics, 2015, Volume: 87, Issue:1 Topics: Amelogenesis Imperfecta; Base Sequence; Cell Adhesion Molecules; Child; Child, Preschool; Epidermolysis Bullosa, Junctional; Female; Genes, Dominant; Humans; Kalinin; Male; Molecular Sequence Data; Pedigree; Sequence Analysis, DNA; Tooth	2015
Novel ENAM and LAMB3 mutations in Chinese families with hypoplastic amelogenesis imperfecta. PloS one, 2015, Volume: 10, Issue:3 Topics: Adolescent; Adult; Amelogenesis Imperfecta; Asian People; Base Sequence; Cell Adhesion Molecules; Child; China; Dental Enamel; Dental Enamel Hypoplasia; Extracellular Matrix Proteins; Female; Humans; Kalinin; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree	2015
A novel de novo mutation in LAMB3 causes localized hypoplastic enamel in the molar region. European journal of oral sciences, 2016, Volume: 124, Issue:4 Topics: Amelogenesis Imperfecta; Cell Adhesion Molecules; Child; Dental Enamel Hypoplasia; Frameshift Mutation; Humans; Kalinin; Male; Molar; Mutation	2016