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Results: 1 to 20 of 100

1.

Conserved transcriptional regulatory mechanisms in aortic valve development and disease.

Wirrig EE, Yutzey KE.

Arterioscler Thromb Vasc Biol. 2014 Apr;34(4):737-41. doi: 10.1161/ATVBAHA.113.302071. Review.

PMID:
24665126
[PubMed - indexed for MEDLINE]
2.

Identification of genetic risk factors for maxillary lateral incisor agenesis.

Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso I.

J Dent Res. 2014 May;93(5):452-8. doi: 10.1177/0022034514523986. Epub 2014 Feb 19.

PMID:
24554542
[PubMed - indexed for MEDLINE]
3.

Oligodontia and curly hair occur with ectodysplasin-a mutations.

Lee KE, Ko J, Shin TJ, Hyun HK, Lee SH, Kim JW.

J Dent Res. 2014 Apr;93(4):371-5. doi: 10.1177/0022034514522059. Epub 2014 Jan 31.

PMID:
24487376
[PubMed - indexed for MEDLINE]
4.

RNA/DNA co-analysis from human menstrual blood and vaginal secretion stains: results of a fourth and fifth collaborative EDNAP exercise.

Haas C, Hanson E, Anjos MJ, Ballantyne KN, Banemann R, Bhoelai B, Borges E, Carvalho M, Courts C, De Cock G, Drobnic K, Dötsch M, Fleming R, Franchi C, Gomes I, Hadzic G, Harbison SA, Harteveld J, Hjort B, Hollard C, Hoff-Olsen P, Hüls C, Keyser C, Maroñas O, McCallum N, Moore D, Morling N, Niederstätter H, Noël F, Parson W, Phillips C, Popielarz C, Roeder AD, Salvaderi L, Sauer E, Schneider PM, Shanthan G, Court DS, Turanská M, van Oorschot RA, Vennemann M, Vidaki A, Zatkalíková L, Ballantyne J.

Forensic Sci Int Genet. 2014 Jan;8(1):203-12. doi: 10.1016/j.fsigen.2013.09.009. Epub 2013 Oct 5.

PMID:
24315610
[PubMed - indexed for MEDLINE]
5.

Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.

Mu YD, Xu Z, Contreras CI, McDaniel JS, Donly KJ, Chen S.

Genet Mol Res. 2013 Oct 10;12(4):4446-58. doi: 10.4238/2013.October.10.10.

PMID:
24222224
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Inductive ability of human developing and differentiated dental mesenchyme.

Zheng L, Warotayanont R, Stahl J, Kunimatsu R, Klein O, DenBesten PK, Zhang Y.

Cells Tissues Organs. 2013;198(2):99-110. doi: 10.1159/000353116. Epub 2013 Jul 30.

PMID:
24192998
[PubMed - indexed for MEDLINE]
7.

A novel multidisciplinary approach toward a better understanding of cranial suture closure: the first evidence of genetic effects in adulthood.

Wolff K, Hadadi E, Vas Z.

Am J Hum Biol. 2013 Nov-Dec;25(6):835-43. doi: 10.1002/ajhb.22459. Epub 2013 Oct 7.

PMID:
24123566
[PubMed - indexed for MEDLINE]
8.

MSX1 and PAX9 investigation in monozygotic twins with variable expression of tooth agenesis.

Lopez SI, Mundstock KS, Paixão-Côrtes VR, Schüler-Faccini L, Mundstock CA, Bortolini MC, Salzano FM.

Twin Res Hum Genet. 2013 Dec;16(6):1112-6. doi: 10.1017/thg.2013.69. Epub 2013 Oct 9.

PMID:
24103583
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.

Arte S, Parmanen S, Pirinen S, Alaluusua S, Nieminen P.

PLoS One. 2013 Aug 22;8(8):e73705. doi: 10.1371/journal.pone.0073705. eCollection 2013.

PMID:
23991204
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

SNPs and interaction analyses of IRF6, MSX1 and PAX9 genes in patients with non‑syndromic cleft lip with or without palate.

Song T, Wu D, Wang Y, Li H, Yin N, Zhao Z.

Mol Med Rep. 2013 Oct;8(4):1228-34. doi: 10.3892/mmr.2013.1617. Epub 2013 Aug 6.

PMID:
23921572
[PubMed - indexed for MEDLINE]
12.

Excess of O-linked N-acetylglucosamine modifies human pluripotent stem cell differentiation.

Maury JJ, Chan KK, Zheng L, Bardor M, Choo AB.

Stem Cell Res. 2013 Sep;11(2):926-37. doi: 10.1016/j.scr.2013.06.004. Epub 2013 Jun 21.

PMID:
23859804
[PubMed - indexed for MEDLINE]
13.

PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.

Wang J, Xu Y, Chen J, Wang F, Huang R, Wu S, Shu L, Qiu J, Yang Z, Xue J, Wang R, Zhao J, Lai W.

J Appl Oral Sci. 2013;21(3):256-64. doi: 10.1590/1679-775720130079.

PMID:
23857653
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.

Ruf S, Klimas D, Hönemann M, Jabir S.

J Orofac Orthop. 2013 Jul;74(4):295-308. doi: 10.1007/s00056-013-0138-z. Epub 2013 Jul 5. Review.

PMID:
23828301
[PubMed - indexed for MEDLINE]
15.

Non-invasive neural stem cells become invasive in vitro by combined FGF2 and BMP4 signaling.

Sailer MH, Gerber A, Tostado C, Hutter G, Cordier D, Mariani L, Ritz MF.

J Cell Sci. 2013 Aug 15;126(Pt 16):3533-40. doi: 10.1242/jcs.125757. Epub 2013 Jun 20.

PMID:
23788430
[PubMed - indexed for MEDLINE]
Free Article
16.

Anomalous findings of number, morphology and size of permanent teeth in 7-10 years children living in the Czech Republic.

Ginzelová K, Kripnerová T, Dostálová T.

Prague Med Rep. 2013;114(2):113-22.

PMID:
23777802
[PubMed - indexed for MEDLINE]
Free Article
17.

A network of transcription factors operates during early tooth morphogenesis.

Zhao M, Gupta V, Raj L, Roussel M, Bei M.

Mol Cell Biol. 2013 Aug;33(16):3099-112. doi: 10.1128/MCB.00524-13. Epub 2013 Jun 10.

PMID:
23754753
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Clinical and genetic evaluation of a Chinese family with isolated oligodontia.

Qin H, Xu HZ, Xuan K.

Arch Oral Biol. 2013 Sep;58(9):1180-6. doi: 10.1016/j.archoralbio.2013.04.007. Epub 2013 May 31.

PMID:
23731659
[PubMed - indexed for MEDLINE]
19.

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

Seo YJ, Park JW, Kim YH, Baek SH.

Angle Orthod. 2013 Nov;83(6):1036-42. doi: 10.2319/020513-104.1. Epub 2013 May 29.

PMID:
23718693
[PubMed - indexed for MEDLINE]
20.

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

Cordell HJ, Bentham J, Topf A, Zelenika D, Heath S, Mamasoula C, Cosgrove C, Blue G, Granados-Riveron J, Setchfield K, Thornborough C, Breckpot J, Soemedi R, Martin R, Rahman TJ, Hall D, van Engelen K, Moorman AF, Zwinderman AH, Barnett P, Koopmann TT, Adriaens ME, Varro A, George AL Jr, dos Remedios C, Bishopric NH, Bezzina CR, O'Sullivan J, Gewillig M, Bu'Lock FA, Winlaw D, Bhattacharya S, Devriendt K, Brook JD, Mulder BJ, Mital S, Postma AV, Lathrop GM, Farrall M, Goodship JA, Keavney BD.

Nat Genet. 2013 Jul;45(7):822-4. doi: 10.1038/ng.2637. Epub 2013 May 26.

PMID:
23708191
[PubMed - indexed for MEDLINE]
Free PMC Article

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