Dystrophin-glycoprotein complex: Post-translational processing and dystroglycan function

被引：325

作者：

Michele, DE

Campbell, KP

机构：

[1] Univ Iowa, Howard Hughes Med Inst, Dept Physiol & Biophys, Iowa City, IA 52242 USA

[2] Univ Iowa, Dept Neurol, Carver Coll Med, Iowa City, IA 52242 USA

来源：

JOURNAL OF BIOLOGICAL CHEMISTRY | 2003年 / 278卷 / 18期

关键词：

D O I：

10.1074/jbc.R200031200

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：15457 / 15460

页数：4

共 66 条

[1] The fukutin protein family - predicted enzymes modifying cell-surface molecules [J].

Aravind, L ;

Koonin, EV .

CURRENT BIOLOGY, 1999, 9 (22) :R836-R837

[2] Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies [J].

Bardoni, A ;

Felisari, G ;

Sironi, M ;

Comi, G ;

Lai, M ;

Robotti, M ;

Bresolin, N .

NEUROMUSCULAR DISORDERS, 2000, 10 (03) :194-199

[3] Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome [J].

Beltran-Valero de Bernabé, D ;

Currier, S ;

Steinbrecher, A ;

Celli, J ;

van Beusekom, E ;

van der Zwaag, B ;

Kayserili, H ;

Merlini, L ;

Chitayat, D ;

Dobyns, WB ;

Cormand, B ;

Lehesjoki, AE ;

Cruces, J ;

Voit, T ;

Walsh, CA ;

van Bokhoven, H ;

Brunner, HG .

AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (05) :1033-1043

[4] IDENTIFICATION AND PURIFICATION OF AN AGRIN RECEPTOR FROM TORPEDO POSTSYNAPTIC MEMBRANES - A HETEROMERIC COMPLEX RELATED TO THE DYSTROGLYCANS [J].

BOWE, MA ;

DEYST, KA ;

LESZYK, JD ;

FALLON, JR .

NEURON, 1994, 12 (05) :1173-1180

[5] ELECTRON-MICROSCOPIC EVIDENCE FOR A MUCIN-LIKE REGION IN CHICK MUSCLE ALPHA-DYSTROGLYCAN [J].

BRANCACCIO, A ;

SCHULTHESS, T ;

GESEMANN, M ;

ENGEL, J .

FEBS LETTERS, 1995, 368 (01) :139-142

[6] Knocking signalling out of the dystrophin complex [J].

Bredt, DS .

NATURE CELL BIOLOGY, 1999, 1 (04) :E89-E91

[7] Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C [J].

Brockington, M ;

Yuva, Y ;

Prandini, P ;

Brown, SC ;

Torelli, S ;

Benson, MA ;

Herrmann, R ;

Anderson, LVB ;

Bashir, R ;

Burgunder, JM ;

Fallet, S ;

Romero, N ;

Fardeau, M ;

Straub, V ;

Storey, G ;

Pollitt, C ;

Richard, I ;

Sewry, CA ;

Bushby, K ;

Voit, T ;

Blake, DJ ;

Muntoni, F .

HUMAN MOLECULAR GENETICS, 2001, 10 (25) :2851-2859

[8] Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin α2 deficiency and abnormal glycosylation of α-dystroglycan [J].

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 .

AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (06) :1198-1209

[9] Enhanced expression of the α7β1 integrin reduces muscular dystrophy and restores viability in dystrophic mice [J].

Burkin, DJ ;

Wallace, GQ ;

Nicol, KJ ;

Kaufman, DJ ;

Kaufman, SJ .

JOURNAL OF CELL BIOLOGY, 2001, 152 (06) :1207-1218

[10] ROLE FOR DYSTROPHIN-ASSOCIATED GLYCOPROTEINS AND UTROPHIN IN AGRIN-INDUCED ACHR CLUSTERING [J].

CAMPANELLI, JT ;

ROBERDS, SL ;

CAMPBELL, KP ;

SCHELLER, RH .

CELL, 1994, 77 (05) :663-674

← 1 2 3 4 5 6 7 →