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Journal Abstract Search

709 related items for PubMed ID: 18392839

  • 1. Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.
    Au CG, Butler TL, Egan JR, Cooper ST, Lo HP, Compton AG, North KN, Winlaw DS.
    Acta Neuropathol; 2008 Sep; 116(3):235-46. PubMed ID: 18392839
    [Abstract] [Full Text] [Related]

  • 2. Aquaporins in skeletal muscle: reassessment of the functional role of aquaporin-4.
    Frigeri A, Nicchia GP, Balena R, Nico B, Svelto M.
    FASEB J; 2004 May; 18(7):905-7. PubMed ID: 15033928
    [Abstract] [Full Text] [Related]

  • 3. Assessing the Role of Aquaporin 4 in Skeletal Muscle Function.
    Aslesh T, Al-Aghbari A, Yokota T.
    Int J Mol Sci; 2023 Jan 12; 24(2):. PubMed ID: 36675000
    [Abstract] [Full Text] [Related]

  • 4. Molecular cloning and protein expression of Duchenne muscular dystrophy gene products in porcine retina.
    Bordais A, Bolaños-Jimenez F, Fort P, Varela C, Sahel JA, Picaud S, Rendon A.
    Neuromuscul Disord; 2005 Jul 12; 15(7):476-87. PubMed ID: 15941659
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  • 7. Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP transgenic mice.
    Rodríguez A, Pérez-Gracia E, Espinosa JC, Pumarola M, Torres JM, Ferrer I.
    Acta Neuropathol; 2006 Nov 12; 112(5):573-85. PubMed ID: 16871401
    [Abstract] [Full Text] [Related]

  • 8. Altered aquaporin-4 expression in human muscular dystrophies: a common feature?
    Frigeri A, Nicchia GP, Repetto S, Bado M, Minetti C, Svelto M.
    FASEB J; 2002 Jul 12; 16(9):1120-2. PubMed ID: 12039847
    [Abstract] [Full Text] [Related]

  • 9. Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies.
    Assereto S, Mastrototaro M, Stringara S, Gazzerro E, Broda P, Nicchia GP, Svelto M, Bruno C, Nigro V, Lisanti MP, Frigeri A, Minetti C.
    Cell Cycle; 2008 Jul 15; 7(14):2199-207. PubMed ID: 18641458
    [Abstract] [Full Text] [Related]

  • 10. Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1.
    Nakamori M, Kimura T, Kubota T, Matsumura T, Sumi H, Fujimura H, Takahashi MP, Sakoda S.
    Neurology; 2008 Feb 26; 70(9):677-85. PubMed ID: 18299519
    [Abstract] [Full Text] [Related]

  • 11. [Altered expression of myostatin gene in the progressive muscular dystrophy patients].
    Zhang Y, Chen Y, Chen JW, Zhu DH.
    Yi Chuan Xue Bao; 2005 Aug 26; 32(8):779-83. PubMed ID: 16231730
    [Abstract] [Full Text] [Related]

  • 12. A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness.
    Kimura S, Ito K, Ueno H, Ikezawa M, Takeshima Y, Yoshioka K, Ozasa S, Nakamura K, Nomura K, Matsukura M, Mitsui K, Matsuo M, Miike T.
    Brain Dev; 2009 Feb 26; 31(2):169-72. PubMed ID: 18430534
    [Abstract] [Full Text] [Related]

  • 13. [Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].
    Wang S, Shen D.
    Zhonghua Yi Xue Za Zhi; 2002 Feb 10; 82(3):155-7. PubMed ID: 11953148
    [Abstract] [Full Text] [Related]

  • 14. Aquaporin 4 changes in rat brain with severe hydrocephalus.
    Mao X, Enno TL, Del Bigio MR.
    Eur J Neurosci; 2006 Jun 10; 23(11):2929-36. PubMed ID: 16819982
    [Abstract] [Full Text] [Related]

  • 15. Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.
    Arning L, Jagiello P, Schara U, Vorgerd M, Dahmen N, Gencikova A, Mortier W, Epplen JT, Gencik M.
    J Neurol; 2004 Jan 10; 251(1):72-8. PubMed ID: 14999492
    [Abstract] [Full Text] [Related]

  • 16. Immunohistochemistry of sarcolemmal membrane-associated proteins in formalin-fixed and paraffin-embedded skeletal muscle tissue: a promising tool for the diagnostic evaluation of common muscular dystrophies.
    Suriyonplengsaeng C, Dejthevaporn C, Khongkhatithum C, Sanpapant S, Tubthong N, Pinpradap K, Srinark N, Waisayarat J.
    Diagn Pathol; 2017 Feb 20; 12(1):19. PubMed ID: 28219397
    [Abstract] [Full Text] [Related]

  • 17. High salt loading alters the expression and localization of glial aquaporins in rat retina.
    Qin Y, Fan J, Ye X, Xu G, Liu W, Da C.
    Exp Eye Res; 2009 Jun 15; 89(1):88-94. PubMed ID: 19268466
    [Abstract] [Full Text] [Related]

  • 18. Reduced expression of aquaporin 4 in human muscles with amyotrophic lateral sclerosis and other neurogenic atrophies.
    Jimi T, Wakayama Y, Matsuzaki Y, Hara H, Inoue M, Shibuya S.
    Pathol Res Pract; 2004 Jun 15; 200(3):203-9. PubMed ID: 15200272
    [Abstract] [Full Text] [Related]

  • 19. Regulation of capacitative calcium entries by alpha1-syntrophin: association of TRPC1 with dystrophin complex and the PDZ domain of alpha1-syntrophin.
    Vandebrouck A, Sabourin J, Rivet J, Balghi H, Sebille S, Kitzis A, Raymond G, Cognard C, Bourmeyster N, Constantin B.
    FASEB J; 2007 Feb 15; 21(2):608-17. PubMed ID: 17202249
    [Abstract] [Full Text] [Related]

  • 20. High-salt loading exacerbates increased retinal content of aquaporins AQP1 and AQP4 in rats with diabetic retinopathy.
    Qin Y, Xu G, Fan J, Witt RE, Da C.
    Exp Eye Res; 2009 Nov 15; 89(5):741-7. PubMed ID: 19596320
    [Abstract] [Full Text] [Related]

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