Wheeler LA - Search Results

1

Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension.

Austin ED, Phillips JA, Cogan JD, Hamid R, Yu C, Stanton KC, Phillips CA, Wheeler LA, Robbins IM, Newman JH, Loyd JE. Austin ED, et al. Among authors: wheeler la. Respir Res. 2009 Sep 28;10(1):87. doi: 10.1186/1465-9921-10-87. Respir Res. 2009. PMID: 19785764 Free PMC article.

2

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32.

Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA 3rd, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Nichols WC, et al. Nat Genet. 1997 Mar;15(3):277-80. doi: 10.1038/ng0397-277. Nat Genet. 1997. PMID: 9054941

3

Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family.

Thomson JR, Machado RD, Pauciulo MW, Morgan NV, Humbert M, Elliott GC, Ward K, Yacoub M, Mikhail G, Rogers P, Newman J, Wheeler L, Higenbottam T, Gibbs JS, Egan J, Crozier A, Peacock A, Allcock R, Corris P, Loyd JE, Trembath RC, Nichols WC. Thomson JR, et al. J Med Genet. 2000 Oct;37(10):741-5. doi: 10.1136/jmg.37.10.741. J Med Genet. 2000. PMID: 11015450 Free PMC article.

4

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension.

Machado RD, Pauciulo MW, Thomson JR, Lane KB, Morgan NV, Wheeler L, Phillips JA 3rd, Newman J, Williams D, Galiè N, Manes A, McNeil K, Yacoub M, Mikhail G, Rogers P, Corris P, Humbert M, Donnai D, Martensson G, Tranebjaerg L, Loyd JE, Trembath RC, Nichols WC. Machado RD, et al. Am J Hum Genet. 2001 Jan;68(1):92-102. doi: 10.1086/316947. Epub 2000 Dec 12. Am J Hum Genet. 2001. PMID: 11115378 Free PMC article.

5

Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred.

Newman JH, Wheeler L, Lane KB, Loyd E, Gaddipati R, Phillips JA 3rd, Loyd JE. Newman JH, et al. N Engl J Med. 2001 Aug 2;345(5):319-24. doi: 10.1056/NEJM200108023450502. N Engl J Med. 2001. PMID: 11484688 Free article.

6

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.

Trembath RC, Thomson JR, Machado RD, Morgan NV, Atkinson C, Winship I, Simonneau G, Galie N, Loyd JE, Humbert M, Nichols WC, Morrell NW, Berg J, Manes A, McGaughran J, Pauciulo M, Wheeler L. Trembath RC, et al. N Engl J Med. 2001 Aug 2;345(5):325-34. doi: 10.1056/NEJM200108023450503. N Engl J Med. 2001. PMID: 11484689 Free article.

7

Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II.

Runo JR, Vnencak-Jones CL, Prince M, Loyd JE, Wheeler L, Robbins IM, Lane KB, Newman JH, Johnson J, Nichols WC, Phillips JA 3rd. Runo JR, et al. Am J Respir Crit Care Med. 2003 Mar 15;167(6):889-94. doi: 10.1164/rccm.200208-861OC. Epub 2002 Nov 21. Am J Respir Crit Care Med. 2003. PMID: 12446270

8

Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary hypertension.

Cogan JD, Vnencak-Jones CL, Phillips JA 3rd, Lane KB, Wheeler LA, Robbins IM, Garrison G, Hedges LK, Loyd JE. Cogan JD, et al. Among authors: wheeler la. Genet Med. 2005 Mar;7(3):169-74. doi: 10.1097/01.gim.0000156525.09595.e9. Genet Med. 2005. PMID: 15775752

9

Serotonin transporter polymorphisms in familial and idiopathic pulmonary arterial hypertension.

Willers ED, Newman JH, Loyd JE, Robbins IM, Wheeler LA, Prince MA, Stanton KC, Cogan JA, Runo JR, Byrne D, Humbert M, Simonneau G, Sztrymf B, Morse JA, Knowles JA, Roberts KE, McElroy JJ, Barst RJ, Phillips JA 3rd. Willers ED, et al. Among authors: wheeler la. Am J Respir Crit Care Med. 2006 Apr 1;173(7):798-802. doi: 10.1164/rccm.200509-1361OC. Epub 2005 Dec 9. Am J Respir Crit Care Med. 2006. PMID: 16339917 Free PMC article.

10

Aberrant signal transduction in pulmonary hypertension.

Lane KB, Blackwell TR, Runo J, Wheeler L, Phillips JA 3rd, Loyd JE. Lane KB, et al. Chest. 2005 Dec;128(6 Suppl):564S-565S. doi: 10.1378/chest.128.6_suppl.564S-a. Chest. 2005. PMID: 16373826 No abstract available.

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