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Items: 1 to 20 of 82

1.

Gene discovery for dental anomalies: a primer for the dental professional.

Pemberton TJ, Gee J, Patel PI.

J Am Dent Assoc. 2006 Jun;137(6):743-52. Review.

PMID:
16803803
2.

Genes underlying familial hypodontia: a review and discussion of the role of dental hygienists in future research.

Nino-Rosales ML, Patel PI.

J Dent Hyg. 2005 Summer;79(3):10. Epub 2005 Jul 1.

PMID:
16197775
3.

Inherited dental anomalies: a review and prospects for the future role of clinicians.

Pemberton TJ, Mendoza G, Gee J, Patel PI.

J Calif Dent Assoc. 2007 May;35(5):324-6, 328-33. Review.

PMID:
17822158
4.

Identification of a novel mutation in the PAX9 gene in a family affected by oligodontia and other dental anomalies.

Tallón-Walton V, Manzanares-Céspedes MC, Arte S, Carvalho-Lobato P, Valdivia-Gandur I, Garcia-Susperregui A, Ventura F, Nieminen P.

Eur J Oral Sci. 2007 Dec;115(6):427-32.

PMID:
18028048
5.

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

Mostowska A, Biedziak B, Zadurska M, Matuszewska-Trojan S, Jagodziński PP.

Eur J Oral Sci. 2015 Feb;123(1):1-8. doi: 10.1111/eos.12165. Epub 2014 Dec 29.

PMID:
25545742
6.

A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia.

Mendoza-Fandino GA, Gee JM, Ben-Dor S, Gonzalez-Quevedo C, Lee K, Kobayashi Y, Hartiala J, Myers RM, Leal SM, Allayee H, Patel PI.

Clin Genet. 2011 Sep;80(3):265-72. doi: 10.1111/j.1399-0004.2010.01529.x. Epub 2010 Sep 8.

PMID:
21443745
7.

Dental agenesis: genetic and clinical perspectives.

De Coster PJ, Marks LA, Martens LC, Huysseune A.

J Oral Pathol Med. 2009 Jan;38(1):1-17. doi: 10.1111/j.1600-0714.2008.00699.x. Epub 2008 Sep 1. Review.

PMID:
18771513
8.

Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review.

Tallón-Walton V, Manzanares-Céspedes MC, Carvalho-Lobato P, Valdivia-Gandur I, Arte S, Nieminen P.

Med Oral Patol Oral Cir Bucal. 2014 May 1;19(3):e248-54. Review.

9.

Genetic basis of non syndromic hypodontia: a DNA investigation performed on three couples of monozygotic twins about PAX9 mutation.

Militi D, Militi A, Cutrupi MC, Portelli M, Rigoli L, Matarese G, Salpietro DC.

Eur J Paediatr Dent. 2011 Mar;12(1):21-4.

PMID:
21434731
10.

The genetic basis of tooth agenesis: basic concepts and genes involved.

Pani SC.

J Indian Soc Pedod Prev Dent. 2011 Apr-Jun;29(2):84-9. doi: 10.4103/0970-4388.84677.

11.

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.

Mostowska A, Kobielak A, Trzeciak WH.

Eur J Oral Sci. 2003 Oct;111(5):365-70. Review.

PMID:
12974677
12.

The genetics of human tooth agenesis: new discoveries for understanding dental anomalies.

Vastardis H.

Am J Orthod Dentofacial Orthop. 2000 Jun;117(6):650-6. Review.

PMID:
10842107
13.

Familial human hypodontia--is it all in the genes?

Cobourne MT.

Br Dent J. 2007 Aug 25;203(4):203-8. Review.

PMID:
17721480
14.

A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

Ahmad W, Brancolini V, ul Faiyaz MF, Lam H, ul Haque S, Haider M, Maimon A, Aita VM, Owen J, Brown D, Zegarelli DJ, Ahmad M, Ott J, Christiano AM.

Am J Hum Genet. 1998 Apr;62(4):987-91. No abstract available.

15.

Classification and genetics of numeric anomalies of dentition.

Burzynski NJ, Escobar VH.

Birth Defects Orig Artic Ser. 1983;19(1):95-106. Review.

PMID:
6362744
16.

Novel PAX9 gene polymorphisms and mutations and susceptibility to tooth agenesis in the Czech population.

Hlousková A, Bonczek O, Izakovicová-Hollá L, Lochman J, Soukalová J, Stembírek J, Mísek I, Cernochová P, Krejcí P, Vanek J, Šerý O.

Neuro Endocrinol Lett. 2015;36(5):452-7.

PMID:
26707046
17.

A 223-kb de novo deletion of PAX9 in a patient with oligodontia.

Haldeman-Englert CR, Biser A, Zackai EH, Ming JE.

J Craniofac Surg. 2010 May;21(3):837-9. doi: 10.1097/SCS.0b013e3181d87912.

PMID:
20485064
18.

Novel PAX9 mutation associated with syndromic tooth agenesis.

Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.

Eur J Oral Sci. 2013 Oct;121(5):403-11. doi: 10.1111/eos.12071. Epub 2013 Jul 13.

PMID:
24028587
19.

Revision of "A 223-kb de novo deletion of PAX9 in a patient with oligodontia".

Haldeman-Englert CR, Biser A, Zackai EH, Ming JE.

J Craniofac Surg. 2012 Mar;23(2):e149-51. doi: 10.1097/SCS.0b013e31824cdcdd.

PMID:
22446453
20.

Deletion of PAX9 and oligodontia: a third family and review of the literature.

Guala A, Falco V, Breedveld G, De Filippi P, Danesino C.

Int J Paediatr Dent. 2008 Nov;18(6):441-5. doi: 10.1111/j.1365-263X.2008.00915.x. Epub 2008 Apr 28. Review.

PMID:
18445003

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