PubMed for id: 20137708

Year	Number of Results
1998	2
1999	3
2000	1
2001	3
2002	1
2003	3
2004	6
2005	4
2006	5
2007	4
2008	2
2009	3
2011	1
2013	2
2014	5
2024	0

1

Fam65b is important for formation of the HDAC6-dysferlin protein complex during myogenic cell differentiation.

Balasubramanian A, Kawahara G, Gupta VA, Rozkalne A, Beauvais A, Kunkel LM, Gussoni E. Balasubramanian A, et al. FASEB J. 2014 Jul;28(7):2955-69. doi: 10.1096/fj.13-246470. Epub 2014 Mar 31. FASEB J. 2014. PMID: 24687993 Free PMC article.

2

Quantitation of the calcium and membrane binding properties of the C2 domains of dysferlin.

Abdullah N, Padmanarayana M, Marty NJ, Johnson CP. Abdullah N, et al. Biophys J. 2014 Jan 21;106(2):382-9. doi: 10.1016/j.bpj.2013.11.4492. Biophys J. 2014. PMID: 24461013 Free PMC article.

3

Crystal structures of the human Dysferlin inner DysF domain.

Sula A, Cole AR, Yeats C, Orengo C, Keep NH. Sula A, et al. BMC Struct Biol. 2014 Jan 17;14:3. doi: 10.1186/1472-6807-14-3. BMC Struct Biol. 2014. PMID: 24438169 Free PMC article.

4

An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

Bian Y, Song C, Cheng K, Dong M, Wang F, Huang J, Sun D, Wang L, Ye M, Zou H. Bian Y, et al. J Proteomics. 2014 Jan 16;96:253-62. doi: 10.1016/j.jprot.2013.11.014. Epub 2013 Nov 22. J Proteomics. 2014. PMID: 24275569 Clinical Trial.

5

Alternate splicing of dysferlin C2A confers Ca²⁺-dependent and Ca²⁺-independent binding for membrane repair.

Fuson K, Rice A, Mahling R, Snow A, Nayak K, Shanbhogue P, Meyer AG, Redpath GM, Hinderliter A, Cooper ST, Sutton RB. Fuson K, et al. Structure. 2014 Jan 7;22(1):104-15. doi: 10.1016/j.str.2013.10.001. Epub 2013 Nov 14. Structure. 2014. PMID: 24239457 Free PMC article.

6

Initial characterization of the human central proteome.

Burkard TR, Planyavsky M, Kaupe I, Breitwieser FP, Bürckstümmer T, Bennett KL, Superti-Furga G, Colinge J. Burkard TR, et al. BMC Syst Biol. 2011 Jan 26;5:17. doi: 10.1186/1752-0509-5-17. BMC Syst Biol. 2011. PMID: 21269460 Free PMC article.

7

Identification and characterisation of human dysferlin transcript variants: implications for dysferlin mutational screening and isoforms.

Pramono ZA, Tan CL, Seah IA, See JS, Kam SY, Lai PS, Yee WC. Pramono ZA, et al. Hum Genet. 2009 May;125(4):413-20. doi: 10.1007/s00439-009-0632-y. Epub 2009 Feb 17. Hum Genet. 2009. PMID: 19221801

8

A new phenotype of dysferlinopathy with congenital onset.

Paradas C, González-Quereda L, De Luna N, Gallardo E, García-Consuegra I, Gómez H, Cabello A, Illa I, Gallano P. Paradas C, et al. Neuromuscul Disord. 2009 Jan;19(1):21-5. doi: 10.1016/j.nmd.2008.09.015. Epub 2008 Dec 11. Neuromuscul Disord. 2009. PMID: 19084402

9

Analysis of the DYSF mutational spectrum in a large cohort of patients.

Krahn M, Béroud C, Labelle V, Nguyen K, Bernard R, Bassez G, Figarella-Branger D, Fernandez C, Bouvenot J, Richard I, Ollagnon-Roman E, Bevilacqua JA, Salvo E, Attarian S, Chapon F, Pellissier JF, Pouget J, Hammouda el H, Laforêt P, Urtizberea JA, Eymard B, Leturcq F, Lévy N. Krahn M, et al. Hum Mutat. 2009 Feb;30(2):E345-75. doi: 10.1002/humu.20910. Hum Mutat. 2009. PMID: 18853459

10

Dysferlin-deficient muscular dystrophy features amyloidosis.

Spuler S, Carl M, Zabojszcza J, Straub V, Bushby K, Moore SA, Bähring S, Wenzel K, Vinkemeier U, Rocken C. Spuler S, et al. Ann Neurol. 2008 Mar;63(3):323-8. doi: 10.1002/ana.21309. Ann Neurol. 2008. PMID: 18306167

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