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Stem Cell Reports
|
April 23, 2021
Automatic identification of small molecules that promote cell conversion and reprogramming
Francesco Napolitano, Trisevgeni Rapakoulia, Patrizia Annunziata, et al.
The EMBO Journal
|
September 15, 2023
TFEB and TFE3 control glucose homeostasis by regulating insulin gene expression
Adrien Pasquier, Nunzia Pastore, Luca D'Orsi, et al.
Cell Reports Methods
|
February 19, 2026
Human neuromuscular organoids mimic cancer-induced muscle cachexia
Pietro Chiolerio, Beatrice Auletta, Camilla Pezzini, et al.
Nature Cell Biology
|
April 27, 2023
Esrrb guides naive pluripotent cells through the formative transcriptional programme
Elena Carbognin, Valentina Carlini, Francesco Panariello, et al.
Journal of Molecular Cell Biology
|
February 2, 2024
Identification of druggable host dependency factors shared by multiple SARS-CoV-2 variants of concern
Ilaria Frasson, Linda Diamante, Manuela Zangrossi, et al.
Biorxiv : the Preprint Server for Biology
|
November 28, 2024
Excitatory Cortical Neurons from CDKL5 Deficiency Disorder Patient-Derived Organoids Show Early Hyperexcitability Not Identified in Neurogenin2 Induced Neurons
Madison R Glass, Dosh Whye, Nickesha C Anderson, et al.
Nature Communications
|
May 29, 2023
Multi-omic approach characterises the neuroprotective role of retromer in regulating lysosomal health
James L Daly, Chris M Danson, Philip A Lewis, et al.
Nature Communications
|
February 11, 2018
Genome-wide tracking of dCas9-methyltransferase footprints
Christina Galonska, Jocelyn Charlton, Alexandra L Mattei, et al.
Neurobiology of Disease
|
September 10, 2025
Excitatory cortical neurons from CDKL5 deficiency disorder patient-derived organoids show early hyperexcitability not identified in neurogenin2 induced neurons
Madison R Glass, Dosh Whye, Nickesha C Anderson, et al.
European Journal of Human Genetics : EJHG
|
December 12, 2024
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomalies
Lucia Micale, Aikaterini Vourlia, Carmela Fusco, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 8
Stem Cell Reports
|
April 23, 2021
Automatic identification of small molecules that promote cell conversion and reprogramming
Francesco Napolitano, Trisevgeni Rapakoulia, Patrizia Annunziata, et al.
The EMBO Journal
|
September 15, 2023
TFEB and TFE3 control glucose homeostasis by regulating insulin gene expression
Adrien Pasquier, Nunzia Pastore, Luca D'Orsi, et al.
Cell Reports Methods
|
February 19, 2026
Human neuromuscular organoids mimic cancer-induced muscle cachexia
Pietro Chiolerio, Beatrice Auletta, Camilla Pezzini, et al.
Nature Cell Biology
|
April 27, 2023
Esrrb guides naive pluripotent cells through the formative transcriptional programme
Elena Carbognin, Valentina Carlini, Francesco Panariello, et al.
Journal of Molecular Cell Biology
|
February 2, 2024
Identification of druggable host dependency factors shared by multiple SARS-CoV-2 variants of concern
Ilaria Frasson, Linda Diamante, Manuela Zangrossi, et al.
Biorxiv : the Preprint Server for Biology
|
November 28, 2024
Excitatory Cortical Neurons from CDKL5 Deficiency Disorder Patient-Derived Organoids Show Early Hyperexcitability Not Identified in Neurogenin2 Induced Neurons
Madison R Glass, Dosh Whye, Nickesha C Anderson, et al.
Nature Communications
|
May 29, 2023
Multi-omic approach characterises the neuroprotective role of retromer in regulating lysosomal health
James L Daly, Chris M Danson, Philip A Lewis, et al.
Nature Communications
|
February 11, 2018
Genome-wide tracking of dCas9-methyltransferase footprints
Christina Galonska, Jocelyn Charlton, Alexandra L Mattei, et al.
Neurobiology of Disease
|
September 10, 2025
Excitatory cortical neurons from CDKL5 deficiency disorder patient-derived organoids show early hyperexcitability not identified in neurogenin2 induced neurons
Madison R Glass, Dosh Whye, Nickesha C Anderson, et al.
European Journal of Human Genetics : EJHG
|
December 12, 2024
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomalies
Lucia Micale, Aikaterini Vourlia, Carmela Fusco, et al.
Page
of 8