Results 21 to 30 of about 5,937 (217)

Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta [PDF]

, 2014
Amelogenesis imperfecta (AI) describes a heterogeneous group of inherited dental enamel defects reflecting failure of normal amelogenesis. Ameloblastin (AMBN) is the second most abundant enamel matrix protein expressed during amelogenesis.
Brookes, SJ, Inglehearn, CF, Kirkham, J, Mighell, AJ, Murillo, G, Parry, DA, Poulter, JA, Silva, S, Smith, CEL   +8 more
core   +1 more source

Cloning, characterization and immunolocalization of human ameloblastin [PDF]

, 2000
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/93555/1/j.1600-0722.2000.108004303.x ...
Berdal, Ariane, Forest, Nadine, Forsman‐semb, Kristina, Gu, Ting Ting, Krebsbach, Paul H., Kärrman Mårdh, Carina, MacDougall, Mary, Mesbah, Michael, Simmons, Darrin, Yamada, Yoishi   +9 more
core   +1 more source

Hypoplastic amelogenesis imperfecta with multiple impacted teeth: report of two cases [PDF]

, 2010
Amelogenesis Imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of all or nearly all the teeth in a more or less equal manner.
Aarthi Nisha, Aarthi, Harish, B.N., Reddy, Sujatha S.   +2 more
core   +1 more source

Amelogenesis imperfecta and localised aggressive periodontitis: A rare clinical entity

Journal of Indian Society of Periodontology, 2013
This case report presents two female patients whose chief complaint was discoloration of teeth. On careful clinical examination it was found that the patients had features of amelogenesis imperfecta and localised aggressive periodontitis.
Gayatri Gundannavar, Radhika M Rosh, Shoba Chandrasekaran, Ahad M Hussain   +3 more
doaj   +1 more source

Regulation of pH During Amelogenesis [PDF]

, 2009
During amelogenesis, extracellular matrix proteins interact with growing hydroxyapatite crystals to create one of the most architecturally complex biological tissues.
Rodrigo S. Lacruz, Antonio Nanci, Ira Kurtz, J. Timothy Wright, Michael L. Paine, CE Smith, JD Bartlett, ML Paine, JD Bartlett, S Sasaki, T Takagi, W Sui, ML Paine, A Nanci, A Nanci, CE Smith, H Warshawsky, M Goldberg, JC Hu, O Ryu, K Iwasaki, P Moffatt, P Moffatt, D Deutsch, K Josephsen, EJ Reith, EJ Reith, T Sasaki, CE Smith, A Boyde, A Boyde, A Boyde, RS Lacruz, ED Eanes, MU Nylen, DF Travis, M Goldberg, RA Young, JP Simmer, CE Smith, T Aoba, T Aoba, GE Lyman, MD McKee, CE Smith, CE Smith, CE Smith, CT Supuran, WS Sly, S Toyosawa, CE Smith, S Pastorekova, P Pan, K Kondo, AA Dogterom, T Sugimoto, M Kakei, HM Lin, C Supanchart, J Sok, DH Retief, T Odajima, RE Primosch, RE Primosch, JT Wright, JT Wright, FS Collins, TJ Sferra, ML Drumm, JR Riordan, RA Frizzell, ID Mandel, FT Cua, CK Arquitt, BH Koller, JN Snouwaert, CL Kiefer, B Illek, A Pushkin, D Dinour, LR Gawenis, J Inatomi, SD McAlear, N Abuladze, MO Bevensee, CE Kurschat, J Lecanda, JF Medina, LR Gawenis, DM Lyaruu, JW Bawden, RS Lacruz, JT Wright, PJ Crawford, DA Parry, FY Demirci, Z Katzir, HS Koppang, T Igarashi, J Elizabeth, TD Azevedo, MP Whyte   +101 more
core   +3 more sources

Molecular Basis of Human Enamel Defects

Balkan Journal of Dental Medicine, 2014
During eruption of teeth in the oral cavity, the effect of gene variations and environmental factors can result in morphological and structural changes in teeth.
Chatzopoulos Georgios, Tziafas Dimitrios
doaj   +1 more source

Target gene analyses of 39 amelogenesis imperfecta kindreds [PDF]

, 2011
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90297/1/EOS_857_sm_FigsS1-S3.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/90297/2/j.1600-0722.2011.00857.x ...
Al-Hashimi, Aldred, Almaani, Backman, Backman, Bartlett, Berkman, Caterina, Chan, Collier, Davit-Beal, Ding, El-Sayed, El-Sayed, El-Sayed, Greene, Gutierrez, Hart, Hart, Hart, Hart, Hart, Hart, Hobson, Hu, Hu, Hyun, Iwasaki, Kang, Kida, Kida, Kim, Kim, Kim, Kim, Kim, Kindelan, Kirzioglu, Krebsbach, Lagerstrom-Fermer, Lee, Lee, Lee, Lee, Lee, Lee, Lench, Lench, Lindemeyer, Lu, Luo, Martelli-Junior, McGrath, Meredith, Meredith, Moffatt, Murrell, Mårdh, Nusier, Ozdemir, Ozdemir, O’Sullivan, Papagerakis, Pavlic, Rajpar, Ravassipour, Sawada, Sekiguchi, Sekiguchi, Simmer, Simmer, Simmer, Sire, Smith, Smith, Sun, Torres-Quintana, Urzua, Witkop, Witkop, Witkop, Wright, Wright, Wright, Wright, Wright   +85 more
core   +1 more source

Enamel renal syndrome: A rare case report

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2012
Enamel renal syndrome is a very rare disorder associating amelogenesis imperfecta with nephrocalcinosis. It is known by various synonyms such as amelogenesis imperfecta nephrocalcinosis syndrome, MacGibbon syndrome, Lubinsky syndrome, and Lubinsky ...
S V Kala Vani, M Varsha, Y Uday Sankar
doaj   +1 more source

Determination of mutation in the coding regions of FAM83H and ENAM genes in patients with imperfect enamel (Amelogenesis Imperfecta)

Journal of Craniomaxillofacial Research, 2020
Introduction: Tooth enamel is a precious and highly mineralized tissue in the human body. Amelogenesis Imperfecta (AI) is a developmental, evolutionary and hereditary disease presents  with the rare abnormal formation of enamel that affects the primary ...
Shamsoulmolouk Najafi, Hasan Roudgari, Reyhaneh Palizgir, Marjan Naderifard, Mohammad Erfan Meighani   +4 more
doaj   +1 more source

Prevalence and distribution of selected dental anomalies among saudi children in Abha, Saudi Arabia [PDF]

, 2016
Dental anomalies are not an unusual finding in routine dental examination. The effect of dental anomalies can lead to functional, esthetic and occlusal problems.
Yassin, Syed M.
core   +1 more source