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Alba Kaci

Staff Engineer, PhD candidate
  • E-mailAlba.Kaci@uib.no
  • Visitor Address
    Haukeland universitetssykehus, Laboratoriebygget
  • Postal Address
    Postboks 7804
    5020 Bergen
  • Malikova, Jana; Kaci, Alba; Bjørkhaug, Lise; Aukrust, Ingvild; Torsvik, Janniche; Vesela, Klara; kankova, Pavla; Njølstad, Pål Rasmus; Pruhova, Stephanka. 2020. Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants. Journal of Clinical Endocrinology and Metabolism.
  • Kaci, Alba. 2019. Precision medicine in MODYdiabetes: Unraveling the disease causality of gene variants and new regulatory mechanisms .
  • Kaci, Alba; Aukrust, Ingvild; Njølstad, Pål Rasmus; Bjørkhaug, Lise; Svalastoga, Pernille; Molnes, Janne. 2019. Functional characterization of diabetes gene variants is important for precision medicine .
  • Kaci, Alba; Aukrust, Ingvild; Bjørkhaug, Lise; Svalastoga, Pernille; Molnes, Janne; Njølstad, Pål Rasmus. 2019. Functional characterization of HNF1A variants identified in Norwegian MODY diabetes registry can implement precision medicine in diabetes clinics.
  • Bjørkhaug, Lise; Kaci, Alba; Keindl, Magdalena; Njølstad, Pål Rasmus; Aukrust, Ingvild. 2018. The E3 SUMO ligase PIAS is a novel interaction partner regulating the activity of diabetes associated hepatocyte nuclear factor-1.
  • Kaci, Alba; Keindl, Magdalena; Solheim, Marie Holm; Njølstad, Pål Rasmus; Bjørkhaug, Lise; Aukrust, Ingvild. 2018. The E3 SUMO ligase PIASy is a novel interaction partner regulating the activity of diabetes associated hepatocyte nuclear factor-1a. Scientific Reports.
  • Bjørkhaug, Lise; Aukrust, Ingvild; Kaci, Alba; Molnes, Janne; Torsvik, Janniche; Irgens, Henrik Underthun; Johansson, Bente Berg; Njølstad, Pål Rasmus. 2018. Functional characterization of HNF1A variants identified in Norwegian diabetes registries can be important for precision medicine in diabetes clinics.
  • Kaci, Alba; Njølstad, Pål Rasmus; Aukrust, Ingvild; Bjørkhaug, Lise. 2017. The E3 SUMO ligase PIASy regulates the activity and stability of the transcription factor hepatocyte nuclear factor 1-alpha.
  • Bjørkhaug, Lise; Hornnes, Lorentze; Kaci, Alba; Madsen, Andre; Cellane-Chantelot, Christine; Hattersley, Andrew; Mellgren, Gunnar; Aukrust, Ingvild; Njølstad, Pål Rasmus. 2017. Functional analysis of various HNF4A variants identifies increased transactivation function of R85W causing the mutation specific phenotype of neonatal hyperinsulinism and Fanconi syndrome.

More information in national current research information system (CRIStin)