Below are the most recent publications written about "Periodontal Diseases" by people in Profiles.
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Costeira R, Aduse-Opoku J, Vernon JJ, Rodriguez-Algarra F, Joseph S, Devine DA, Marsh PD, Rakyan V, Curtis MA, Bell JT. Hemin availability induces coordinated DNA methylation and gene expression changes in Porphyromonas gingivalis. mSystems. 2023 08 31; 8(4):e0119322.
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Michael M, Begum R, Chan GK, Whitewood AJ, Matthews DR, Goult BT, McGrath JA, Parsons M. Kindlin-1 Regulates Epidermal Growth Factor?Receptor Signaling. J Invest Dermatol. 2019 02; 139(2):369-379.
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Zhang G, Gu Y, Begum R, Chen H, Gao X, McGrath JA, Parsons M, Song B. Kindlin-1 Regulates Keratinocyte Electrotaxis. J Invest Dermatol. 2016 11; 136(11):2229-2239.
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Gelato MC, Schoenfeld E, Hou W, Michalowicz B, Seaquist E, Oates T, Tripathy D, Engebretson S, Hyman L. Changes in diabetes medications in the Diabetes and Periodontal Therapy Trial and their effect on hemoglobin A1c (HbA1c). Contemp Clin Trials. 2016 09; 50:21-7.
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Barzegar M, Asadi-Kani Z, Mozafari N, Vahidnezhad H, Kariminejad A, Toossi P. Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran. Int J Dermatol. 2015 Oct; 54(10):e416-23.
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Almeida HL, Goetze FM, Fong K, Lai-Cheong J, McGrath J. Is adermatoglyphia an additional feature of Kindler Syndrome? An Bras Dermatol. 2015 Jul-Aug; 90(4):592-3.
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Rognoni E, Widmaier M, Jakobson M, Ruppert R, Ussar S, Katsougkri D, B?ttcher RT, Lai-Cheong JE, Rifkin DB, McGrath JA, F?ssler R. Kindlin-1 controls Wnt and TGF-? availability to regulate cutaneous stem cell proliferation. Nat Med. 2014 Apr; 20(4):350-9.
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Almeida HL, Heckler GT, Fong K, Lai-Cheong J, McGrath J. Sporadic Kindler syndrome with a novel mutation. An Bras Dermatol. 2013 Nov-Dec; 88(6 Suppl 1):212-5.
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Pressman GS, Qasim A, Verma N, Miyamae M, Arishiro K, Notohara Y, Crudu V, Figueredo VM. Periodontal disease is an independent predictor of intracardiac calcification. Biomed Res Int. 2013; 2013:854340.
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Has C, Kiritsi D, Mellerio JE, Franzke CW, Wedgeworth E, Tantcheva-Poor I, Kernland-Lang K, Itin P, Simpson MA, Dopping-Hepenstal PJ, Fujimoto W, McGrath JA, Bruckner-Tuderman L. The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndrome. J Invest Dermatol. 2014 Mar; 134(3):845-849.