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The Journal of Biological Chemistry
|
July 26, 2011
Hepatic nuclear factor 1alpha (HNF1alpha) dysfunction down-regulates X-box-binding protein 1 (XBP1) and sensitizes beta-cells to endoplasmic reticulum stress
Clare L Kirkpatrick, Andreas Wiederkehr, Mathurin Baquié, et al.
Nature Genetics
|
December 14, 2011
GATA6 haploinsufficiency causes pancreatic agenesis in humans
Hana Lango Allen, Sarah E Flanagan, Charles Shaw-Smith, et al.
Cell Reports
|
April 14, 2021
Neonatal diabetes mutations disrupt a chromatin pioneering function that activates the human insulin gene
Ildem Akerman, Miguel Angel Maestro, Elisa De Franco, et al.
Nature Communications
|
September 22, 2020
A predictable conserved DNA base composition signature defines human core DNA replication origins
Ildem Akerman, Bahar Kasaai, Alina Bazarova, et al.
Biorxiv : the Preprint Server for Biology
|
June 5, 2026
High-purity stem cell-derived β-cells recapitulate key transcriptional and functional features of human islets
Rémi B Fiancette, Junyue Huang, Christine Stephens, et al.
JCI Insight
|
July 15, 2021
Prolyl-4-hydroxylase 3 maintains β cell glucose metabolism during fatty acid excess in mice
Daniela Nasteska, Federica Cuozzo, Katrina Viloria, et al.
JCI Insight
|
April 13, 2021
Systemic and adipocyte transcriptional and metabolic dysregulation in idiopathic intracranial hypertension
Connar Sj Westgate, Hannah F Botfield, Zerin Alimajstorovic, et al.
Nature Communications
|
January 30, 2021
PDX1<sup>LOW</sup> MAFA<sup>LOW</sup> β-cells contribute to islet function and insulin release
Daniela Nasteska, Nicholas H F Fine, Fiona B Ashford, et al.
Nature Communications
|
July 21, 2021
Author Correction: PDX1<sup>LOW</sup> MAFA<sup>LOW</sup> β-cells contribute to islet function and insulin release
Daniela Nasteska, Nicholas H F Fine, Fiona B Ashford, et al.
Nature Communications
|
July 2, 2025
A heterozygous CEBPA mutation disrupting the bZIP domain in a RUNX1 and SRSF2 mutational background causes MDS disease progression
Ruba Almaghrabi, Yara Alyahyawi, Peter Keane, et al.
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of 3
Search research articles
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Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
The Journal of Biological Chemistry
|
July 26, 2011
Hepatic nuclear factor 1alpha (HNF1alpha) dysfunction down-regulates X-box-binding protein 1 (XBP1) and sensitizes beta-cells to endoplasmic reticulum stress
Clare L Kirkpatrick, Andreas Wiederkehr, Mathurin Baquié, et al.
Nature Genetics
|
December 14, 2011
GATA6 haploinsufficiency causes pancreatic agenesis in humans
Hana Lango Allen, Sarah E Flanagan, Charles Shaw-Smith, et al.
Cell Reports
|
April 14, 2021
Neonatal diabetes mutations disrupt a chromatin pioneering function that activates the human insulin gene
Ildem Akerman, Miguel Angel Maestro, Elisa De Franco, et al.
Nature Communications
|
September 22, 2020
A predictable conserved DNA base composition signature defines human core DNA replication origins
Ildem Akerman, Bahar Kasaai, Alina Bazarova, et al.
Biorxiv : the Preprint Server for Biology
|
June 5, 2026
High-purity stem cell-derived β-cells recapitulate key transcriptional and functional features of human islets
Rémi B Fiancette, Junyue Huang, Christine Stephens, et al.
JCI Insight
|
July 15, 2021
Prolyl-4-hydroxylase 3 maintains β cell glucose metabolism during fatty acid excess in mice
Daniela Nasteska, Federica Cuozzo, Katrina Viloria, et al.
JCI Insight
|
April 13, 2021
Systemic and adipocyte transcriptional and metabolic dysregulation in idiopathic intracranial hypertension
Connar Sj Westgate, Hannah F Botfield, Zerin Alimajstorovic, et al.
Nature Communications
|
January 30, 2021
PDX1<sup>LOW</sup> MAFA<sup>LOW</sup> β-cells contribute to islet function and insulin release
Daniela Nasteska, Nicholas H F Fine, Fiona B Ashford, et al.
Nature Communications
|
July 21, 2021
Author Correction: PDX1<sup>LOW</sup> MAFA<sup>LOW</sup> β-cells contribute to islet function and insulin release
Daniela Nasteska, Nicholas H F Fine, Fiona B Ashford, et al.
Nature Communications
|
July 2, 2025
A heterozygous CEBPA mutation disrupting the bZIP domain in a RUNX1 and SRSF2 mutational background causes MDS disease progression
Ruba Almaghrabi, Yara Alyahyawi, Peter Keane, et al.
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