MacLennan DH - Search Results

1

Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotype.

De Crescenzo V, Fogarty KE, Lefkowitz JJ, Bellve KD, Zvaritch E, MacLennan DH, Walsh JV Jr. De Crescenzo V, et al. Among authors: maclennan dh. Proc Natl Acad Sci U S A. 2012 Jan 10;109(2):610-5. doi: 10.1073/pnas.1115111108. Epub 2011 Dec 27. Proc Natl Acad Sci U S A. 2012. PMID: 22203976 Free PMC article.

2

An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line.

Zvaritch E, Depreux F, Kraeva N, Loy RE, Goonasekera SA, Boncompagni S, Kraev A, Gramolini AO, Dirksen RT, Franzini-Armstrong C, Seidman CE, Seidman JG, Maclennan DH. Zvaritch E, et al. Among authors: maclennan dh. Proc Natl Acad Sci U S A. 2007 Nov 20;104(47):18537-42. doi: 10.1073/pnas.0709312104. Epub 2007 Nov 14. Proc Natl Acad Sci U S A. 2007. PMID: 18003898 Free PMC article.

3

Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods.

Zvaritch E, Kraeva N, Bombardier E, McCloy RA, Depreux F, Holmyard D, Kraev A, Seidman CE, Seidman JG, Tupling AR, MacLennan DH. Zvaritch E, et al. Among authors: maclennan dh. Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21813-8. doi: 10.1073/pnas.0912126106. Epub 2009 Dec 3. Proc Natl Acad Sci U S A. 2009. PMID: 19959667 Free PMC article.

4

Muscle spindles exhibit core lesions and extensive degeneration of intrafusal fibers in the Ryr1(I4895T/wt) mouse model of core myopathy.

Zvaritch E, MacLennan DH. Zvaritch E, et al. Among authors: maclennan dh. Biochem Biophys Res Commun. 2015 Apr 24;460(1):34-9. doi: 10.1016/j.bbrc.2015.01.056. Epub 2015 Jan 22. Biochem Biophys Res Commun. 2015. PMID: 25619131

5

Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum.

Loy RE, Orynbayev M, Xu L, Andronache Z, Apostol S, Zvaritch E, MacLennan DH, Meissner G, Melzer W, Dirksen RT. Loy RE, et al. Among authors: maclennan dh. J Gen Physiol. 2011 Jan;137(1):43-57. doi: 10.1085/jgp.201010523. Epub 2010 Dec 13. J Gen Physiol. 2011. PMID: 21149547 Free PMC article.

6

Mechanistic models for muscle diseases and disorders originating in the sarcoplasmic reticulum.

Maclennan DH, Zvaritch E. Maclennan DH, et al. Biochim Biophys Acta. 2011 May;1813(5):948-64. doi: 10.1016/j.bbamcr.2010.11.009. Epub 2010 Nov 27. Biochim Biophys Acta. 2011. PMID: 21118704 Free article. Review.

7

Novel excitation-contraction uncoupled RYR1 mutations in patients with central core disease.

Kraeva N, Zvaritch E, Rossi AE, Goonasekera SA, Zaid H, Frodis W, Kraev A, Dirksen RT, Maclennan DH, Riazi S. Kraeva N, et al. Among authors: maclennan dh. Neuromuscul Disord. 2013 Feb;23(2):120-32. doi: 10.1016/j.nmd.2012.08.007. Epub 2012 Nov 24. Neuromuscul Disord. 2013. PMID: 23183335 Free PMC article.

8

Identification of biochemical adaptations in hyper- or hypocontractile hearts from phospholamban mutant mice by expression proteomics.

Pan Y, Kislinger T, Gramolini AO, Zvaritch E, Kranias EG, MacLennan DH, Emili A. Pan Y, et al. Among authors: maclennan dh. Proc Natl Acad Sci U S A. 2004 Feb 24;101(8):2241-6. doi: 10.1073/pnas.0308174101. Proc Natl Acad Sci U S A. 2004. PMID: 14982994 Free PMC article.

9

Crystal structure of type I ryanodine receptor amino-terminal beta-trefoil domain reveals a disease-associated mutation "hot spot" loop.

Amador FJ, Liu S, Ishiyama N, Plevin MJ, Wilson A, MacLennan DH, Ikura M. Amador FJ, et al. Among authors: maclennan dh. Proc Natl Acad Sci U S A. 2009 Jul 7;106(27):11040-4. doi: 10.1073/pnas.0905186106. Epub 2009 Jun 18. Proc Natl Acad Sci U S A. 2009. PMID: 19541610 Free PMC article.

10

CASQ1 gene is an unlikely candidate for malignant hyperthermia susceptibility in the North American population.

Kraeva N, Zvaritch E, Frodis W, Sizova O, Kraev A, MacLennan DH, Riazi S. Kraeva N, et al. Among authors: maclennan dh. Anesthesiology. 2013 Feb;118(2):344-9. doi: 10.1097/01.anes.0000530185.78660.da. Anesthesiology. 2013. PMID: 23460944

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