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Items: 1 to 20 of 30

1.

Advances in analyzing RNA diversity in eukaryotic transcriptomes: peering through the Omics lens.

Bangru S, Kalsotra A.

F1000Res. 2016 Nov 14;5:2668. eCollection 2016 Nov 14. Review.

2.

A novel TERC CR4/CR5 domain mutation causes telomere disease via decreased TERT binding.

Boyraz B, Bellomo CM, Fleming MD, Cutler CS, Agarwal S.

Blood. 2016 Oct 20;128(16):2089-2092. doi: 10.1182/blood-2016-04-710160. Epub 2016 Sep 1. No abstract available.

PMID:
27587879
3.

Hematopoietic lineage skewing and intestinal epithelia degeneration in aged mice with telomerase RNA component deletion.

Chen J, Bryant MA, Dent JJ, Sun Y, Desierto MJ, Young NS.

Exp Gerontol. 2015 Dec;72:251-60. doi: 10.1016/j.exger.2015.10.016. Epub 2015 Oct 30.

4.

Reversibility of Defective Hematopoiesis Caused by Telomere Shortening in Telomerase Knockout Mice.

Raval A, Behbehani GK, Nguyen le XT, Thomas D, Kusler B, Garbuzov A, Ramunas J, Holbrook C, Park CY, Blau H, Nolan GP, Artandi SE, Mitchell BS.

PLoS One. 2015 Jul 2;10(7):e0131722. doi: 10.1371/journal.pone.0131722. eCollection 2015 Jul 2.

5.

Naive T-cells in myelodysplastic syndrome display intrinsic human telomerase reverse transcriptase (hTERT) deficiency.

Yang L, Mailloux A, Rollison DE, Painter JS, Maciejewski J, Paquette RL, Loughran TP, McGraw K, Makishima H, Radhakrishnan R, Wei S, Ren X, Komrokji R, List AF, Epling-Burnette PK.

Leukemia. 2013 Apr;27(4):897-906. doi: 10.1038/leu.2012.300. Epub 2012 Oct 17.

6.

The genetics of dyskeratosis congenita.

Mason PJ, Bessler M.

Cancer Genet. 2011 Dec;204(12):635-45. doi: 10.1016/j.cancergen.2011.11.002. Review.

7.

It all comes together at the ends: telomerase structure, function, and biogenesis.

Podlevsky JD, Chen JJ.

Mutat Res. 2012 Feb 1;730(1-2):3-11. doi: 10.1016/j.mrfmmm.2011.11.002. Epub 2011 Nov 7. Review.

8.

Architecture of human telomerase RNA.

Zhang Q, Kim NK, Feigon J.

Proc Natl Acad Sci U S A. 2011 Dec 20;108(51):20325-32. doi: 10.1073/pnas.1100279108. Epub 2011 Aug 15.

9.

Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis.

Alder JK, Cogan JD, Brown AF, Anderson CJ, Lawson WE, Lansdorp PM, Phillips JA 3rd, Loyd JE, Chen JJ, Armanios M.

PLoS Genet. 2011 Mar;7(3):e1001352. doi: 10.1371/journal.pgen.1001352. Epub 2011 Mar 31.

10.

Medical genetics and epigenetics of telomerase.

Koziel JE, Fox MJ, Steding CE, Sprouse AA, Herbert BS.

J Cell Mol Med. 2011 Mar;15(3):457-67. doi: 10.1111/j.1582-4934.2011.01276.x. Review.

11.

Investigation of human telomerase holoenzyme assembly, activity, and processivity using disease-linked subunit variants.

Robart AR, Collins K.

J Biol Chem. 2010 Feb 12;285(7):4375-86. doi: 10.1074/jbc.M109.088575. Epub 2009 Dec 17.

12.

Single-molecule analysis of the human telomerase RNA.dyskerin interaction and the effect of dyskeratosis congenita mutations.

Ashbridge B, Orte A, Yeoman JA, Kirwan M, Vulliamy T, Dokal I, Klenerman D, Balasubramanian S.

Biochemistry. 2009 Nov 24;48(46):10858-65. doi: 10.1021/bi901373e.

13.
14.

Telomere dysfunction in human diseases: the long and short of it!

Carroll KA, Ly H.

Int J Clin Exp Pathol. 2009 May 10;2(6):528-43.

15.

Telomeres and disease.

Lansdorp PM.

EMBO J. 2009 Sep 2;28(17):2532-40. doi: 10.1038/emboj.2009.172. Epub 2009 Jul 23. Review.

16.

Sex hormones, acting on the TERT gene, increase telomerase activity in human primary hematopoietic cells.

Calado RT, Yewdell WT, Wilkerson KL, Regal JA, Kajigaya S, Stratakis CA, Young NS.

Blood. 2009 Sep 10;114(11):2236-43. doi: 10.1182/blood-2008-09-178871. Epub 2009 Jun 26.

17.

Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia.

Calado RT, Regal JA, Hills M, Yewdell WT, Dalmazzo LF, Zago MA, Lansdorp PM, Hogge D, Chanock SJ, Estey EH, Falc√£o RP, Young NS.

Proc Natl Acad Sci U S A. 2009 Jan 27;106(4):1187-92. doi: 10.1073/pnas.0807057106. Epub 2009 Jan 15.

18.

Accelerated telomere shortening precedes development of therapy-related myelodysplasia or acute myelogenous leukemia after autologous transplantation for lymphoma.

Chakraborty S, Sun CL, Francisco L, Sabado M, Li L, Chang KL, Forman S, Bhatia S, Bhatia R.

J Clin Oncol. 2009 Feb 10;27(5):791-8. doi: 10.1200/JCO.2008.17.1033. Epub 2009 Jan 5.

19.

Dyskeratosis congenita mutations in the H/ACA domain of human telomerase RNA affect its assembly into a pre-RNP.

Trahan C, Dragon F.

RNA. 2009 Feb;15(2):235-43. doi: 10.1261/rna.1354009. Epub 2008 Dec 17.

20.

Characterization of primitive hematopoietic cells from patients with dyskeratosis congenita.

Goldman FD, Aubert G, Klingelhutz AJ, Hills M, Cooper SR, Hamilton WS, Schlueter AJ, Lambie K, Eaves CJ, Lansdorp PM.

Blood. 2008 May 1;111(9):4523-31. doi: 10.1182/blood-2007-10-120204. Epub 2008 Feb 29.

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