Justyna Janikiewicz

3 Pasteur St
Warsaw, MZ 02093, Poland

Last Updated: 09/26/2026

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Found 28 publications

Compositional recalibrations of cardiolipin integrate loss of stearoyl-CoA desaturase 1 activity with mitochondrial decay in lipid-laden pancreatic β-cells.

Compositional recalibrations of cardiolipin integrate loss of stearoyl-CoA desaturase 1 activity with mitochondrial decay in lipid-laden pancreatic β-cells.

Journal: Cell communication and signaling : CCS

Published: November 07, 2025

Autophagy-related proteomics reveals lysosomal alterations linked to C19orf12 mutations and candidate biomarkers in MPAN patients' fibroblasts.

Autophagy-related proteomics reveals lysosomal alterations linked to C19orf12 mutations and candidate biomarkers in MPAN patients' fibroblasts.

Journal: Neurobiology of disease

Published: October 24, 2025

Distinct Neurodegenerative Pathways in Two NBIA Subtypes: Inflammatory Activation in C19orf12 but Not in PANK2 Mutation Carriers.

Distinct Neurodegenerative Pathways in Two NBIA Subtypes: Inflammatory Activation in C19orf12 but Not in PANK2 Mutation Carriers.

Journal: Cells

Published: October 16, 2025

Metformin promotes lipid droplet-mitochondria coupling and improves insulin secretion in pancreatic β-cells exposed to lipotoxicity.

Metformin promotes lipid droplet-mitochondria coupling and improves insulin secretion in pancreatic β-cells exposed to lipotoxicity.

Journal: Biochimica et biophysica acta. Molecular and cell biology of lipids

Published: March 03, 2025

From potential to practice: Overcoming the immaturity of iPSC-derived cardiomyocytes for regenerative medicine.

From potential to practice: Overcoming the immaturity of iPSC-derived cardiomyocytes for regenerative medicine.

Journal: Kardiologia polska

Published: January 20, 2025

Metabolic alterations in fibroblasts of patients presenting with the MPAN subtype of neurodegeneration with brain iron accumulation (NBIA).

Metabolic alterations in fibroblasts of patients presenting with the MPAN subtype of neurodegeneration with brain iron accumulation (NBIA).

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: May 23, 2024

Metabolic impairments in neurodegeneration with brain iron accumulation.

Metabolic impairments in neurodegeneration with brain iron accumulation.

Journal: Biochimica et biophysica acta. Bioenergetics

Published: April 20, 2024

Stearoyl-CoA desaturase 1 deficiency exacerbates palmitate-induced lipotoxicity by the formation of small lipid droplets in pancreatic β-cells.

Stearoyl-CoA desaturase 1 deficiency exacerbates palmitate-induced lipotoxicity by the formation of small lipid droplets in pancreatic β-cells.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: December 13, 2022

Inhibition of stearoyl-CoA desaturase 1 in the mouse impairs pancreatic islet morphogenesis and promotes loss of β-cell identity and α-cell expansion in the mature pancreas.

Inhibition of stearoyl-CoA desaturase 1 in the mouse impairs pancreatic islet morphogenesis and promotes loss of β-cell identity and α-cell expansion in the mature pancreas.

Journal: Molecular metabolism

Published: August 22, 2022

Mitochondria-targeted anti-oxidant AntiOxCIN4 improved liver steatosis in Western diet-fed mice by preventing lipid accumulation due to upregulation of fatty acid oxidation, quality control mechanism and antioxidant defense systems.

Mitochondria-targeted anti-oxidant AntiOxCIN4 improved liver steatosis in Western diet-fed mice by preventing lipid accumulation due to upregulation of fatty acid oxidation, quality control mechanism and antioxidant defense systems.

Journal: Redox biology

Published: April 27, 2022

An intact zinc finger motif of the C1B domain is critical for stability and activity of diacylglycerol kinase-ε.

An intact zinc finger motif of the C1B domain is critical for stability and activity of diacylglycerol kinase-ε.

Journal: The international journal of biochemistry & cell biology

Published: April 11, 2022

Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study.

Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study.

Journal: Metabolomics : Official journal of the Metabolomic Society

Published: July 28, 2021

Showing 1-12 of 28

Last Updated: 09/26/2026