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Items: 1 to 20 of 106

1.

Non-redundant function of dystroglycan and β1 integrins in radial sorting of axons.

Berti C, Bartesaghi L, Ghidinelli M, Zambroni D, Figlia G, Chen ZL, Quattrini A, Wrabetz L, Feltri ML.

Development. 2011 Sep;138(18):4025-37. doi: 10.1242/dev.065490.

2.

Expression of laminin receptors in schwann cell differentiation: evidence for distinct roles.

Previtali SC, Nodari A, Taveggia C, Pardini C, Dina G, Villa A, Wrabetz L, Quattrini A, Feltri ML.

J Neurosci. 2003 Jul 2;23(13):5520-30.

3.

Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice.

Saito F, Masaki T, Saito Y, Nakamura A, Takeda S, Shimizu T, Toda T, Matsumura K.

J Neurochem. 2007 Jun;101(6):1712-22. Epub 2007 Feb 26.

4.

α6β1 and α7β1 integrins are required in Schwann cells to sort axons.

Pellegatta M, De Arcangelis A, D'Urso A, Nodari A, Zambroni D, Ghidinelli M, Matafora V, Williamson C, Georges-Labouesse E, Kreidberg J, Mayer U, McKee KK, Yurchenco PD, Quattrini A, Wrabetz L, Feltri ML.

J Neurosci. 2013 Nov 13;33(46):17995-8007. doi: 10.1523/JNEUROSCI.3179-13.2013.

5.

Beta1 integrin activates Rac1 in Schwann cells to generate radial lamellae during axonal sorting and myelination.

Nodari A, Zambroni D, Quattrini A, Court FA, D'Urso A, Recchia A, Tybulewicz VL, Wrabetz L, Feltri ML.

J Cell Biol. 2007 Jun 18;177(6):1063-75.

6.

Conditional disruption of beta 1 integrin in Schwann cells impedes interactions with axons.

Feltri ML, Graus Porta D, Previtali SC, Nodari A, Migliavacca B, Cassetti A, Littlewood-Evans A, Reichardt LF, Messing A, Quattrini A, Mueller U, Wrabetz L.

J Cell Biol. 2002 Jan 7;156(1):199-209. Epub 2002 Jan 3.

7.

Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.

Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, Endo T, Kobayashi K, Campbell KP, Toda T.

Hum Mol Genet. 2009 Feb 15;18(4):621-31. doi: 10.1093/hmg/ddn387. Epub 2008 Nov 18.

8.

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.

Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, Khalil N, Feng L, Saran RK, Voit T, Merlini L, Sewry CA, Brown SC, Muntoni F.

Hum Mol Genet. 2003 Nov 1;12(21):2853-61. Epub 2003 Sep 9.

PMID:
12966029
9.

Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier.

Occhi S, Zambroni D, Del Carro U, Amadio S, Sirkowski EE, Scherer SS, Campbell KP, Moore SA, Chen ZL, Strickland S, Di Muzio A, Uncini A, Wrabetz L, Feltri ML.

J Neurosci. 2005 Oct 12;25(41):9418-27.

10.

Giant scaffolding protein AHNAK1 interacts with β-dystroglycan and controls motility and mechanical properties of Schwann cells.

von Boxberg Y, Soares S, Féréol S, Fodil R, Bartolami S, Taxi J, Tricaud N, Nothias F.

Glia. 2014 Sep;62(9):1392-406. doi: 10.1002/glia.22685. Epub 2014 May 3.

PMID:
24796807
11.

Identification of dystroglycan as a second laminin receptor in oligodendrocytes, with a role in myelination.

Colognato H, Galvin J, Wang Z, Relucio J, Nguyen T, Harrison D, Yurchenco PD, Ffrench-Constant C.

Development. 2007 May;134(9):1723-36. Epub 2007 Mar 29.

12.

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.

Brockington M, Blake DJ, Prandini P, Brown SC, Torelli S, Benson MA, Ponting CP, Estournet B, Romero NB, Mercuri E, Voit T, Sewry CA, Guicheney P, Muntoni F.

Am J Hum Genet. 2001 Dec;69(6):1198-209. Epub 2001 Oct 8.

13.

Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of α-dystroglycan.

Kuga A, Kanagawa M, Sudo A, Chan YM, Tajiri M, Manya H, Kikkawa Y, Nomizu M, Kobayashi K, Endo T, Lu QL, Wada Y, Toda T.

J Biol Chem. 2012 Mar 16;287(12):9560-7. doi: 10.1074/jbc.M111.271767. Epub 2012 Jan 23.

14.

Lck tyrosine kinase mediates β1-integrin signalling to regulate Schwann cell migration and myelination.

Ness JK, Snyder KM, Tapinos N.

Nat Commun. 2013;4:1912. doi: 10.1038/ncomms2928.

15.

Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy.

Brockington M, Torelli S, Prandini P, Boito C, Dolatshad NF, Longman C, Brown SC, Muntoni F.

Hum Mol Genet. 2005 Mar 1;14(5):657-65. Epub 2005 Jan 20.

PMID:
15661757
16.

Zebrafish models for human FKRP muscular dystrophies.

Kawahara G, Guyon JR, Nakamura Y, Kunkel LM.

Hum Mol Genet. 2010 Feb 15;19(4):623-33. doi: 10.1093/hmg/ddp528. Epub 2009 Dec 1.

17.

Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP).

Thornhill P, Bassett D, Lochmüller H, Bushby K, Straub V.

Brain. 2008 Jun;131(Pt 6):1551-61. doi: 10.1093/brain/awn078. Epub 2008 May 13.

PMID:
18477595
18.

Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy.

Beedle AM, Turner AJ, Saito Y, Lueck JD, Foltz SJ, Fortunato MJ, Nienaber PM, Campbell KP.

J Clin Invest. 2012 Sep;122(9):3330-42. doi: 10.1172/JCI63004. Epub 2012 Aug 27.

19.

Distinct roles for laminin globular domains in laminin alpha1 chain mediated rescue of murine laminin alpha2 chain deficiency.

Gawlik KI, Akerlund M, Carmignac V, Elamaa H, Durbeej M.

PLoS One. 2010 Jul 19;5(7):e11549. doi: 10.1371/journal.pone.0011549.

20.

A laminin-2, dystroglycan, utrophin axis is required for compartmentalization and elongation of myelin segments.

Court FA, Hewitt JE, Davies K, Patton BL, Uncini A, Wrabetz L, Feltri ML.

J Neurosci. 2009 Mar 25;29(12):3908-19. doi: 10.1523/JNEUROSCI.5672-08.2009.

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