Zobrazeno 1 - 10
of 83
pro vyhledávání: '"David Israeli"'
Autor:
Mathilde Sanson, Ai Vu Hong, Emmanuelle Massourides, Nathalie Bourg, Laurence Suel, Fatima Amor, Guillaume Corre, Paule Bénit, Inès Barthelemy, Stephane Blot, Anne Bigot, Christian Pinset, Pierre Rustin, Laurent Servais, Thomas Voit, Isabelle Richard, David Israeli
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/0c77b6003e324539b6d84c264c47812e
Autor:
Fatima Amor, Ai Vu Hong, Guillaume Corre, Mathilde Sanson, Laurence Suel, Stephanie Blaie, Laurent Servais, Thomas Voit, Isabelle Richard, David Israeli
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 3, Pp 677-693 (2021)
Abstract Background Duchenne muscular dystrophy (DMD) is a lethal muscle disease detected in approximately 1:5000 male births. DMD is caused by mutations in the DMD gene, encoding a critical protein that links the cytoskeleton and the extracellular m
Externí odkaz:
https://doaj.org/article/f5d408807f4241a8853b7739e99b7ed0
Publikováno v:
European Journal of Translational Myology (2021)
We recetly identified a signaling pathway that links the upregulation of miR-379 with a mitochondrial response in dystrophic muscle. In the present commentary, we explain the significance that this pathway may have in mitochondrial dysfunction in Duc
Externí odkaz:
https://doaj.org/article/1926c63cbc56400a9c3850d80aa316b0
Autor:
David Israeli, Jérémie Cosette, Guillaume Corre, Fatima Amor, Jérôme Poupiot, Daniel Stockholm, Marie Montus, Bernard Gjata, Isabelle Richard
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 13, Iss , Pp 494-502 (2019)
Sarcoglycanopathies are rare autosomic limb girdle muscular dystrophies caused by mutations in one of the genes coding for sarcoglycans. Sarcoglycans form a complex, which is an important part of the dystrophin-associated glycoprotein complex and whi
Externí odkaz:
https://doaj.org/article/ee8e06cdf9eb4628b70c764a33633dd6
Publikováno v:
Non-Coding RNA, Vol 8, Iss 4, p 48 (2022)
It is now well-established that microRNA dysregulation is a hallmark of human diseases, and that aberrant expression of miRNA is not randomly associated with human pathologies but plays a causal role in the pathological process. Investigations of the
Externí odkaz:
https://doaj.org/article/b8a8894b826d4bb08311b4b56f484f7b
Autor:
Nathalie Bourg, Ai Vu Hong, William Lostal, Abbass Jaber, Nicolas Guerchet, Guillaume Tanniou, Fanny Bordier, Emilie Bertil-Froidevaux, Christophe Georger, Nathalie Daniele, Isabelle Richard, David Israeli
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 4, p 2016 (2022)
Duchenne muscular dystrophy (DMD) is the most common and cureless muscle pediatric genetic disease, which is caused by the lack or the drastically reduced expression of dystrophin. Experimental therapeutic approaches for DMD have been mainly focused
Externí odkaz:
https://doaj.org/article/b33d5a168eaa421083eccfe1b5d5b3d0
Autor:
Zipora Yablonka-Reuveni, Frank Stockdale, Uri Nudel, David Israeli, Helen M. Blau, Asher Shainberg, Sara Neuman, Gania Kessler-Icekson, Erica Meghid Krull, Bruce Paterson, Ora Saxel Fuchs, David Greenberg, Rachel Sarig, Orna Halevy, Eijiro Ozawa, Don J. Katcoff
Publikováno v:
European Journal of Translational Myology (2020)
It is with great sadness that we have learned about the passing of Professor David Yaffe (1929-2020, Israel). Yehi Zichro Baruch - May his memory be a blessing. David was a man of family, science and nature. A native of Israel, David grew up in the h
Externí odkaz:
https://doaj.org/article/cef8fab63df3412d95691da602433ed6
Autor:
Anouar Boucheham, Vivien Sommard, Farida Zehraoui, Adnane Boualem, Mohamed Batouche, Abdelhafid Bendahmane, David Israeli, Fariza Tahi
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179787 (2017)
Many computational tools have been proposed during the two last decades for predicting piRNAs, which are molecules with important role in post-transcriptional gene regulation. However, these tools are mostly based on only one feature that is generall
Externí odkaz:
https://doaj.org/article/b4a45a5000e54894b18197d1ab9ec5df
Publikováno v:
International Journal of Biological Sciences, Vol 7, Iss 1, Pp 1-8 (2011)
The development of imaging methodologies for detecting blood-brain-barrier (BBB) disruption may help predict stroke patient's propensity to develop hemorrhagic complications following reperfusion. We have developed a delayed contrast extravasation MR
Externí odkaz:
https://doaj.org/article/e98f7180ffb545a3a94495a6e3cc1d34
Autor:
Nicolas Vignier, Fatima Amor, Paul Fogel, Angélique Duvallet, Jérôme Poupiot, Sabine Charrier, Michel Arock, Marie Montus, Isabelle Nelson, Isabelle Richard, Lucie Carrier, Laurent Servais, Thomas Voit, Gisèle Bonne, David Israeli
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e55281 (2013)
Biomarkers are critically important for disease diagnosis and monitoring. In particular, close monitoring of disease evolution is eminently required for the evaluation of therapeutic treatments. Classical monitoring methods in muscular dystrophies ar
Externí odkaz:
https://doaj.org/article/5331d55271d5433a82a47bf22aaec121