Results 51 to 60 of about 5,937 (217)

Reduced Dietary Protein Induces Changes in the Dental Proteome

Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, Volume 346, Issue 2, Page 107-127, March 2026.
Low dietary protein (10%) from normal (20%) does change protein expression in tooth proteome and alter developmental pathways. Among the significant protein expressions changes are actin‐based myosins, tooth, and bone development proteins. Perplexingly tooth size is not altered, suggesting more nuanced phenotypic response to low dietary protein in ...
Robert W. Burroughs, Christopher J. Percival, Natasha S. Vitek   +2 more
wiley   +1 more source

Amelogenezis imperfektalı iki hastada estetik ve fonksiyonun sağlanması: olgu sunumu

Cumhuriyet Dental Journal, 2011
Amelogenesis imperfecta is a rare hereditarycondition in which enamel structure without evidence of sistemic disorders. Amelogenesis imperfecta is a disorder, requiring treatment due to esthetical, functional and related psychosocial problems.
Behiye Bolgul, Buket Ayna, Emrah Ayna, Nihal Hamamci, Sema Celenk   +4 more
doaj   +3 more sources

Auto-percepção dos portadores de Amelogênese Imperfeita e Displasia [PDF]

, 2012
TCC (graduação) - Universidade Federal de Santa Catarina. Centro de Ciências da Saúde. Odontologia.A Amelogênese Imperfeita é um distúrbio hereditário caracterizado pela formação anormal de esmalte, o que gera dentes com alteração de cor, sensibilidade e
Klita, Ana Paula Haisi
core  

Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta [PDF]

, 2017
We identified two homozygous missense variants (c.428C>T, p.(T143M) and c.746C>T, p.(P249L)) in ACPT, the gene encoding Acid Phosphatase, Testicular, which segregate with hypoplastic Amelogenesis imperfecta (AI) in two unrelated families.
Alan J Mighell, B Backman, CE Smith, CEL Smith, Chris F Inglehearn, Claire EL Smith, DA Parry, F Seymen, Francesca Soldani, GA Van der Auwera, H Choi, H Fleisig, H Li, James A Poulter, Jennifer Kirkham, Laura LE Whitehouse, M Goldberg, NA Romas, Peter F Day, ST Sherry, Steven J Brookes   +20 more
core   +1 more source

WDR72 Is Required for Urinary Acidification and Normal H+‐ATPase Activity in Intercalated Cells in Mice

Acta Physiologica, Volume 242, Issue 3, March 2026.
ABSTRACT Aim Biallelic inactivating WDR72 variants are linked to distal renal tubular acidosis (dRTA), nephrocalcinosis, and amelogenesis imperfecta. The kidney shows high WDR72 expression; its precise localization and function remain unclear. WDR72 is a member of the WD40 repeat domain protein family—a large group of scaffold proteins involved in ...
Hannah Auwerx, Moana Busch‐Dohr, Xiaoxu Li, Carsten A. Wagner, Soline Bourgeois   +4 more
wiley   +1 more source

Diagnosis, treatment planning, and full-mouth rehabilitation in a case of amelogenesis imperfecta

Contemporary Clinical Dentistry, 2018
Amelogenesis imperfecta is a genetic condition affecting the teeth resulting in aberrations of the structure and clinical appearance of enamel. The treatment of amelogenesis imperfecta involves a multidisciplinary treatment approach requiring a ...
Mayuri Naik, Siddharth Bansal
doaj   +1 more source

FAM20A Deficiency Drives Transcriptomic Dysregulation and Functional Impairment in Gingival Fibroblasts

Cell Proliferation, Volume 59, Issue 2, February 2026.
FAM20A variants cause AI1G, marked by enamel defects, gingival overgrowth and ectopic calcifications. RNA sequencing of patient‐derived gingival fibroblasts showed dysregulated genes in adhesion, proliferation and signalling pathways. Functional assays revealed increased cell proliferation, impaired ECM interactions and osteogenesis, suggesting FAM20A ...
Kanokwan Sriwattanapong, Sermporn Thaweesapphithak, Chompak Khamwachirapitak, Pannagorn Sae‐ear, Sasiprapa Prommanee, Noppadol Sa‐Ard‐Iam, Suphalak Phothichailert, Han Sung Jung, Vorasuk Shotelersuk, Thantrira Porntaveetus   +9 more
wiley   +1 more source

Amelogenesis imperfecta in a family

Revista Cubana de Estomatología, 2018
Introduction: amelogenesis imperfecta consists of a group of hereditary disorders that affect the development of the dental enamel in such a way that the clinical appearance of all or almost all primary and permanent teeth is compromised.
Paula Hurtado-Villa, Fabián Tobar-Tosse, Julio Osorio, Freddy Moreno   +3 more
doaj  

FAM20C Functions Intracellularly Within Both Ameloblasts and Odontoblasts In Vivo [PDF]

, 2013
FAM20C, also known as Golgi casein kinase (G‐CK), is proposed to be the archetype for a family of secreted kinases that phosphorylate target proteins in the Golgi and in extracellular matrices, but FAM20C serving an extracellular function is ...
Al-Hashimi, Brunati, Chan, Delgado, Duncan, Feng, Fincham, Ishikawa, Kawasaki, Nadanaka, Nalbant, O'Sullivan, Ryu, Simmer, Simpson, Tagliabracci, Tagliabracci, Wang, Wang, Yamakoshi   +19 more
core   +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, Shashikant, Katkade, Roshan Noor, Mohamed, Rachappa, Mallikarjuna   +3 more
openaire   +2 more sources