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832. In Vitro Assessment of GNE-Wt Plasmid for Management of Hereditary Inclusion Body Myopathy 2 (HIBM2)
Molecular Therapy
◽
10.1016/s1525-0016(16)40235-2
◽
2008
◽
Vol 16
◽
pp. S311
Keyword(s):
Inclusion Body
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
◽
In Vitro Assessment
Download Full-text
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References
G.P.5.06 In vitro assessment of AAV8 based gene delivery for hereditary inclusion body myopathy
Neuromuscular Disorders
◽
10.1016/j.nmd.2009.06.084
◽
2009
◽
Vol 19
(8-9)
◽
pp. 569
Author(s):
M. Telem
◽
Z. Shlomai
◽
S. Mitrani-Rosenbaum
Keyword(s):
Gene Delivery
◽
Inclusion Body
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
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In Vitro Assessment
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Consequences of the hereditary inclusion-body myopathy-characteristic GNE mutations on muscle proteins in vivo and in vitro
Muscle Aging, Inclusion-Body Myositis and Myopathies
◽
10.1002/9781444398311.ch13
◽
2011
◽
pp. 199-205
◽
Cited By ~ 1
Author(s):
Aldobrando Broccolini
◽
Massimiliano Mirabella
Keyword(s):
Inclusion Body
◽
Muscle Proteins
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
Download Full-text
G.P.29 Results from a pilot study of muscle strength and function in adults with Hereditary Inclusion Body Myopathy (HIBM)
Neuromuscular Disorders
◽
10.1016/j.nmd.2012.06.051
◽
2012
◽
Vol 22
(9-10)
◽
pp. 817
Author(s):
A.M. Skrinar
◽
J.E. Mayhew
◽
M.L. Maurer
◽
E. Kakkis
Keyword(s):
Pilot Study
◽
Muscle Strength
◽
Inclusion Body
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
◽
And Function
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The hereditary inclusion body myopathy enigma and its future therapy
Neurotherapeutics
◽
10.1016/j.nurt.2008.07.004
◽
2008
◽
Vol 5
(4)
◽
pp. 633-637
◽
Cited By ~ 22
Author(s):
Zohar Argov
◽
Stella Mitrani-Rosenbaum
Keyword(s):
Inclusion Body
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
◽
Future Therapy
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Autophagy in a Mouse Model of Distal Myopathy with Rimmed Vacuoles or Hereditary Inclusion Body Myopathy
Autophagy
◽
10.4161/auto.4270
◽
2007
◽
Vol 3
(4)
◽
pp. 396-398
◽
Cited By ~ 34
Author(s):
May Christine V. Malicdan
◽
Satoru Noguchi
◽
Ichizo Nishino
Keyword(s):
Mouse Model
◽
Inclusion Body
◽
Distal Myopathy
◽
Rimmed Vacuoles
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
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The homozygous M712T mutation of UDP-N -acetylglucosamine 2-epimerase/N -acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy
FEBS Letters
◽
10.1016/j.febslet.2004.04.013
◽
2004
◽
Vol 566
(1-3)
◽
pp. 105-109
◽
Cited By ~ 54
Author(s):
Stephan Hinderlich
◽
Ilan Salama
◽
Iris Eisenberg
◽
Tamara Potikha
◽
Lars R. Mantey
◽
...
Keyword(s):
Inclusion Body
◽
Enzyme Activities
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
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Hereditary Inclusion Body Myopathy Maps to Chromosome 9p1-q1
Human Molecular Genetics
◽
10.1093/hmg/5.1.159
◽
1996
◽
Vol 5
(1)
◽
pp. 159-163
◽
Cited By ~ 62
Author(s):
S. Mitrani-Rosenbaum
◽
Z. Argov
◽
A. Blumenfeld
◽
C. E. Seidman
◽
J. G. Seidman
Keyword(s):
Inclusion Body
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
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A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
Brazilian Journal of Medical and Biological Research
◽
10.1590/s0100-879x2011007500028
◽
2011
◽
Vol 44
(4)
◽
pp. 374-380
◽
Cited By ~ 14
Author(s):
R.D. Fanganiello
◽
V.E. Kimonis
◽
C.C. Côrte
◽
R. Nitrini
◽
M.R. Passos-Bueno
Keyword(s):
Frontotemporal Dementia
◽
Inclusion Body
◽
Inclusion Body Myopathy
◽
Paget Disease Of Bone
◽
Paget Disease
◽
Hereditary Inclusion Body Myopathy
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GNE Myopathy (Hereditary Inclusion-Body Myopathy/Distal Myopathy with Rimmed Vacuoles): Clinical Features and Epidemiology
Muscle Aging, Inclusion-Body Myositis and Myopathies
◽
10.1002/9781444398311.ch12
◽
2011
◽
pp. 191-198
Author(s):
Zohar Argov
◽
Ichizo Nishino
◽
Ikuya Nonaka
Keyword(s):
Inclusion Body
◽
Clinical Features
◽
Distal Myopathy
◽
Rimmed Vacuoles
◽
Inclusion Body Myopathy
◽
Gne Myopathy
◽
Hereditary Inclusion Body Myopathy
Download Full-text
564. Correction of Hyposialylation in Hereditary Inclusion Body Myopathy, by Ex-Vivo Therapy
Molecular Therapy
◽
10.1016/j.ymthe.2006.08.637
◽
2006
◽
Vol 13
◽
pp. S217
Author(s):
Zoé Coulombe
◽
Dominic Gagné
◽
Jacques P. Tremblay
Keyword(s):
Inclusion Body
◽
Ex Vivo
◽
Inclusion Body Myopathy
◽
Hereditary Inclusion Body Myopathy
Download Full-text
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