136 related articles for article (PubMed ID: 15326183)
1. The structure of the N-terminal region of murine skeletal muscle alpha-dystroglycan discloses a modular architecture.
Bozic D; Sciandra F; Lamba D; Brancaccio A
J Biol Chem; 2004 Oct; 279(43):44812-6. PubMed ID: 15326183
[TBL] [Abstract][Full Text] [Related]
2. A second Ig-like domain identified in dystroglycan by molecular modelling and dynamics.
De Rosa MC; Pirolli D; Bozzi M; Sciandra F; Giardina B; Brancaccio A
J Mol Graph Model; 2011 Aug; 29(8):1015-24. PubMed ID: 21605994
[TBL] [Abstract][Full Text] [Related]
3. α-dystroglycan is a potential target of matrix metalloproteinase MMP-2.
Sbardella D; Sciandra F; Gioia M; Marini S; Gori A; Giardina B; Tarantino U; Coletta M; Brancaccio A; Bozzi M
Matrix Biol; 2015 Jan; 41():2-7. PubMed ID: 25483986
[TBL] [Abstract][Full Text] [Related]
4. An extracellular pathway for dystroglycan function in acetylcholine receptor aggregation and laminin deposition in skeletal myotubes.
Tremblay MR; Carbonetto S
J Biol Chem; 2006 May; 281(19):13365-13373. PubMed ID: 16531403
[TBL] [Abstract][Full Text] [Related]
5. In vitro developmental expression of dystroglycan and laminin-alpha2 in human skeletal muscle.
Chen L; Burgunder JM
Cell Biol Int; 2005 Jul; 29(7):506-13. PubMed ID: 15982904
[TBL] [Abstract][Full Text] [Related]
6. An evaluation of the evolution of the gene structure of dystroglycan.
Brancaccio A; Adams JC
BMC Res Notes; 2017 Jan; 10(1):19. PubMed ID: 28057052
[TBL] [Abstract][Full Text] [Related]
7. Binding of laminin alpha1-chain LG4-5 domain to alpha-dystroglycan causes tyrosine phosphorylation of syntrophin to initiate Rac1 signaling.
Zhou YW; Thomason DB; Gullberg D; Jarrett HW
Biochemistry; 2006 Feb; 45(7):2042-52. PubMed ID: 16475793
[TBL] [Abstract][Full Text] [Related]
8. The Structure of the T190M Mutant of Murine α-Dystroglycan at High Resolution: Insight into the Molecular Basis of a Primary Dystroglycanopathy.
Bozzi M; Cassetta A; Covaceuszach S; Bigotti MG; Bannister S; Hübner W; Sciandra F; Lamba D; Brancaccio A
PLoS One; 2015; 10(5):e0124277. PubMed ID: 25932631
[TBL] [Abstract][Full Text] [Related]
9. Dystroglycan is not required for localization of dystrophin, syntrophin, and neuronal nitric-oxide synthase at the sarcolemma but regulates integrin alpha 7B expression and caveolin-3 distribution.
Côté PD; Moukhles H; Carbonetto S
J Biol Chem; 2002 Feb; 277(7):4672-9. PubMed ID: 11741881
[TBL] [Abstract][Full Text] [Related]
10. Distinct requirements for heparin and alpha-dystroglycan binding revealed by structure-based mutagenesis of the laminin alpha2 LG4-LG5 domain pair.
Wizemann H; Garbe JH; Friedrich MV; Timpl R; Sasaki T; Hohenester E
J Mol Biol; 2003 Sep; 332(3):635-42. PubMed ID: 12963372
[TBL] [Abstract][Full Text] [Related]
11. High degree of conservation of the enzymes synthesizing the laminin-binding glycoepitope of α-dystroglycan.
Bigotti MG; Brancaccio A
Open Biol; 2021 Sep; 11(9):210104. PubMed ID: 34582712
[TBL] [Abstract][Full Text] [Related]
12. Structural basis of laminin binding to the LARGE glycans on dystroglycan.
Briggs DC; Yoshida-Moriguchi T; Zheng T; Venzke D; Anderson ME; Strazzulli A; Moracci M; Yu L; Hohenester E; Campbell KP
Nat Chem Biol; 2016 Oct; 12(10):810-4. PubMed ID: 27526028
[TBL] [Abstract][Full Text] [Related]
13. Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy.
Saito F; Blank M; Schröder J; Manya H; Shimizu T; Campbell KP; Endo T; Mizutani M; Kröger S; Matsumura K
FEBS Lett; 2005 Apr; 579(11):2359-63. PubMed ID: 15848172
[TBL] [Abstract][Full Text] [Related]
14. The N-terminal region of alpha-dystroglycan is an autonomous globular domain.
Brancaccio A; Schulthess T; Gesemann M; Engel J
Eur J Biochem; 1997 May; 246(1):166-72. PubMed ID: 9210479
[TBL] [Abstract][Full Text] [Related]
15. Site mapping and characterization of O-glycan structures on alpha-dystroglycan isolated from rabbit skeletal muscle.
Stalnaker SH; Hashmi S; Lim JM; Aoki K; Porterfield M; Gutierrez-Sanchez G; Wheeler J; Ervasti JM; Bergmann C; Tiemeyer M; Wells L
J Biol Chem; 2010 Aug; 285(32):24882-91. PubMed ID: 20507986
[TBL] [Abstract][Full Text] [Related]
16. Mini-dystrophin efficiently incorporates into the dystrophin protein complex in living cells.
Draviam RA; Wang B; Li J; Xiao X; Watkins SC
J Muscle Res Cell Motil; 2006; 27(1):53-67. PubMed ID: 16496225
[TBL] [Abstract][Full Text] [Related]
17. Hypoglycosylation of dystroglycan due to T192M mutation: a molecular insight behind the fact.
Bhattacharya S; Das A; Ghosh S; Dasgupta R; Bagchi A
Gene; 2014 Mar; 537(1):108-14. PubMed ID: 24361964
[TBL] [Abstract][Full Text] [Related]
18. Identification of the beta-dystroglycan binding epitope within the C-terminal region of alpha-dystroglycan.
Sciandra F; Schneider M; Giardina B; Baumgartner S; Petrucci TC; Brancaccio A
Eur J Biochem; 2001 Aug; 268(16):4590-7. PubMed ID: 11502221
[TBL] [Abstract][Full Text] [Related]
19. Concerted mutation of Phe residues belonging to the beta-dystroglycan ectodomain strongly inhibits the interaction with alpha-dystroglycan in vitro.
Bozzi M; Sciandra F; Ferri L; Torreri P; Pavoni E; Petrucci TC; Giardina B; Brancaccio A
FEBS J; 2006 Nov; 273(21):4929-43. PubMed ID: 17018058
[TBL] [Abstract][Full Text] [Related]
20. Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin.
Tisi D; Talts JF; Timpl R; Hohenester E
EMBO J; 2000 Apr; 19(7):1432-40. PubMed ID: 10747011
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
