Slor H - Search Results

1

Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair.

Nakazawa Y, Sasaki K, Mitsutake N, Matsuse M, Shimada M, Nardo T, Takahashi Y, Ohyama K, Ito K, Mishima H, Nomura M, Kinoshita A, Ono S, Takenaka K, Masuyama R, Kudo T, Slor H, Utani A, Tateishi S, Yamashita S, Stefanini M, Lehmann AR, Yoshiura K, Ogi T. Nakazawa Y, et al. Among authors: slor h. Nat Genet. 2012 May;44(5):586-92. doi: 10.1038/ng.2229. Nat Genet. 2012. PMID: 22466610 Free article.

2

Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6.

Falik-Zaccai TC, Laskar M, Kfir N, Nasser W, Slor H, Khayat M. Falik-Zaccai TC, et al. Among authors: slor h. Am J Med Genet A. 2008 Jun 1;146A(11):1423-9. doi: 10.1002/ajmg.a.32309. Am J Med Genet A. 2008. PMID: 18446857

3

The versatile DNA nucleotide excision repair (NER) and its medical significance.

Falik-Zaccai TC, Keren Z, Slor H. Falik-Zaccai TC, et al. Among authors: slor h. Pediatr Endocrinol Rev. 2009 Dec;7(2):37-42. Pediatr Endocrinol Rev. 2009. PMID: 20118892 Review.

4

[Clinical, biochemical and molecular characterization of rare genetic disorders, related to nucleotide excision repair (NER) system].

Falik-Zaccai T, Kfir N, Laskar M, Segel R, Khyat M, Slor H. Falik-Zaccai T, et al. Among authors: slor h. Harefuah. 2006 Dec;145(12):889-94, 942. Harefuah. 2006. PMID: 17220027 Hebrew.

5

A novel XPD mutation in a compound heterozygote; the mutation in the second allele is present in three homozygous patients with mild sun sensitivity.

Falik-Zaccai TC, Erel-Segal R, Horev L, Bitterman-Deutsch O, Koka S, Chaim S, Keren Z, Kalfon L, Gross B, Segal Z, Orgal S, Shoval Y, Slor H, Spivak G, Hanawalt PC. Falik-Zaccai TC, et al. Among authors: slor h. Environ Mol Mutagen. 2012 Aug;53(7):505-14. doi: 10.1002/em.21716. Epub 2012 Jul 23. Environ Mol Mutagen. 2012. PMID: 22826098

6

Clinical utility gene card for: Xeroderma pigmentosum.

Schubert S, Lehmann J, Kalfon L, Slor H, Falik-Zaccai TC, Emmert S. Schubert S, et al. Among authors: slor h. 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.

7

The effect of chlorpromazine and haloperidol on DNA transcription.

Barak Y, Ron IG, Sirota P, Sobe T, Slor H. Barak Y, et al. Among authors: slor h. Int Clin Psychopharmacol. 1996 Sep;11(3):193-7. doi: 10.1097/00004850-199609000-00006. Int Clin Psychopharmacol. 1996. PMID: 8923098

8

Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life.

Slor H, Batko S, Khan SG, Sobe T, Emmert S, Khadavi A, Frumkin A, Busch DB, Albert RB, Kraemer KH. Slor H, et al. J Invest Dermatol. 2000 Dec;115(6):974-80. doi: 10.1046/j.1523-1747.2000.00190.x. J Invest Dermatol. 2000. PMID: 11121128 Free article.

9

DNA repair and recovery of RNA synthesis in uremic patients.

Malachi T, Zevin D, Gafter U, Chagnac A, Slor H, Levi J. Malachi T, et al. Among authors: slor h. Kidney Int. 1993 Aug;44(2):385-9. doi: 10.1038/ki.1993.256. Kidney Int. 1993. PMID: 7690862 Free article.

10

Pronounced depressed ability of DNA repair in uremic human lymphocytes.

Friedman J, Levi J, Malachi T, Slor H. Friedman J, et al. Among authors: slor h. Transplantation. 1988 Mar;45(3):665-6. doi: 10.1097/00007890-198803000-00036. Transplantation. 1988. PMID: 3347940 No abstract available.

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