Gratchev A - Search Results

1

Xeroderma pigmentosum-variant patients from America, Europe, and Asia.

Inui H, Oh KS, Nadem C, Ueda T, Khan SG, Metin A, Gozukara E, Emmert S, Slor H, Busch DB, Baker CC, DiGiovanna JJ, Tamura D, Seitz CS, Gratchev A, Wu WH, Chung KY, Chung HJ, Azizi E, Woodgate R, Schneider TD, Kraemer KH. Inui H, et al. Among authors: gratchev a. J Invest Dermatol. 2008 Aug;128(8):2055-68. doi: 10.1038/jid.2008.48. Epub 2008 Mar 27. J Invest Dermatol. 2008. PMID: 18368133 Free PMC article.

2

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: gratchev a. 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.

3

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. Among authors: gratchev a. 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

4

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: gratchev a. Exp Dermatol. 2013 Jan;22(1):24-9. doi: 10.1111/exd.12052. Epub 2012 Nov 22. Exp Dermatol. 2013. PMID: 23173980

5

Molecular genetics of Xeroderma pigmentosum variant.

Gratchev A, Strein P, Utikal J, Sergij G. Gratchev A, et al. Exp Dermatol. 2003 Oct;12(5):529-36. doi: 10.1034/j.1600-0625.2003.00124.x. Exp Dermatol. 2003. PMID: 14705792 Review.

6

Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes.

Schäfer A, Gratchev A, Seebode C, Hofmann L, Schubert S, Laspe P, Apel A, Ohlenbusch A, Tzvetkov M, Weishaupt C, Oji V, Schön MP, Emmert S. Schäfer A, et al. Among authors: gratchev a. Exp Dermatol. 2013 Jul;22(7):486-9. doi: 10.1111/exd.12166. Exp Dermatol. 2013. PMID: 23800062

7

Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.

Kleijer WJ, Laugel V, Berneburg M, Nardo T, Fawcett H, Gratchev A, Jaspers NG, Sarasin A, Stefanini M, Lehmann AR. Kleijer WJ, et al. Among authors: gratchev a. DNA Repair (Amst). 2008 May 3;7(5):744-50. doi: 10.1016/j.dnarep.2008.01.014. Epub 2008 Mar 10. DNA Repair (Amst). 2008. PMID: 18329345

8

The nucleotide excision repair of DNA in human cells and its association with xeroderma pigmentosum.

Gratchev A. Gratchev A. Adv Exp Med Biol. 2008;637:113-9. doi: 10.1007/978-0-387-09599-8_12. Adv Exp Med Biol. 2008. PMID: 19181116 Review. No abstract available.

9

Phenotypical and molecular profiling of the extraneuronal cholinergic system of the skin.

Kurzen H, Berger H, Jäger C, Hartschuh W, Näher H, Gratchev A, Goerdt S, Deichmann M. Kurzen H, et al. Among authors: gratchev a. J Invest Dermatol. 2004 Nov;123(5):937-49. doi: 10.1111/j.0022-202X.2004.23425.x. J Invest Dermatol. 2004. PMID: 15482483 Free article.

10

[Cutaneous non-Langerhans' cell histiocytoses].

Utikal J, Klemke CD, Gratchev A, Goerdt S. Utikal J, et al. Among authors: gratchev a. J Dtsch Dermatol Ges. 2003 Jun;1(6):471-91; quiz 492-3. doi: 10.1046/j.1610-0387.2003.03551.x. J Dtsch Dermatol Ges. 2003. PMID: 16295142 Review. German. No abstract available.

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