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Children (Basel, Switzerland)
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September 28, 2023
Metabolic Profile of Patients with Smith-Magenis Syndrome: An Observational Study with Literature Review
Clelia Cipolla, Linda Sessa, Giulia Rotunno, et al.
Stem Cell Research
|
October 22, 2022
Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3
Elisa Maria Turco, Angela Maria Giada Giovenale, Giovannina Rotundo, et al.
Stem Cell Research
|
September 16, 2018
Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7
Elisa Maria Turco, Ersilia Vinci, Filomena Altieri, et al.
International Journal of Molecular Sciences
|
February 2, 2021
Known Drugs Identified by Structure-Based Virtual Screening Are Able to Bind Sigma-1 Receptor and Increase Growth of Huntington Disease Patient-Derived Cells
Theo Battista, Gianmarco Pascarella, David Sasah Staid, et al.
Circulation Research
|
November 3, 2007
Nitric oxide modulates chromatin folding in human endothelial cells via protein phosphatase 2A activation and class II histone deacetylases nuclear shuttling
Barbara Illi, Claudio Dello Russo, Claudia Colussi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 7, 2009
Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy
Claudia Colussi, Aymone Gurtner, Jessica Rosati, et al.
Stem Cell Research
|
June 9, 2024
Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)
Alessia Casamassa, Giovannina Rotundo, Chiara Ceresoni, et al.
Stem Cell Research
|
September 8, 2019
Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA)
Eris Bidollari, Giovannina Rotundo, Filomena Altieri, et al.
Stem Cell Research
|
September 11, 2024
Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region
Angela Maria Giada Giovenale, Elisa Maria Turco, Martina Mazzoni, et al.
Stem Cell Research & Therapy
|
January 17, 2019
DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient
Simona Ruggieri, Luigi Viggiano, Tiziana Annese, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 69) with videos related to
Sort By:
Page
of 7
Children (Basel, Switzerland)
|
September 28, 2023
Metabolic Profile of Patients with Smith-Magenis Syndrome: An Observational Study with Literature Review
Clelia Cipolla, Linda Sessa, Giulia Rotunno, et al.
Stem Cell Research
|
October 22, 2022
Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3
Elisa Maria Turco, Angela Maria Giada Giovenale, Giovannina Rotundo, et al.
Stem Cell Research
|
September 16, 2018
Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7
Elisa Maria Turco, Ersilia Vinci, Filomena Altieri, et al.
International Journal of Molecular Sciences
|
February 2, 2021
Known Drugs Identified by Structure-Based Virtual Screening Are Able to Bind Sigma-1 Receptor and Increase Growth of Huntington Disease Patient-Derived Cells
Theo Battista, Gianmarco Pascarella, David Sasah Staid, et al.
Circulation Research
|
November 3, 2007
Nitric oxide modulates chromatin folding in human endothelial cells via protein phosphatase 2A activation and class II histone deacetylases nuclear shuttling
Barbara Illi, Claudio Dello Russo, Claudia Colussi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 7, 2009
Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy
Claudia Colussi, Aymone Gurtner, Jessica Rosati, et al.
Stem Cell Research
|
June 9, 2024
Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)
Alessia Casamassa, Giovannina Rotundo, Chiara Ceresoni, et al.
Stem Cell Research
|
September 8, 2019
Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA)
Eris Bidollari, Giovannina Rotundo, Filomena Altieri, et al.
Stem Cell Research
|
September 11, 2024
Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region
Angela Maria Giada Giovenale, Elisa Maria Turco, Martina Mazzoni, et al.
Stem Cell Research & Therapy
|
January 17, 2019
DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient
Simona Ruggieri, Luigi Viggiano, Tiziana Annese, et al.
Page
of 7