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                             29 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactome Blandin, Gaëlle
2013
3 1 artikel
2 BMP-9 expression in human traumatic heterotopic ossification: a case report Grenier, Guillaume
2013
3 1 artikel
3 Bone marrow derived cells in adult skeletal muscle tissue in humans Strömberg, Anna
2013
3 1 artikel
4 Canonical Wnt signaling induces BMP-4 to specify slow myofibrogenesis of fetal myoblasts Kuroda, Kazuki
2013
3 1 artikel
5 Comparison of endogenous and overexpressed MyoD shows enhanced binding of physiologically bound sites Yao, Zizhen
2013
3 1 artikel
6 Control of mRNA stability contributes to low levels of nuclear poly(A) binding protein 1 (PABPN1) in skeletal muscle Apponi, Luciano H
2013
3 1 artikel
7 Differential response of skeletal muscles to mTORC1 signaling during atrophy and hypertrophy Bentzinger, C Florian
2013
3 1 artikel
8 Distinct roles for Ste20-like kinase SLK in muscle function and regeneration Storbeck, Christopher J
2013
3 1 artikel
9 Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy Boyer, Justin G
2013
3 1 artikel
10 Genome-wide binding of the basic helix-loop-helix myogenic inhibitor musculin has substantial overlap with MyoD: implications for buffering activity MacQuarrie, Kyle L
2013
3 1 artikel
11 Idiopathic inflammatory myopathies: pathogenic mechanisms of muscle weakness Rayavarapu, Sree
2013
3 1 artikel
12 Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research Yoon, Soonsang
2013
3 1 artikel
13 Increased sphingosine-1-phosphate improves muscle regeneration in acutely injured mdx mice Ieronimakis, Nicholas
2013
3 1 artikel
14 Inhibition of extracellular signal-regulated kinase 1/2 signaling has beneficial effects on skeletal muscle in a mouse model of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutation Muchir, Antoine
2013
3 1 artikel
15 Krüppel-like factor 6 (KLF6) promotes cell proliferation in skeletal myoblasts in response to TGFβ/Smad3 signaling Dionyssiou, Mathew G
2013
3 1 artikel
16 Linking cytoarchitecture to metabolism: sarcolemma-associated plectin affects glucose uptake by destabilizing microtubule networks in mdx myofibers Raith, Marianne
2013
3 1 artikel
17 Live cell imaging reveals marked variability in myoblast proliferation and fate Gross, Sean M
2013
3 1 artikel
18 Measuring microRNA reporter activity in skeletal muscle using hydrodynamic limb vein injection of plasmid DNA combined with in vivo imaging Guess, Martin G
2013
3 1 artikel
19 MG53′s new identity Levy, Jennifer R
2013
3 1 artikel
20 Mice with RyR1 mutation (Y524S) undergo hypermetabolic response to simvastatin Knoblauch, Mark
2013
3 1 artikel
21 Murine Fig4 is dispensable for muscle development but required for muscle function Reifler, Aaron
2013
3 1 artikel
22 Rb1 loss modifies but does not initiate alveolar rhabdomyosarcoma Kikuchi, Ken
2013
3 1 artikel
23 Retraction: MyoD-dependent regulation of NF-κB activity couples cell-cycle withdrawal to myogenic differentiation Parker, Maura H
2013
3 1 artikel
24 Sarcospan: a small protein with large potential for Duchenne muscular dystrophy Marshall, Jamie L
2013
3 1 artikel
25 Satellite cell therapy – from mice to men Bareja, Akshay
2013
3 1 artikel
26 Trip12, a HECT domain E3 ubiquitin ligase, targets Sox6 for proteasomal degradation and affects fiber type-specific gene expression in muscle cells An, Chung-Il
2013
3 1 artikel
27 TWEAK promotes exercise intolerance by decreasing skeletal muscle oxidative phosphorylation capacity Sato, Shuichi
2013
3 1 artikel
28 Vascular-targeted therapies for Duchenne muscular dystrophy Ennen, James P
2013
3 1 artikel
29 Viral-mediated expression of desmin mutants to create mouse models of myofibrillar myopathy Joanne, Pierre
2013
3 1 artikel
                             29 gevonden resultaten
 
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