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Items: 1 to 20 of 57

1.

MicroRNAs promote skeletal muscle differentiation of mesodermal iPSC-derived progenitors.

Giacomazzi G, Holvoet B, Trenson S, Caluwé E, Kravic B, Grosemans H, Cortés-Calabuig Á, Deroose CM, Huylebroeck D, Hashemolhosseini S, Janssens S, McNally E, Quattrocelli M, Sampaolesi M.

Nat Commun. 2017 Nov 1;8(1):1249. doi: 10.1038/s41467-017-01359-w.

2.

Genetic modifiers of muscular dystrophy act on sarcolemmal resealing and recovery from injury.

Quattrocelli M, Capote J, Ohiri JC, Warner JL, Vo AH, Earley JU, Hadhazy M, Demonbreun AR, Spencer MJ, McNally EM.

PLoS Genet. 2017 Oct 24;13(10):e1007070. doi: 10.1371/journal.pgen.1007070. eCollection 2017 Oct.

3.

Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular Dystrophy


.

Nghiem PP, Bello L, Stoughton WB, López SM, Vidal AH, Hernandez BV, Hulbert KN, Gourley TR, Bettis AK, Balog-Alvarez CJ, Heath-Barnett H, Kornegay JN.

Yale J Biol Med. 2017 Sep 25;90(3):351-360. eCollection 2017 Sep.

4.

Creation of a Novel Humanized Dystrophic Mouse Model of Duchenne Muscular Dystrophy and Application of a CRISPR/Cas9 Gene Editing Therapy.

Young CS, Mokhonova E, Quinonez M, Pyle AD, Spencer MJ.

J Neuromuscul Dis. 2017;4(2):139-145. doi: 10.3233/JND-170218.

5.

Intermittent glucocorticoid steroid dosing enhances muscle repair without eliciting muscle atrophy.

Quattrocelli M, Barefield DY, Warner JL, Vo AH, Hadhazy M, Earley JU, Demonbreun AR, McNally EM.

J Clin Invest. 2017 Jun 1;127(6):2418-2432. doi: 10.1172/JCI91445. Epub 2017 May 8.

6.

Outside in: The matrix as a modifier of muscular dystrophy.

Quattrocelli M, Spencer MJ, McNally EM.

Biochim Biophys Acta. 2017 Mar;1864(3):572-579. doi: 10.1016/j.bbamcr.2016.12.020. Epub 2016 Dec 21. Review.

PMID:
28011285
7.

Severe murine limb-girdle muscular dystrophy type 2C pathology is diminished by FTY720 treatment.

Heydemann A.

Muscle Nerve. 2017 Sep;56(3):486-494. doi: 10.1002/mus.25503. Epub 2017 Mar 26.

8.

Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy.

Bello L, Flanigan KM, Weiss RB; United Dystrophinopathy Project, Spitali P, Aartsma-Rus A, Muntoni F, Zaharieva I, Ferlini A, Mercuri E, Tuffery-Giraud S, Claustres M, Straub V, Lochmüller H, Barp A, Vianello S, Pegoraro E, Punetha J, Gordish-Dressman H, Giri M, McDonald CM, Hoffman EP; Cooperative International Neuromuscular Research Group.

Am J Hum Genet. 2016 Nov 3;99(5):1163-1171. doi: 10.1016/j.ajhg.2016.08.023. Epub 2016 Oct 13.

9.

Genetic Background Limits Generalizability of Genotype-Phenotype Relationships.

Sittig LJ, Carbonetto P, Engel KA, Krauss KS, Barrios-Camacho CM, Palmer AA.

Neuron. 2016 Sep 21;91(6):1253-1259. doi: 10.1016/j.neuron.2016.08.013. Epub 2016 Sep 8.

10.

Overexpression of Latent TGFβ Binding Protein 4 in Muscle Ameliorates Muscular Dystrophy through Myostatin and TGFβ.

Lamar KM, Bogdanovich S, Gardner BB, Gao QQ, Miller T, Earley JU, Hadhazy M, Vo AH, Wren L, Molkentin JD, McNally EM.

PLoS Genet. 2016 May 5;12(5):e1006019. doi: 10.1371/journal.pgen.1006019. eCollection 2016 May.

11.

Muscular dystrophy in a dish: engineered human skeletal muscle mimetics for disease modeling and drug discovery.

Smith AST, Davis J, Lee G, Mack DL, Kim DH.

Drug Discov Today. 2016 Sep;21(9):1387-1398. doi: 10.1016/j.drudis.2016.04.013. Epub 2016 Apr 22. Review.

12.

Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype.

Capote J, Kramerova I, Martinez L, Vetrone S, Barton ER, Sweeney HL, Miceli MC, Spencer MJ.

J Cell Biol. 2016 Apr 25;213(2):275-88. doi: 10.1083/jcb.201510086. Epub 2016 Apr 18.

13.

Enhanced Muscular Dystrophy from Loss of Dysferlin Is Accompanied by Impaired Annexin A6 Translocation after Sarcolemmal Disruption.

Demonbreun AR, Allen MV, Warner JL, Barefield DY, Krishnan S, Swanson KE, Earley JU, McNally EM.

Am J Pathol. 2016 Jun;186(6):1610-22. doi: 10.1016/j.ajpath.2016.02.005. Epub 2016 Apr 9.

14.

Role of Transforming Growth Factor-β1 and Smads Signaling Pathway in Intrauterine Adhesion.

Salma U, Xue M, Ali Sheikh MS, Guan X, Xu B, Zhang A, Huang L, Xu D.

Mediators Inflamm. 2016;2016:4158287. doi: 10.1155/2016/4158287. Epub 2016 Feb 21.

15.

Effect of genetic background on the dystrophic phenotype in mdx mice.

Coley WD, Bogdanik L, Vila MC, Yu Q, Van Der Meulen JH, Rayavarapu S, Novak JS, Nearing M, Quinn JL, Saunders A, Dolan C, Andrews W, Lammert C, Austin A, Partridge TA, Cox GA, Lutz C, Nagaraju K.

Hum Mol Genet. 2016 Jan 1;25(1):130-45. doi: 10.1093/hmg/ddv460. Epub 2015 Nov 12.

16.

Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.

Barp A, Bello L, Politano L, Melacini P, Calore C, Polo A, Vianello S, Sorarù G, Semplicini C, Pantic B, Taglia A, Picillo E, Magri F, Gorni K, Messina S, Vita GL, Vita G, Comi GP, Ermani M, Calvo V, Angelini C, Hoffman EP, Pegoraro E.

PLoS One. 2015 Oct 29;10(10):e0141240. doi: 10.1371/journal.pone.0141240. eCollection 2015.

17.

The matrix protein Fibulin-5 is at the interface of tissue stiffness and inflammation in fibrosis.

Nakasaki M, Hwang Y, Xie Y, Kataria S, Gund R, Hajam EY, Samuel R, George R, Danda D, M J P, Nakamura T, Shen Z, Briggs S, Varghese S, Jamora C.

Nat Commun. 2015 Oct 15;6:8574. doi: 10.1038/ncomms9574.

18.

Modifier genes and their effect on Duchenne muscular dystrophy.

Vo AH, McNally EM.

Curr Opin Neurol. 2015 Oct;28(5):528-34. doi: 10.1097/WCO.0000000000000240. Review.

19.

Abnormal Activation of BMP Signaling Causes Myopathy in Fbn2 Null Mice.

Sengle G, Carlberg V, Tufa SF, Charbonneau NL, Smaldone S, Carlson EJ, Ramirez F, Keene DR, Sakai LY.

PLoS Genet. 2015 Jun 26;11(6):e1005340. doi: 10.1371/journal.pgen.1005340. eCollection 2015 Jun.

20.

Biochemical and Functional Comparisons of mdx and Sgcg(-/-) Muscular Dystrophy Mouse Models.

Roberts NW, Holley-Cuthrell J, Gonzalez-Vega M, Mull AJ, Heydemann A.

Biomed Res Int. 2015;2015:131436. doi: 10.1155/2015/131436. Epub 2015 May 3.

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