Bruckner-Tuderman L - Search Results

1

UV-B-induced cutaneous inflammation and prospects for antioxidant treatment in Kindler syndrome.

Maier K, He Y, Wölfle U, Esser PR, Brummer T, Schempp C, Bruckner-Tuderman L, Has C. Maier K, et al. Hum Mol Genet. 2016 Dec 15;25(24):5339-5352. doi: 10.1093/hmg/ddw350. Hum Mol Genet. 2016. PMID: 27798104

2

Induction of phenotype modifying cytokines by FERMT1 mutations.

Heinemann A, He Y, Zimina E, Boerries M, Busch H, Chmel N, Kurz T, Bruckner-Tuderman L, Has C. Heinemann A, et al. Hum Mutat. 2011 Apr;32(4):397-406. doi: 10.1002/humu.21449. Epub 2011 Mar 1. Hum Mutat. 2011. PMID: 21309038 Free article.

3

Kindlin-1 and -2 have overlapping functions in epithelial cells implications for phenotype modification.

He Y, Esser P, Heinemann A, Bruckner-Tuderman L, Has C. He Y, et al. Am J Pathol. 2011 Mar;178(3):975-82. doi: 10.1016/j.ajpath.2010.11.053. Am J Pathol. 2011. PMID: 21356350 Free PMC article.

4

Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.

Has C, Castiglia D, del Rio M, Diez MG, Piccinni E, Kiritsi D, Kohlhase J, Itin P, Martin L, Fischer J, Zambruno G, Bruckner-Tuderman L. Has C, et al. Hum Mutat. 2011 Nov;32(11):1204-12. doi: 10.1002/humu.21576. Epub 2011 Sep 20. Hum Mutat. 2011. PMID: 21936020 Review.

5

The genetics of skin fragility.

Has C, Bruckner-Tuderman L. Has C, et al. Annu Rev Genomics Hum Genet. 2014;15:245-68. doi: 10.1146/annurev-genom-090413-025540. Epub 2014 May 29. Annu Rev Genomics Hum Genet. 2014. PMID: 24898041 Review.

6

Molecular and diagnostic aspects of genetic skin fragility.

Has C, Bruckner-Tuderman L. Has C, et al. J Dermatol Sci. 2006 Dec;44(3):129-44. doi: 10.1016/j.jdermsci.2006.08.003. Epub 2006 Sep 22. J Dermatol Sci. 2006. PMID: 16996720 Review.

7

Role of kindlin-2 in fibroblast functions: implications for wound healing.

He Y, Esser P, Schacht V, Bruckner-Tuderman L, Has C. He Y, et al. J Invest Dermatol. 2011 Jan;131(1):245-56. doi: 10.1038/jid.2010.273. Epub 2010 Sep 23. J Invest Dermatol. 2011. PMID: 20861856 Free article.

8

Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity.

Pigors M, Kiritsi D, Krümpelmann S, Wagner N, He Y, Podda M, Kohlhase J, Hausser I, Bruckner-Tuderman L, Has C. Pigors M, et al. Hum Mol Genet. 2011 May 1;20(9):1811-9. doi: 10.1093/hmg/ddr064. Epub 2011 Feb 14. Hum Mol Genet. 2011. PMID: 21320868

9

Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa.

Kiritsi D, Kern JS, Schumann H, Kohlhase J, Has C, Bruckner-Tuderman L. Kiritsi D, et al. J Med Genet. 2011 Jul;48(7):450-7. doi: 10.1136/jmg.2010.086751. Epub 2011 Feb 28. J Med Genet. 2011. PMID: 21357940 Free article.

10

Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination.

Kiritsi D, He Y, Pasmooij AM, Onder M, Happle R, Jonkman MF, Bruckner-Tuderman L, Has C. Kiritsi D, et al. J Clin Invest. 2012 May;122(5):1742-6. doi: 10.1172/JCI61976. Epub 2012 Apr 2. J Clin Invest. 2012. PMID: 22466645 Free PMC article.

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