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Valosin-containing protein (VCP)–Adaptor Interactions are Exceptionally Dynamic and Subject to Differential Modulation by a VCP Inhibitor
Xue, Liang, Blythe, Emily E., Freiberger, Elyse C., Mamrosh, Jennifer L., Hebert, Alexander S., Reitsma, Justin M., Hess, Sonja, Coon, Joshua J., Deshaies, Raymond J.
Published in Molecular & cellular proteomics (01.09.2016)
Published in Molecular & cellular proteomics (01.09.2016)
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Phenotypic variability in three families with valosin-containing protein mutation
Spina, S., Van Laar, A. D., Murrell, J. R., Hamilton, R. L., Kofler, J. K., Epperson, F., Farlow, M. R., Lopez, O. L., Quinlan, J., DeKosky, S. T., Ghetti, B.
Published in European journal of neurology (01.02.2013)
Published in European journal of neurology (01.02.2013)
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Autoantibodies to nuclear valosin-containing protein-like protein: systemic sclerosis-specific antibodies revealed by in vitro human proteome
Matsuda, Kazuki M, Kotani, Hirohito, Yamaguchi, Kei, Ono, Chihiro, Okumura, Taishi, Ogawa, Koji, Miya, Ayako, Sato, Ayaka, Uchino, Rikako, Yumi, Murakami, Matsunaka, Hiroshi, Kono, Masanori, Norimatsu, Yuta, Hisamoto, Teruyoshi, Kawanabe, Ruriko, Kuzumi, Ai, Fukasawa, Takemichi, Yoshizaki-Ogawa, Asako, Okamura, Tomohisa, Shoda, Hirofumi, Fujio, Keishi, Matsushita, Takashi, Goshima, Naoki, Sato, Shinichi, Yoshizaki, Ayumi
Published in Rheumatology (Oxford, England) (01.10.2024)
Published in Rheumatology (Oxford, England) (01.10.2024)
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215P Evaluating the responsiveness of patient reported outcome measures (PROs) to change in valosin-containing protein multisystem proteinopathy (MSP1) over 24 months
Iammarino, M., Reash, N., Lowes, L., Pietruszewski, L., Adderley, K., Humphrey, L., Beale, A., Steiner, C., Smith, M., Alfano, L.
Published in Neuromuscular disorders : NMD (01.10.2024)
Published in Neuromuscular disorders : NMD (01.10.2024)
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Combining Valosin-containing Protein (VCP) Inhibition and Suberanilohydroxamic Acid (SAHA) Treatment Additively Enhances the Folding, Trafficking, and Function of Epilepsy-associated γ-Aminobutyric Acid, Type A (GABAA) Receptors
Han, Dong-Yun, Di, Xiao-Jing, Fu, Yan-Lin, Mu, Ting-Wei
Published in The Journal of biological chemistry (02.01.2015)
Published in The Journal of biological chemistry (02.01.2015)
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P.179 Clinical trial readiness and validation of onsite and remote evaluation in valosin containing protein-associated multisystem proteinopathy
Alfano, L., Peck, A., Iammarino, M., Patel, S., Reash, N., Almomen, M., Mendell, J., Sabo, B., Long, A., Pietruszewski, L., Lowes, L., Peck, N.
Published in Neuromuscular disorders : NMD (01.10.2022)
Published in Neuromuscular disorders : NMD (01.10.2022)
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O06 Clinical trial readiness and validation of onsite and remote evaluation in valosin-containing protein-associated multisystem proteinopathy: a 24-month longitudinal study
Reash, N., Iammarino, M., Pietruszewski, L., Lowes, L., Mendell, J., Connolly, A., Adderley, K., Peck, N., Peck, A., Alfano, L.
Published in Neuromuscular disorders : NMD (01.10.2023)
Published in Neuromuscular disorders : NMD (01.10.2023)
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Case report: Frontotemporal dementia and amyotrophic lateral sclerosis caused by a missense variant (p.Arg89Trp) in the valosin-containing protein gene
Miura, Shiroh, Hiruki, Shigeyoshi, Okada, Tomohisa, Takei, Satoko Itani, Senzaki, Kensuke, Okada, Yoko, Ochi, Masayuki, Tanabe, Yuki, Ochi, Hirofumi, Igase, Michiya, Ohyagi, Yasumasa, Shibata, Hiroki
Published in Frontiers in genetics (26.05.2023)
Published in Frontiers in genetics (26.05.2023)
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Valosin-containing protein immunoreactivity in tauopathies, synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease
Mori, Fumiaki, Tanji, Kunikazu, Toyoshima, Yasuko, Sasaki, Hidenao, Yoshida, Mari, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi
Published in Neuropathology (01.12.2013)
Published in Neuropathology (01.12.2013)
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Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant
Ayaki, Takashi, Ito, Hidefumi, Fukushima, Hiroko, Inoue, Takeshi, Kondo, Takayuki, Ikemoto, Akito, Asano, Takeshi, Shodai, Akemi, Fujita, Takuji, Fukui, Satoshi, Morino, Hiroyuki, Nakano, Satoshi, Kusaka, Hirofumi, Yamashita, Hirofumi, Ihara, Masafumi, Matsumoto, Riki, Kawamata, Jun, Urushitani, Makoto, Kawakami, Hideshi, Takahashi, Ryosuke
Published in Acta neuropathologica communications (10.12.2014)
Published in Acta neuropathologica communications (10.12.2014)
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Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone
Lucas, Gavin J.A., Mehta, Sarju G., Hocking, Lynne J., Stewart, Tracy L., Cundy, Tim, Nicholson, Geoff C., Walsh, John P., Fraser, William D., Watts, Giles D.J., Ralston, Stuart H., Kimonis, Virginia E.
Published in Bone (New York, N.Y.) (01.02.2006)
Published in Bone (New York, N.Y.) (01.02.2006)
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Valosin-Containing Protein is a Novel Autoantigen in Patients with Glaucoma
Lee, Koon-Ja, Jeong, Seon-Mi, Hoehn, Benjamin Douglass, Hong, Young Jae, Lee, Sung Ho
Published in Optometry and vision science (01.01.2011)
Published in Optometry and vision science (01.01.2011)
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A clinicopathologic study of malignancy in VCP-associated multisystem proteinopathy
Shmara, Alyaa, Perez-Rosendahl, Mari, Murphy, Kady, Kwon, Ashley, Smith, Charles, Kimonis, Virginia
Published in Orphanet journal of rare diseases (15.07.2022)
Published in Orphanet journal of rare diseases (15.07.2022)
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Role of Cdc48/p97 as a SUMO-targeted segregase curbing Rad51–Rad52 interaction
Bergink, Steven, Ammon, Tim, Kern, Maximilian, Schermelleh, Lothar, Leonhardt, Heinrich, Jentsch, Stefan
Published in Nature cell biology (01.05.2013)
Published in Nature cell biology (01.05.2013)
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Structure and functions of the chaperone-like p97/CDC48 in plants
Bègue, Hervé, Jeandroz, Sylvain, Blanchard, Cécile, Wendehenne, David, Rosnoblet, Claire
Published in Biochimica et biophysica acta. General subjects (01.01.2017)
Published in Biochimica et biophysica acta. General subjects (01.01.2017)
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Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia
Mehta, SG, Khare, M, Ramani, R, Watts, GDJ, Simon, M, Osann, KE, Donkervoort, S, Dec, E, Nalbandian, A, Platt, J, Pasquali, M, Wang, A, Mozaffar, T, Smith, CD, Kimonis, VE
Published in Clinical genetics (01.05.2013)
Published in Clinical genetics (01.05.2013)
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A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family
Gu, Jie-Mei, Ke, Yao-Hua, Yue, Hua, Liu, Yu-Juan, Zhang, Zeng, Zhang, Hao, Hu, Wei-Wei, Wang, Chun, He, Jin-Wei, Hu, Yun-Qiu, Li, Miao, Fu, Wen-Zhen, Zhang, Zhen-Lin
Published in Bone (New York, N.Y.) (01.01.2013)
Published in Bone (New York, N.Y.) (01.01.2013)
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Critical role of proteostasis-imbalance in pathogenesis of COPD and severe emphysema
Min, Taehong, Bodas, Manish, Mazur, Steven, Vij, Neeraj
Published in Journal of molecular medicine (Berlin, Germany) (01.06.2011)
Published in Journal of molecular medicine (Berlin, Germany) (01.06.2011)
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