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Items: 1 to 20 of 21

1.

Temporomandibular joint damage in K/BxN arthritic mice.

Kuchler-Bopp S, Mariotte A, Strub M, Po C, De Cauwer A, Schulz G, Van Bellinghen X, Fioretti F, Clauss F, Georgel P, Benkirane-Jessel N, Bornert F.

Int J Oral Sci. 2020 Feb 6;12(1):5. doi: 10.1038/s41368-019-0072-z.

2.

Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders.

de La Dure-Molla M, Fournier BP, Manzanares MC, Acevedo AC, Hennekam RC, Friedlander L, Boy-Lefèvre ML, Kerner S, Toupenay S, Garrec P, Vi-Fane B, Felizardo R, Berteretche MV, Jordan L, Ferré F, Clauss F, Jung S, de Chalendar M, Troester S, Kawczynski M, Chaloyard J; International Group of Dental Nomenclature, Manière MC, Berdal A, Bloch-Zupan A.

Am J Med Genet A. 2019 Oct;179(10):1913-1981. doi: 10.1002/ajmg.a.61316. Epub 2019 Aug 29.

PMID:
31468724
3.

Application of Chitosan in Bone and Dental Engineering.

Aguilar A, Zein N, Harmouch E, Hafdi B, Bornert F, Offner D, Clauss F, Fioretti F, Huck O, Benkirane-Jessel N, Hua G.

Molecules. 2019 Aug 19;24(16). pii: E3009. doi: 10.3390/molecules24163009. Review.

4.

Polymer-Based Instructive Scaffolds for Endodontic Regeneration.

Zein N, Harmouch E, Lutz JC, Fernandez De Grado G, Kuchler-Bopp S, Clauss F, Offner D, Hua G, Benkirane-Jessel N, Fioretti F.

Materials (Basel). 2019 Jul 24;12(15). pii: E2347. doi: 10.3390/ma12152347. Review.

5.

Periodontal Tissues, Maxillary Jaw Bone, and Tooth Regeneration Approaches: From Animal Models Analyses to Clinical Applications.

Batool F, Strub M, Petit C, Bugueno IM, Bornert F, Clauss F, Huck O, Kuchler-Bopp S, Benkirane-Jessel N.

Nanomaterials (Basel). 2018 May 16;8(5). pii: E337. doi: 10.3390/nano8050337. Review.

6.

Maxillary Bone Regeneration Based on Nanoreservoirs Functionalized ε-Polycaprolactone Biomembranes in a Mouse Model of Jaw Bone Lesion.

Strub M, Van Bellinghen X, Fioretti F, Bornert F, Benkirane-Jessel N, Idoux-Gillet Y, Kuchler-Bopp S, Clauss F.

Biomed Res Int. 2018 Feb 26;2018:7380389. doi: 10.1155/2018/7380389. eCollection 2018.

7.

Temporomandibular Joint Regenerative Medicine.

Van Bellinghen X, Idoux-Gillet Y, Pugliano M, Strub M, Bornert F, Clauss F, Schwinté P, Keller L, Benkirane-Jessel N, Kuchler-Bopp S, Lutz JC, Fioretti F.

Int J Mol Sci. 2018 Feb 2;19(2). pii: E446. doi: 10.3390/ijms19020446. Review.

8.

[Preventive and therapeutic advantages of sugar-free chewing gums in orthodontics. A study conducted on practitioners and patients].

Ferney P, Clauss F, Offner D, Wagner D.

Orthod Fr. 2017 Sep;88(3):275-281. doi: 10.1051/orthodfr/2017020. Epub 2017 Oct 18. French.

9.

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.

Prasad MK, Geoffroy V, Vicaire S, Jost B, Dumas M, Le Gras S, Switala M, Gasse B, Laugel-Haushalter V, Paschaki M, Leheup B, Droz D, Dalstein A, Loing A, Grollemund B, Muller-Bolla M, Lopez-Cazaux S, Minoux M, Jung S, Obry F, Vogt V, Davideau JL, Davit-Beal T, Kaiser AS, Moog U, Richard B, Morrier JJ, Duprez JP, Odent S, Bailleul-Forestier I, Rousset MM, Merametdijan L, Toutain A, Joseph C, Giuliano F, Dahlet JC, Courval A, El Alloussi M, Laouina S, Soskin S, Guffon N, Dieux A, Doray B, Feierabend S, Ginglinger E, Fournier B, de la Dure Molla M, Alembik Y, Tardieu C, Clauss F, Berdal A, Stoetzel C, Manière MC, Dollfus H, Bloch-Zupan A.

J Med Genet. 2016 Feb;53(2):98-110. doi: 10.1136/jmedgenet-2015-103302. Epub 2015 Oct 26.

10.

Angiotensin-converting enzyme inhibition prevents myocardial infarction-induced increase in renal cortical cGMP and cAMP phosphodiesterase activities.

Clauss F, Charloux A, Piquard F, Doutreleau S, Talha S, Zoll J, Lugnier C, Geny B.

Fundam Clin Pharmacol. 2015 Aug;29(4):352-61. doi: 10.1111/fcp.12124. Epub 2015 May 25.

PMID:
25939307
11.

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.

Huckert M, Stoetzel C, Morkmued S, Laugel-Haushalter V, Geoffroy V, Muller J, Clauss F, Prasad MK, Obry F, Raymond JL, Switala M, Alembik Y, Soskin S, Mathieu E, Hemmerlé J, Weickert JL, Dabovic BB, Rifkin DB, Dheedene A, Boudin E, Caluseriu O, Cholette MC, Mcleod R, Antequera R, Gellé MP, Coeuriot JL, Jacquelin LF, Bailleul-Forestier I, Manière MC, Van Hul W, Bertola D, Dollé P, Verloes A, Mortier G, Dollfus H, Bloch-Zupan A.

Hum Mol Genet. 2015 Jun 1;24(11):3038-49. doi: 10.1093/hmg/ddv053. Epub 2015 Feb 10.

12.

Bone defects and future regenerative nanomedicine approach using stem cells in the mutant Tabby mouse model.

Noordijk M, Davideau JL, Eap S, Huck O, Fioretti F, Stoltz JF, Bacon W, Benkirane-Jessel N, Clauss F.

Biomed Mater Eng. 2015;25(1 Suppl):111-9. doi: 10.3233/BME-141246. Review.

PMID:
25538062
13.

Nanostructured thick 3D nanofibrous scaffold can induce bone.

Eap S, Morand D, Clauss F, Huck O, Stoltz JF, Lutz JC, Gottenberg JE, Benkirane-Jessel N, Keller L, Fioretti F.

Biomed Mater Eng. 2015;25(1 Suppl):79-85. doi: 10.3233/BME-141248.

PMID:
25538059
14.

Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.

Clauss F, Waltmann E, Barriere P, Hadj-Rabia S, Manière MC, Schmittbuhl M.

J Craniomaxillofac Surg. 2014 Sep;42(6):e346-51. doi: 10.1016/j.jcms.2014.01.037. Epub 2014 Jan 15. Review.

PMID:
24702986
15.

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.

16.

Hemostatic management in pediatric patients with type I von Willebrand disease undergoing oral surgery: case report and literature review.

Bornert F, Clauss F, Gros CI, Faradji A, Schmittbuhl M, Manière MC, Feki A.

J Oral Maxillofac Surg. 2011 Aug;69(8):2086-91. doi: 10.1016/j.joms.2011.03.073. Review. No abstract available.

PMID:
21783000
17.

Subtle Morphological Changes in the Mandible of Tabby Mice Revealed by Micro-CT Imaging and Elliptical Fourier Quantification.

Bornert F, Choquet P, Gros CI, Aubertin G, Perrin-Schmitt F, Clauss F, Lesot H, Constantinesco A, Schmittbuhl M.

Front Physiol. 2011 Apr 20;2:15. doi: 10.3389/fphys.2011.00015. eCollection 2011.

18.

Targeted apc;twist double-mutant mice: a new model of spontaneous osteosarcoma that mimics the human disease.

Entz-Werlé N, Choquet P, Neuville A, Kuchler-Bopp S, Clauss F, Danse JM, Simo-Noumbissie P, Guérin E, Gaub MP, Freund JN, Boehm N, Constantinesco A, Lutz P, Guenot D, Perrin-Schmitt F.

Transl Oncol. 2010 Dec 1;3(6):344-53.

19.

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.

Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A.

Hum Mutat. 2011 Jan;32(1):70-2. doi: 10.1002/humu.21384.

PMID:
20979233
20.

Orodental phenotype and genotype findings in all subtypes of hypophosphatasia.

Reibel A, Manière MC, Clauss F, Droz D, Alembik Y, Mornet E, Bloch-Zupan A.

Orphanet J Rare Dis. 2009 Feb 21;4:6. doi: 10.1186/1750-1172-4-6.

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