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Digenic inheritance in epidermolysis bullosa simplex.
J Invest Dermatol. 2012 Dec;132(12):2852-4. doi: 10.1038/jid.2012.229. Epub 2012 Jul 26.
J Invest Dermatol. 2012.
PMID: 22832485
Free article.
No abstract available.
Semidominant inheritance in epidermolytic ichthyosis.
Nousbeck J, Padalon-Brauch G, Fuchs-Telem D, Israeli S, Sarig O, Sheffer R, Sprecher E.
Nousbeck J, et al. Among authors: padalon brauch g.
J Invest Dermatol. 2013 Nov;133(11):2626-2628. doi: 10.1038/jid.2013.193. Epub 2013 Apr 19.
J Invest Dermatol. 2013.
PMID: 23604102
Free article.
No abstract available.
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Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility.
Lin Z, Li S, Feng C, Yang S, Wang H, Ma D, Zhang J, Gou M, Bu D, Zhang T, Kong X, Wang X, Sarig O, Ren Y, Dai L, Liu H, Zhang J, Li F, Hu Y, Padalon-Brauch G, Vodo D, Zhou F, Chen T, Deng H, Sprecher E, Yang Y, Tan X.
Lin Z, et al. Among authors: padalon brauch g.
Nat Genet. 2016 Dec;48(12):1508-1516. doi: 10.1038/ng.3701. Epub 2016 Oct 31.
Nat Genet. 2016.
PMID: 27798626
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Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9.
Fuchs-Telem D, Padalon-Brauch G, Sarig O, Sprecher E.
Fuchs-Telem D, et al. Among authors: padalon brauch g.
Clin Exp Dermatol. 2013 Mar;38(2):189-92: quiz 192. doi: 10.1111/ced.12059. Epub 2013 Feb 9.
Clin Exp Dermatol. 2013.
PMID: 23397986
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The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12.
Goldsmith T, Fuchs-Telem D, Israeli S, Sarig O, Padalon-Brauch G, Bergman R, Indelman M, Sprecher E, Nousbeck J.
Goldsmith T, et al. Among authors: padalon brauch g.
Exp Dermatol. 2013 Apr;22(4):251-4. doi: 10.1111/exd.12110.
Exp Dermatol. 2013.
PMID: 23528209
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Pyoderma gangrenosum, acne and ulcerative colitis in a patient with a novel mutation in the PSTPIP1 gene.
Zeeli T, Padalon-Brauch G, Ellenbogen E, Gat A, Sarig O, Sprecher E.
Zeeli T, et al. Among authors: padalon brauch g.
Clin Exp Dermatol. 2015 Jun;40(4):367-72. doi: 10.1111/ced.12585. Epub 2015 Feb 16.
Clin Exp Dermatol. 2015.
PMID: 25683018
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Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.
Sarig O, Nahum S, Rapaport D, Ishida-Yamamoto A, Fuchs-Telem D, Qiaoli L, Cohen-Katsenelson K, Spiegel R, Nousbeck J, Israeli S, Borochowitz ZU, Padalon-Brauch G, Uitto J, Horowitz M, Shalev S, Sprecher E.
Sarig O, et al. Among authors: padalon brauch g.
Am J Hum Genet. 2012 Aug 10;91(2):337-42. doi: 10.1016/j.ajhg.2012.06.003. Epub 2012 Jul 26.
Am J Hum Genet. 2012.
PMID: 22840363
Free PMC article.
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Small RNAs encoded within genetic islands of Salmonella typhimurium show host-induced expression and role in virulence.
Padalon-Brauch G, Hershberg R, Elgrably-Weiss M, Baruch K, Rosenshine I, Margalit H, Altuvia S.
Padalon-Brauch G, et al.
Nucleic Acids Res. 2008 Apr;36(6):1913-27. doi: 10.1093/nar/gkn050. Epub 2008 Feb 11.
Nucleic Acids Res. 2008.
PMID: 18267966
Free PMC article.
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