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M Raynaud

Showing results (21-30 of 64) with videos related to

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European Journal of Human Genetics : EJHG|June 15, 2000
Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three familiesM Raynaud, M P Moizard, B Dessay, et al.
Physical Review. E|March 19, 2021
Ultrashort high energy electron bunches from tunable surface plasma waves driven with laser wavefront rotationS Marini, P S Kleij, F Pisani, et al.
Biological Psychiatry|September 15, 1996
X chromosome and infantile autismE Petit, J Hérault, M Raynaud, et al.
American Journal of Medical Genetics|April 6, 1999
Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screeningM P Moizard, A Toutain, D Fournier, et al.
Stem Cell Research|August 28, 2013
Endothelial cells provide a niche for placental hematopoietic stem/progenitor cell expansion through broad transcriptomic modificationChristophe M Raynaud, Jason M Butler, Najeeb M Halabi, et al.
Heart (British Cardiac Society)|October 20, 1999
Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods?D Babuty, L Fauchier, D Tena-Carbi, et al.
Plos One|January 24, 2013
Human embryonic stem cell derived mesenchymal progenitors express cardiac markers but do not form contractile cardiomyocytesChristophe M Raynaud, Najeeb Halabi, David A Elliott, et al.
The American Journal of Cardiology|November 24, 1999
Significance of late ventricular potentials in myotonic dystrophyD Babuty, L Fauchier, D Tena-Carbi, et al.
Clinical Genetics|April 24, 2010
Novel missense mutations in the ubiquitination-related gene UBE2A cause a recognizable X-linked mental retardation syndromeB Budny, M Badura-Stronka, A Materna-Kiryluk, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|June 15, 2000
Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three familiesM Raynaud, M P Moizard, B Dessay, et al.
Physical Review. E|March 19, 2021
Ultrashort high energy electron bunches from tunable surface plasma waves driven with laser wavefront rotationS Marini, P S Kleij, F Pisani, et al.
Biological Psychiatry|September 15, 1996
X chromosome and infantile autismE Petit, J Hérault, M Raynaud, et al.
American Journal of Medical Genetics|April 6, 1999
Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screeningM P Moizard, A Toutain, D Fournier, et al.
Stem Cell Research|August 28, 2013
Endothelial cells provide a niche for placental hematopoietic stem/progenitor cell expansion through broad transcriptomic modificationChristophe M Raynaud, Jason M Butler, Najeeb M Halabi, et al.
Heart (British Cardiac Society)|October 20, 1999
Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods?D Babuty, L Fauchier, D Tena-Carbi, et al.
Plos One|January 24, 2013
Human embryonic stem cell derived mesenchymal progenitors express cardiac markers but do not form contractile cardiomyocytesChristophe M Raynaud, Najeeb Halabi, David A Elliott, et al.
The American Journal of Cardiology|November 24, 1999
Significance of late ventricular potentials in myotonic dystrophyD Babuty, L Fauchier, D Tena-Carbi, et al.
Clinical Genetics|April 24, 2010
Novel missense mutations in the ubiquitination-related gene UBE2A cause a recognizable X-linked mental retardation syndromeB Budny, M Badura-Stronka, A Materna-Kiryluk, et al.
Pageof 7