Works matching DE "DENTINOGENESIS imperfecta"

Results: 225

Dental Management of Heritable Dental Developmental Anomalies.

Published in:: Pediatric Dentistry, 2017, v. 39, n. 6, p. 348
Publication type:: Article

Guideline on Dental Management of Heritable Dental Developmental Anomalies.

Published in:: 2016
Publication type:: journal article

Osteogenesis imperfecta and the teeth, eyes, and ears—a study of non-skeletal phenotypes in adults.

Published in:

Osteoporosis International, 2018, v. 29, n. 12, p. 2781, doi. 10.1007/s00198-018-4663-x

By:

Hald, J.D.;
Folkestad, L.;
Swan, C.Z.;
Wanscher, J.;
Schmidt, M.;
Gjørup, H.;
Haubek, D.;
Leonhard, C.-H.;
Larsen, D.A.;
Hjortdal, J.Ø.;
Harsløf, T.;
Duno, M.;
Lund, A.M.;
Jensen, J.-E.B.;
Brixen, K.;
Langdahl, B.

Publication type:

Article

Novel mutations in the SEC24D gene in Chinese families with autosomal recessive osteogenesis imperfecta.

Published in:

Osteoporosis International, 2017, v. 28, n. 4, p. 1473, doi. 10.1007/s00198-016-3866-2

By:

Zhang, H.;
Yue, H.;
Wang, C.;
Gu, J.;
He, J.;
Fu, W.;
Hu, W.;
Zhang, Z.

Publication type:

Article

OSTEOGENESIS IMPERFECTA: GENETICS AND TREATMENT.

Published in:

2018

By:

Pinnell, Jonathan;
Chaudhuri, Kaushik

Publication type:

Case Study

DENTINOGENESIS IMPERFECTA.

Published in:

Guident, 2011, v. 4, n. 12, p. 40

By:

Hasan, Shamimul;
Khan, Nabeel Ishrat;
Khan, Mohd. Rashid

Publication type:

Article

Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfecta.

Published in:

2003

By:

Malmgren, Barbro;
Lindskog, Sven

Publication type:

journal article

Genotype–phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 6, p. 642, doi. 10.1038/ejhg.2009.242

By:

Rauch, Frank;
Lalic, Liljana;
Roughley, Peter;
Glorieux, Francis H.

Publication type:

Article

A novel mutation in PAX9 causes familial form of molar oligodontia.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 2, p. 173, doi. 10.1038/sj.ejhg.5201536

By:

Mostowska, Adrianna;
Biedziak, Barbara;
Trzeciak, Wieslaw H.

Publication type:

Article

Tooth-bone morphogenesis during postnatal stages of mouse first molar development.

Published in:

Journal of Anatomy, 2011, v. 218, n. 6, p. 699, doi. 10.1111/j.1469-7580.2011.01367.x

By:

Lungová, Vlasta;
Radlanski, Ralf J.;
Tucker, Abigail S.;
Renz, Herbert;
Míšek, Ivan;
Matalová, Eva

Publication type:

Article

Transgenic expression of dentin phosphoprotein (DPP) partially rescued the dentin defects of DSPP-null mice.

Published in:

PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0195854

By:

Zhang, Hua;
Xie, Xiaohua;
Liu, Peihong;
Liang, Tian;
Lu, Yongbo;
Qin, Chunlin

Publication type:

Article

Dentinogenesis imperfecta type II in Swedish children and adolescents.

Published in:

2018

By:

Andersson, K.;
Malmgren, B.;
Åström, E.;
Dahllöf, G.;
Åström, E;
Dahllöf, G

Publication type:

journal article

A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.

Published in:

Nature Genetics, 2005, v. 37, n. 8, p. 803, doi. 10.1038/ng1603

By:

Aubin, Isabelle;
Adams, Carolyn P.;
Opsahl, Sibylle;
Septier, Dominique;
Bishop, Colin E.;
Auge, Nathalie;
Salvayre, Robert;
Negre-Salvayre, Anne;
Goldberg, Michel;
Guénet, Jean-Louis;
Poirier, Christophe

Publication type:

Article

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.

Published in:: Nature Genetics, 2001, v. 27, n. 3, p. 345
Publication type:: Article

Soundbites.

Published in:

Nature Genetics, 2001, v. 27, n. 2, p. 129, doi. 10.1038/84728

By:

Patel, Pragna I

Publication type:

Article

DSPP mutation in dentinogenesis imperfecta Shields type II.

Published in:

Nature Genetics, 2001, v. 27, n. 2, p. 151, doi. 10.1038/84765

By:

Zhang, Xiaohai;
Zhao, Jun;
Li, Changfu;
Gao, Shan;
Qiu, Changchun;
Liu, Ping;
Wu, Guanyun;
Qiang, Boqin;
Lo, Wilson H.Y.;
Shen, Yan

Publication type:

Article

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.

Published in:

Nature Genetics, 2001, v. 27, n. 2, p. 201, doi. 10.1038/84848

By:

Xiao, Shangxi;
Yu, Chuan;
Chou, Xueming;
Yuan, Wenjuan;
Wang, Ying;
Bu, Lei;
Fu, Gang;
Qian, Meiqian;
Yang, Jun;
Shi, Yaozhou;
Hu, Landian;
Han, Bin;
Wang, Zhengmin;
Huang, Wei;
Liu, Jing;
Chen, Zhu;
Zhao, Guoping;
Kong, Xiangyin

Publication type:

Article

The dental perspective on osteogenesis imperfecta in a Danish adult population.

Published in:

BMC Oral Health, 2018, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12903-018-0639-7

By:

Thuesen, Kirstine Juhl;
Haubek, Dorte;
Gjørup, Hans;
Hald, Jannie Dahl;
Harsløf, Torben;
Langdahl, Bente;
Schmidt, Malene

Publication type:

Article

Dentinogenesis imperfecta: An update.

Published in:

Journal of Research & Practice on the Musculoskeletal System (JRPMS), 2022, v. 6, n. 1, p. 9, doi. 10.22540/JRPMS-06-009

By:

Tsoukala, Efthimia;
Chochtoula, Georgia;
Theodorou, Iosifina;
Lambrou, George I.

Publication type:

Article

Genetic studies of craniofacial anomalies: clinical implications and applications.

Published in:

Orthodontics & Craniofacial Research, 2009, v. 12, n. 3, p. 212, doi. 10.1111/j.1601-6343.2009.01455.x

By:

Hart, T. C.;
Hart, P. S.

Publication type:

Article

Developmental biology and genetics of dental malformations.

Published in:

Orthodontics & Craniofacial Research, 2007, v. 10, n. 2, p. 45, doi. 10.1111/j.1601-6343.2007.00384.x

By:

Hu, J. C.-C.;
Simmer, J. P.

Publication type:

Article

CD 95 mediated apoptosis in embryogenesis: implication in tooth development.

Published in:

Orthodontics & Craniofacial Research, 2006, v. 9, n. 3, p. 123, doi. 10.1111/j.1601-6343.2006.00365.x

By:

Matalov, E.;
Šetkov, J.;
Blackburn, J.;
Míšek, I.;
Sharpe, P. T.

Publication type:

Article

Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype.

Published in:

2006

By:

Gerits, A.;
Nieminen, P.;
De Muynck, S.;
Carels, C.

Publication type:

journal article

Radiological features of hereditary opalescent dentin.

Published in:

Dentomaxillofacial Radiology, 1998, v. 27, n. 4, p. 251, doi. 10.1038/sj.dmfr.4600350

By:

Tanaka, T;
Murakami, T

Publication type:

Article

3 Dimensional Diagnosis Unravelling Prognosis of Multiple Impacted Teeth - A Case Report.

Published in:

2013

By:

Gopinath, Adusumilli;
Reddy, Naveen Admala;
Rohra, Mayur G.

Publication type:

Case Study

Brittle teeth with brittle bone in a family for four generations: Case report and literature review.

Published in:

2012

By:

P. S. SHILPA;
CHAYA M. DAVID;
KAUL, RACHNA;
C. J. SANJAY;
NARAYAN, B. K. RAM

Publication type:

Case Study

Prosthodontic rehabilitation of dentinogenesis imperfecta.

Published in:

2011

By:

GOUD, ANIL;
DESHPANDE, SAEE

Publication type:

Case Study

Successful Bleaching of Teeth with Dentinogenesis Imperfecta Discoloration: A Case Report.

Published in:

Journal of Esthetic & Restorative Dentistry, 2011, v. 23, n. 1, p. 3, doi. 10.1111/j.1708-8240.2010.00379.x

By:

BIDRA, AVINASH S.;
URIBE, FLAVIO

Publication type:

Article

COMMENTARY.

Published in:

Journal of Esthetic & Restorative Dentistry, 2011, v. 23, n. 1, p. 11, doi. 10.1111/j.1708-8240.2010.00380.x

By:

Li, Yiming

Publication type:

Article

Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.

Published in:

European Journal of Oral Sciences, 2011, v. 119, p. 158, doi. 10.1111/j.1600-0722.2011.00874.x

By:

Wang, Shih‐Kai;
Chan, Hui‐Chen;
Rajderkar, Sudha;
Milkovich, Rachel N.;
Uston, Karen A.;
Kim, Jung‐Wook;
Simmer, James P.;
Hu, Jan C‐C.

Publication type:

Article

De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family.

Published in:

European Journal of Oral Sciences, 2009, v. 117, n. 6, p. 691, doi. 10.1111/j.1600-0722.2009.00683.x

By:

Kida, Miyuki;
Tsutsumi, Tomonori;
Shindoh, Masanobu;
Ikeda, Hisami;
Ariga, Tadashi

Publication type:

Article

Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II.

Published in:

European Journal of Oral Sciences, 2006, v. 114, n. 5, p. 381, doi. 10.1111/j.1600-0722.2006.00391.x

By:

Holappa, Heidi;
Nieminen, Pekka;
Tolva, Liisa;
Lukinmaa, Pirjo‐Liisa;
Alaluusua, Satu

Publication type:

Article

Involvement of matrix metalloproteinases in the onset of dentin mineralization.

Published in:

European Journal of Oral Sciences, 2004, v. 112, n. 2, p. 171, doi. 10.1111/j.1600-0722.2004.00120.x

By:

Fanchon, Stephanie;
Bourd, Katia;
Septier, Dominique;
Everts, Vincent;
Beertsen, Wouter;
Menashi, Suzanne;
Goldberg, Michel

Publication type:

Article

Dentin matrix proteins.

Published in:

European Journal of Oral Sciences, 1998, v. 106, p. 204, doi. 10.1111/j.1600-0722.1998.tb02177.x

By:

Butler, William T.

Publication type:

Article

Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci.

Published in:

European Journal of Oral Sciences, 1998, v. 106, p. 227, doi. 10.1111/j.1600-0722.1998.tb02180.x

By:

MacDougall, Mary

Publication type:

Article

Novel PAX9 and COL1A2 Missense Mutations Causing Tooth Agenesis and OI/DGI without Skeletal Abnormalities.

Published in:

PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051533

By:

Shih-Kai Wang;
Hui-Chen Chan;
Makovey, Igor;
Simmer, James P.;
Hu, Jan C-C.

Publication type:

Article

A Novel Splicing Mutation Alters DSPP Transcription and Leads to Dentinogenesis Imperfecta Type II.

Published in:

PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0027982

By:

Jun Zhang;
Jiucun Wang;
Yanyun Ma;
Wenqi Du;
Siyang Zhao;
Zuowei Zhang;
Xiaojiao Zhang;
Yue Liu;
Huasheng Xiao;
Hongyan Wang;
Li Jin;
Jie Liu

Publication type:

Article

Early Rehabilitation of Incisors with Dentinogenesis Imperfecta Type II - Case Report.

Published in:

2017

By:

Beltrame, Ana Paula C. A.;
Rosa, Maíra Mery;
Noschang, Ricardo A. T.;
Almeida, Izabel C. S.;
Beltrame, Ana Paula Ca;
Noschang, Ricardo At;
Almeida, Izabel Cs

Publication type:

journal article

Multiple Teeth Fractures in Dentinogenesis Imperfecta: A Case Report.

Published in:

2014

By:

Min, B.;
Song, J. S.;
Lee, J. H.;
Choi, B. J.;
Kim, K. M.;
Kim, S. O.

Publication type:

Case Study

Tratamiento quirúrgico de mesiodents en Odontopediatría.

Published in:

Revista Oral, 2011, v. 12, n. 39, p. 770

By:

de Oliveira, Camila Fávero;
Sacono, Nancy Tomoko;
Muñoz, Eduardo Mariscal;
Hebling, Josemeri;
Giro, Elisa María Aparecida;
de Souza Costa, Carlos Alberto

Publication type:

Article

Efficiency in the detection of the mesiopalatine canal in upper first molars, through clinical eye, 3.5 X magnifying glass and dental microscope.

Published in:

Revista Oral, 2011, v. 12, n. 36, p. 673

By:

Sánchez Huerta, Héctor Antonio;
Robles Romero, David Martín;
Hernández Hernández, María de Jesús;
Flores Soto, Cecilio Oswaldo

Publication type:

Article

Eficacia en la detección del conducto mesiopalatino en primeros molares superiores mediante ojo clínico, lupas 3.5 X y microscopio dental.

Published in:

Revista Oral, 2011, v. 12, n. 36, p. 673

By:

Sánchez Huerta, Héctor Antonio;
Robles Romero, David Martín;
Hernández Hernández, María de Jesús;
Flores Soto, Cecilio Oswaldo

Publication type:

Article

The Leucine-Rich Amelogenin Peptide Alters the Amelogenin Null Enamel Phenotype.

Published in:

Cells Tissues Organs, 2008, v. 189, n. 1-4, p. 169, doi. 10.1159/000151384

By:

Gibson, Carolyn W.;
Yong Li;
Daly, Bill;
Suggs, Cynthia;
Zhi-an Yuan;
Fong, Hanson;
Simmons, Darrin;
Aragon, Melissa;
Kulkarni, Ashok B.;
Wright, J. Timothy

Publication type:

Article

Dynamic Analysis of the Expression of the TGFβ/SMAD2 Pathway and CCN2/CTGF during Early Steps of Tooth Development.

Published in:

Cells Tissues Organs, 2007, v. 187, n. 3, p. 199, doi. 10.1159/000112640

By:

Pacheco, Marcos S.;
Reis, Alice H.;
Aguiar, Diego P.;
Lyons, Karen M.;
Abreu, José G.

Publication type:

Article

Disorders of Human Dentin.

Published in:

Cells Tissues Organs, 2007, v. 186, n. 1, p. 70, doi. 10.1159/000102682

By:

Hart, P. Suzanne;
Hart, Thomas C.

Publication type:

Article

Author and Subject Index Vol. 186, No. 1, 2007.

Published in:: Cells Tissues Organs, 2007, v. 186, n. 1, p. 94, doi. 10.1159/000105382
Publication type:: Article

Characterization of Ectomesenchymal Cells Isolated from the First Branchial Arch during Multilineage Differentiation.

Published in:

Cells Tissues Organs, 2006, v. 183, n. 3, p. 123, doi. 10.1159/000095986

By:

Zhengbin Yan;
Yunfeng Lin;
Xiaohui Jiao;
Zhiyong Li;
Ling Wu;
Wei Jing;
Ju Qiao;
Lei Liu;
Wei Tang;
Xiaohui Zheng;
Weidong Tian

Publication type:

Article

Overexpression of TRAP in the Enamel Matrix Does Not Alter the Enamel Structural Hierarchy.

Published in:

Cells Tissues Organs, 2004, v. 176, n. 1-3, p. 7, doi. 10.1159/000075023

By:

Paine, Michael L.;
Dan-Hong Zhu, Michael L.;
Wen Luo;
Snead, Malcolm L.

Publication type:

Article

Congenital oral anomalies in Argentinian children.

Published in:

Community Dentistry & Oral Epidemiology, 1975, v. 3, n. 2, p. 61, doi. 10.1111/j.1600-0528.1975.tb00281.x

By:

Sedano, Heddie O.

Publication type:

Article

Prosthetic treatment in dentinogenesis imperfecta type II: a case report.

Published in:

2016

By:

Güven, Sedat;
Demirci, Fatih;
Tanik, Abdulsamet;
Koparal, Mahmut

Publication type:

Case Study