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Page 1
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity.
Pace RA, Peat RA, Baker NL, Zamurs L, Mörgelin M, Irving M, Adams NE, Bateman JF, Mowat D, Smith NJ, Lamont PJ, Moore SA, Mathews KD, North KN, Lamandé SR. Pace RA, et al. Among authors: bateman jf. Ann Neurol. 2008 Sep;64(3):294-303. doi: 10.1002/ana.21439. Ann Neurol. 2008. PMID: 18825676 Free PMC article.
Molecular consequences of dominant Bethlem myopathy collagen VI mutations.
Baker NL, Mörgelin M, Pace RA, Peat RA, Adams NE, Gardner RJ, Rowland LP, Miller G, De Jonghe P, Ceulemans B, Hannibal MC, Edwards M, Thompson EM, Jacobson R, Quinlivan RC, Aftimos S, Kornberg AJ, North KN, Bateman JF, Lamandé SR. Baker NL, et al. Among authors: bateman jf. Ann Neurol. 2007 Oct;62(4):390-405. doi: 10.1002/ana.21213. Ann Neurol. 2007. PMID: 17886299
Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophy.
Tooley LD, Zamurs LK, Beecher N, Baker NL, Peat RA, Adams NE, Bateman JF, North KN, Baldock C, Lamandé SR. Tooley LD, et al. Among authors: bateman jf. J Biol Chem. 2010 Oct 22;285(43):33567-33576. doi: 10.1074/jbc.M110.152520. Epub 2010 Aug 21. J Biol Chem. 2010. PMID: 20729548 Free PMC article.
The role of the alpha3(VI) chain in collagen VI assembly. Expression of an alpha3(VI) chain lacking N-terminal modules N10-N7 restores collagen VI assembly, secretion, and matrix deposition in an alpha3(VI)-deficient cell line.
Lamandé SR, Sigalas E, Pan TC, Chu ML, Dziadek M, Timpl R, Bateman JF. Lamandé SR, et al. Among authors: bateman jf. J Biol Chem. 1998 Mar 27;273(13):7423-30. doi: 10.1074/jbc.273.13.7423. J Biol Chem. 1998. PMID: 9516440 Free article.
211 results