Schubert S - Search Results

1

Transcription factor/microRNA axis blocks melanoma invasion program by miR-211 targeting NUAK1.

Bell RE, Khaled M, Netanely D, Schubert S, Golan T, Buxbaum A, Janas MM, Postolsky B, Goldberg MS, Shamir R, Levy C. Bell RE, et al. Among authors: schubert s. J Invest Dermatol. 2014 Feb;134(2):441-451. doi: 10.1038/jid.2013.340. Epub 2013 Aug 9. J Invest Dermatol. 2014. PMID: 23934065 Free article.

2

Intronic miR-211 assumes the tumor suppressive function of its host gene in melanoma.

Levy C, Khaled M, Iliopoulos D, Janas MM, Schubert S, Pinner S, Chen PH, Li S, Fletcher AL, Yokoyama S, Scott KL, Garraway LA, Song JS, Granter SR, Turley SJ, Fisher DE, Novina CD. Levy C, et al. Among authors: schubert s. Mol Cell. 2010 Dec 10;40(5):841-9. doi: 10.1016/j.molcel.2010.11.020. Epub 2010 Nov 25. Mol Cell. 2010. PMID: 21109473 Free PMC article.

3

Feed-forward microprocessing and splicing activities at a microRNA-containing intron.

Janas MM, Khaled M, Schubert S, Bernstein JG, Golan D, Veguilla RA, Fisher DE, Shomron N, Levy C, Novina CD. Janas MM, et al. Among authors: schubert s. PLoS Genet. 2011 Oct;7(10):e1002330. doi: 10.1371/journal.pgen.1002330. Epub 2011 Oct 20. PLoS Genet. 2011. PMID: 22028668 Free PMC article.

4

Characterization of three XPG-defective patients identifies three missense mutations that impair repair and transcription.

Schäfer A, Schubert S, Gratchev A, Seebode C, Apel A, Laspe P, Hofmann L, Ohlenbusch A, Mori T, Kobayashi N, Schürer A, Schön MP, Emmert S. Schäfer A, et al. Among authors: schubert s. J Invest Dermatol. 2013 Jul;133(7):1841-9. doi: 10.1038/jid.2013.54. Epub 2013 Jan 31. J Invest Dermatol. 2013. PMID: 23370536 Free article.

5

Clinical utility gene card for: Xeroderma pigmentosum.

Schubert S, Lehmann J, Kalfon L, Slor H, Falik-Zaccai TC, Emmert S. Schubert S, et al. Eur J Hum Genet. 2014 Jul;22(7). doi: 10.1038/ejhg.2013.233. Epub 2013 Oct 9. Eur J Hum Genet. 2014. PMID: 24105368 Free PMC article. Review. No abstract available.

6

An unusual mutation in the XPG gene leads to an internal in-frame deletion and a XP/CS complex phenotype.

Lehmann J, Schubert S, Schäfer A, Apel A, Laspe P, Schiller S, Ohlenbusch A, Gratchev A, Emmert S. Lehmann J, et al. Among authors: schubert s. Br J Dermatol. 2014 Oct;171(4):903-5. doi: 10.1111/bjd.13035. Epub 2014 Jul 26. Br J Dermatol. 2014. PMID: 24702031 No abstract available.

7

A novel mutation in the XPA gene results in two truncated protein variants and leads to a severe XP/neurological symptoms phenotype.

Lehmann J, Schubert S, Schäfer A, Laspe P, Haenssle HA, Ohlenbusch A, Gratchev A, Emmert S. Lehmann J, et al. Among authors: schubert s. J Eur Acad Dermatol Venereol. 2015 Dec;29(12):2479-82. doi: 10.1111/jdv.12841. Epub 2014 Nov 13. J Eur Acad Dermatol Venereol. 2015. PMID: 25393472

8

Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations.

Schäfer A, Hofmann L, Gratchev A, Laspe P, Schubert S, Schürer A, Ohlenbusch A, Tzvetkov M, Hallermann C, Reichrath J, Schön MP, Emmert S. Schäfer A, et al. Among authors: schubert s. Exp Dermatol. 2013 Jan;22(1):24-9. doi: 10.1111/exd.12052. Epub 2012 Nov 22. Exp Dermatol. 2013. PMID: 23173980

9

A unique chromosomal in-frame deletion identified among seven XP-C patients.

Schubert S, Rieper P, Ohlenbusch A, Seebode C, Lehmann J, Gratchev A, Emmert S. Schubert S, et al. Photodermatol Photoimmunol Photomed. 2016 Sep;32(5-6):276-283. doi: 10.1111/phpp.12251. Epub 2016 Jul 27. Photodermatol Photoimmunol Photomed. 2016. PMID: 27387384

10

Skin cancer in organ transplant recipients: effects of immunosuppressive medications on DNA repair.

Kuschal C, Thoms KM, Schubert S, Schäfer A, Boeckmann L, Schön MP, Emmert S. Kuschal C, et al. Among authors: schubert s. Exp Dermatol. 2012 Jan;21(1):2-6. doi: 10.1111/j.1600-0625.2011.01413.x. Exp Dermatol. 2012. PMID: 22151386 Free article. Review.

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