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Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 9, 2017
AAV-PHP.B-Mediated Global-Scale Expression in the Mouse Nervous System Enables GBA1 Gene Therapy for Wide Protection from Synucleinopathy
Giuseppe Morabito, Serena G Giannelli, Gabriele Ordazzo, et al.
American Journal of Human Genetics
|
June 24, 2008
FOXG1 is responsible for the congenital variant of Rett syndrome
Francesca Ariani, Giuseppe Hayek, Dalila Rondinella, et al.
The Journal of Clinical Investigation
|
June 18, 2014
Remote control of induced dopaminergic neurons in parkinsonian rats
Maria Teresa Dell'Anno, Massimiliano Caiazzo, Damiana Leo, et al.
Nature Communications
|
February 8, 2017
Two factor-based reprogramming of rodent and human fibroblasts into Schwann cells
Pietro Giuseppe Mazzara, Luca Massimino, Marta Pellegatta, et al.
Plos One
|
September 17, 2008
Magic-factor 1, a partial agonist of Met, induces muscle hypertrophy by protecting myogenic progenitors from apoptosis
Marco Cassano, Stefano Biressi, Amanda Finan, et al.
Neuron
|
April 20, 2010
The apical complex couples cell fate and cell survival to cerebral cortical development
Seonhee Kim, Maria K Lehtinen, Alessandro Sessa, et al.
Plos One
|
July 25, 2019
Correction: Magic-Factor 1, a Partial Agonist of Met, Induces Muscle Hypertrophy by Protecting Myogenic Progenitors from Apoptosis
Marco Cassano, Stefano Biressi, Amanda Finan, et al.
Nature Communications
|
July 1, 2021
SETBP1 accumulation induces P53 inhibition and genotoxic stress in neural progenitors underlying neurodegeneration in Schinzel-Giedion syndrome
Federica Banfi, Alicia Rubio, Mattia Zaghi, et al.
Diabetologia
|
November 9, 2024
A WFS1 variant disrupting acceptor splice site uncovers the impact of alternative splicing on beta cell apoptosis in a patient with Wolfram syndrome
Raniero Chimienti, Silvia Torchio, Gabriel Siracusano, et al.
EMBO Molecular Medicine
|
August 13, 2016
Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration
Daniel I Orellana, Paolo Santambrogio, Alicia Rubio, et al.
Page
of 14
Search research articles
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Showing results (101-110 of 131) with videos related to
Sort By:
Page
of 14
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 9, 2017
AAV-PHP.B-Mediated Global-Scale Expression in the Mouse Nervous System Enables GBA1 Gene Therapy for Wide Protection from Synucleinopathy
Giuseppe Morabito, Serena G Giannelli, Gabriele Ordazzo, et al.
American Journal of Human Genetics
|
June 24, 2008
FOXG1 is responsible for the congenital variant of Rett syndrome
Francesca Ariani, Giuseppe Hayek, Dalila Rondinella, et al.
The Journal of Clinical Investigation
|
June 18, 2014
Remote control of induced dopaminergic neurons in parkinsonian rats
Maria Teresa Dell'Anno, Massimiliano Caiazzo, Damiana Leo, et al.
Nature Communications
|
February 8, 2017
Two factor-based reprogramming of rodent and human fibroblasts into Schwann cells
Pietro Giuseppe Mazzara, Luca Massimino, Marta Pellegatta, et al.
Plos One
|
September 17, 2008
Magic-factor 1, a partial agonist of Met, induces muscle hypertrophy by protecting myogenic progenitors from apoptosis
Marco Cassano, Stefano Biressi, Amanda Finan, et al.
Neuron
|
April 20, 2010
The apical complex couples cell fate and cell survival to cerebral cortical development
Seonhee Kim, Maria K Lehtinen, Alessandro Sessa, et al.
Plos One
|
July 25, 2019
Correction: Magic-Factor 1, a Partial Agonist of Met, Induces Muscle Hypertrophy by Protecting Myogenic Progenitors from Apoptosis
Marco Cassano, Stefano Biressi, Amanda Finan, et al.
Nature Communications
|
July 1, 2021
SETBP1 accumulation induces P53 inhibition and genotoxic stress in neural progenitors underlying neurodegeneration in Schinzel-Giedion syndrome
Federica Banfi, Alicia Rubio, Mattia Zaghi, et al.
Diabetologia
|
November 9, 2024
A WFS1 variant disrupting acceptor splice site uncovers the impact of alternative splicing on beta cell apoptosis in a patient with Wolfram syndrome
Raniero Chimienti, Silvia Torchio, Gabriel Siracusano, et al.
EMBO Molecular Medicine
|
August 13, 2016
Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration
Daniel I Orellana, Paolo Santambrogio, Alicia Rubio, et al.
Page
of 14