Agarwal S - Search Results

1

Hepatic vascular remodelling in a patient with dyskeratosis congenita.

Boyraz B, Agarwal S, Pratt DS, Simoneau T, Bhan I, Markmann JF, Misdraji J. Boyraz B, et al. Among authors: agarwal s. Histopathology. 2022 Jan;80(2):450-453. doi: 10.1111/his.14530. Epub 2021 Sep 8. Histopathology. 2022. PMID: 34327718 No abstract available.

2

Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients.

Agarwal S, Loh YH, McLoughlin EM, Huang J, Park IH, Miller JD, Huo H, Okuka M, Dos Reis RM, Loewer S, Ng HH, Keefe DL, Goldman FD, Klingelhutz AJ, Liu L, Daley GQ. Agarwal S, et al. Nature. 2010 Mar 11;464(7286):292-6. doi: 10.1038/nature08792. Epub 2010 Feb 17. Nature. 2010. PMID: 20164838 Free PMC article.

3

Telomere dynamics in dyskeratosis congenita: the long and the short of iPS.

Agarwal S, Daley GQ. Agarwal S, et al. Cell Res. 2011 Aug;21(8):1157-60. doi: 10.1038/cr.2011.120. Epub 2011 Jul 26. Cell Res. 2011. PMID: 21788988 Free PMC article. No abstract available.

4

CTC1 Mutations in a patient with dyskeratosis congenita.

Keller RB, Gagne KE, Usmani GN, Asdourian GK, Williams DA, Hofmann I, Agarwal S. Keller RB, et al. Among authors: agarwal s. Pediatr Blood Cancer. 2012 Aug;59(2):311-4. doi: 10.1002/pbc.24193. Epub 2012 Apr 24. Pediatr Blood Cancer. 2012. PMID: 22532422 Free PMC article.

5

Poly(A)-specific ribonuclease (PARN) mediates 3'-end maturation of the telomerase RNA component.

Moon DH, Segal M, Boyraz B, Guinan E, Hofmann I, Cahan P, Tai AK, Agarwal S. Moon DH, et al. Among authors: agarwal s. Nat Genet. 2015 Dec;47(12):1482-8. doi: 10.1038/ng.3423. Epub 2015 Oct 19. Nat Genet. 2015. PMID: 26482878 Free PMC article.

6

Posttranscriptional manipulation of TERC reverses molecular hallmarks of telomere disease.

Boyraz B, Moon DH, Segal M, Muosieyiri MZ, Aykanat A, Tai AK, Cahan P, Agarwal S. Boyraz B, et al. Among authors: agarwal s. J Clin Invest. 2016 Sep 1;126(9):3377-82. doi: 10.1172/JCI87547. Epub 2016 Aug 2. J Clin Invest. 2016. PMID: 27482890 Free PMC article.

7

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

Boyraz B, Bellomo CM, Fleming MD, Cutler CS, Agarwal S. Boyraz B, et al. Among authors: agarwal s. Blood. 2016 Oct 20;128(16):2089-2092. doi: 10.1182/blood-2016-04-710160. Epub 2016 Sep 1. Blood. 2016. PMID: 27587879 Free PMC article. No abstract available.

8

Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders.

Khincha PP, Bertuch AA, Agarwal S, Townsley DM, Young NS, Keel S, Shimamura A, Boulad F, Simoneau T, Justino H, Kuo C, Artandi S, McCaslin C, Cox DW, Chaffee S, Collins BF, Giri N, Alter BP, Raghu G, Savage SA. Khincha PP, et al. Among authors: agarwal s. Eur Respir J. 2017 Jan 25;49(1):1601640. doi: 10.1183/13993003.01640-2016. Print 2017 Jan. Eur Respir J. 2017. PMID: 27824607 Free PMC article.

9

Exudative Vitreoretinopathy in Dyskeratosis Congenita.

Indaram M, Agarwal S, Yonekawa Y. Indaram M, et al. Among authors: agarwal s. Ophthalmology. 2017 Aug;124(8):1246. doi: 10.1016/j.ophtha.2017.01.044. Ophthalmology. 2017. PMID: 28734336 No abstract available.

10

Evaluation and Management of Hematopoietic Failure in Dyskeratosis Congenita.

Agarwal S. Agarwal S. Hematol Oncol Clin North Am. 2018 Aug;32(4):669-685. doi: 10.1016/j.hoc.2018.04.003. Epub 2018 May 28. Hematol Oncol Clin North Am. 2018. PMID: 30047419 Free PMC article. Review.

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