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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1985 2
1986 1
1987 2
1988 2
1989 3
1990 3
1991 6
1992 4
1993 9
1994 6
1995 5
1996 10
1997 5
1998 4
1999 6
2000 10
2001 6
2002 13
2003 7
2004 7
2005 11
2006 7
2007 12
2008 16
2009 9
2010 13
2011 6
2012 6
2013 7
2014 7
2015 6
2016 5
2017 4
2018 9
2019 6
2020 5
2021 2
2022 3
2023 15
2024 2

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249 results

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Page 1
PCYT2-regulated lipid biosynthesis is critical to muscle health and ageing.
Cikes D, Elsayad K, Sezgin E, Koitai E, Torma F, Orthofer M, Yarwood R, Heinz LX, Sedlyarov V, Miranda ND, Taylor A, Grapentine S, Al-Murshedi F, Abot A, Weidinger A, Kutchukian C, Sanchez C, Cronin SJF, Novatchkova M, Kavirayani A, Schuetz T, Haubner B, Haas L, Hagelkruys A, Jackowski S, Kozlov AV, Jacquemond V, Knauf C, Superti-Furga G, Rullman E, Gustafsson T, McDermot J, Lowe M, Radak Z, Chamberlain JS, Bakovic M, Banka S, Penninger JM. Cikes D, et al. Among authors: chamberlain js. Nat Metab. 2023 Mar;5(3):495-515. doi: 10.1038/s42255-023-00766-2. Epub 2023 Mar 20. Nat Metab. 2023. PMID: 36941451
Assessment of systemic AAV-microdystrophin gene therapy in the GRMD model of Duchenne muscular dystrophy.
Birch SM, Lawlor MW, Conlon TJ, Guo LJ, Crudele JM, Hawkins EC, Nghiem PP, Ahn M, Meng H, Beatka MJ, Fickau BA, Prieto JC, Styner MA, Struharik MJ, Shanks C, Brown KJ, Golebiowski D, Bettis AK, Balog-Alvarez CJ, Clement N, Coleman KE, Corti M, Pan X, Hauschka SD, Gonzalez JP, Morris CA, Schneider JS, Duan D, Chamberlain JS, Byrne BJ, Kornegay JN. Birch SM, et al. Among authors: chamberlain js. Sci Transl Med. 2023 Jan 4;15(677):eabo1815. doi: 10.1126/scitranslmed.abo1815. Epub 2023 Jan 4. Sci Transl Med. 2023. PMID: 36599002
Micro-dystrophin gene therapy demonstrates long-term cardiac efficacy in a severe Duchenne muscular dystrophy model.
Piepho AB, Lowe J, Cumby LR, Dorn LE, Lake DM, Rastogi N, Gertzen MD, Sturgill SL, Odom GL, Ziolo MT, Accornero F, Chamberlain JS, Rafael-Fortney JA. Piepho AB, et al. Among authors: chamberlain js. Mol Ther Methods Clin Dev. 2023 Feb 9;28:344-354. doi: 10.1016/j.omtm.2023.02.001. eCollection 2023 Mar 9. Mol Ther Methods Clin Dev. 2023. PMID: 36874243 Free PMC article.
Clinical potential of microdystrophin as a surrogate endpoint.
Boehler JF, Brown KJ, Beatka M, Gonzalez JP, Donisa Dreghici R, Soustek-Kramer M, McGonigle S, Ganot A, Palmer T, Lowie C, Chamberlain JS, Lawlor MW, Morris CA. Boehler JF, et al. Among authors: chamberlain js. Neuromuscul Disord. 2023 Jan;33(1):40-49. doi: 10.1016/j.nmd.2022.12.007. Epub 2022 Dec 14. Neuromuscul Disord. 2023. PMID: 36575103 Free article. Review.
Duchenne muscular dystrophy.
Chamberlain JS. Chamberlain JS. Curr Opin Genet Dev. 1991 Jun;1(1):11-4. doi: 10.1016/0959-437x(91)80033-i. Curr Opin Genet Dev. 1991. PMID: 1840869 Free article. Review.
Viral vector-mediated gene therapies.
Hollinger K, Chamberlain JS. Hollinger K, et al. Among authors: chamberlain js. Curr Opin Neurol. 2015 Oct;28(5):522-7. doi: 10.1097/WCO.0000000000000241. Curr Opin Neurol. 2015. PMID: 26263476 Free PMC article. Review.
AAV-based gene therapies for the muscular dystrophies.
Crudele JM, Chamberlain JS. Crudele JM, et al. Among authors: chamberlain js. Hum Mol Genet. 2019 Oct 1;28(R1):R102-R107. doi: 10.1093/hmg/ddz128. Hum Mol Genet. 2019. PMID: 31238336 Free PMC article. Review.
249 results