Hjem
  • E-postluiza.ghila@uib.no
  • Besøksadresse
    Barne- og ungdomssjukehuset (BUS1)
    Haukelandsbakken 15
    5021 Bergen
    Rom 
    6th floor, room 6110
  • Postadresse
    Postboks 7804
    5020 Bergen
Vitenskapelig artikkel
  • Vis forfatter(e) (2024). Targeted Gene Silencing by Using GapmeRs in Differentiating Human-Induced Pluripotent Stem Cells (hiPSC) Toward Pancreatic Progenitors. Methods in molecular biology. 23-38.
  • Vis forfatter(e) (2024). Glucose Concentration in Regulating Induced Pluripotent Stem Cells Differentiation Toward Insulin-Producing Cells. Transplant International.
  • Vis forfatter(e) (2023). Modulation of Unfolded Protein Response Restores Survival and Function of β-Cells Exposed to the Endocrine Disruptor Bisphenol A. International Journal of Molecular Sciences.
  • Vis forfatter(e) (2023). Global proteomics reveals insulin abundance as a marker of human islet homeostasis alterations. Acta Physiologica. 15 sider.
  • Vis forfatter(e) (2022). Spatial Environment Affects HNF4A Mutation-Specific Proteome Signatures and Cellular Morphology in hiPSC-Derived β-Like Cells. Diabetes. 862-869.
  • Vis forfatter(e) (2022). Islet cell replacement and transplantation immunology in a mouse strain with inducible diabetes. Scientific Reports.
  • Vis forfatter(e) (2021). Chronically elevated exogenous glucose elicits antipodal effects on the proteome signature of differentiating human ipsc-derived pancreatic progenitors. International Journal of Molecular Sciences.
  • Vis forfatter(e) (2021). A Method for Encapsulation and Transplantation into Diabetic Mice of Human Induced Pluripotent Stem Cells (hiPSC)-Derived Pancreatic Progenitors. Methods in molecular biology.
  • Vis forfatter(e) (2020). In vivo environment swiftly restricts human pancreatic progenitors toward mono-hormonal identity via a HNF1A/HNF4A mechanism. Frontiers in Cell and Developmental Biology. 1-14.
  • Vis forfatter(e) (2020). Encapsulation boosts islet-cell signature in differentiating human induced pluripotent stem cells via integrin signalling . Scientific Reports. 1-16.
  • Vis forfatter(e) (2020). Bioinformatic analyses of miRNA-mRNA signature during hiPSC differentiation towards insulin-producing cells upon HNF4α mutation. Biomedicines. 1-20.
  • Vis forfatter(e) (2019). The effect of WnT pathway modulators on human iPSC-derived pancreatic beta cell maturation. Frontiers in Endocrinology. 1-13.
  • Vis forfatter(e) (2019). Reprogrammed cells display distinct proteomic signaturesAssociated with colony morphology variability. Stem Cells International. 1-16.
  • Vis forfatter(e) (2019). In vivo hyperglycemia exposure elicits distinct period-dependent effects on human pancreatic progenitor differentiation, conveyed by oxidative stress. Acta Physiologica. 1-16.
  • Vis forfatter(e) (2019). Encapsulation boosts islet-cell signature in differentiating human induced pluripotent stem cells via integrin signalling. bioRxiv.
  • Vis forfatter(e) (2019). Diabetes relief in mice by glucose-sensing insulin-secreting human α-cells. Nature. 43-48.
  • Vis forfatter(e) (2018). Pancreatic islet-autonomous insulin and smoothened-mediated signalling modulate identity changes of glucagon+ α-cells. Nature Cell Biology. 1267-1277.
  • Vis forfatter(e) (2018). Novel protein signatures suggest progression to muscular invasiveness in bladder cancer. PLOS ONE. 1-15.
  • Vis forfatter(e) (2017). Probing the missing mature β-cell proteomic landscape in differentiating patient iPSC-derived cells. Scientific Reports. 1-14.
Faglig foredrag
  • Vis forfatter(e) (2023). Hnf1a Is An Important Regulator in Ageing And Maturation Of Pancreatic Islets.
  • Vis forfatter(e) (2023). Exploring the role of transcription factors HNF1A, HNF1B, and HNF4A in human pancreatic islet cell differentiation.
  • Vis forfatter(e) (2023). Exploring the role of transcription factors HNF1A, HNF1B, and HNF4A in human induced pluripotent stem cell-derived pancreatic islet cell differentiation.
  • Vis forfatter(e) (2022). Mapping tumour heterogeneity and predictive cancer signatures in vivo.
  • Vis forfatter(e) (2022). Chronically Elevated Exogenous Glucose Elicits Antipodal Effects on the Proteome Signature of Differentiating Human iPSC-Derived Pancreatic Progenitors.
Vitenskapelig foredrag
  • Vis forfatter(e) (2023). Islet maturation and ageing is governed by the Hnf1a transcription factor.
Leder
  • Vis forfatter(e) (2022). Editorial: Beta-Cell Fate: From Gene Circuits to Disease Mechanisms. Frontiers in Genetics.
Populærvitenskapelig artikkel
  • Vis forfatter(e) (2021). Islet transplantation tolerance in animals with defined histocompatibility and diabetes. bioRxiv.
Sammendrag/abstract
  • Vis forfatter(e) (2021). 402.2: High Glucose Concentration Increases KATP Channel Activity but Suppresses Mitochondrial Respiration Ability in Insulin-producing Cells Regenerated From Stem Cells. Transplantation. S27-S27.
Poster
  • Vis forfatter(e) (2023). Mapping predictive bladder cancer signatures in a mouse model.
  • Vis forfatter(e) (2023). Mapping islet architecture changes upon high fat diet challenge in a HNF1A-MODY mouse model.
  • Vis forfatter(e) (2023). Investigating the developmental role of HNF1A, HNF1B and HNF4A in human pancreatic islet cell differentiation.
  • Vis forfatter(e) (2023). Human induced pluripotent stem cells as a model for environmental impact on diabetes.
  • Vis forfatter(e) (2022). Molecular mechanisms affecting islet like cell fate acquisition in differentiating iPSC derived β-like cells”.
  • Vis forfatter(e) (2022). Mind your background!
  • Vis forfatter(e) (2022). Know your background, know your data.
  • Vis forfatter(e) (2022). Investigating the developmental role of HNF1A, HNF1B and HNF4A in human pancreatic islet cell differentiation.
  • Vis forfatter(e) (2022). Investigating the developmental role of HNF1A in human pancreatic islet cell differentiation.
  • Vis forfatter(e) (2022). Hnf1a is a key regulator of β-cell identity and function.
  • Vis forfatter(e) (2021). Glucose during in vitro pancreatic beta cells regeneration: friends or for?
Vitenskapelig oversiktsartikkel/review
  • Vis forfatter(e) (2019). Tissue repair brakes: A common paradigm in the biology of regeneration: Concise review. Stem Cells. 330-339.

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