Russell MW - Search Results

1

Pleiotropic phenotype of a genomic knock-in of an RGS-insensitive G184S Gnai2 allele.

Huang X, Fu Y, Charbeneau RA, Saunders TL, Taylor DK, Hankenson KD, Russell MW, D'Alecy LG, Neubig RR. Huang X, et al. Among authors: russell mw. Mol Cell Biol. 2006 Sep;26(18):6870-9. doi: 10.1128/MCB.00314-06. Mol Cell Biol. 2006. PMID: 16943428 Free PMC article.

2

Targeted deletion of the zebrafish obscurin A RhoGEF domain affects heart, skeletal muscle and brain development.

Raeker MO, Bieniek AN, Ryan AS, Tsai HJ, Zahn KM, Russell MW. Raeker MO, et al. Among authors: russell mw. Dev Biol. 2010 Jan 15;337(2):432-43. doi: 10.1016/j.ydbio.2009.11.018. Epub 2009 Nov 26. Dev Biol. 2010. PMID: 19931525 Free PMC article.

3

Deficient cMyBP-C protein expression during cardiomyocyte differentiation underlies human hypertrophic cardiomyopathy cellular phenotypes in disease specific human ES cell derived cardiomyocytes.

Monteiro da Rocha A, Guerrero-Serna G, Helms A, Luzod C, Mironov S, Russell M, Jalife J, Day SM, Smith GD, Herron TJ. Monteiro da Rocha A, et al. J Mol Cell Cardiol. 2016 Oct;99:197-206. doi: 10.1016/j.yjmcc.2016.09.004. Epub 2016 Sep 10. J Mol Cell Cardiol. 2016. PMID: 27620334 Free PMC article.

4

Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity.

Stefanelli CB, Rosenthal A, Borisov AB, Ensing GJ, Russell MW. Stefanelli CB, et al. Among authors: russell mw. Mol Genet Metab. 2004 Sep-Oct;83(1-2):188-96. doi: 10.1016/j.ymgme.2004.04.013. Mol Genet Metab. 2004. PMID: 15464434

5

Developmental expression and differential cellular localization of obscurin and obscurin-associated kinase in cardiac muscle cells.

Borisov AB, Raeker MO, Russell MW. Borisov AB, et al. Among authors: russell mw. J Cell Biochem. 2008 Apr 1;103(5):1621-35. doi: 10.1002/jcb.21551. J Cell Biochem. 2008. PMID: 18041765 Free PMC article.

6

In vivo, Pikfyve generates PI(3,5)P2, which serves as both a signaling lipid and the major precursor for PI5P.

Zolov SN, Bridges D, Zhang Y, Lee WW, Riehle E, Verma R, Lenk GM, Converso-Baran K, Weide T, Albin RL, Saltiel AR, Meisler MH, Russell MW, Weisman LS. Zolov SN, et al. Among authors: russell mw. Proc Natl Acad Sci U S A. 2012 Oct 23;109(43):17472-7. doi: 10.1073/pnas.1203106109. Epub 2012 Oct 9. Proc Natl Acad Sci U S A. 2012. PMID: 23047693 Free PMC article.

7

The Impact of Extracellular Histones and Absence of Toll-like Receptors on Cardiac Functional and Electrical Disturbances in Mouse Hearts.

Loaiza R, Fattahi F, Kalbitz M, Grailer JJ, Russell MW, Jalife J, Valdivia HH, Zetoune FS, Ward PA. Loaiza R, et al. Among authors: russell mw. Int J Mol Sci. 2024 Aug 8;25(16):8653. doi: 10.3390/ijms25168653. Int J Mol Sci. 2024. PMID: 39201339 Free PMC article.

8

Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.

Russell MW, Raeker MO, Geisler SB, Thomas PE, Simmons TA, Bernat JA, Thorsson T, Innis JW. Russell MW, et al. Hum Mol Genet. 2014 Aug 15;23(16):4272-84. doi: 10.1093/hmg/ddu144. Epub 2014 Apr 2. Hum Mol Genet. 2014. PMID: 24694933

9

Identification, tissue expression and chromosomal localization of human Obscurin-MLCK, a member of the titin and Dbl families of myosin light chain kinases.

Russell MW, Raeker MO, Korytkowski KA, Sonneman KJ. Russell MW, et al. Gene. 2002 Jan 9;282(1-2):237-46. doi: 10.1016/s0378-1119(01)00795-8. Gene. 2002. PMID: 11814696

10

Essential role of obscurin in cardiac myofibrillogenesis and hypertrophic response: evidence from small interfering RNA-mediated gene silencing.

Borisov AB, Sutter SB, Kontrogianni-Konstantopoulos A, Bloch RJ, Westfall MV, Russell MW. Borisov AB, et al. Among authors: russell mw. Histochem Cell Biol. 2006 Mar;125(3):227-38. doi: 10.1007/s00418-005-0069-x. Epub 2005 Oct 5. Histochem Cell Biol. 2006. PMID: 16205939 Free article.

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