Works matching DE "TEETH abnormality genetics"

Results: 84

Triplets with bilateral palatally displaced canines in association with third molar agenesis: an example of biologically related dental anomaly patterns?

Published in:

Journal of Orthodontics, 2013, v. 40, n. 2, p. 172, doi. 10.1179/1465312513Z.00000000081

By:

Harte, Criona;
Juggins, Karen

Publication type:

Article

Tooth agenesis related to a novel KDF1 variant: A case report and literature review.

Published in:

Oral Diseases, 2024, v. 30, n. 8, p. 5195, doi. 10.1111/odi.14930

By:

Intarak, Narin;
Manaspon, Chawan;
Theerapanon, Thanakorn;
Prommanee, Sasiprapa;
Samaranayake, Lakshman;
Shotelersuk, Vorasuk;
Porntaveetus, Thantrira

Publication type:

Article

Eight EDA mutations in Chinese patients with tooth agenesis and genotype–phenotype analysis.

Published in:

Oral Diseases, 2024, v. 30, n. 7, p. 4598, doi. 10.1111/odi.14878

By:

Yu, Kang;
Sheng, Yihan;
Wang, Feng;
Yang, Shuwen;
Wan, Futang;
Lei, Ming;
Wu, Yiqun

Publication type:

Article

Identified a novel splicing mutation at EDA gene in a hypohidrotic ectodermal dysplasia pedigree.

Published in:

Oral Diseases, 2023, v. 29, n. 8, p. 3164, doi. 10.1111/odi.14362

By:

Zhou, Yuan;
Yin, Bin;
Shi, Bing;
Zheng, Li‐Wei;
Jia, Zhong‐Lin

Publication type:

Article

A novel ENAM mutation causes hypoplastic amelogenesis imperfecta.

Published in:

Oral Diseases, 2022, v. 28, n. 6, p. 1610, doi. 10.1111/odi.13877

By:

Yu, Shunlan;
Zhang, Chenying;
Zhu, Ce;
Quan, Junkang;
Liu, Dandan;
Wang, Xiaozhe;
Zheng, Shuguo

Publication type:

Article

Dentin dysplasia type I—A dental disease with genetic heterogeneity.

Published in:

Oral Diseases, 2019, v. 25, n. 2, p. 439, doi. 10.1111/odi.12861

By:

Chen, D;
Li, X;
Lu, F;
Wang, Y;
Xiong, F;
Li, Q

Publication type:

Article

A novel <italic>PITX2</italic> mutation in non‐syndromic orodental anomalies.

Published in:

Oral Diseases, 2018, v. 24, n. 4, p. 611, doi. 10.1111/odi.12804

By:

Intarak, N.;
Theerapanon, T.;
Ittiwut, C.;
Suphapeetiporn, K.;
Porntaveetus, T.;
Shotelersuk, V.

Publication type:

Article

<italic>GREM2</italic> nucleotide variants and the risk of tooth agenesis.

Published in:

Oral Diseases, 2018, v. 24, n. 4, p. 591, doi. 10.1111/odi.12793

By:

Mostowska, A.;
Biedziak, B.;
Zadurska, M.;
Bogdanowicz, A.;
Olszewska, A.;
Cieślińska, K.;
Firlej, E.;
Jagodziński, P. P.

Publication type:

Article

Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.

Published in:

Oral Diseases, 2017, v. 23, n. 3, p. 360, doi. 10.1111/odi.12621

By:

Li, F;
Liu, Y;
Liu, H;
Yang, J;
Zhang, F;
Feng, H

Publication type:

Article

Autoinflammatory disease with corneal and mucosal dyskeratosis caused by a novel NLRP1 variant.

Published in:

Rheumatology, 2020, v. 59, n. 9, p. 2334, doi. 10.1093/rheumatology/kez612

By:

Herlin, Troels;
Jørgensen, Sofie E;
Høst, Christian;
Mitchell, Patrick S;
Christensen, Maria Hønholt;
Laustsen, Mira;
Larsen, Dorthe A;
Schmidt, Florian I;
Christiansen, Mette;
Mogensen, Trine H

Publication type:

Article

The familial line, studied by a new line of reference.

Published in:

European Journal of Orthodontics, 2007, v. 29, p. i65, doi. 10.1093/ejo/cjl074

By:

De Coster, Lucien

Publication type:

Article

Dental transposition as a disorder of genetic origin.

Published in:

European Journal of Orthodontics, 2006, v. 28, n. 2, p. 145, doi. 10.1093/ejo/cji092

By:

Ely, Nicola J.;
Sherriff, Martyn;
Cobourne, Martyn T.

Publication type:

Article

Root growth in the permanent teeth of 45,X/46,XX females.

Published in:

European Journal of Orthodontics, 2006, v. 28, n. 4, p. 339, doi. 10.1093/ejo/cji121

By:

Lähdesmäki, Raija;
Alvesalo, Lassi

Publication type:

Article

Those with dental phobia more likely to have cavities or missing teeth, study confirms.

Published in:: IDA Times, 2017, v. 13, n. 12, p. 16
Publication type:: Article

Nfic Gene Disruption Inhibits Differentiation of Odontoblasts Responsible for Root Formation and Results in Formation of Short and Abnormal Roots in Mice.

Published in:

Journal of Periodontology, 2007, v. 78, n. 9, p. 1795, doi. 10.1902/jop.2007.060363

By:

Joo Cheol Park;
Yeek Herr;
Heung-Joong Kim;
Gronostajski, Richard M.;
Moon-Il Cho

Publication type:

Article

Non-Extraction Treatment of a Crowded Class II Division 2 Adult Patient with Crozat Appliances and Eureka Springs.

Published in:

2008

By:

Marasa, Frank K.

Publication type:

Case Study

Análisis mutacional del gen MSX1 en pacientes con FLPNS e hipodoncia.

Published in:

Universitas Médica, 2009, v. 50, n. 3, p. 346

By:

PRIETO, SANDRA JANETH GUTIÉRREZ;
LÓPEZ, DIANA MARÍA TORRES;
CUBILLOS, JORGE ARTURO REY;
BALCÁZAR, IGNACIO BRICEÑO

Publication type:

Article

Dental abnormalities observed in the oculo-facio-cardio-dental (OFCD) syndrome present in two Czech families bearing novel de novo BCOR pathogenic variants.

Published in:

BMC Oral Health, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12903-024-05005-y

By:

Batkova, M.;
Havlovicova, M.;
Nocar, A.;
Dudakova, L.;
Macek, M.;
Liskova, Petra;
Dostalova, Tatjana

Publication type:

Article

Segregation analysis of mandibular prognathism in Korean orthognathic surgery patients and their families.

Published in:

Angle Orthodontist, 2013, v. 83, n. 6, p. 1027, doi. 10.2319/021313-130.1

By:

Jeong-Min Ko;
Young Ju Suh;
Jongrak Hong;
Jun-Young Paeng;
Seung-Hak Baek;
Young Ho Kim

Publication type:

Article

Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients.

Published in:

Angle Orthodontist, 2013, v. 83, n. 6, p. 1036, doi. 10.2319/020513-104.1

By:

Yu-Jin Seo;
Ji Wan Park;
Young Ho Kim;
Seung-Hak Baek

Publication type:

Article

Witkop Tooth and Nail Syndrome and Orthodontics.

Published in:

2008

By:

Altug-Atac, Ayse T.;
Iseri, Haluk

Publication type:

Case Study

Missing Lateral with a Transposed Canine.

Published in:

2011

By:

Kalman, Les

Publication type:

Case Study

TRATAMENTUL ANODONŢIEI DE INCISIV LATERAL SUPERIOR - PREZENTAREA A DOUă CAZURI CLINICE.

Published in:

2012

By:

Bozga, Andreea;
Stanciu, Radu Patru;
Bartok, Ruxandra Ioana;
Stanciu1, Dragoş

Publication type:

Case Study

MEZIODENSUL FAMILIAL.

Published in:

Romanian Journal of Stomatology / Revista Romana de Stomatologie, 2009, v. 55, n. 4, p. 293

By:

Severin, Emilia;
Purcărea, Răzvan;
Albu, Crenguţa;
Albu, Dinu F.;
Ionescu, Ecaterina;
Stanciu, Dragoş

Publication type:

Article

LRP4 mutations, dental anomalies, and oral exostoses.

Published in:

International Journal of Paediatric Dentistry, 2024, v. 34, n. 4, p. 432, doi. 10.1111/ipd.13141

By:

Kantaputra, Piranit;
Panichkul, Weena;
Sillapasorn, Parisri;
Adisornkanj, Ploy;
Kitsadayurach, Panita;
Kaewgaya, Massupa;
Intachai, Worrachet;
Olsen, Bjorn;
Ngamphiw, Chumpol;
Leethanakul, Chidchanok;
Jatooratthawichot, Peeranat;
Ketudat Cairns, James R.;
Tongsima, Sissades

Publication type:

Article

Clinical Case Prize.

Published in:: 2019
Publication type:: Case Study

Comproving the multifactorial etiology of molar incisor hypomineralization.

Published in:

2019

By:

Teixeira, Rafael José Pio Barbosa;
Andrade, Natália Silva;
Queiroz, Lisanca Carvalho Cavalcante;
Mendes, Fausto Medeiros;
Moura, Marcoeli Silva de;
Moura, Lúcia de Fátima Almeida de Deus;
Lima, Marina de Deus Moura de

Publication type:

Letter to the Editor

On the genetics contribution to molar incisor hypomineralization.

Published in:

2019

By:

Vieira, Alexandre R.

Publication type:

Letter to the Editor

Exploring the association between genetic and environmental factors and molar incisor hypomineralization: evidence from a twin study.

Published in:

International Journal of Paediatric Dentistry, 2018, v. 28, n. 2, p. 198, doi. 10.1111/ipd.12327

By:

BARBOSA TEIXEIRA, RAFAEL JOSÉ PIO;
ANDRADE, NATÁLIA SILVA;
QUEIROZ, LISANCA CARVALHO CAVALCANTE;
MENDES, FAUSTO MEDEIROS;
MOURA, MARCOELI SILVA;
DE FÁTIMA ALMEIDA DE DEUS MOURA, LÚCIA;
MOURA LIMA, MARINA DEUS

Publication type:

Article

Gene links skull and teeth abnormalities.

Published in:: British Dental Journal, 2011, v. 211, n. 4, p. 155, doi. 10.1038/sj.bdj.2011.694
Publication type:: Article

GENETICS AND TOOTH ANOMALIES - AN UPDATE.

Published in:

Oral & Maxillofacial Pathology Journal, 2013, v. 4, n. 1, p. 334

By:

Raj R., Aswathy;
M. S., Deepa.;
Farooqi T., Ahmed Hasan;
Brahmanandan, Aswathy

Publication type:

Article

Use of a combination of orthodontics and prosthodontics to treat congenitally missing maxillary lateral incisors: A case report.

Published in:

1994

By:

Kocadereli, İlken;
Şahmali, Sevil M.

Publication type:

Case Study

Polymorphism in the Msx1 gene associated with hypodontia in a Brazilian family.

Published in:

Journal of Oral Science, 2009, v. 51, n. 3, p. 341, doi. 10.2334/josnusd.51.341

By:

Silva, Elisângela R.;
Reis-Filho, Cláudio R.;
Napimoga, Marcelo H.;
Alves, José B.

Publication type:

Article

Dental Anomalies with Genetic Influence of ABO Blood Group in Malaysian Orthodontic Patients.

Published in:

International Medical Journal, 2018, v. 25, n. 1, p. 9

By:

Alam, Mohammad Khursheed;
Wan Ab Rahman, Wan Suriana;
Ng Yee Theng, Yvonne

Publication type:

Article

X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings.

Published in:

Clinical Genetics, 2010, v. 78, n. 3, p. 257, doi. 10.1111/j.1399-0004.2010.01376.x

By:

Clauss, F.;
Chassaing, N.;
Smahi, A.;
Vincent, M. C.;
Calvas, P.;
Molla, M.;
Lesot, H.;
Alembik, Y.;
Hadj-Rabia, S.;
Bodemer, C.;
Manière, M. C.;
Schmittbuhl, M.

Publication type:

Article

Correction of Class II malocclusion and soft tissue profile in an adult patient.

Published in:

2016

By:

GAUR, ADITI;
MAHESHWARI, SANDHYA;
VERMA, SANJEEV KUMAR

Publication type:

Case Study

Inactivation of Fam20B in the dental epithelium of mice leads to supernumerary incisors.

Published in:

European Journal of Oral Sciences, 2015, v. 123, n. 6, p. 396, doi. 10.1111/eos.12222

By:

Tian, Ye;
Ma, Pan;
Liu, Chao;
Yang, Xiudong;
Crawford, Derrick M.;
Yan, Wenjuan;
Bai, Ding;
Qin, Chunlin;
Wang, Xiaofang

Publication type:

Article

WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.

Published in:

European Journal of Oral Sciences, 2015, v. 123, n. 1, p. 1, doi. 10.1111/eos.12165

By:

Mostowska, Adrianna;
Biedziak, Barbara;
Zadurska, Małgorzata;
Matuszewska‐Trojan, Sylwia;
Jagodziński, Paweł P.

Publication type:

Article

Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/ MH4.

Published in:

European Journal of Oral Sciences, 2014, v. 122, n. 1, p. 15, doi. 10.1111/eos.12105

By:

Kimura, Masashi;
Machida, Junichiro;
Yamaguchi, Seishi;
Shibata, Akio;
Tatematsu, Tadashi;
Miyachi, Hitoshi;
Jezewski, Peter A.;
Nakayama, Atsuo;
Higashi, Yujiro;
Shimozato, Kazuo;
Tokita, Yoshihito

Publication type:

Article

Functional evaluation of a novel tooth agenesis-associated bone morphogenetic protein 4 prodomain mutation.

Published in:

European Journal of Oral Sciences, 2013, v. 121, n. 4, p. 313, doi. 10.1111/eos.12055

By:

Huang, Yanyu;
Lu, Yongbo;
Mues, Gabriele;
Wang, Suzhen;
Bonds, John;
D'Souza, Rena

Publication type:

Article

Novel PAX 9 mutation associated with syndromic tooth agenesis.

Published in:

European Journal of Oral Sciences, 2013, v. 121, n. 5, p. 403, doi. 10.1111/eos.12071

By:

Mostowska, Adrianna;
Zadurska, Małgorzata;
Rakowska, Adriana;
Lianeri, Margarita;
Jagodziński, Paweł P.

Publication type:

Article

Novel mutation of the initiation codon of PAX9 causes oligodontia.

Published in:

2005

By:

Klein, M. L.;
Nieminen, P.;
Lammi, L.;
Niebuhr, E.;
Kreiborg, S.

Publication type:

journal article

MSX1, PAX9, and TGFA Contribute to Tooth Agenesis in Humans.

Published in:

Journal of Dental Research, 2004, v. 83, n. 9, p. 723, doi. 10.1177/154405910408300913

By:

Vieira, A. R.;
Meira, R.;
Modesto, A.;
Murray, J. C.

Publication type:

Article

Characteristics of Incisor-Premolar Hypodontia in Families.

Published in:

Journal of Dental Research, 2001, v. 80, n. 5, p. 1445, doi. 10.1177/00220345010800051201

By:

Arte, S.;
Nieminen, P.;
Apajalahti, S.;
Haavikko, K.;
Thesleff, I.;
Pirinen, S.

Publication type:

Article

Guideline on Oral Health Care/Dental Management of Heritable Dental Developmental Anomalies.

Published in:: Pediatric Dentistry, 2012, v. 34, n. 6, p. 252
Publication type:: Article

Diagnosis and esthetic functional rehabilitation of a patient with amelogenesis imperfecta.

Published in:

Quintessence International, 2011, v. 42, n. 6, p. 463

By:

Costa Sousa Oliveira, Ilione Kruschewsky;
de Fátima Barbosa Fonseca, Jussara;
do Amaral, Flavia Lucisano Botelho;
Arias Pecorari, Vanessa Gallego;
Basting, Roberta Tarkany;
Gomes França, Fabiana Mantovani

Publication type:

Article

Freeman-Sheldon syndrome: A case report.

Published in:

Quintessence International, 2003, v. 34, n. 4, p. 307

By:

Aren, Gamze;
Yurdabakan, Zuhal;
Özcan, Ilknur

Publication type:

Article

Dens evaginatus of anterior teeth (talon cusp): Report of five cases.

Published in:

Quintessence International, 2003, v. 34, n. 4, p. 272

By:

Segura-Egea, Juan J.;
Jiménez-Rubio, Alicia;
Ríos-Santos, José V.;
VeIasco-Ortega, Eugenio

Publication type:

Article

Hereditary Enamel Hypoplasia in a Prehistoric Indian Child.

Published in:

Journal of Dental Research, 1980, v. 59, n. 9, p. 1522, doi. 10.1177/00220345800590091601

By:

COOK, DELLA COLLINS

Publication type:

Article

Agenesis and Peg-Shaped Permanent Maxillary Lateral Incisors in Kalahari Bushmen.

Published in:

Journal of Dental Research, 1970, v. 49, n. 2, p. 457, doi. 10.1177/00220345700490024501

By:

CLEATON-JONES, P.

Publication type:

Article