These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Alpha7beta1 integrin does not alleviate disease in a mouse model of limb girdle muscular dystrophy type 2F. Milner DJ; Kaufman SJ Am J Pathol; 2007 Feb; 170(2):609-19. PubMed ID: 17255329 [TBL] [Abstract][Full Text] [Related]
7. Valproic acid activates the PI3K/Akt/mTOR pathway in muscle and ameliorates pathology in a mouse model of Duchenne muscular dystrophy. Gurpur PB; Liu J; Burkin DJ; Kaufman SJ Am J Pathol; 2009 Mar; 174(3):999-1008. PubMed ID: 19179609 [TBL] [Abstract][Full Text] [Related]
8. Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin. Rooney JE; Welser JV; Dechert MA; Flintoff-Dye NL; Kaufman SJ; Burkin DJ J Cell Sci; 2006 Jun; 119(Pt 11):2185-95. PubMed ID: 16684813 [TBL] [Abstract][Full Text] [Related]
9. PTEN contributes to profound PI3K/Akt signaling pathway deregulation in dystrophin-deficient dog muscle. Feron M; Guevel L; Rouger K; Dubreil L; Arnaud MC; Ledevin M; Megeney LA; Cherel Y; Sakanyan V Am J Pathol; 2009 Apr; 174(4):1459-70. PubMed ID: 19264909 [TBL] [Abstract][Full Text] [Related]
10. Levels of α7 integrin and laminin-α2 are increased following prednisone treatment in the mdx mouse and GRMD dog models of Duchenne muscular dystrophy. Wuebbles RD; Sarathy A; Kornegay JN; Burkin DJ Dis Model Mech; 2013 Sep; 6(5):1175-84. PubMed ID: 23846963 [TBL] [Abstract][Full Text] [Related]
11. A growth stimulus is needed for IGF-1 to induce skeletal muscle hypertrophy in vivo. Shavlakadze T; Chai J; Maley K; Cozens G; Grounds G; Winn N; Rosenthal N; Grounds MD J Cell Sci; 2010 Mar; 123(Pt 6):960-71. PubMed ID: 20179101 [TBL] [Abstract][Full Text] [Related]
12. SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models. Mázala DA; Pratt SJP; Chen D; Molkentin JD; Lovering RM; Chin ER Am J Physiol Cell Physiol; 2015 May; 308(9):C699-709. PubMed ID: 25652448 [TBL] [Abstract][Full Text] [Related]
14. Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy. Guo C; Willem M; Werner A; Raivich G; Emerson M; Neyses L; Mayer U Hum Mol Genet; 2006 Mar; 15(6):989-98. PubMed ID: 16476707 [TBL] [Abstract][Full Text] [Related]
15. Perturbation of PI3K/Akt signaling affected autophagy modulation in dystrophin-deficient myoblasts. Yazid MD; Hung-Chih C Cell Commun Signal; 2021 Oct; 19(1):105. PubMed ID: 34706731 [TBL] [Abstract][Full Text] [Related]
17. PTRH2 gene mutation causes progressive congenital skeletal muscle pathology. Doe J; Kaindl AM; Jijiwa M; de la Vega M; Hu H; Griffiths GS; Fontelonga TM; Barraza P; Cruz V; Van Ry P; Ramos JW; Burkin DJ; Matter ML Hum Mol Genet; 2017 Apr; 26(8):1458-1464. PubMed ID: 28175314 [TBL] [Abstract][Full Text] [Related]
18. Expression of a NOS transgene in dystrophin-deficient muscle reduces muscle membrane damage without increasing the expression of membrane-associated cytoskeletal proteins. Tidball JG; Wehling-Henricks M Mol Genet Metab; 2004 Aug; 82(4):312-20. PubMed ID: 15308129 [TBL] [Abstract][Full Text] [Related]
19. Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy. Church JE; Trieu J; Chee A; Naim T; Gehrig SM; Lamon S; Angelini C; Russell AP; Lynch GS Exp Physiol; 2014 Apr; 99(4):675-87. PubMed ID: 24443351 [TBL] [Abstract][Full Text] [Related]
20. Altered activity of signaling pathways in diaphragm and tibialis anterior muscle of dystrophic mice. Lang JM; Esser KA; Dupont-Versteegden EE Exp Biol Med (Maywood); 2004 Jun; 229(6):503-11. PubMed ID: 15169969 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]