Search research articles
Contact Us
Filters
Showing results (151-160 of 358) with videos related to
Page
of 36
Sort By:
Stem Cell Research
|
January 16, 2018
Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850)
Jessica Rosati, Filomena Altieri, Silvia Tardivo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 5, 2007
Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements
Oronzo Scarciolla, Francesco Brancati, Enza Maria Valente, et al.
Stem Cell Research
|
March 17, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene
Manuela Mura, Federica Pisano, Manuela Stefanello, et al.
Autophagy
|
April 4, 2017
PINK1 and BECN1 relocalize at mitochondria-associated membranes during mitophagy and promote ER-mitochondria tethering and autophagosome formation
Vania Gelmetti, Priscilla De Rosa, Liliana Torosantucci, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2021
Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal Study
Francesco Testa, Andrea Sodi, Sabrina Signorini, et al.
Human Mutation
|
December 13, 2006
Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum
Roberta Marongiu, Francesco Brancati, Angelo Antonini, et al.
World Journal of Hepatology
|
February 2, 2019
High prevalence of occult hepatitis C infection in predialysis patients
Luís Henrique Bezerra Cavalcanti Sette, Edmundo Pessoa de Almeida Lopes, Nathália Campello Guedes Dos Anjos, et al.
Plos One
|
October 28, 2016
Brain Connectivity Changes in Autosomal Recessive Parkinson Disease: A Model for the Sporadic Form
Elena Makovac, Mara Cercignani, Laura Serra, et al.
Journal of Clinical Medicine
|
February 24, 2024
Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements
Adriana Prato, Lara Cirnigliaro, Federica Maugeri, et al.
Stem Cell Research
|
June 16, 2019
Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome
Filomena Altieri, Angela D'Anzi, Francesco Martello, et al.
Page
of 36
Search research articles
Search
Showing results (151-160 of 358) with videos related to
Sort By:
Page
of 36
Stem Cell Research
|
January 16, 2018
Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850)
Jessica Rosati, Filomena Altieri, Silvia Tardivo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 5, 2007
Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements
Oronzo Scarciolla, Francesco Brancati, Enza Maria Valente, et al.
Stem Cell Research
|
March 17, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene
Manuela Mura, Federica Pisano, Manuela Stefanello, et al.
Autophagy
|
April 4, 2017
PINK1 and BECN1 relocalize at mitochondria-associated membranes during mitophagy and promote ER-mitochondria tethering and autophagosome formation
Vania Gelmetti, Priscilla De Rosa, Liliana Torosantucci, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2021
Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal Study
Francesco Testa, Andrea Sodi, Sabrina Signorini, et al.
Human Mutation
|
December 13, 2006
Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum
Roberta Marongiu, Francesco Brancati, Angelo Antonini, et al.
World Journal of Hepatology
|
February 2, 2019
High prevalence of occult hepatitis C infection in predialysis patients
Luís Henrique Bezerra Cavalcanti Sette, Edmundo Pessoa de Almeida Lopes, Nathália Campello Guedes Dos Anjos, et al.
Plos One
|
October 28, 2016
Brain Connectivity Changes in Autosomal Recessive Parkinson Disease: A Model for the Sporadic Form
Elena Makovac, Mara Cercignani, Laura Serra, et al.
Journal of Clinical Medicine
|
February 24, 2024
Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements
Adriana Prato, Lara Cirnigliaro, Federica Maugeri, et al.
Stem Cell Research
|
June 16, 2019
Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome
Filomena Altieri, Angela D'Anzi, Francesco Martello, et al.
Page
of 36