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Giornale Italiano Di Cardiologia (2006)
|
August 30, 2016
[ANMCO/SIC Consensus document: The heart failure network: organization of outpatient care]
Nadia Aspromonte, Michele Massimo Gulizia, Andrea Di Lenarda, et al.
Molecular Autism
|
November 19, 2020
High-throughput screening identifies histone deacetylase inhibitors that modulate GTF2I expression in 7q11.23 microduplication autism spectrum disorder patient-derived cortical neurons
Francesca Cavallo, Flavia Troglio, Giovanni Fagà, et al.
Molecular Psychiatry
|
February 22, 2025
YY1 mutations disrupt corticogenesis through a cell type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programs
Marlene F Pereira, Veronica Finazzi, Ludovico Rizzuti, et al.
Biorxiv : the Preprint Server for Biology
|
February 26, 2024
YY1 mutations disrupt corticogenesis through a cell-type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programs
Marlene F Pereira, Veronica Finazzi, Ludovico Rizzuti, et al.
Autophagy
|
July 21, 2021
Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders
Katrin Linda, Elly I Lewerissa, Anouk H A Verboven, et al.
Scientific Reports
|
June 26, 2024
Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients
Claudio Peter D'Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
European Journal of Internal Medicine
|
May 2, 2026
Hospital-to-community care pathways for patients with heart failure, an inter-society consensus document
Mario Mallardo, Pasquale Perrone Filardi, Claudio Micheletto, et al.
Nature Structural & Molecular Biology
|
August 25, 2025
The mitotic STAG3-cohesin complex shapes male germline nucleome
Masahiro Nagano, Bo Hu, Kosuke Ogata, et al.
American Journal of Human Genetics
|
June 3, 2017
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction
Michele Gabriele, Anneke T Vulto-van Silfhout, Pierre-Luc Germain, et al.
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Search research articles
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Showing results (21-30 of 29) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 29 results.
Giornale Italiano Di Cardiologia (2006)
|
August 30, 2016
[ANMCO/SIC Consensus document: The heart failure network: organization of outpatient care]
Nadia Aspromonte, Michele Massimo Gulizia, Andrea Di Lenarda, et al.
Molecular Autism
|
November 19, 2020
High-throughput screening identifies histone deacetylase inhibitors that modulate GTF2I expression in 7q11.23 microduplication autism spectrum disorder patient-derived cortical neurons
Francesca Cavallo, Flavia Troglio, Giovanni Fagà, et al.
Molecular Psychiatry
|
February 22, 2025
YY1 mutations disrupt corticogenesis through a cell type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programs
Marlene F Pereira, Veronica Finazzi, Ludovico Rizzuti, et al.
Biorxiv : the Preprint Server for Biology
|
February 26, 2024
YY1 mutations disrupt corticogenesis through a cell-type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programs
Marlene F Pereira, Veronica Finazzi, Ludovico Rizzuti, et al.
Autophagy
|
July 21, 2021
Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders
Katrin Linda, Elly I Lewerissa, Anouk H A Verboven, et al.
Scientific Reports
|
June 26, 2024
Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients
Claudio Peter D'Incal, Elisa Cappuyns, Kaoutar Choukri, et al.
European Journal of Internal Medicine
|
May 2, 2026
Hospital-to-community care pathways for patients with heart failure, an inter-society consensus document
Mario Mallardo, Pasquale Perrone Filardi, Claudio Micheletto, et al.
Nature Structural & Molecular Biology
|
August 25, 2025
The mitotic STAG3-cohesin complex shapes male germline nucleome
Masahiro Nagano, Bo Hu, Kosuke Ogata, et al.
American Journal of Human Genetics
|
June 3, 2017
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction
Michele Gabriele, Anneke T Vulto-van Silfhout, Pierre-Luc Germain, et al.
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of 3