Keywords: Amelogenesis imperfecta; Amelogenesis; Enamel; Biomineralization; TRAP; MMP20;
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: Kohlschutter-Tonz syndrome; ROGDI homolog (Drosophila) (FLJ22386); amelogenesis imperfecta; epilepsy; intellectual impairment;
Keywords: Amelogenesis imperfecta; Longevity; Restorative treatment; Survival probability; Dental material;
Keywords: Moderate hypodontia; Severe hypodontia; Amelogenesis imperfecta; Quality of life; Self esteem;
Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene
Keywords: Jalili syndrome; Cone-rod dystrophy; Amelogenesis imperfecta; CNNM4; Mutation;
Altered Ca2+ signaling in enamelopathies
Keywords: Hap; hydroxyapatite; SOCE; store-operated Ca2+ entry; RA; ruffled-ended ameloblast; SA; smooth-ended ameloblast; AI; amelogenesis imperfecta; Enamel; Ameloblasts; Ca2+ signaling; Channelopathy;
Deciphering defective amelogenesis using in vitro culture systems
Keywords: Amelogenesis imperfecta; Cell-cell interaction; Cell-matrix interaction; Dental epithelial cell; Genetic disease; In vitro amelogenesis imperfecta model; Phenotypic screening; Sp6;
CRAC channels in dental enamel cells
Keywords: AI; amelogenesis imperfecta; CRAC; Ca2+ release activated Ca2+ channels; ED; ectodermal dysplasia; TAM; tubular aggregate myopathy; SOCE; store-operated Ca2+ entry; Enamel; CRAC channels; Mutations; Amelogenesis imperfecta; Hypoplasia;
Integrin αvβ6: Structure, function and role in health and disease
Keywords: DC; dendritic cells; EBV; Epstein-Barr virus; ECM; extracellular matrix; EGFR; epidermal growth factor receptor; EMT; epithelial-to-mesenchymal transformation; ERK; extracellular signal-regulated kinase; FMDV; foot-and-mouth disease virus; HSV; herpes s
ZespóÅ szkliwno-nerkowy (ERS) - charakterystyczne objawy w jamie ustnej
Keywords: amelogenesis imperfecta; nefrokacynoza; wÅókniakowatoÅÄ dziÄ
seÅ; FAM20A; choroby nerek; Amelogenesis imperfecta; Nephrocalcinosis syndrome; Gingival fibromatosis; FAM20A; Kidney diseases;
A novel AMELX mutation causes hypoplastic amelogenesis imperfecta
Keywords: AMELX; Amelogenesis imperfecta; X-linked; Enamel; Pre-mRNA splicing;
Overexpression of constitutively active MAP3K7 in ameloblasts causes enamel defects of mouse teeth
Keywords: Ameloblast; Amelogenesis imperfecta; Transforming growth factor -β-activating kinase 1; Amelotin; Transgenic mice;
Novel splice site mutation in CNNM4 gene in a family with Jalili syndrome
Keywords: Amelogenesis imperfecta; CNNM4; Cone-rod dystrophy; Jalili syndrome; Splice site mutation;
Comprehensive rehabilitation of a case of Amelogenesis imperfecta
Keywords: Amelogenesis imperfecta; Full mouth rehabilitation; Hypoplasia;
Improved protocol to purify untagged amelogenin – Application to murine amelogenin containing the equivalent P70 → T point mutation observed in human amelogenesis imperfecta
Keywords: Amelogenesis imperfecta; Intrinsic disorder; Amelogenin; Tooth enamel; Biomineralization; NMR spectroscopy
Effects of Fam83h overexpression on enamel and dentine formation
Keywords: Amelogenesis imperfecta; Dentinogenesis; Tooth; Family with sequence similarity 83, member h;
Amelogenesis imperfecta - Functional and esthetic rehabilitation of a mutilated dentition
Keywords: Amelogenesis imperfecta; Rehabilitation; Hereditary disorder; Esthetics;
A solution NMR investigation into the impaired self-assembly properties of two murine amelogenins containing the point mutations T21→I or P41→T
Keywords: Amelogenesis imperfecta; Intrinsic disorder; Amelogenin; Enamel; Biomineralization; Nanospheres
Full mouth rehabilitation of hypomaturation type amelogenesis imperfecta: A clinical report
Keywords: Amelogenesis imperfecta; Hypoplasia; Hypocalcification; Hypomaturation; Full mouth rehabilitation
Candidate-gene exclusion in a family with inherited non-syndromic dental disorders
Keywords: AI; Amelogenesis imperfecta; ADAI; Amelogenesis imperfecta with autosomal dominant inheritance; ARAI; Amelogenesis imperfecta with autosomal recessive inheritance; X-linked AI; Amelogenesis imperfecta related to X chromosome; ENAM; Enamelin; DLX3; Distal-
Treatment of enamel hypoplasia in a patient with Usher syndrome
Keywords: Composites; dental veneers; permanent dental restorations; amelogenesis imperfecta; Usher syndromeUSH: Usher syndrome; USH1: Usher syndrome type I; USH2: Usher syndrome type II; USH3: Usher syndrome type III
Histological and immunohistochemical analyses of molar tooth germ in enamelin-deficient mouse
Keywords: Amelogenesis imperfecta; Enamelin; Amelogenin; Immunohistochemistry; Mouse
β-Catenin/LEF1 activated enamelin expression in ameloblast-like cells
Keywords: Enamelin; Wnt/β-catenin; LEF1; Amelogenesis imperfecta; Tooth development
Enamel defects in extracted and exfoliated teeth from patients with Amelogenesis Imperfecta, measured using the extended enamel defects index and image analysis
Keywords: Amelogenesis Imperfecta; Enamel defects; Image analysis; EDI;
ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia
Keywords: ORAI1; STIM1; CRAC; calcium channel; Ca2+; store-operated Ca2+ entry; T cells; immunodeficiency; signal transduction; congenital myopathy; anhydrotic ectodermal dysplasia; dental enamel; amelogenesis imperfecta; CRAC; Ca2+ release activated Ca2+; EDA; Ect
Identifying polymorphism in enamelin gene in amelogenesis imperfecta (AI)
Keywords: Dental enamel; Amelogenesis imperfecta; Enamelin gene; Mutation
Cytomegalovirus inhibition of embryonic mouse tooth development: A model of the human amelogenesis imperfecta phenocopy
Keywords: Odontogenesis; Cytomegalovirus; Amelogenesis imperfecta; Fibronectin; NF-κB; β-Catenin
The genetic basis of inherited anomalies of the teeth: Part 1: Clinical and molecular aspects of non-syndromic dental disorders
Keywords: Genetics; Amelogenesis imperfecta; Dentinogenesis imperfecta; Oligodontia; Review
Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta
Keywords: Amelogenesis imperfecta; Enamelin gene; Hypoplastic; Autosomal-dominant; Mutation
Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185–13186insAG and 8344delG
Keywords: Dental enamel; Enamel ultrastructure; Amelogenesis imperfecta; Enamelin mutations
Msx2 −/− transgenic mice develop compound amelogenesis imperfecta, dentinogenesis imperfecta and periodental osteopetrosis
Keywords: Msx2; Amelogenesis imperfecta; Dentinogenesis imperfecta; Odontogenic tumour; Alveolar bone osteopetrosis
Sensorineural deafness, enamel abnormalities and nail abnormalities: a case report of Heimler syndrome in identical twin girls
Keywords: Sensorineural hearing loss; Amelogenesis imperfecta; Nails; Monozygotic twins; Child; Syndrome
Orthodontic correction of a skeletal Class III malocclusion with impacted maxillary second molars and amelogenesis imperfecta
Keywords: Orthognathic surgery; Impacted second molars; Amelogenesis imperfecta
Ameloblastin gene polymorphisms in healthy Japanese
Keywords: Ameloblastin; Amelogenesis imperfecta; Gene polymorphisms; Japanese;
Case report of a rare syndrome associating amelogenesis imperfecta and nephrocalcinosis in a consanguineous family
Keywords: Amelogenesis imperfecta; Nephrocalcinosis; Phenotype;
The psychosocial impact of developmental dental defects in people with hereditary amelogenesis imperfecta
Keywords: Amelogenesis imperfecta; psychosocial effects; fear; distress;