Uncoupling in the gamma-butyrobetaine hydroxylase reaction by D- and L-carnitine

Community and stakeholders' engagement in the prevention and management of Type 2 diabetes: a qualitative study in socioeconomically disadvantaged suburbs in region Stockholm.

Global health action·2019

Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.

Journal of inherited metabolic disease·2015

Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.

The British journal of ophthalmology·2010

Progressive encephalopathy and complex I deficiency associated with mutations in MTND1.

Neuropediatrics·2008

Deficiency of mitochondrial ATP synthase of nuclear genetic origin.

Neuromuscular disorders : NMD·2006

Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene.

Neuromuscular disorders : NMD·2006

Promoting astrocytic activity genetically and pharmacologically increases locomotor function after spinal cord injury in mice.

Biochemical and biophysical research communications·2026

Integrative characterization of cell-surface proximity interactions using DTSSP crosslinking and high-dimensional profiling.

Biochemical and biophysical research communications·2026

Correlative insights into luteolin regulating the macrophage-p53-CCNB1/CDK1 axis associated with cell-cycle control in hepatocellular carcinoma.

Biochemical and biophysical research communications·2026

Biotransformation of notoginsenoside Fe into compound K by β-glucanase: Mechanistic insights.

Biochemical and biophysical research communications·2026

Nanotechnology-based metal, metalloid, and hybrid strategies against urinary tract infections: a narrative review.

Biochemical and biophysical research communications·2026

Silencing FGL2 alleviates rhabdomyolysis-induced acute kidney injury by activating the Nrf2 signaling to suppress ferroptosis.

Biochemical and biophysical research communications·2026

Visualizing Cell Type-Specific Glycan Profiles in Tissue Sections With Glycan Painting.

Bio-protocol·2026

Genomic profiling of estrogen-related receptor identifies adult adipocyte-specific targets in Drosophila.

G3 (Bethesda, Md.)·2026

Sphingolipid Dysregulation in Type 2 Diabetes and Its Microvascular Complications.

International journal of molecular sciences·2026

β-cell adaptation to increased insulin demand is a swift and dynamic process orchestrated by unfolded protein response.

Cell communication and signaling : CCS·2026

Dual purine starvation triggers an Iml1-Whi2-dependent autophagy pathway for survival in yeast.

Autophagy·2026

Ubiquitylation of unbranched glycogen and glycogenin-1 in branching enzyme-deficient cells.

Biochemical and biophysical research communications·2026

Uncoupling in the gamma-butyrobetaine hydroxylase reaction by D- and L-carnitine

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Community and stakeholders' engagement in the prevention and management of Type 2 diabetes: a qualitative study in socioeconomically disadvantaged suburbs in region Stockholm.

Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.

Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.

Progressive encephalopathy and complex I deficiency associated with mutations in MTND1.

Deficiency of mitochondrial ATP synthase of nuclear genetic origin.

Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene.

Promoting astrocytic activity genetically and pharmacologically increases locomotor function after spinal cord injury in mice.

Integrative characterization of cell-surface proximity interactions using DTSSP crosslinking and high-dimensional profiling.

Correlative insights into luteolin regulating the macrophage-p53-CCNB1/CDK1 axis associated with cell-cycle control in hepatocellular carcinoma.

Biotransformation of notoginsenoside Fe into compound K by β-glucanase: Mechanistic insights.

Nanotechnology-based metal, metalloid, and hybrid strategies against urinary tract infections: a narrative review.

Silencing FGL2 alleviates rhabdomyolysis-induced acute kidney injury by activating the Nrf2 signaling to suppress ferroptosis.

Visualizing Cell Type-Specific Glycan Profiles in Tissue Sections With Glycan Painting.

Genomic profiling of estrogen-related receptor identifies adult adipocyte-specific targets in Drosophila.

Sphingolipid Dysregulation in Type 2 Diabetes and Its Microvascular Complications.

β-cell adaptation to increased insulin demand is a swift and dynamic process orchestrated by unfolded protein response.

Dual purine starvation triggers an Iml1-Whi2-dependent autophagy pathway for survival in yeast.

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Uncoupling in the gamma-butyrobetaine hydroxylase reaction by D- and L-carnitine

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