Rudarakanchana N - Search Results

1

Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension.

Machado RD, Rudarakanchana N, Atkinson C, Flanagan JA, Harrison R, Morrell NW, Trembath RC. Machado RD, et al. Among authors: rudarakanchana n. Hum Mol Genet. 2003 Dec 15;12(24):3277-86. doi: 10.1093/hmg/ddg365. Epub 2003 Oct 28. Hum Mol Genet. 2003. PMID: 14583445

2

Functional analysis of bone morphogenetic protein type II receptor mutations underlying primary pulmonary hypertension.

Rudarakanchana N, Flanagan JA, Chen H, Upton PD, Machado R, Patel D, Trembath RC, Morrell NW. Rudarakanchana N, et al. Hum Mol Genet. 2002 Jun 15;11(13):1517-25. doi: 10.1093/hmg/11.13.1517. Hum Mol Genet. 2002. PMID: 12045205

3

Primary pulmonary hypertension: molecular basis and potential for therapy.

Rudarakanchana N, Morrell NW. Rudarakanchana N, et al. Expert Rev Mol Med. 2004 Mar 9;6(6):1-15. doi: 10.1017/S1462399404007483. Expert Rev Mol Med. 2004. PMID: 15005857 Review.

4

BMPR2 mutations have short lifetime expectancy in primary pulmonary hypertension.

Sankelo M, Flanagan JA, Machado R, Harrison R, Rudarakanchana N, Morrell N, Dixon M, Halme M, Puolijoki H, Kere J, Elomaa O, Kupari M, Räisänen-Sokolowski A, Trembath RC, Laitinen T. Sankelo M, et al. Among authors: rudarakanchana n. Hum Mutat. 2005 Aug;26(2):119-24. doi: 10.1002/humu.20200. Hum Mutat. 2005. PMID: 15965979

5

Stoichiometric imbalance in the receptor complex contributes to dysfunctional BMPR-II mediated signalling in pulmonary arterial hypertension.

Nasim MT, Ghouri A, Patel B, James V, Rudarakanchana N, Morrell NW, Trembath RC. Nasim MT, et al. Among authors: rudarakanchana n. Hum Mol Genet. 2008 Jun 1;17(11):1683-94. doi: 10.1093/hmg/ddn059. Epub 2008 Mar 4. Hum Mol Genet. 2008. PMID: 18321866

6

Failure of bone morphogenetic protein receptor trafficking in pulmonary arterial hypertension: potential for rescue.

Sobolewski A, Rudarakanchana N, Upton PD, Yang J, Crilley TK, Trembath RC, Morrell NW. Sobolewski A, et al. Among authors: rudarakanchana n. Hum Mol Genet. 2008 Oct 15;17(20):3180-90. doi: 10.1093/hmg/ddn214. Epub 2008 Jul 21. Hum Mol Genet. 2008. PMID: 18647753

7

Dysfunctional Smad signaling contributes to abnormal smooth muscle cell proliferation in familial pulmonary arterial hypertension.

Yang X, Long L, Southwood M, Rudarakanchana N, Upton PD, Jeffery TK, Atkinson C, Chen H, Trembath RC, Morrell NW. Yang X, et al. Among authors: rudarakanchana n. Circ Res. 2005 May 27;96(10):1053-63. doi: 10.1161/01.RES.0000166926.54293.68. Epub 2005 Apr 21. Circ Res. 2005. PMID: 15845886

8

New insights into the pathogenesis and treatment of primary pulmonary hypertension.

Rudarakanchana N, Trembath RC, Morrell NW. Rudarakanchana N, et al. Thorax. 2001 Nov;56(11):888-90. doi: 10.1136/thorax.56.11.888. Thorax. 2001. PMID: 11641516 Free PMC article. Review. No abstract available.

9

Serotonin increases susceptibility to pulmonary hypertension in BMPR2-deficient mice.

Long L, MacLean MR, Jeffery TK, Morecroft I, Yang X, Rudarakanchana N, Southwood M, James V, Trembath RC, Morrell NW. Long L, et al. Among authors: rudarakanchana n. Circ Res. 2006 Mar 31;98(6):818-27. doi: 10.1161/01.RES.0000215809.47923.fd. Epub 2006 Feb 23. Circ Res. 2006. PMID: 16497988

10

Trapping of BMP receptors in distinct membrane domains inhibits their function in pulmonary arterial hypertension.

Jiang Y, Nohe A, Bragdon B, Tian C, Rudarakanchana N, Morrell NW, Petersen NO. Jiang Y, et al. Among authors: rudarakanchana n. Am J Physiol Lung Cell Mol Physiol. 2011 Aug;301(2):L218-27. doi: 10.1152/ajplung.00300.2010. Epub 2011 May 27. Am J Physiol Lung Cell Mol Physiol. 2011. PMID: 21622843 Free article.

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