These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 15725589)

  • 21. (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
    Neuromuscul Disord; 2005 Feb; 15(2):185-90. PubMed ID: 15694141
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Late onset oculopharyngeal muscular dystrophy with prominent neurogenic features and short GCG trinucleotide expansion.
    Piccolo G; Cortese A; Tavazzi E; Piccolo L; Sassone J; Ciammola A; Alfonsi E; Colombo I; Moggio M
    Muscle Nerve; 2011 Jan; 43(1):141-2. PubMed ID: 21171103
    [No Abstract]   [Full Text] [Related]  

  • 23. Unique PABPN1 gene mutation in a large Bulgarian family with OPMD.
    Mihaylova V; Müller T; Petrova I; Tournev I; Cherninkova S; Walter MC; Deschauer M
    J Neurol; 2008 Apr; 255(4):609-11. PubMed ID: 18274805
    [No Abstract]   [Full Text] [Related]  

  • 24. Oculopharyngeal muscular dystrophy: phenotypic and genotypic characteristics of 9 Polish patients.
    Nadaj-Pakleza A; Richard P; Lusakowska A; Gajewska J; Jamrozik Z; Kostera-Pruszczyk A; Kwieciński H; Kamińska A
    Neurol Neurochir Pol; 2009; 43(2):113-20. PubMed ID: 19484687
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Wild-type PABPN1 is anti-apoptotic and reduces toxicity of the oculopharyngeal muscular dystrophy mutation.
    Davies JE; Sarkar S; Rubinsztein DC
    Hum Mol Genet; 2008 Apr; 17(8):1097-108. PubMed ID: 18178579
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [A late-onset case of oculopharyngeal muscular dystrophy carrying a (GCG)8 repeat expansion in the PAPBN1 gene].
    Tokutake T; Ikeuchi T; Tanaka K; Onodera O; Nishizawa M
    Rinsho Shinkeigaku; 2005 Jun; 45(6):437-40. PubMed ID: 16022469
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Oculopharyngeal muscle dystrophy: fine structure and mRNA expression levels of PABPN1.
    Schröder JM; Klossok T; Weis J
    Clin Neuropathol; 2011; 30(3):94-103. PubMed ID: 21545772
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic heterogeneity in 30 German patients with oculopharyngeal muscular dystrophy.
    Müller T; Deschauer M; Kolbe-Fehr F; Zierz S
    J Neurol; 2006 Jul; 253(7):892-5. PubMed ID: 16619122
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Modeling oculopharyngeal muscular dystrophy in myotube cultures reveals reduced accumulation of soluble mutant PABPN1 protein.
    Raz V; Routledge S; Venema A; Buijze H; van der Wal E; Anvar S; Straasheijm KR; Klooster R; Antoniou M; van der Maarel SM
    Am J Pathol; 2011 Oct; 179(4):1988-2000. PubMed ID: 21854744
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Two different PABPN1 expanded alleles in a Mexican population with oculopharyngeal muscular dystrophy arising from independent founder effects.
    Rivera D; Mejia-Lopez H; Pompa-Mera EN; Villanueva-Mendoza C; Nava-Castañeda A; Garnica-Hayashi L; Cuevas-Covarrubias S; Zenteno JC
    Br J Ophthalmol; 2008 Jul; 92(7):998-1002. PubMed ID: 18577654
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Progress in understanding the pathogenesis of oculopharyngeal muscular dystrophy.
    Fan X; Rouleau GA
    Can J Neurol Sci; 2003 Feb; 30(1):8-14. PubMed ID: 12619777
    [TBL] [Abstract][Full Text] [Related]  

  • 32. HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.
    Fan X; Messaed C; Dion P; Laganiere J; Brais B; Karpati G; Rouleau GA
    Can J Neurol Sci; 2003 Aug; 30(3):244-51. PubMed ID: 12945950
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a Chinese population.
    Shan J; Chen B; Lin P; Li D; Luo Y; Ji K; Zheng J; Yuan Y; Yan C
    Neuromolecular Med; 2014 Dec; 16(4):782-6. PubMed ID: 25283883
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dropped-head in recessive oculopharyngeal muscular dystrophy.
    Garibaldi M; Pennisi EM; Bruttini M; Bizzarri V; Bucci E; Morino S; Talerico C; Stoppacciaro A; Renieri A; Antonini G
    Neuromuscul Disord; 2015 Nov; 25(11):869-72. PubMed ID: 26494409
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy.
    Gambelli S; Malandrini A; Ginanneschi F; Berti G; Cardaioli E; De Stefano R; Franci M; Salvadori C; Mari F; Bruttini M; Rossi A; Federico A; Renieri A
    Eur Neurol; 2004; 51(3):144-7. PubMed ID: 14988608
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy.
    Dubbioso R; Moretta P; Manganelli F; Fiorillo C; Iodice R; Trojano L; Santoro L
    J Neurol; 2012 May; 259(5):833-7. PubMed ID: 21956377
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Oculopharyngeal muscular dystrophy: potential therapies for an aggregate-associated disorder.
    Davies JE; Berger Z; Rubinsztein DC
    Int J Biochem Cell Biol; 2006; 38(9):1457-62. PubMed ID: 16530457
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A Case of Oculopharyngeal Muscular Dystrophy Caused by a Novel PABPN1 c.34G > T (p.Gly12Trp) Point Mutation without Polyalanine Expansion.
    Takahashi Y; Morimoto N; Nada T; Morimoto M; Eura N; Minami N; Nishino I
    J Neuromuscul Dis; 2023; 10(3):459-463. PubMed ID: 36847015
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy.
    Davies JE; Sarkar S; Rubinsztein DC
    Hum Mol Genet; 2006 Jan; 15(1):23-31. PubMed ID: 16311254
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Animal model of oculopharyngeal muscular dystrophy.
    Uyama E; Hino H; Araki K; Takeya M; Uchino M; Yamamura K
    Acta Myol; 2005 Oct; 24(2):84-8. PubMed ID: 16550922
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.