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Items: 1 to 50 of 60

1.

A genetic mouse model of severe iron-deficiency anemia reveals tissue-specific transcriptional stress responses and cardiac remodeling.

Schwartz AJ, Converso-Baran K, Michele DE, Shah YM.

J Biol Chem. 2019 Aug 15. pii: jbc.RA119.009578. doi: 10.1074/jbc.RA119.009578. [Epub ahead of print]

2.

Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients.

Eisen B, Ben Jehuda R, Cuttitta AJ, Mekies LN, Shemer Y, Baskin P, Reiter I, Willi L, Freimark D, Gherghiceanu M, Monserrat L, Scherr M, Hilfiker-Kleiner D, Arad M, Michele DE, Binah O.

J Cell Mol Med. 2019 Mar;23(3):2125-2135. doi: 10.1111/jcmm.14124. Epub 2019 Jan 8.

3.

Fibro-Adipogenic Remodeling of the Diaphragm in Obesity-Associated Respiratory Dysfunction.

Buras ED, Converso-Baran K, Davis CS, Akama T, Hikage F, Michele DE, Brooks SV, Chun TH.

Diabetes. 2019 Jan;68(1):45-56. doi: 10.2337/db18-0209. Epub 2018 Oct 25.

4.

Generation of Duchenne muscular dystrophy patient-specific induced pluripotent stem cell line lacking exons 45-50 of the dystrophin gene (IITi001-A).

Eisen B, Ben Jehuda R, Cuttitta AJ, Mekies LN, Reiter I, Ramchandren S, Arad M, Michele DE, Binah O.

Stem Cell Res. 2018 May;29:111-114. doi: 10.1016/j.scr.2018.03.023. Epub 2018 Apr 3.

5.

Potential association of LMNA-associated generalized lipodystrophy with juvenile dermatomyositis.

Sahinoz M, Khairi S, Cuttitta A, Brady GF, Rupani A, Meral R, Tayeh MK, Thomas P, Riebschleger M, Camelo-Piragua S, Innis JW, Bishr Omary M, Michele DE, Oral EA.

Clin Diabetes Endocrinol. 2018 Mar 27;4:6. doi: 10.1186/s40842-018-0058-3. eCollection 2018.

6.

Ensuring due process in the IACUC and animal welfare setting: considerations in developing noncompliance policies and procedures for institutional animal care and use committees and institutional officials.

Hansen BC, Gografe S, Pritt S, Jen KC, McWhirter CA, Barman SM, Comuzzie A, Greene M, McNulty JA, Michele DE, Moaddab N, Nelson RJ, Norris K, Uray KD, Banks R, Westlund KN, Yates BJ, Silverman J, Hansen KD, Redman B.

FASEB J. 2017 Oct;31(10):4216-4225. doi: 10.1096/fj.201601250R. Epub 2017 Aug 15. Review.

7.

Dilated cardiomyopathy mutations in δ-sarcoglycan exert a dominant-negative effect on cardiac myocyte mechanical stability.

Campbell MD, Witcher M, Gopal A, Michele DE.

Am J Physiol Heart Circ Physiol. 2016 May 1;310(9):H1140-50. doi: 10.1152/ajpheart.00521.2015. Epub 2016 Mar 11.

8.

Differential protein expression and basal lamina remodeling in human heart failure.

Kim EH, Galchev VI, Kim JY, Misek SA, Stevenson TK, Campbell MD, Pagani FD, Day SM, Johnson TC, Washburn JG, Vikstrom KL, Michele DE, Misek DE, Westfall MV.

Proteomics Clin Appl. 2016 May;10(5):585-96. doi: 10.1002/prca.201500099. Epub 2016 Jan 25.

9.

Dystrophin-glycoprotein complex regulates muscle nitric oxide production through mechanoregulation of AMPK signaling.

Garbincius JF, Michele DE.

Proc Natl Acad Sci U S A. 2015 Nov 3;112(44):13663-8. doi: 10.1073/pnas.1512991112. Epub 2015 Oct 19.

10.

Voluntary Exercise Improves Estrous Cyclicity in Prenatally Androgenized Female Mice Despite Programming Decreased Voluntary Exercise: Implications for Polycystic Ovary Syndrome (PCOS).

Homa LD, Burger LL, Cuttitta AJ, Michele DE, Moenter SM.

Endocrinology. 2015 Dec;156(12):4618-28. doi: 10.1210/en.2015-1593. Epub 2015 Sep 10.

11.

Proinflammatory effects of interferon gamma in mouse adenovirus 1 myocarditis.

McCarthy MK, Procario MC, Twisselmann N, Wilkinson JE, Archambeau AJ, Michele DE, Day SM, Weinberg JB.

J Virol. 2015 Jan;89(1):468-79. doi: 10.1128/JVI.02077-14. Epub 2014 Oct 15.

12.

Prevalence of lesions detected at upper endoscopy: an Italian survey.

Zullo A, Esposito G, Ridola L, Hassan C, Lahner E, Perri F, Bianco MA, De Francesco V, Buscarini E, Di Giulio E, Annibale B; AIGO-SIED study group; AIGO-SIED study group.

Eur J Intern Med. 2014 Oct;25(8):772-6. doi: 10.1016/j.ejim.2014.08.010. Epub 2014 Sep 20.

PMID:
25245606
13.

Rapid actin-cytoskeleton-dependent recruitment of plasma membrane-derived dysferlin at wounds is critical for muscle membrane repair.

McDade JR, Archambeau A, Michele DE.

FASEB J. 2014 Aug;28(8):3660-70. doi: 10.1096/fj.14-250191. Epub 2014 May 1.

14.

Conditional knockout of pik3c3 causes a murine muscular dystrophy.

Reifler A, Li X, Archambeau AJ, McDade JR, Sabha N, Michele DE, Dowling JJ.

Am J Pathol. 2014 Jun;184(6):1819-30. doi: 10.1016/j.ajpath.2014.02.012. Epub 2014 Apr 13.

15.

Membrane-myofibril cross-talk in myofibrillogenesis and in muscular dystrophy pathogenesis: lessons from the zebrafish.

Raeker MÖ, Shavit JA, Dowling JJ, Michele DE, Russell MW.

Front Physiol. 2014 Jan 28;5:14. doi: 10.3389/fphys.2014.00014. eCollection 2014.

16.

Membrane damage-induced vesicle-vesicle fusion of dysferlin-containing vesicles in muscle cells requires microtubules and kinesin.

McDade JR, Michele DE.

Hum Mol Genet. 2014 Apr 1;23(7):1677-86. doi: 10.1093/hmg/ddt557. Epub 2013 Nov 7.

17.

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.

Cirak S, Foley AR, Herrmann R, Willer T, Yau S, Stevens E, Torelli S, Brodd L, Kamynina A, Vondracek P, Roper H, Longman C, Korinthenberg R, Marrosu G, Nürnberg P; UK10K Consortium, Michele DE, Plagnol V, Hurles M, Moore SA, Sewry CA, Campbell KP, Voit T, Muntoni F.

Brain. 2013 Jan;136(Pt 1):269-81. doi: 10.1093/brain/aws312. Epub 2013 Jan 3.

18.

Muscle-specific expression of LARGE restores neuromuscular transmission deficits in dystrophic LARGE(myd) mice.

Gumerson JD, Davis CS, Kabaeva ZT, Hayes JM, Brooks SV, Michele DE.

Hum Mol Genet. 2013 Feb 15;22(4):757-68. doi: 10.1093/hmg/dds483. Epub 2012 Dec 6.

19.

The dystrophin-glycoprotein complex in the prevention of muscle damage.

Gumerson JD, Michele DE.

J Biomed Biotechnol. 2011;2011:210797. doi: 10.1155/2011/210797. Epub 2011 Oct 5. Review.

20.

Sarcolemma instability during mechanical activity in Largemyd cardiac myocytes with loss of dystroglycan extracellular matrix receptor function.

Kabaeva Z, Meekhof KE, Michele DE.

Hum Mol Genet. 2011 Sep 1;20(17):3346-55. doi: 10.1093/hmg/ddr240. Epub 2011 May 30.

21.

COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans.

Labelle-Dumais C, Dilworth DJ, Harrington EP, de Leau M, Lyons D, Kabaeva Z, Manzini MC, Dobyns WB, Walsh CA, Michele DE, Gould DB.

PLoS Genet. 2011 May;7(5):e1002062. doi: 10.1371/journal.pgen.1002062. Epub 2011 May 19.

22.

Altering α-dystroglycan receptor affinity of LCMV pseudotyped lentivirus yields unique cell and tissue tropism.

Dylla DE, Xie L, Michele DE, Kunz S, McCray PB Jr.

Genet Vaccines Ther. 2011 Apr 8;9:8. doi: 10.1186/1479-0556-9-8.

23.

Lateral transmission of force is impaired in skeletal muscles of dystrophic mice and very old rats.

Ramaswamy KS, Palmer ML, van der Meulen JH, Renoux A, Kostrominova TY, Michele DE, Faulkner JA.

J Physiol. 2011 Mar 1;589(Pt 5):1195-208. doi: 10.1113/jphysiol.2010.201921. Epub 2011 Jan 10.

24.

Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I.

Mathews KD, Stephan CM, Laubenthal K, Winder TL, Michele DE, Moore SA, Campbell KP.

Neurology. 2011 Jan 11;76(2):194-5. doi: 10.1212/WNL.0b013e3182061ad4. No abstract available.

25.

Soleus muscle in glycosylation-deficient muscular dystrophy is protected from contraction-induced injury.

Gumerson JD, Kabaeva ZT, Davis CS, Faulkner JA, Michele DE.

Am J Physiol Cell Physiol. 2010 Dec;299(6):C1430-40. doi: 10.1152/ajpcell.00192.2010. Epub 2010 Sep 15.

26.

Inhibition of calpain prevents muscle weakness and disruption of sarcomere structure during hindlimb suspension.

Salazar JJ, Michele DE, Brooks SV.

J Appl Physiol (1985). 2010 Jan;108(1):120-7. doi: 10.1152/japplphysiol.01080.2009. Epub 2009 Nov 5.

27.

Identification of alpha-dystroglycan binding sequences in the laminin alpha2 chain LG4-5 module.

Suzuki N, Hozumi K, Urushibata S, Yoshimura T, Kikkawa Y, Gumerson JD, Michele DE, Hoffman MP, Yamada Y, Nomizu M.

Matrix Biol. 2010 Mar;29(2):143-51. doi: 10.1016/j.matbio.2009.09.006. Epub 2009 Sep 29.

28.

Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage.

Michele DE, Kabaeva Z, Davis SL, Weiss RM, Campbell KP.

Circ Res. 2009 Nov 6;105(10):984-93. doi: 10.1161/CIRCRESAHA.109.199489. Epub 2009 Sep 24.

29.

Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan.

Han R, Kanagawa M, Yoshida-Moriguchi T, Rader EP, Ng RA, Michele DE, Muirhead DE, Kunz S, Moore SA, Iannaccone ST, Miyake K, McNeil PL, Mayer U, Oldstone MB, Faulkner JA, Campbell KP.

Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12573-9. doi: 10.1073/pnas.0906545106. Epub 2009 Jul 24.

30.

Basolateral entry and release of New and Old World arenaviruses from human airway epithelia.

Dylla DE, Michele DE, Campbell KP, McCray PB Jr.

J Virol. 2008 Jun;82(12):6034-8. doi: 10.1128/JVI.00100-08. Epub 2008 Apr 16.

31.

Blebbistatin extends culture life of adult mouse cardiac myocytes and allows efficient and stable transgene expression.

Kabaeva Z, Zhao M, Michele DE.

Am J Physiol Heart Circ Physiol. 2008 Apr;294(4):H1667-74. doi: 10.1152/ajpheart.01144.2007. Epub 2008 Feb 22.

32.

Limb-girdle muscular dystrophy in the United States.

Moore SA, Shilling CJ, Westra S, Wall C, Wicklund MP, Stolle C, Brown CA, Michele DE, Piccolo F, Winder TL, Stence A, Barresi R, King N, King W, Florence J, Campbell KP, Fenichel GM, Stedman HH, Kissel JT, Griggs RC, Pandya S, Mathews KD, Pestronk A, Serrano C, Darvish D, Mendell JR.

J Neuropathol Exp Neurol. 2006 Oct;65(10):995-1003.

PMID:
17021404
33.

Interactions of intermediate filament protein synemin with dystrophin and utrophin.

Bhosle RC, Michele DE, Campbell KP, Li Z, Robson RM.

Biochem Biophys Res Commun. 2006 Aug 4;346(3):768-77. Epub 2006 Jun 9.

PMID:
16777071
34.

Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function.

Kanagawa M, Michele DE, Satz JS, Barresi R, Kusano H, Sasaki T, Timpl R, Henry MD, Campbell KP.

FEBS Lett. 2005 Aug 29;579(21):4792-6.

35.

Dystrophic heart failure blocked by membrane sealant poloxamer.

Yasuda S, Townsend D, Michele DE, Favre EG, Day SM, Metzger JM.

Nature. 2005 Aug 18;436(7053):1025-9. Epub 2005 Jul 17.

36.

Parvalbumin gene delivery improves diastolic function in the aged myocardium in vivo.

Michele DE, Szatkowski ML, Albayya FP, Metzger JM.

Mol Ther. 2004 Aug;10(2):399-403.

37.

Molecular recognition by LARGE is essential for expression of functional dystroglycan.

Kanagawa M, Saito F, Kunz S, Yoshida-Moriguchi T, Barresi R, Kobayashi YM, Muschler J, Dumanski JP, Michele DE, Oldstone MB, Campbell KP.

Cell. 2004 Jun 25;117(7):953-64.

38.

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP.

Nat Med. 2004 Jul;10(7):696-703. Epub 2004 Jun 6.

39.

POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.

Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, Sakuta R, Mochizuki M, Michele DE, Campbell KP, Nonaka I, Nishino I.

Neurology. 2004 Mar 23;62(6):1009-11.

PMID:
15037715
40.

Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.

Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP.

Proc Natl Acad Sci U S A. 2003 Jul 22;100(15):8910-5. Epub 2003 Jul 8.

41.

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

Michele DE, Campbell KP.

J Biol Chem. 2003 May 2;278(18):15457-60. Epub 2003 Jan 29. Review. No abstract available.

42.

Sarcomere thin filament regulatory isoforms. Evidence of a dominant effect of slow skeletal troponin I on cardiac contraction.

Metzger JM, Michele DE, Rust EM, Borton AR, Westfall MV.

J Biol Chem. 2003 Apr 11;278(15):13118-23. Epub 2003 Jan 27.

43.

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, Williamson RA, Campbell KP.

Cell. 2002 Sep 6;110(5):639-48.

44.
45.

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

Moore SA, Saito F, Chen J, Michele DE, Henry MD, Messing A, Cohn RD, Ross-Barta SE, Westra S, Williamson RA, Hoshi T, Campbell KP.

Nature. 2002 Jul 25;418(6896):422-5.

PMID:
12140559
46.

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.

Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP.

Nature. 2002 Jul 25;418(6896):417-22.

PMID:
12140558
47.

Divergent abnormal muscle relaxation by hypertrophic cardiomyopathy and nemaline myopathy mutant tropomyosins.

Michele DE, Coutu P, Metzger JM.

Physiol Genomics. 2002;9(2):103-11. Epub 2002 Mar 26.

PMID:
12006676
48.

IDAF (intensity-duration-area frequency) curves of extreme storm rainfall: a scaling approach.

De MC, Kottegoda NT, Rosso R.

Water Sci Technol. 2002;45(2):83-90.

PMID:
11888186
49.
50.

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