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Items: 12

1.

Metabolic Syndrome Induces Over Expression of the Human AT1R: A Haplotype-Dependent Effect With Implications on Cardio-Renal Function.

Jain S, Puri N, Rana A, Sirianni N, Mopidevi B, Kumar A.

Am J Hypertens. 2018 Mar 10;31(4):495-503. doi: 10.1093/ajh/hpx176.

2.

Ivabradine in the treatment of postural tachycardia syndrome (POTS), a single center experience.

Ruzieh M, Sirianni N, Ammari Z, Dasa O, Alhazmi L, Karabin B, Grubb B.

Pacing Clin Electrophysiol. 2017 Nov;40(11):1242-1245. doi: 10.1111/pace.13182. Epub 2017 Sep 20.

PMID:
28846151
3.

The transcriptional regulation of the human angiotensinogen gene after high-fat diet is haplotype-dependent: Novel insights into the gene-regulatory networks and implications for human hypertension.

Rana A, Jain S, Puri N, Kaw M, Sirianni N, Eren D, Mopidevi BR, Kumar A.

PLoS One. 2017 May 3;12(5):e0176373. doi: 10.1371/journal.pone.0176373. eCollection 2017.

4.

Closed-Tube Barcoding.

Sirianni NM, Yuan H, Rice JE, Kaufman RS, Deng J, Fulton C, Wangh LJ.

Genome. 2016 Nov;59(11):1049-1061. Epub 2016 Aug 30.

5.

Auranofin protects against anthrax lethal toxin-induced activation of the Nlrp1b inflammasome.

Newman ZL, Sirianni N, Mawhinney C, Lee MS, Leppla SH, Moayeri M, Johansen LM.

Antimicrob Agents Chemother. 2011 Mar;55(3):1028-35. doi: 10.1128/AAC.00772-10. Epub 2010 Dec 13.

7.

Human papillomavirus-16 associated squamous cell carcinoma of the head and neck (SCCHN): a natural disease model provides insights into viral carcinogenesis.

Ferris RL, Martinez I, Sirianni N, Wang J, López-Albaitero A, Gollin SM, Johnson JT, Khan S.

Eur J Cancer. 2005 Mar;41(5):807-15.

PMID:
15763658
8.

Effect of human papillomavirus-16 infection on CD8+ T-cell recognition of a wild-type sequence p53264-272 peptide in patients with squamous cell carcinoma of the head and neck.

Sirianni N, Ha PK, Oelke M, Califano J, Gooding W, Westra W, Whiteside TL, Koch WM, Schneck JP, DeLeo A, Ferris RL.

Clin Cancer Res. 2004 Oct 15;10(20):6929-37.

9.
10.

MeCP2 mutations in children with and without the phenotype of Rett syndrome.

Hoffbuhr K, Devaney JM, LaFleur B, Sirianni N, Scacheri C, Giron J, Schuette J, Innis J, Marino M, Philippart M, Narayanan V, Umansky R, Kronn D, Hoffman EP, Naidu S.

Neurology. 2001 Jun 12;56(11):1486-95.

PMID:
11402105
11.

Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.

Sirianni N, Naidu S, Pereira J, Pillotto RF, Hoffman EP.

Am J Hum Genet. 1998 Nov;63(5):1552-8. No abstract available.

12.

Selection and use of ligands for receptor-mediated gene delivery to myogenic cells.

Feero WG, Li S, Rosenblatt JD, Sirianni N, Morgan JE, Partridge TA, Huang L, Hoffman EP.

Gene Ther. 1997 Jul;4(7):664-74.

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