Search research articles
Contact Us
Filters
Showing results (81-90 of 103) with videos related to
Page
of 11
Sort By:
American Journal of Human Genetics
|
July 29, 2008
Evolutionary forces shape the human RFPL1,2,3 genes toward a role in neocortex development
Jérôme Bonnefont, Sergey I Nikolaev, Anselme L Perrier, et al.
Science Translational Medicine
|
December 22, 2017
Human ESC-derived retinal epithelial cell sheets potentiate rescue of photoreceptor cell loss in rats with retinal degeneration
Karim Ben M'Barek, Walter Habeler, Alexandra Plancheron, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 8, 2015
In vitro modeling of hyperpigmentation associated to neurofibromatosis type 1 using melanocytes derived from human embryonic stem cells
Jennifer Allouche, Nathalia Bellon, Manoubia Saidani, et al.
The Lancet. Neurology
|
March 21, 2006
Effect of fetal neural transplants in patients with Huntington's disease 6 years after surgery: a long-term follow-up study
Anne-Catherine Bachoud-Lévi, Véronique Gaura, Pierre Brugières, et al.
Human Molecular Genetics
|
June 9, 2012
Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells
Maxime Feyeux, Fany Bourgois-Rocha, Amanda Redfern, et al.
Biomaterials
|
November 17, 2019
Clinical-grade production and safe delivery of human ESC derived RPE sheets in primates and rodents
Karim Ben M'Barek, Stéphane Bertin, Elena Brazhnikova, et al.
Stem Cells Translational Medicine
|
March 7, 2014
Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with hutchinson-gilford progeria syndrome
Sophie Blondel, Anne-Laure Jaskowiak, Anne-Laure Egesipe, et al.
Journal of Cell Science
|
February 28, 2013
mTOR-dependent proliferation defect in human ES-derived neural stem cells affected by myotonic dystrophy type 1
Jérôme Alexandre Denis, Morgane Gauthier, Latif Rachdi, et al.
Human Molecular Genetics
|
August 8, 2013
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1
Morgane Gauthier, Antoine Marteyn, Jérôme Alexandre Denis, et al.
Neuron
|
December 2, 2004
Functional recovery in a primate model of Parkinson's disease following motor cortex stimulation
Xavier Drouot, Satoru Oshino, Bechir Jarraya, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 103) with videos related to
Sort By:
Page
of 11
American Journal of Human Genetics
|
July 29, 2008
Evolutionary forces shape the human RFPL1,2,3 genes toward a role in neocortex development
Jérôme Bonnefont, Sergey I Nikolaev, Anselme L Perrier, et al.
Science Translational Medicine
|
December 22, 2017
Human ESC-derived retinal epithelial cell sheets potentiate rescue of photoreceptor cell loss in rats with retinal degeneration
Karim Ben M'Barek, Walter Habeler, Alexandra Plancheron, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 8, 2015
In vitro modeling of hyperpigmentation associated to neurofibromatosis type 1 using melanocytes derived from human embryonic stem cells
Jennifer Allouche, Nathalia Bellon, Manoubia Saidani, et al.
The Lancet. Neurology
|
March 21, 2006
Effect of fetal neural transplants in patients with Huntington's disease 6 years after surgery: a long-term follow-up study
Anne-Catherine Bachoud-Lévi, Véronique Gaura, Pierre Brugières, et al.
Human Molecular Genetics
|
June 9, 2012
Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells
Maxime Feyeux, Fany Bourgois-Rocha, Amanda Redfern, et al.
Biomaterials
|
November 17, 2019
Clinical-grade production and safe delivery of human ESC derived RPE sheets in primates and rodents
Karim Ben M'Barek, Stéphane Bertin, Elena Brazhnikova, et al.
Stem Cells Translational Medicine
|
March 7, 2014
Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with hutchinson-gilford progeria syndrome
Sophie Blondel, Anne-Laure Jaskowiak, Anne-Laure Egesipe, et al.
Journal of Cell Science
|
February 28, 2013
mTOR-dependent proliferation defect in human ES-derived neural stem cells affected by myotonic dystrophy type 1
Jérôme Alexandre Denis, Morgane Gauthier, Latif Rachdi, et al.
Human Molecular Genetics
|
August 8, 2013
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1
Morgane Gauthier, Antoine Marteyn, Jérôme Alexandre Denis, et al.
Neuron
|
December 2, 2004
Functional recovery in a primate model of Parkinson's disease following motor cortex stimulation
Xavier Drouot, Satoru Oshino, Bechir Jarraya, et al.
Page
of 11