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Journal Abstract Search

134 related items for PubMed ID: 31740511

  • 21. [Inclusion Body Myopathy, Paget's Disease, and Fronto-temporal Dementia: a VCP-related Multi-systemic Proteinopathy].
    Mengel D, Librizzi D, Schoser B, Gläser D, Clemen CS, Dodel R, Schröder R.
    Fortschr Neurol Psychiatr; 2018 Jul; 86(7):434-438. PubMed ID: 30029282
    [Abstract] [Full Text] [Related]

  • 22. Cross-sectional study of patients with VCP multisystem proteinopathy 1 using dual-energy x-ray absorptiometry.
    Columbres RCA, Luu V, Nguyen M, Kimonis V.
    Muscle Nerve; 2024 Jun; 69(6):699-707. PubMed ID: 38551101
    [Abstract] [Full Text] [Related]

  • 23. Valosin-containing protein (VCP/p97) inhibitors relieve Mitofusin-dependent mitochondrial defects due to VCP disease mutants.
    Zhang T, Mishra P, Hay BA, Chan D, Guo M.
    Elife; 2017 Mar 21; 6():. PubMed ID: 28322724
    [Abstract] [Full Text] [Related]

  • 24. Characteristics of VCP mutation-associated cardiomyopathy.
    Wang SC, Smith CD, Lombardo DM, Kimonis V.
    Neuromuscul Disord; 2021 Aug 21; 31(8):701-705. PubMed ID: 34244020
    [Abstract] [Full Text] [Related]

  • 25. Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels.
    Bartolome F, Wu HC, Burchell VS, Preza E, Wray S, Mahoney CJ, Fox NC, Calvo A, Canosa A, Moglia C, Mandrioli J, Chiò A, Orrell RW, Houlden H, Hardy J, Abramov AY, Plun-Favreau H.
    Neuron; 2013 Apr 10; 78(1):57-64. PubMed ID: 23498975
    [Abstract] [Full Text] [Related]

  • 26. Hereditary inclusion-body myopathies.
    Broccolini A, Mirabella M.
    Biochim Biophys Acta; 2015 Apr 10; 1852(4):644-50. PubMed ID: 25149037
    [Abstract] [Full Text] [Related]

  • 27. Ubiquitin- and ATP-dependent unfoldase activity of P97/VCP•NPLOC4•UFD1L is enhanced by a mutation that causes multisystem proteinopathy.
    Blythe EE, Olson KC, Chau V, Deshaies RJ.
    Proc Natl Acad Sci U S A; 2017 May 30; 114(22):E4380-E4388. PubMed ID: 28512218
    [Abstract] [Full Text] [Related]

  • 28. Adolescent-onset multisystem proteinopathy due to a novel VCP variant.
    Soontrapa P, Seven NA, Liewluck T, Cui G, Mer G, Milone M.
    Neuromuscul Disord; 2024 Jan 30; 34():89-94. PubMed ID: 38159460
    [Abstract] [Full Text] [Related]

  • 29. [Inclusion body myositis, Paget's disease of the bone and frontotemporal dementia: early involvement of the heart and respiratory muscles].
    Ponfick M, Ludolph AC, Dekomien G, Uttner I, Kassubek J, Gdynia HJ.
    Fortschr Neurol Psychiatr; 2012 Jun 30; 80(6):344-7. PubMed ID: 22644520
    [Abstract] [Full Text] [Related]

  • 30. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.
    Kim HJ, Kim NC, Wang YD, Scarborough EA, Moore J, Diaz Z, MacLea KS, Freibaum B, Li S, Molliex A, Kanagaraj AP, Carter R, Boylan KB, Wojtas AM, Rademakers R, Pinkus JL, Greenberg SA, Trojanowski JQ, Traynor BJ, Smith BN, Topp S, Gkazi AS, Miller J, Shaw CE, Kottlors M, Kirschner J, Pestronk A, Li YR, Ford AF, Gitler AD, Benatar M, King OD, Kimonis VE, Ross ED, Weihl CC, Shorter J, Taylor JP.
    Nature; 2013 Mar 28; 495(7442):467-73. PubMed ID: 23455423
    [Abstract] [Full Text] [Related]

  • 31. Axonal hyperpolarization in inclusion-body myopathy, Paget disease of the bone, and frontotemporal dementia (IBMPFD).
    Kumar KR, Liang C, Needham M, Burke D, Sue CM, Ng K.
    Muscle Nerve; 2011 Aug 28; 44(2):191-6. PubMed ID: 21607982
    [Abstract] [Full Text] [Related]

  • 32. Neuronal-specific overexpression of a mutant valosin-containing protein associated with IBMPFD promotes aberrant ubiquitin and TDP-43 accumulation and cognitive dysfunction in transgenic mice.
    Rodriguez-Ortiz CJ, Hoshino H, Cheng D, Liu-Yescevitz L, Blurton-Jones M, Wolozin B, LaFerla FM, Kitazawa M.
    Am J Pathol; 2013 Aug 28; 183(2):504-15. PubMed ID: 23747512
    [Abstract] [Full Text] [Related]

  • 33. VCP/p97 controls signals of the ERK1/2 pathway transmitted via the Shoc2 scaffolding complex: novel insights into IBMPFD pathology.
    Jang H, Jang ER, Wilson PG, Anderson D, Galperin E.
    Mol Biol Cell; 2019 Jul 01; 30(14):1655-1663. PubMed ID: 31091164
    [Abstract] [Full Text] [Related]

  • 34. A case of progressive quadriceps weakness and elevated creatine kinase level mimicking inclusion body myositis.
    Leung DG, Taylor HA, Lindy AS, Basehore MJ, Mammen AL.
    Arthritis Care Res (Hoboken); 2014 Feb 01; 66(2):328-33. PubMed ID: 24022920
    [No Abstract] [Full Text] [Related]

  • 35. A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.
    Gu JM, Ke YH, Yue H, Liu YJ, Zhang Z, Zhang H, Hu WW, Wang C, He JW, Hu YQ, Li M, Fu WZ, Zhang ZL.
    Bone; 2013 Jan 01; 52(1):9-16. PubMed ID: 23000505
    [Abstract] [Full Text] [Related]

  • 36. A progressive translational mouse model of human valosin-containing protein disease: the VCP(R155H/+) mouse.
    Nalbandian A, Llewellyn KJ, Badadani M, Yin HZ, Nguyen C, Katheria V, Watts G, Mukherjee J, Vesa J, Caiozzo V, Mozaffar T, Weiss JH, Kimonis VE.
    Muscle Nerve; 2013 Feb 01; 47(2):260-70. PubMed ID: 23169451
    [Abstract] [Full Text] [Related]

  • 37. Targeted excision of VCP R155H mutation by Cre-LoxP technology as a promising therapeutic strategy for valosin-containing protein disease.
    Nalbandian A, Llewellyn KJ, Nguyen C, Monuki ES, Kimonis VE.
    Hum Gene Ther Methods; 2015 Feb 01; 26(1):13-24. PubMed ID: 25545721
    [Abstract] [Full Text] [Related]

  • 38. Multisystem Proteinopathy Associated with a VCP G156S Mutation in a French Canadian Family.
    Pellerin D, Ellezam B, Korathanakhun P, Renaud M, Dicaire MJ, Pilote L, Levy JP, Karamchandani J, Ducharme S, Massie R, Brais B.
    Can J Neurol Sci; 2020 May 01; 47(3):412-415. PubMed ID: 32036797
    [No Abstract] [Full Text] [Related]

  • 39. Structural and Functional Analysis of Disease-Linked p97 ATPase Mutant Complexes.
    Nandi P, Li S, Columbres RCA, Wang F, Williams DR, Poh YP, Chou TF, Chiu PL.
    Int J Mol Sci; 2021 Jul 28; 22(15):. PubMed ID: 34360842
    [Abstract] [Full Text] [Related]

  • 40.
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