Trembath RC - 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: trembath rc. 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

Familial and sporadic primary pulmonary hypertension is caused by BMPR2 gene mutations resulting in haploinsufficiency of the bone morphogenetic protein tùype II receptor.

Thomson J, Machado R, Pauciulo M, Morgan N, Yacoub M, Corris P, McNeil K, Loyd J, Nichols W, Trembath R. Thomson J, et al. J Heart Lung Transplant. 2001 Feb;20(2):149. doi: 10.1016/s1053-2498(01)00259-5. J Heart Lung Transplant. 2001. PMID: 11250205 No abstract available.

3

A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies.

Lloyd DJ, Trembath RC, Shackleton S. Lloyd DJ, et al. Among authors: trembath rc. Hum Mol Genet. 2002 Apr 1;11(7):769-77. doi: 10.1093/hmg/11.7.769. Hum Mol Genet. 2002. PMID: 11929849

4

Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor.

Atkinson C, Stewart S, Upton PD, Machado R, Thomson JR, Trembath RC, Morrell NW. Atkinson C, et al. Among authors: trembath rc. Circulation. 2002 Apr 9;105(14):1672-8. doi: 10.1161/01.cir.0000012754.72951.3d. Circulation. 2002. PMID: 11940546

5

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. Among authors: trembath rc. Hum Mol Genet. 2002 Jun 15;11(13):1517-25. doi: 10.1093/hmg/11.13.1517. Hum Mol Genet. 2002. PMID: 12045205

6

Insights into the genetic and molecular basis of primary pulmonary hypertension.

Trembath RC, Harrison R. Trembath RC, et al. Pediatr Res. 2003 Jun;53(6):883-8. doi: 10.1203/01.PDR.0000061565.22500.E7. Epub 2003 Mar 5. Pediatr Res. 2003. PMID: 12621102

7

BMP4 inhibits proliferation and promotes myocyte differentiation of lung fibroblasts via Smad1 and JNK pathways.

Jeffery TK, Upton PD, Trembath RC, Morrell NW. Jeffery TK, et al. Among authors: trembath rc. Am J Physiol Lung Cell Mol Physiol. 2005 Feb;288(2):L370-8. doi: 10.1152/ajplung.00242.2004. Epub 2004 Oct 29. Am J Physiol Lung Cell Mol Physiol. 2005. PMID: 15516492 Free article.

8

Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood.

Harrison RE, Berger R, Haworth SG, Tulloh R, Mache CJ, Morrell NW, Aldred MA, Trembath RC. Harrison RE, et al. Among authors: trembath rc. Circulation. 2005 Feb 1;111(4):435-41. doi: 10.1161/01.CIR.0000153798.78540.87. Circulation. 2005. PMID: 15687131

9

Investigation of second genetic hits at the BMPR2 locus as a modulator of disease progression in familial pulmonary arterial hypertension.

Machado RD, James V, Southwood M, Harrison RE, Atkinson C, Stewart S, Morrell NW, Trembath RC, Aldred MA. Machado RD, et al. Among authors: trembath rc. Circulation. 2005 Feb 8;111(5):607-13. doi: 10.1161/01.CIR.0000154543.07679.08. Circulation. 2005. PMID: 15699281

10

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: trembath rc. 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

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