Results 51 to 60 of about 12,368 (291)

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

New Perspectives on Amelotin and Amelogenesis [PDF]

Journal of Dental Research, 2015
This issue reports the first enamel malformations in amelotin (Amtn)-ablated mice (Nakayama et al. 2015). Among the proteins necessary for enamel formation, amelotin is one of the more recently discovered. It was discovered independently by 2 different laboratories (Iwasaki et al. 2005; Moffatt et al. 2006). The amelotin protein is enriched in proline,
John D. Bartlett, James P. Simmer
openalex   +4 more sources

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

A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta

Human Molecular Genetics, 2020
Amelogenesis is the process of enamel formation. For amelogenesis to proceed, the cells of the inner enamel epithelium (IEE) must first proliferate and then differentiate into the enamel-producing ameloblasts.
Claire E L Smith, Laura L E Whitehouse, J. Poulter, Laura Wilkinson Hewitt, Fatima Nadat, B. Jackson, I. Manfield, T. Edwards, H. Rodd, C. Inglehearn, A. Mighell   +10 more
semanticscholar   +1 more source

Teeth restoration features for patients with amelogenesis imperfecta

Эндодонтия Today, 2019
Amelogenesis Imperfecta is a serious disease which affects not only the oral health, but although the general health and the quality of life of the patients. This article describes the causes of amelogenesis imperfecta and associated pathologies.
V. V. Vedmitskaya, O. S. Kovylina, L. A. Khromova, Yu. A. Mitronin   +3 more
doaj   +1 more source

Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations [PDF]

, 2014
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects. Commonly described as an isolated trait, it may be observed concomitantly with other orodental and/or systemic features such as ...
Acevedo, A-C, Berdal, A, Bloch-Zupan, A, De La Dure-Molla, M, Huckert, M, Mighell, AJ, Quentric, M, Vikkula, M, Yamaguti, PM   +8 more
core   +1 more source

Alteration of Exon Definition Causes Amelogenesis Imperfecta

Journal of dentistry research, 2020
Amelogenesis imperfecta (AI) is a collection of genetic disorders affecting the quality and/or quantity of tooth enamel. More than 20 genes are, so far, known to be responsible for this condition.
Yong-Ik Kim, Jenny Kang, F. Seymen, M. Koruyucu, Hong Zhang, Y. Kasımoğlu, M. Bayram, E. B. Tuna-İnce, Ş. Bayrak, N. Tuloglu, J. Hu, J. Simmer, J. Kim   +12 more
semanticscholar   +1 more source

FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta

Journal of dentistry research, 2020
Autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI; OMIM #130900) is a genetic disorder exhibiting severe hardness defects and reduced fracture toughness of dental enamel. While the condition is nonsyndromic, it can be associated with other
S.K. Wang, H. Zhang, C. Hu, J.F. Liu, S. Chadha, J. Kim, J. Simmer, J. Hu   +7 more
semanticscholar   +1 more source

Amelogenesis imperfecta with bilateral nephrocalcinosis [PDF]

BMJ Case Reports, 2013
A 12-year-old patient presented with a severe delay of eruption in permanent maxillary and mandibular incisors. On examination, there was over-retained primary teeth and delayed eruption of permanent teeth. Retained primary teeth showed light yellow discolouration whereas permanent teeth were distinct yellow with thin or little enamel.
P Poornima, Rachappa Mallikarjuna, Shashikant Katkade, Roshan Noor Mohamed   +3 more
openaire   +3 more sources

Evaluation of the esthetic properties of developmental defects of enamel: a spectrophotometric clinical study [PDF]

, 2015
Objectives. Detailed clinical quantification of optical properties of developmental defect of enamel is possible with spectropho- tometric evaluation. Developmental defects of enamel (DDE) are daily encountered in clinical practice. DDE are an alteration
Corridore, Denise, Debora, Pasqualotto, Guerra, Fabrizio, Mazur, Marta Danuta, Nardi, Gianna Maria, Ottolenghi, Livia   +5 more
core   +4 more sources