Zobrazeno 1 - 10
of 1 042
pro vyhledávání: '"Caiozzo V"'
Autor:
Bhatnagar C; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA., Shah J; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA., Ramani B; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA., Surampalli A; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA., Avanti M; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA., Radom-Aizik S; Pediatric Exercise & Genomics Research Center, Department of Pediatrics, University of California, Irvine, USA., Knight M; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA., Weiss L; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA., Caiozzo V; Department of Orthopedic Surgery, University of California, Irvine, USA., Kimonis V; Department of Pediatrics, Neurology and Pathology, Division of Genetics and Genomic Medicine, University of California, Irvine School of Medicine, 101 The City Drive South, ZC4482, Orange, CA, USA; Department of Neurology, University of California, Irvine School of Medicine, Orange, CA, USA; Department of Pathology & Laboratory Medicine, University of California, Irvine School of Medicine, Orange, CA, USA. Electronic address: vkimonis@uci.edu.
Publikováno v:
Neuromuscular disorders : NMD [Neuromuscul Disord] 2022 Apr; Vol. 32 (4), pp. 284-294. Date of Electronic Publication: 2022 Feb 17.
Autor:
Huang, Shuting1,2,3 (AUTHOR), Tam, Ming Yik1 (AUTHOR), Ho, Wai Hon Caleb1 (AUTHOR), Wong, Hong Ki1 (AUTHOR), Zhou, Meng4 (AUTHOR), Zeng, Chun5 (AUTHOR), Xie, Denghui5 (AUTHOR), Elmer Ker, Dai Fei3,6 (AUTHOR), Ling, Samuel KK.3,4 (AUTHOR), Tuan, Rocky S.1,2,3,4 (AUTHOR), Wang, Dan Michelle1,2,3,4 (AUTHOR) wangmd@cuhk.edu.hk
Publikováno v:
Biological Procedures Online. 10/4/2024, Vol. 26 Issue 1, p1-23. 23p.
Autor:
Powers SK; Department of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL, USA.
Publikováno v:
The Journal of physiology [J Physiol] 2024 Oct; Vol. 602 (19), pp. 4729-4752. Date of Electronic Publication: 2024 Aug 31.
Autor:
Kolobe, T. H. A, Christy, J. B, Gannotti, M. E, Heathcock, J. C, Damiano, D. L, Taub, E., Majsak, M. J, Gordon, A. M, Fuchs, R. K, O'Neil, M. E, Caiozzo, V. J
Publikováno v:
Kolobe, T. H. A; Christy, J. B; Gannotti, M. E; Heathcock, J. C; Damiano, D. L; Taub, E.; et al.(2014). Research Summit III Proceedings on Dosing in Children With an Injured Brain or Cerebral Palsy: Executive Summary. Physical Therapy, 94(7), 907-920. doi: 10.2522/ptj.20130024. UC Irvine: Institute for Clinical and Translational Science. Retrieved from: http://www.escholarship.org/uc/item/1w83z503
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::4d611156ca0a0b877c823d03aa99153a
http://www.escholarship.org/uc/item/1w83z503
http://www.escholarship.org/uc/item/1w83z503
Autor:
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
Publikováno v:
Nalbandian, A; Llewellyn, KJ; Badadani, M; Yin, HZ; Nguyen, C; Katheria, V; et al.(2013). A progressive translational mouse model of human valosin-containing protein disease: The VCPR155H/+mouse. Muscle and Nerve, 47(2), 260-270. doi: 10.1002/mus.23522. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/6fv693w5
Introduction: Mutations in the valosin-containing protein (VCP) gene cause hereditary inclusion body myopathy (IBM) associated with Paget disease of bone (PDB), and frontotemporal dementia (FTD). More recently, these mutations have been linked to 2%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::c9520552e3ef636047637174141db719
http://www.escholarship.org/uc/item/6fv693w5
http://www.escholarship.org/uc/item/6fv693w5
Autor:
Sorrentino, Riccardo G.1,2 (AUTHOR), Avila‐Mirèles, Edwin1,3 (AUTHOR), Babič, Jan1 (AUTHOR), Supej, Matej4 (AUTHOR), Mekjavic, Igor B.1 (AUTHOR) igor.mekjavic@ijs.si, McDonnell, Adam C.1 (AUTHOR)
Publikováno v:
Physiological Reports. Jul2024, Vol. 12 Issue 13, p1-13. 13p.
Publikováno v:
Journal of Applied Physiology; Jul2009, Vol. 107 Issue 1, p39-46, 8p, 1 Chart, 15 Graphs
Autor:
Pontifex, Carly S.1 (AUTHOR) cspontif@ucalgary.ca, Zaman, Mashiat1,2,3 (AUTHOR) mashiat.zaman1@ucalgary.ca, Fanganiello, Roberto D.4 (AUTHOR) robertofanganiello@gmail.com, Shutt, Timothy E.1,2,3 (AUTHOR) timothy.shutt@ucalgary.ca, Pfeffer, Gerald1,2,5 (AUTHOR) gerald.pfeffer@ucalgary.ca
Publikováno v:
International Journal of Molecular Sciences. Jun2024, Vol. 25 Issue 11, p5633. 23p.