PubMed (cited) for id: 164300

Year	Number of Results
1951	1
1962	1
1963	1
1964	2
1965	1
1968	1
1973	1
1980	1
1981	1
1982	1
1984	2
1991	2
1995	1
1996	1
1997	1
1998	1
1999	1
2000	2
2001	1
2003	2
2004	2
2005	3
2006	2
2009	1
2010	1
2024	0

1

Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres.

Trollet C, Anvar SY, Venema A, Hargreaves IP, Foster K, Vignaud A, Ferry A, Negroni E, Hourde C, Baraibar MA, 't Hoen PA, Davies JE, Rubinsztein DC, Heales SJ, Mouly V, van der Maarel SM, Butler-Browne G, Raz V, Dickson G. Trollet C, et al. Hum Mol Genet. 2010 Jun 1;19(11):2191-207. doi: 10.1093/hmg/ddq098. Epub 2010 Mar 5. Hum Mol Genet. 2010. PMID: 20207626

2

Prevention of oculopharyngeal muscular dystrophy by muscular expression of Llama single-chain intrabodies in vivo.

Chartier A, Raz V, Sterrenburg E, Verrips CT, van der Maarel SM, Simonelig M. Chartier A, et al. Hum Mol Genet. 2009 May 15;18(10):1849-59. doi: 10.1093/hmg/ddp101. Epub 2009 Mar 3. Hum Mol Genet. 2009. PMID: 19258344

3

Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutation.

Robinson DO, Wills AJ, Hammans SR, Read SP, Sillibourne J. Robinson DO, et al. J Med Genet. 2006 May;43(5):e23. doi: 10.1136/jmg.2005.037598. J Med Genet. 2006. PMID: 16648376 Free PMC article.

4

Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy.

Davies JE, Sarkar S, Rubinsztein DC. Davies JE, et al. Hum Mol Genet. 2006 Jan 1;15(1):23-31. doi: 10.1093/hmg/ddi422. Epub 2005 Nov 25. Hum Mol Genet. 2006. PMID: 16311254

5

Oculopharyngeal muscular dystrophy with PABPN1 mutation in a Chinese Malaysian woman.

Goh KJ, Wong KT, Nishino I, Minami N, Nonaka I. Goh KJ, et al. Neuromuscul Disord. 2005 Mar;15(3):262-4. doi: 10.1016/j.nmd.2004.10.016. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15725589

6

(GCG)11 founder mutation in the PABPN1 gene of OPMD Uruguayan families.

Rodríguez M, Camejo C, Bertoni B, Braida C, Rodríguez MM, Brais B, Medici M, Roche L. Rodríguez M, et al. Neuromuscul Disord. 2005 Feb;15(2):185-90. doi: 10.1016/j.nmd.2004.10.012. Epub 2005 Jan 11. Neuromuscul Disord. 2005. PMID: 15694141

7

Progressive dystrophy of the external ocular muscles (ocular myopathy).

KILOH LG, NEVIN S. KILOH LG, et al. Brain. 1951;74(2):115-43. doi: 10.1093/brain/74.2.115. Brain. 1951. PMID: 14858744 No abstract available.

8

Congo red, doxycycline, and HSP70 overexpression reduce aggregate formation and cell death in cell models of oculopharyngeal muscular dystrophy.

Bao YP, Sarkar S, Uyama E, Rubinsztein DC. Bao YP, et al. J Med Genet. 2004 Jan;41(1):47-51. doi: 10.1136/jmg.2003.014548. J Med Genet. 2004. PMID: 14729833 Free PMC article. No abstract available.

9

Myopathy phenotype in transgenic mice expressing mutated PABPN1 as a model of oculopharyngeal muscular dystrophy.

Hino H, Araki K, Uyama E, Takeya M, Araki M, Yoshinobu K, Miike K, Kawazoe Y, Maeda Y, Uchino M, Yamamura K. Hino H, et al. Hum Mol Genet. 2004 Jan 15;13(2):181-90. doi: 10.1093/hmg/ddh017. Epub 2003 Nov 25. Hum Mol Genet. 2004. PMID: 14645203

10

OCULAR MYOPATHY WITH DYSPHAGIA.

BRAY GM, KAARSOO M, ROSS RT. BRAY GM, et al. Neurology. 1965 Jul;15:678-84. doi: 10.1212/wnl.15.7.678. Neurology. 1965. PMID: 14306330 No abstract available.

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