Search research articles
Contact Us
Filters
Showing results (151-160 of 346) with videos related to
Page
of 35
Sort By:
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1984
Embryonic----Fetal Hb switch in humans: studies on erythroid bursts generated by embryonic progenitors from yolk sac and liver
C Peschle, A R Migliaccio, G Migliaccio, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 22, 2021
Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical model
Margherita Bersani, Mafalda Rizzuti, Elisa Pagliari, et al.
Journal of Neurology
|
May 1, 1993
Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency
N Bresolin, G P Comi, F Fortunato, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
September 10, 2005
Multipotentiality, homing properties, and pyramidal neurogenesis of CNS-derived LeX(ssea-1)+/CXCR4+ stem cells
Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Journal of Neuroscience Research
|
November 22, 2002
Neuroectodermal and microglial differentiation of bone marrow cells in the mouse spinal cord and sensory ganglia
S Corti, F Locatelli, C Donadoni, et al.
Experimental Neurology
|
November 14, 2002
Modulated generation of neuronal cells from bone marrow by expansion and mobilization of circulating stem cells with in vivo cytokine treatment
S Corti, F Locatelli, S Strazzer, et al.
Brain : a Journal of Neurology
|
February 1, 1994
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates
G P Comi, A Prelle, N Bresolin, et al.
Neurology
|
August 23, 2000
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy
G Felisari, F Martinelli Boneschi, A Bardoni, et al.
Journal of the Neurological Sciences
|
September 23, 2008
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion
S Lucchiari, S Pagliarani, S Corti, et al.
Human Molecular Genetics
|
July 24, 2010
Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosis
Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Page
of 35
Search research articles
Search
Showing results (151-160 of 346) with videos related to
Sort By:
Page
of 35
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1984
Embryonic----Fetal Hb switch in humans: studies on erythroid bursts generated by embryonic progenitors from yolk sac and liver
C Peschle, A R Migliaccio, G Migliaccio, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 22, 2021
Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical model
Margherita Bersani, Mafalda Rizzuti, Elisa Pagliari, et al.
Journal of Neurology
|
May 1, 1993
Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency
N Bresolin, G P Comi, F Fortunato, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
September 10, 2005
Multipotentiality, homing properties, and pyramidal neurogenesis of CNS-derived LeX(ssea-1)+/CXCR4+ stem cells
Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Journal of Neuroscience Research
|
November 22, 2002
Neuroectodermal and microglial differentiation of bone marrow cells in the mouse spinal cord and sensory ganglia
S Corti, F Locatelli, C Donadoni, et al.
Experimental Neurology
|
November 14, 2002
Modulated generation of neuronal cells from bone marrow by expansion and mobilization of circulating stem cells with in vivo cytokine treatment
S Corti, F Locatelli, S Strazzer, et al.
Brain : a Journal of Neurology
|
February 1, 1994
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates
G P Comi, A Prelle, N Bresolin, et al.
Neurology
|
August 23, 2000
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy
G Felisari, F Martinelli Boneschi, A Bardoni, et al.
Journal of the Neurological Sciences
|
September 23, 2008
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion
S Lucchiari, S Pagliarani, S Corti, et al.
Human Molecular Genetics
|
July 24, 2010
Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosis
Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Page
of 35