Morse JH - Search Results

1

Pulmonary arterial hypertension: future directions: report of a National Heart, Lung and Blood Institute/Office of Rare Diseases workshop.

Newman JH, Fanburg BL, Archer SL, Badesch DB, Barst RJ, Garcia JG, Kao PN, Knowles JA, Loyd JE, McGoon MD, Morse JH, Nichols WC, Rabinovitch M, Rodman DM, Stevens T, Tuder RM, Voelkel NF, Gail DB; National Heart, Lung and Blood Institute/Office of Rare Diseases. Newman JH, et al. Among authors: morse jh. Circulation. 2004 Jun 22;109(24):2947-52. doi: 10.1161/01.CIR.0000132476.87231.6F. Circulation. 2004. PMID: 15210611 No abstract available.

2

Comparative analysis of BMPR2 gene and its mutations in idiopathic pulmonary arterial hypertension.

Wong WP, Knowles JA, Morse JH. Wong WP, et al. Among authors: morse jh. Chest. 2005 Dec;128(6 Suppl):615S. doi: 10.1378/chest.128.6_suppl.615S-a. Chest. 2005. PMID: 16373869 No abstract available.

3

Genetic aspects of pulmonary arterial hypertension.

Morse JH, Deng Z, Knowles JA. Morse JH, et al. Ann Med. 2001 Dec;33(9):596-603. doi: 10.3109/07853890109002105. Ann Med. 2001. PMID: 11817654 Free article. Review.

4

BMPR2 mutations in pulmonary arterial hypertension with congenital heart disease.

Roberts KE, McElroy JJ, Wong WP, Yen E, Widlitz A, Barst RJ, Knowles JA, Morse JH. Roberts KE, et al. Among authors: morse jh. Eur Respir J. 2004 Sep;24(3):371-4. doi: 10.1183/09031936.04.00018604. Eur Respir J. 2004. PMID: 15358693 Free article.

5

Bone morphogenetic protein receptor type II C-terminus interacts with c-Src: implication for a role in pulmonary arterial hypertension.

Wong WK, Knowles JA, Morse JH. Wong WK, et al. Among authors: morse jh. Am J Respir Cell Mol Biol. 2005 Nov;33(5):438-46. doi: 10.1165/rcmb.2005-0103OC. Epub 2005 Jul 7. Am J Respir Cell Mol Biol. 2005. PMID: 16002577 Free PMC article.

6

Bone morphogenetic protein receptor 2 mutations in adults and children with idiopathic pulmonary arterial hypertension: association with thyroid disease.

Roberts KE, Barst RJ, McElroy JJ, Widlitz A, Chada K, Knowles JA, Morse JH. Roberts KE, et al. Among authors: morse jh. Chest. 2005 Dec;128(6 Suppl):618S. doi: 10.1378/chest.128.6_suppl.618S. Chest. 2005. PMID: 16373874 No abstract available.

7

Detection of familial primary pulmonary hypertension by genetic testing.

Morse JH, Barst RJ. Morse JH, et al. N Engl J Med. 1997 Jul 17;337(3):202-3. doi: 10.1056/NEJM199707173370315. N Engl J Med. 1997. PMID: 9221353 No abstract available.

8

Evidence for the association of unexplained pulmonary hypertension in children with the major histocompatibility complex.

Barst RJ, Flaster ER, Menon A, Fotino M, Morse JH. Barst RJ, et al. Among authors: morse jh. Circulation. 1992 Jan;85(1):249-58. doi: 10.1161/01.cir.85.1.249. Circulation. 1992. PMID: 1728456

9

Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32.

Morse JH, Jones AC, Barst RJ, Hodge SE, Wilhelmsen KC, Nygaard TG. Morse JH, et al. Circulation. 1997 Jun 17;95(12):2603-6. doi: 10.1161/01.cir.95.12.2603. Circulation. 1997. PMID: 9193425

10

Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasia.

Abdalla SA, Gallione CJ, Barst RJ, Horn EM, Knowles JA, Marchuk DA, Letarte M, Morse JH. Abdalla SA, et al. Among authors: morse jh. Eur Respir J. 2004 Mar;23(3):373-7. doi: 10.1183/09031936.04.00085504. Eur Respir J. 2004. PMID: 15065824 Free article.

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