Selig S - Search Results

1

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, Selig S, Lapointe JY, Zelikovic I, Skorecki K. Magen D, et al. Among authors: selig s. N Engl J Med. 2010 Mar 25;362(12):1102-9. doi: 10.1056/NEJMoa0905647. N Engl J Med. 2010. PMID: 20335586 Free article.

2

Position effect of human telomeric repeats on replication timing.

Ofir R, Wong AC, McDermid HE, Skorecki KL, Selig S. Ofir R, et al. Among authors: selig s. Proc Natl Acad Sci U S A. 1999 Sep 28;96(20):11434-9. doi: 10.1073/pnas.96.20.11434. Proc Natl Acad Sci U S A. 1999. PMID: 10500194 Free PMC article.

3

Telomeres and telomerase in human health and disease.

Tzukerman M, Selig S, Skorecki K. Tzukerman M, et al. Among authors: selig s. J Pediatr Endocrinol Metab. 2002 Mar;15(3):229-40. doi: 10.1515/jpem.2002.15.3.229. J Pediatr Endocrinol Metab. 2002. PMID: 11924925 Review.

4

Replication and/or separation of some human telomeres is delayed beyond S-phase in pre-senescent cells.

Ofir R, Yalon-Hacohen M, Segev Y, Schultz A, Skorecki KL, Selig S. Ofir R, et al. Among authors: selig s. Chromosoma. 2002 Sep;111(3):147-55. doi: 10.1007/s00412-002-0199-z. Epub 2002 Jul 25. Chromosoma. 2002. PMID: 12355203

5

Sister chromatid separation at human telomeric regions.

Yalon M, Gal S, Segev Y, Selig S, Skorecki KL. Yalon M, et al. Among authors: selig s. J Cell Sci. 2004 Apr 15;117(Pt 10):1961-70. doi: 10.1242/jcs.01032. Epub 2004 Mar 23. J Cell Sci. 2004. PMID: 15039457

6

The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males.

Rosenberg S, Templeton AR, Feigin PD, Lancet D, Beckmann JS, Selig S, Hamer DH, Skorecki K. Rosenberg S, et al. Among authors: selig s. Hum Genet. 2006 Nov;120(4):447-59. doi: 10.1007/s00439-006-0198-x. Epub 2006 Aug 2. Hum Genet. 2006. PMID: 16896926

7

Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions.

Yehezkel S, Segev Y, Viegas-Péquignot E, Skorecki K, Selig S. Yehezkel S, et al. Among authors: selig s. Hum Mol Genet. 2008 Sep 15;17(18):2776-89. doi: 10.1093/hmg/ddn177. Epub 2008 Jun 16. Hum Mol Genet. 2008. PMID: 18558631

8

African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.

Behar DM, Rosset S, Tzur S, Selig S, Yudkovsky G, Bercovici S, Kopp JB, Winkler CA, Nelson GW, Wasser WG, Skorecki K. Behar DM, et al. Among authors: selig s. Hum Mol Genet. 2010 May 1;19(9):1816-27. doi: 10.1093/hmg/ddq040. Epub 2010 Feb 9. Hum Mol Genet. 2010. PMID: 20144966 Free PMC article.

9

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.

Tzur S, Rosset S, Shemer R, Yudkovsky G, Selig S, Tarekegn A, Bekele E, Bradman N, Wasser WG, Behar DM, Skorecki K. Tzur S, et al. Among authors: selig s. Hum Genet. 2010 Sep;128(3):345-50. doi: 10.1007/s00439-010-0861-0. Epub 2010 Jul 16. Hum Genet. 2010. PMID: 20635188 Free PMC article.

10

Reprogramming of telomeric regions during the generation of human induced pluripotent stem cells and subsequent differentiation into fibroblast-like derivatives.

Yehezkel S, Rebibo-Sabbah A, Segev Y, Tzukerman M, Shaked R, Huber I, Gepstein L, Skorecki K, Selig S. Yehezkel S, et al. Among authors: selig s. Epigenetics. 2011 Jan;6(1):63-75. doi: 10.4161/epi.6.1.13390. Epub 2011 Jan 1. Epigenetics. 2011. PMID: 20861676 Free PMC article.

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