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Ferdinando Squitieri

Showing results (91-100 of 147) with videos related to

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Stem Cell Research|January 18, 2018
Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington DiseaseJessica Rosati, Eris Bidollari, Giovannina Rotundo, et al.
Autophagy|July 20, 2017
Polyglutamine tracts regulate autophagyAvraham Ashkenazi, Carla F Bento, Thomas Ricketts, et al.
Nature|April 27, 2017
Polyglutamine tracts regulate beclin 1-dependent autophagyAvraham Ashkenazi, Carla F Bento, Thomas Ricketts, et al.
Parkinsonism & Related Disorders|October 30, 2012
The influence of gender on phenotype and disease progression in patients with Huntington's diseaseDaniel Zielonka, Johan Marinus, Raymund A C Roos, et al.
Molecular Brain|December 17, 2013
Changes of peripheral TGF-β1 depend on monocytes-derived macrophages in Huntington diseaseAlba Di Pardo, Silvia Alberti, Vittorio Maglione, et al.
Human Mutation|December 6, 2005
Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locusChristina L Liquori, Michel J Berg, Ferdinando Squitieri, et al.
Stem Cell Research|February 28, 2018
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stageEris Bidollari, Giovannina Rotundo, Daniela Ferrari, et al.
Stem Cell Research|April 29, 2018
Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's DiseaseGiovannina Rotundo, Eris Bidollari, Daniela Ferrari, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Frequency of the loss of CAA interruption in the HTT CAG tract and implications for Huntington disease in the reduced penetrance rangeHailey Findlay Black, Galen E B Wright, Jennifer A Collins, et al.
Neurogenetics|December 7, 2007
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohortsChristina L Liquori, Silvana Penco, Judith Gault, et al.
Pageof 15

Showing results (91-100 of 147) with videos related to

Sort By:
Pageof 15
Stem Cell Research|January 18, 2018
Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington DiseaseJessica Rosati, Eris Bidollari, Giovannina Rotundo, et al.
Autophagy|July 20, 2017
Polyglutamine tracts regulate autophagyAvraham Ashkenazi, Carla F Bento, Thomas Ricketts, et al.
Nature|April 27, 2017
Polyglutamine tracts regulate beclin 1-dependent autophagyAvraham Ashkenazi, Carla F Bento, Thomas Ricketts, et al.
Parkinsonism & Related Disorders|October 30, 2012
The influence of gender on phenotype and disease progression in patients with Huntington's diseaseDaniel Zielonka, Johan Marinus, Raymund A C Roos, et al.
Molecular Brain|December 17, 2013
Changes of peripheral TGF-β1 depend on monocytes-derived macrophages in Huntington diseaseAlba Di Pardo, Silvia Alberti, Vittorio Maglione, et al.
Human Mutation|December 6, 2005
Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locusChristina L Liquori, Michel J Berg, Ferdinando Squitieri, et al.
Stem Cell Research|February 28, 2018
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stageEris Bidollari, Giovannina Rotundo, Daniela Ferrari, et al.
Stem Cell Research|April 29, 2018
Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's DiseaseGiovannina Rotundo, Eris Bidollari, Daniela Ferrari, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Frequency of the loss of CAA interruption in the HTT CAG tract and implications for Huntington disease in the reduced penetrance rangeHailey Findlay Black, Galen E B Wright, Jennifer A Collins, et al.
Neurogenetics|December 7, 2007
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohortsChristina L Liquori, Silvana Penco, Judith Gault, et al.
Pageof 15