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Items: 1 to 50 of 163

1.

Genetics: The Future Is Now with Interprofessional Collaboration.

Regier DS, Hart TC.

Dent Clin North Am. 2016 Oct;60(4):943-9. doi: 10.1016/j.cden.2016.03.005. Review.

PMID:
27671963
2.

Invited commentary: The need for human genetics and genomics in dental school curricula.

Hart PS, Hart TC.

Mol Genet Genomic Med. 2016 Mar 17;4(2):123-5. doi: 10.1002/mgg3.216. eCollection 2016 Mar. No abstract available.

3.

Interleukin 1 genetic tests provide no support for reduction of preventive dental care.

Diehl SR, Kuo F, Hart TC.

J Am Dent Assoc. 2015 Mar;146(3):164-173.e4. doi: 10.1016/j.adaj.2014.12.018.

PMID:
25726343
4.

The American Dental Association Caries Classification System for clinical practice: a report of the American Dental Association Council on Scientific Affairs.

Young DA, Nový BB, Zeller GG, Hale R, Hart TC, Truelove EL; American Dental Association Council on Scientific Affairs; American Dental Association Council on Scientific Affairs.

J Am Dent Assoc. 2015 Feb;146(2):79-86. doi: 10.1016/j.adaj.2014.11.018. Erratum in: J Am Dent Assoc. 2015 Jun ;146(6):364-5.

PMID:
25637205
5.

Craniodentofacial Manifestations in a Rare Syndrome: Orofaciodigital Type IV (Mohr-Majewski Syndrome).

Ozdemir-Karatas M, Ozdemir-Ozenen D, Hart PS, Hart TC.

Case Rep Dent. 2014;2014:605892. doi: 10.1155/2014/605892. Epub 2014 Dec 21.

6.

Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1.

Bleyer AJ, Kmoch S, Antignac C, Robins V, Kidd K, Kelsoe JR, Hladik G, Klemmer P, Knohl SJ, Scheinman SJ, Vo N, Santi A, Harris A, Canaday O, Weller N, Hulick PJ, Vogel K, Rahbari-Oskoui FF, Tuazon J, Deltas C, Somers D, Megarbane A, Kimmel PL, Sperati CJ, Orr-Urtreger A, Ben-Shachar S, Waugh DA, McGinn S, Bleyer AJ Jr, Hodanová K, Vylet'al P, Živná M, Hart TC, Hart PS.

Clin J Am Soc Nephrol. 2014 Mar;9(3):527-35. doi: 10.2215/CJN.06380613. Epub 2014 Feb 7.

7.

Proteomic analyses of human gingival and periodontal ligament fibroblasts.

McKnight H, Kelsey WP, Hooper DA, Hart TC, Mariotti A.

J Periodontol. 2014 Jun;85(6):810-8. doi: 10.1902/jop.2013.130161. Epub 2013 Oct 30.

PMID:
24171499
8.

The utility of hybrid promotion and tenure tracks for dental school faculty.

Costello BJ, Marshall KL, Schafer T, Phillips S, Hart TC.

J Dent Educ. 2013 Jun;77(6):706-15. Review.

9.

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

Jaureguiberry G, De la Dure-Molla M, Parry D, Quentric M, Himmerkus N, Koike T, Poulter J, Klootwijk E, Robinette SL, Howie AJ, Patel V, Figueres ML, Stanescu HC, Issler N, Nicholson JK, Bockenhauer D, Laing C, Walsh SB, McCredie DA, Povey S, Asselin A, Picard A, Coulomb A, Medlar AJ, Bailleul-Forestier I, Verloes A, Le Caignec C, Roussey G, Guiol J, Isidor B, Logan C, Shore R, Johnson C, Inglehearn C, Al-Bahlani S, Schmittbuhl M, Clauss F, Huckert M, Laugel V, Ginglinger E, Pajarola S, Spartà G, Bartholdi D, Rauch A, Addor MC, Yamaguti PM, Safatle HP, Acevedo AC, Martelli-Júnior H, dos Santos Netos PE, Coletta RD, Gruessel S, Sandmann C, Ruehmann D, Langman CB, Scheinman SJ, Ozdemir-Ozenen D, Hart TC, Hart PS, Neugebauer U, Schlatter E, Houillier P, Gahl WA, Vikkula M, Bloch-Zupan A, Bleich M, Kitagawa H, Unwin RJ, Mighell A, Berdal A, Kleta R.

Nephron Physiol. 2012;122(1-2):1-6. doi: 10.1159/000349989. Epub 2013 Feb 23.

10.

Do X-linked diseases affect periodontal health?

Chien HH, Hart TC.

Periodontol 2000. 2013 Feb;61(1):266-78. doi: 10.1111/j.1600-0757.2012.00441.x. Review.

PMID:
23240954
11.

A characterization of the oral microbiome in allogeneic stem cell transplant patients.

Ames NJ, Sulima P, Ngo T, Barb J, Munson PJ, Paster BJ, Hart TC.

PLoS One. 2012;7(10):e47628. doi: 10.1371/journal.pone.0047628. Epub 2012 Oct 29.

12.

Error propagation models to examine the effects of geocoding quality on spatial analysis of individual-level datasets.

Zandbergen PA, Hart TC, Lenzer KE, Camponovo ME.

Spat Spatiotemporal Epidemiol. 2012 Apr;3(1):69-82. doi: 10.1016/j.sste.2012.02.007. Epub 2012 Feb 11.

13.

Identification of microbial and proteomic biomarkers in early childhood caries.

Hart TC, Corby PM, Hauskrecht M, Hee Ryu O, Pelikan R, Valko M, Oliveira MB, Hoehn GT, Bretz WA.

Int J Dent. 2011;2011:196721. doi: 10.1155/2011/196721. Epub 2011 Oct 16.

14.

Amelogenesis imperfecta: genotype-phenotype studies in 71 families.

Wright JT, Torain M, Long K, Seow K, Crawford P, Aldred MJ, Hart PS, Hart TC.

Cells Tissues Organs. 2011;194(2-4):279-83. doi: 10.1159/000324339. Epub 2011 May 19.

15.

Periodontal disease in children.

Alrayyes S, Hart TC.

Dis Mon. 2011 Apr;57(4):184-91. doi: 10.1016/j.disamonth.2011.03.004. Review. No abstract available.

PMID:
21569881
16.

Periodontal disease for the primary care physician.

Kawar N, Gajendrareddy PK, Hart TC, Nouneh R, Maniar N, Alrayyes S.

Dis Mon. 2011 Apr;57(4):174-83. doi: 10.1016/j.disamonth.2011.03.003. Review. No abstract available.

PMID:
21569880
17.

Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone.

Bleyer AJ, Zivná M, Hulková H, Hodanová K, Vyletal P, Sikora J, Zivný J, Sovová J, Hart TC, Adams JN, Elleder M, Kapp K, Haws R, Cornell LD, Kmoch S, Hart PS.

Clin Nephrol. 2010 Dec;74(6):411-22.

18.

Mutant DLX 3 disrupts odontoblast polarization and dentin formation.

Choi SJ, Song IS, Feng JQ, Gao T, Haruyama N, Gautam P, Robey PG, Hart TC.

Dev Biol. 2010 Aug 15;344(2):682-92. doi: 10.1016/j.ydbio.2010.05.499. Epub 2010 May 25.

19.

Novel cathepsin C mutation in a Brazilian family with Papillon-Lefèvre syndrome: case report and mutation update.

Pallos D, Acevedo AC, Mestrinho HD, Cordeiro I, Hart TC.

J Dent Child (Chic). 2010 Jan-Apr;77(1):36-41.

20.

More on clinical renal genetics.

Grünfeld JP, Hwu W, Chien Y, Lee N, Chiang S, Dobrovolny R, Huang A, Yeh H, Chao M, Lin S, Kitagawa T, Desnick R, Hsu L, Van Keimpema L, Nevens F, Vanslembrouck R, Van Oijen G, Hoffmann A, Dekker H, De Man R, Drenth J, Alamovitch S, Plaisier E, Favrole P, Prost C, Chen Z, Van Agrmael T, Marro B, Ronco P, Zivna M, Hulkova H, Matignon M, Hodanova K, Vylet'al P, Kalbacova M, Baresova V, Sikora J, Blazkova H, Zivny J, Ivanek R, Stranecky V, Sovova J, Claes K, Lerut E, Fryns J, Hart P, Hart T, Adams J, Pawtowski A, Clemessy M, Gasc J, Gubler M, Antignac C, Elleder M, Kapp K, Grimbert P, Bleyer A, Kmoch S, Brown E, Schlöndorff J, Becker Dj, Tsukaguchi H, Uschinski A, Higgs H, Henderson J, Pollak M.

Clin J Am Soc Nephrol. 2010 Apr;5(4):563-7. doi: 10.2215/CJN.01720210. Epub 2010 Mar 25. No abstract available.

21.

Craniofacial and dental findings in cystinosis.

Bassim CW, Gautam P, Domingo DL, Balog JZ, Guadagnini JP, Gahl WA, Hart TC.

Oral Dis. 2010 Jul;16(5):488-95. doi: 10.1111/j.1601-0825.2010.01662.x. Epub 2010 Mar 9.

22.

Oral rehabilitation of a patient with amelogenesis imperfecta.

Cogulu D, Becerik S, Emingil G, Hart PS, Hart TC.

Pediatr Dent. 2009 Nov-Dec;31(7):523-7.

23.

Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure.

Zivná M, Hůlková H, Matignon M, Hodanová K, Vylet'al P, Kalbácová M, Baresová V, Sikora J, Blazková H, Zivný J, Ivánek R, Stránecký V, Sovová J, Claes K, Lerut E, Fryns JP, Hart PS, Hart TC, Adams JN, Pawtowski A, Clemessy M, Gasc JM, Gübler MC, Antignac C, Elleder M, Kapp K, Grimbert P, Bleyer AJ, Kmoch S.

Am J Hum Genet. 2009 Aug;85(2):204-13. doi: 10.1016/j.ajhg.2009.07.010. Epub 2009 Aug 6.

24.

Genetic studies of craniofacial anomalies: clinical implications and applications.

Hart TC, Hart PS.

Orthod Craniofac Res. 2009 Aug;12(3):212-20. doi: 10.1111/j.1601-6343.2009.01455.x. Review.

25.

Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.

Becerik S, Cogulu D, Emingil G, Han T, Hart PS, Hart TC.

Am J Med Genet A. 2009 Jul;149A(7):1392-8. doi: 10.1002/ajmg.a.32885.

26.

Phenotypic variation in FAM83H-associated amelogenesis imperfecta.

Wright JT, Frazier-Bowers S, Simmons D, Alexander K, Crawford P, Han ST, Hart PS, Hart TC.

J Dent Res. 2009 Apr;88(4):356-60. doi: 10.1177/0022034509333822.

27.

Hutchinson-Gilford progeria syndrome: oral and craniofacial phenotypes.

Domingo DL, Trujillo MI, Council SE, Merideth MA, Gordon LB, Wu T, Introne WJ, Gahl WA, Hart TC.

Oral Dis. 2009 Apr;15(3):187-95. doi: 10.1111/j.1601-0825.2009.01521.x. Epub 2009 Feb 19.

28.

Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.

Hart PS, Becerik S, Cogulu D, Emingil G, Ozdemir-Ozenen D, Han ST, Sulima PP, Firatli E, Hart TC.

Clin Genet. 2009 Apr;75(4):401-4. doi: 10.1111/j.1399-0004.2008.01112.x. Epub 2009 Feb 11. No abstract available.

29.

Enamel defects and salivary methylmalonate in methylmalonic acidemia.

Bassim CW, Wright JT, Guadagnini JP, Muralidharan R, Sloan J, Domingo DL, Venditti CP, Hart TC.

Oral Dis. 2009 Apr;15(3):196-205. doi: 10.1111/j.1601-0825.2008.01509.x. Epub 2009 Jan 9.

30.

The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P.

Choi SJ, Marazita ML, Hart PS, Sulima PP, Field LL, McHenry TG, Govil M, Cooper ME, Letra A, Menezes R, Narayanan S, Mansilla MA, Granjeiro JM, Vieira AR, Lidral AC, Murray JC, Hart TC.

Eur J Hum Genet. 2009 Jun;17(6):774-84. doi: 10.1038/ejhg.2008.245. Epub 2008 Dec 17.

31.

Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta.

McKnight DA, Simmer JP, Hart PS, Hart TC, Fisher LW.

J Dent Res. 2008 Dec;87(12):1108-11. Erratum in: J Dent Res. 2009 Jan;88(1):95.

32.

In vivo impact of a 4 bp deletion mutation in the DLX3 gene on bone development.

Choi SJ, Roodman GD, Feng JQ, Song IS, Amin K, Hart PS, Wright JT, Haruyama N, Hart TC.

Dev Biol. 2009 Jan 1;325(1):129-37. doi: 10.1016/j.ydbio.2008.10.014. Epub 2008 Oct 25.

33.

A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features.

Dumitrescu CE, Kelly MH, Khosravi A, Hart TC, Brahim J, White KE, Farrow EG, Nathan MH, Murphey MD, Collins MT.

Osteoporos Int. 2009 Jul;20(7):1273-8. doi: 10.1007/s00198-008-0775-z. Epub 2008 Nov 4.

34.
35.

Oral and dental phenotype of dyskeratosis congenita.

Atkinson JC, Harvey KE, Domingo DL, Trujillo MI, Guadagnini JP, Gollins S, Giri N, Hart TC, Alter BP.

Oral Dis. 2008 Jul;14(5):419-27.

36.

Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4.

Wright JT, Hart TC, Hart PS, Simmons D, Suggs C, Daley B, Simmer J, Hu J, Bartlett JD, Li Y, Yuan ZA, Seow WK, Gibson CW.

Cells Tissues Organs. 2009;189(1-4):224-9. doi: 10.1159/000151378. Epub 2008 Aug 19.

37.

A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene.

McKnight DA, Suzanne Hart P, Hart TC, Hartsfield JK, Wilson A, Wright JT, Fisher LW.

Hum Mutat. 2008 Dec;29(12):1392-404. doi: 10.1002/humu.20783.

38.

Genetics and its implications for clinical dental practice and education: report of panel 3 of the Macy study.

Johnson L, Genco RJ, Damsky C, Haden NK, Hart S, Hart TC, Shuler CF, Tabak LA, tedesco LA.

J Dent Educ. 2008 Feb;72(2 Suppl):86-94. No abstract available.

39.

Inheritance of occlusal topography: a twin study.

Su CY, Corby PM, Elliot MA, Studen-Pavlovich DA, Ranalli DN, Rosa B, Wessel J, Schork NJ, Hart TC, Bretz WA.

Eur Arch Paediatr Dent. 2008 Mar;9(1):19-24.

40.

Phenotype and course of Hutchinson-Gilford progeria syndrome.

Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith AC, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B, Brooks BP, Gerber LH, Turner ML, Domingo DL, Hart TC, Graf J, Reynolds JC, Gropman A, Yanovski JA, Gerhard-Herman M, Collins FS, Nabel EG, Cannon RO 3rd, Gahl WA, Introne WJ.

N Engl J Med. 2008 Feb 7;358(6):592-604. doi: 10.1056/NEJMoa0706898.

41.

Heritability of oral microbial species in caries-active and caries-free twins.

Corby PM, Bretz WA, Hart TC, Schork NJ, Wessel J, Lyons-Weiler J, Paster BJ.

Twin Res Hum Genet. 2007 Dec;10(6):821-8. doi: 10.1375/twin.10.6.821.

42.

Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome.

Domingo DL, Freeman AF, Davis J, Puck JM, Tianxia W, Holland SM, Hart TC.

Oral Dis. 2008 Jan;14(1):73-81. doi: 10.1111/j.1601-0825.2007.01363.x.

PMID:
18173452
43.

Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.

Doherty ES, Lacbawan F, Hadley DW, Brewer C, Zalewski C, Kim HJ, Solomon B, Rosenbaum K, Domingo DL, Hart TC, Brooks BP, Immken L, Lowry RB, Kimonis V, Shanske AL, Jehee FS, Bueno MR, Knightly C, McDonald-McGinn D, Zackai EH, Muenke M.

Am J Med Genet A. 2007 Dec 15;143A(24):3204-15.

PMID:
18000976
44.

A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitro.

Choi SJ, Song IS, Ryu OH, Choi SW, Hart PS, Wu WW, Shen RF, Hart TC.

Bone. 2008 Jan;42(1):162-71. Epub 2007 Sep 19.

45.

Mendelian forms of periodontitis.

Hart TC, Atkinson JC.

Periodontol 2000. 2007;45:95-112. Review. No abstract available.

PMID:
17850451
46.

Gingival epithelial cell expression of macrophage inflammatory protein-1alpha induced by interleukin-1beta and lipopolysaccharide.

Ryu OH, Choi SJ, Linares AM, Song IS, Kim YJ, Jang KT, Hart TC.

J Periodontol. 2007 Aug;78(8):1627-34.

PMID:
17668983
47.

Gingival Epithelial Cell Expression of Macrophage Inflammatory Protein-1α Induced by Interleukin-1β and Lipopolysaccharide.

Ryu OH, Choi SJ, Linares AMG, Song IS, Kim YJ, Jang KT, Hart TC.

J Periodontol. 2007 Aug;78(8):1627-1634. doi: 10.1902/jop.2007.070066.

PMID:
29539188
48.

Disorders of human dentin.

Hart PS, Hart TC.

Cells Tissues Organs. 2007;186(1):70-7.

49.

Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosis.

Jang SI, Lee EJ, Hart PS, Ramaswami M, Pallos D, Hart TC.

J Biol Chem. 2007 Jul 13;282(28):20245-55. Epub 2007 May 17.

50.

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.

Santos MC, Hart PS, Ramaswami M, Kanno CM, Hart TC, Line SR.

Head Face Med. 2007 Jan 31;3:8.

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