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Items: 1 to 20 of 118


Recurrent Bullous Eruption on the Feet in a Child.

Weber FP.

Proc R Soc Med. 1926;19(Dermatol Sect):72. No abstract available.


A systematic review of randomized controlled trials of treatments for inherited forms of epidermolysis bullosa.

Langan SM, Williams HC.

Clin Exp Dermatol. 2009 Jan;34(1):20-5. doi: 10.1111/j.1365-2230.2008.02789.x. Epub 2008 Sep 25. Review.


Dual-specificity phosphatases in the hypo-osmotic stress response of keratin-defective epithelial cell lines.

Liovic M, Lee B, Tomic-Canic M, D'Alessandro M, Bolshakov VN, Lane EB.

Exp Cell Res. 2008 Jun 10;314(10):2066-75. doi: 10.1016/j.yexcr.2008.02.020. Epub 2008 Mar 8.


The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.

Fine JD, Eady RA, Bauer EA, Bauer JW, Bruckner-Tuderman L, Heagerty A, Hintner H, Hovnanian A, Jonkman MF, Leigh I, McGrath JA, Mellerio JE, Murrell DF, Shimizu H, Uitto J, Vahlquist A, Woodley D, Zambruno G.

J Am Acad Dermatol. 2008 Jun;58(6):931-50. doi: 10.1016/j.jaad.2008.02.004. Epub 2008 Apr 18.


SMaRT technology enables gene expression repair in skin gene therapy.

Hengge UR.

J Invest Dermatol. 2008 Mar;128(3):499-500. doi: 10.1038/sj.jid.5701241. Review.


KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.

Lugassy J, McGrath JA, Itin P, Shemer R, Verbov J, Murphy HR, Ishida-Yamamoto A, Digiovanna JJ, Bercovich D, Karin N, Vitenshtein A, Uitto J, Bergman R, Richard G, Sprecher E.

J Invest Dermatol. 2008 Jun;128(6):1517-24. Epub 2007 Nov 29.


The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.

Szeverenyi I, Cassidy AJ, Chung CW, Lee BT, Common JE, Ogg SC, Chen H, Sim SY, Goh WL, Ng KW, Simpson JA, Chee LL, Eng GH, Li B, Lunny DP, Chuon D, Venkatesh A, Khoo KH, McLean WH, Lim YP, Lane EB.

Hum Mutat. 2008 Mar;29(3):351-60.


Reprogramming of keratin biosynthesis by sulforaphane restores skin integrity in epidermolysis bullosa simplex.

Kerns ML, DePianto D, Dinkova-Kostova AT, Talalay P, Coulombe PA.

Proc Natl Acad Sci U S A. 2007 Sep 4;104(36):14460-5. Epub 2007 Aug 27.


Induction of inflammatory cytokines by a keratin mutation and their repression by a small molecule in a mouse model for EBS.

Lu H, Chen J, Planko L, Zigrino P, Klein-Hitpass L, Magin TM.

J Invest Dermatol. 2007 Dec;127(12):2781-9. Epub 2007 Jun 21.


Induction of the phase 2 response in mouse and human skin by sulforaphane-containing broccoli sprout extracts.

Dinkova-Kostova AT, Fahey JW, Wade KL, Jenkins SN, Shapiro TA, Fuchs EJ, Kerns ML, Talalay P.

Cancer Epidemiol Biomarkers Prev. 2007 Apr;16(4):847-51.


Preclinical and clinical evaluation of sulforaphane for chemoprevention in the breast.

Cornblatt BS, Ye L, Dinkova-Kostova AT, Erb M, Fahey JW, Singh NK, Chen MS, Stierer T, Garrett-Mayer E, Argani P, Davidson NE, Talalay P, Kensler TW, Visvanathan K.

Carcinogenesis. 2007 Jul;28(7):1485-90. Epub 2007 Mar 7.


Keratin function in skin epithelia: a broadening palette with surprising shades.

Gu LH, Coulombe PA.

Curr Opin Cell Biol. 2007 Feb;19(1):13-23. Epub 2006 Dec 18. Review.


Safety, tolerance, and metabolism of broccoli sprout glucosinolates and isothiocyanates: a clinical phase I study.

Shapiro TA, Fahey JW, Dinkova-Kostova AT, Holtzclaw WD, Stephenson KK, Wade KL, Ye L, Talalay P.

Nutr Cancer. 2006;55(1):53-62.


Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14.

Lugassy J, Itin P, Ishida-Yamamoto A, Holland K, Huson S, Geiger D, Hennies HC, Indelman M, Bercovich D, Uitto J, Bergman R, McGrath JA, Richard G, Sprecher E.

Am J Hum Genet. 2006 Oct;79(4):724-30. Epub 2006 Aug 25.


The quest for the mechanism of melanin transfer.

Van Den Bossche K, Naeyaert JM, Lambert J.

Traffic. 2006 Jul;7(7):769-78. Review.


Keratin 17 modulates hair follicle cycling in a TNFalpha-dependent fashion.

Tong X, Coulombe PA.

Genes Dev. 2006 May 15;20(10):1353-64.


Epidermolysis bullosa simplex with mottled pigmentation resulting from a recurrent mutation in KRT14.

Harel A, Bergman R, Indelman M, Sprecher E.

J Invest Dermatol. 2006 Jul;126(7):1654-7. Epub 2006 Apr 6. No abstract available.


A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis.

McGowan KA, Aradhya S, Fuchs H, de Angelis MH, Barsh GS.

J Invest Dermatol. 2006 May;126(5):1013-6.


Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.

Betz RC, Planko L, Eigelshoven S, Hanneken S, Pasternack SM, Bussow H, Van Den Bogaert K, Wenzel J, Braun-Falco M, Rutten A, Rogers MA, Ruzicka T, Nöthen MM, Magin TM, Kruse R.

Am J Hum Genet. 2006 Mar;78(3):510-9. Epub 2006 Jan 19.

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