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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Vahidnezhad H, Youssefian L, Saeidian AH, Mahmoudi H, Touati A, Abiri M, Kajbafzadeh AM, Aristodemou S, Liu L, McGrath JA, Ertel A, Londin E, Kariminejad A, Zeinali S, Fortina P, Uitto J. Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biol. 2018 03; 66:22-33.
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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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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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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.
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Wada M, Masuda K, Tsuruta D, Tamai K, Lai-Cheong JE, McGrath JA, Katoh N. Case of Kindler syndrome resulting from mutation in the FERMT1 gene. J Dermatol. 2012 Dec; 39(12):1057-8.