Below are the most recent publications written about "Photosensitivity Disorders" by people in Profiles.
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McSweeney SM, Sarkany R, Fassihi H, Tziotzios C, McGrath JA. Pathogenesis of solar urticaria: Classic perspectives and emerging concepts. Exp Dermatol. 2022 04; 31(4):586-593.
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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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Fong K, Bailey CV, Tuttle P, Cunningham B, McGrath JA, Cho RJ. Questioning the Clinical Utility of Exome Sequencing in Developing Countries. Pediatr Dermatol. 2017 Jan; 34(1):e32-e34.
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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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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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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.