Li H - Search Results

1

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.

Mohapatra B, Casey B, Li H, Ho-Dawson T, Smith L, Fernbach SD, Molinari L, Niesh SR, Jefferies JL, Craigen WJ, Towbin JA, Belmont JW, Ware SM. Mohapatra B, et al. Among authors: li h. Hum Mol Genet. 2009 Mar 1;18(5):861-71. doi: 10.1093/hmg/ddn411. Epub 2008 Dec 8. Hum Mol Genet. 2009. PMID: 19064609 Free PMC article.

2

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA. Vatta M, et al. Among authors: li h. Hum Mol Genet. 2002 Feb 1;11(3):337-45. doi: 10.1093/hmg/11.3.337. Hum Mol Genet. 2002. PMID: 11823453

3

Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy.

Arola AM, Sanchez X, Murphy RT, Hasle A, Li H, Elliott PM, McKenna WJ, Towbin JA, Bowles NE. Arola AM, et al. Among authors: li h. Mol Genet Metab. 2007 Apr;90(4):435-40. doi: 10.1016/j.ymgme.2006.12.008. Epub 2007 Jan 24. Mol Genet Metab. 2007. PMID: 17254821

4

Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.

Wang Z, Li H, Moss AJ, Robinson J, Zareba W, Knilans T, Bowles NE, Towbin JA. Wang Z, et al. Among authors: li h. Mol Genet Metab. 2002 Apr;75(4):308-16. doi: 10.1016/S1096-7192(02)00007-0. Mol Genet Metab. 2002. PMID: 12051962

5

Novel mutations in domain I of SCN5A cause Brugada syndrome.

Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA. Vatta M, et al. Among authors: li h. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963

6

Genetics and cardiac arrhythmias.

Towbin JA, Vatta M, Li H, Bowles NE. Towbin JA, et al. Among authors: li h. Adv Pediatr. 2002;49:87-129. Adv Pediatr. 2002. PMID: 12214781 Review.

7

A role for Toll-like receptor 3 variants in host susceptibility to enteroviral myocarditis and dilated cardiomyopathy.

Gorbea C, Makar KA, Pauschinger M, Pratt G, Bersola JL, Varela J, David RM, Banks L, Huang CH, Li H, Schultheiss HP, Towbin JA, Vallejo JG, Bowles NE. Gorbea C, et al. Among authors: li h. J Biol Chem. 2010 Jul 23;285(30):23208-23. doi: 10.1074/jbc.M109.047464. Epub 2010 May 14. J Biol Chem. 2010. PMID: 20472559 Free PMC article.

8

Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Yang Z, Bowles NE, Scherer SE, Taylor MD, Kearney DL, Ge S, Nadvoretskiy VV, DeFreitas G, Carabello B, Brandon LI, Godsel LM, Green KJ, Saffitz JE, Li H, Danieli GA, Calkins H, Marcus F, Towbin JA. Yang Z, et al. Among authors: li h. Circ Res. 2006 Sep 15;99(6):646-55. doi: 10.1161/01.RES.0000241482.19382.c6. Epub 2006 Aug 17. Circ Res. 2006. PMID: 16917092

9

Cardiotropic viruses in the myocardium of children with end-stage heart disease.

Francalanci P, Chance JL, Vatta M, Jimenez S, Li H, Towbin JA, Bowles NE. Francalanci P, et al. Among authors: li h. J Heart Lung Transplant. 2004 Sep;23(9):1046-52. doi: 10.1016/j.healun.2003.08.015. J Heart Lung Transplant. 2004. PMID: 15454170

10

Analysis of the coxsackievirus B-adenovirus receptor gene in patients with myocarditis or dilated cardiomyopathy.

Bowles NE, Javier Fuentes-Garcia F, Makar KA, Li H, Gibson J, Soto F, Schwimmbeck PL, Schultheiss HP, Pauschinger M. Bowles NE, et al. Among authors: li h. Mol Genet Metab. 2002 Nov;77(3):257-9. doi: 10.1016/s1096-7192(02)00168-3. Mol Genet Metab. 2002. PMID: 12409275

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