Results 111 to 120 of about 12,368 (291)

Relationships between protein and mineral during enamel development in normal and genetically altered mice [PDF]

, 2011
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90093/1/EOS_871_sm_SupportingInformation.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/90093/2/j.1600-0722.2011.00871.x ...
Bartlett, John D., Hu, Jan C‐C., Hu, Yuan Yuan, Richardson, Amelia S., Simmer, James P., Smith, Charles E.   +5 more
core   +1 more source

Amelogenesis imperfecta

TandartsPraktijk, 2017
SamenvattingAmelogenesis imperfecta is een erfelijke aandoening waarbij de dikte en/of de vorm van de glazuurlaag afwijken. We onderscheiden drie verschijningsvormen: hypoplasie, hypocalcificatie en hypomaturatie.
Marcel Linssen, Hans Pelt
semanticscholar   +1 more source

Amelogenesis imperfecta with Class III malocclusion, reduced crown size and decreased OVD: A multi‐disciplinary management and a 5‐year follow‐up

Clinical Case Reports, 2020
This clinical report describes the oral rehabilitation of a 22‐year‐old‐man diagnosed with a variant of hypoplastic amelogenesis imperfecta. The treatment approach was multi‐disciplinary, and it included the surgical procedure of Lefort I osteotomy ...
A. Labidi, Sana Bekri, Yosra Mabrouk, J. Ben Mustapha, M. Omezzine, S. Ghoul-Mazgar, L. Mansour   +6 more
semanticscholar   +1 more source

Structural Variants in COL1A1 and COL1A2 in Osteogenesis Imperfecta

American Journal of Medical Genetics Part A, Volume 197, Issue 3, March 2025.
ABSTRACT Osteogenesis Imperfecta (OI) is a heterogeneous skeletal dysplasia characterized by bone fragility, skeletal deformities, and short stature. Most commonly, it is caused by autosomal dominant variants in the type I collagen genes, COL1A1 or COL1A2.
Dominyka Batkovskyte, Diana Swolin‐Eide, Anna Hammarsjö, Kristine Bilgrav Sæther, Sofia Thunström, Johanna Lundin, Jesper Eisfeldt, Anna Lindstrand, Ann Nordgren, Eva Åström, Giedre Grigelioniene   +10 more
wiley   +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

Experiences of Being a Parent to a Child with Amelogenesis Imperfecta

Dental journal, 2019
Amelogenesis imperfecta (AI) is a hereditary developmental disorder affecting the enamel of teeth. Affected patients present with tooth hypersensitivity, rapid tooth wear, or fractures of enamel as well as alterations in color and shape, all of which ...
G. Pousette Lundgren, T. Hasselblad, A. Johansson, A. Johansson, G. Dahllöf   +4 more
semanticscholar   +1 more source

A Missense Variant Affecting the N‐Terminal Domain of the Laminin‐332 β3 Chain Results in a Distinct Form of Junctional Epidermolysis Bullosa With Altered Granulation Tissue Response and No New Blistering: A Second Family Report

Pediatric Dermatology, Volume 42, Issue 2, Page 410-412, March/April 2025.
ABSTRACT Junctional epidermolysis bullosa (JEB) is a rare genodermatosis characterized by fragility of the skin and mucous membranes due to alterations in the dermal epidermal junction. This condition manifests as mechanically induced bullous lesions that heal with hypertrophic granulation tissue and/or atrophic scars.
Marina Goldoni, Barbara Torres, Maurizio Pettinato, Alessia Gennaro, Tommaso Biagini, Angelo Giuseppe Condorelli, Rosanna Monetta, Tommaso Mazza, Laura Bernardini, Teresa Mattina   +9 more
wiley   +1 more source

Protein Phosphorylation and Mineral Binding Affect the Secondary Structure of the Leucine-Rich Amelogenin Peptide

Frontiers in Physiology, 2017
Previously, we have shown that serine-16 phosphorylation in native full-length porcine amelogenin (P173) and the Leucine-Rich Amelogenin Peptide (LRAP(+P)), an alternative amelogenin splice product, affects protein assembly and mineralization in vitro ...
Hajime Yamazaki, Hajime Yamazaki, Elia Beniash, Yasuo Yamakoshi, James P. Simmer, Henry C. Margolis, Henry C. Margolis   +6 more
doaj   +1 more source

Epithelial‐specific knockout of the Rac1 gene leads to enamel defects [PDF]

, 2011
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90135/1/j.1600-0722.2011.00904.x ...
Albertinazzi, Bei, Biz, Boyde, Castilho, Cerny, Chrostek, Couwenhoven, Cutroneo, DeMali, Filipenko, Fincham, Fukumoto, Fukumoto, Fukumoto, Gibson, Gibson, Glogauer, Hart, Hart, Hatakeyama, Huang, Hunter, Jernvall, Krebsbach, Li, Li, Liu, Nishikawa, Noritake, Paine, Rajpar, Reith, Snead, Snead, Sugihara, Thesleff, Thomas, Vidali, Wright, Xu   +40 more
core   +1 more source

Revisiting Linear Enamel Hypoplasia in Cayo Santiago Rhesus Macaques (Macaca mulatta): How a Stress Marker Relates to Environment and Maternal Lineage in a Rare Rhesus Colony With Known Life History

American Journal of Primatology, Volume 87, Issue 2, February 2025.
Linear enamel hypoplasia (LEH) prevalence in the teeth of Cayo Santiago rhesus monkeys (Macaca mulatta). Defects matched on right and left teeth and the increase in the frequency of LEH by decade. ABSTRACT Linear enamel hypoplasias (LEHs) are development defects appearing as lines or grooves on enamel surfaces.
Debbie Guatelli‐Steinberg, Julianna Watson, Liya Samuel, Emma Showalter, Finn Lerner, Emilie Dixon, Terry B. Kensler, George Francis, Elizabeth Maldonado, Luci A. P. Kohn, Martin Q. Zhao, Qian Wang   +11 more
wiley   +1 more source