[PDF][PDF] Stockholm

SE Stockholm - SE: International Research Group on Wood …, 2013 - kartor.118700.se
BAKGRUND Stockholm Vatten AB (SVOA) har genomfort en upphandlmg avseende"
SCADA-och Labbsystem". Upphandlingen har genomforts I syfte att mstallera ett nytt gemensamt …

Molecular adaptations of neuromuscular disease‐associated proteins in response to eccentric exercise in human skeletal muscle

L Feasson, D Stockholm, D Freyssenet… - The Journal of …, 2002 - Wiley Online Library
The molecular events by which eccentric muscle contractions induce muscle damage and
remodelling remain largely unknown. We assessed whether eccentric exercise modulates the …

Intracellular trafficking of adeno-associated virus vectors: routing to the late endosomal compartment and proteasome degradation

AM Douar, K Poulard, D Stockholm, O Danos - Journal of virology, 2001 - Am Soc Microbiol
… (D) HeLa cells were infected for 2 h with rAAV-Luc at an MOI of 2, 25, or 100, in the presence
of increasing doses of bafilomycin A 1 . Values are given with the standard deviations (n = 3…

Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IκBα/nuclear factor κB pathway perturbation in mice

…, S Baghdiguian, M Herasse, D Stockholm… - The Journal of cell …, 2000 - rupress.org
Calpain 3 is known as the skeletal muscle–specific member of the calpains, a family of
intracellular nonlysosomal cysteine proteases. It was previously shown that defects in the human …

[HTML][HTML] The origin of phenotypic heterogeneity in a clonal cell population in vitro

D Stockholm, R Benchaouir, J Picot, P Rameau… - PloS one, 2007 - journals.plos.org
… Four representative images (a, b, c and d) are shown from regions with different cell densities…
The c and d patterns are significantly different from a random pattern, because the values of …

A lentiviral vector encoding the human Wiskott–Aldrich syndrome protein corrects immune and cytoskeletal defects in WASP knockout mice

S Charrier, D Stockholm, K Seye, P Opolon, M Taveau… - Gene therapy, 2005 - nature.com
Wiskott–Aldrich syndrome (WAS) is an immune deficiency with thrombopenia resulting from
mutations in the WASP gene. This gene normally encodes the Wiskott–Aldrich syndrome …

Imaging calpain protease activity by multiphoton FRET in living mice

D Stockholm, M Bartoli, G Sillon, N Bourg… - Journal of molecular …, 2005 - Elsevier
… Several peaked distributions of FRETeff values were obtained in individual fibers (Figure
5(d), histograms ROIs 1–8) and consistently, our biochemical assay showed partial calpain-…

Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events

…, D Stockholm, C Beley, D Montarras… - … and cellular biology, 1999 - Taylor & Francis
Calpain 3 is a nonlysosomal cysteine protease whose biological functions remain unknown.
We previously demonstrated that this protease is altered in limb girdle muscular dystrophy …

[HTML][HTML] Lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy

…, M Pryadkina, P Borel, L Suel, JA Roche, D Stockholm… - PloS one, 2012 - journals.plos.org
Mutations in the dysferlin gene are the cause of Limb-girdle Muscular Dystrophy type 2B
and Miyoshi Myopathy. The dysferlin protein has been implicated in sarcolemmal resealing, …

Natural history of LGMD 2A for delineating outcome measures in clinical trials

I Richard, JY Hogrel, D Stockholm… - Annals of clinical …, 2016 - Wiley Online Library
… 5D). The observation of the respective decline between the different mutation types of the
MMT, QMT, and MFM evaluations (Fig. 6) also confirmed a steeper decline for the M3 group. …