Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation

Competitive intramolecular C-C vs. C-O bond coupling reactions toward C6 ring-fused 2-pyridone synthesis.

Organic & biomolecular chemistry·2016

Glucosylation of flavonoids in petals of Petunia hybrida.

Planta·2013

Modification of the B-ring during flavonoid synthesis in Petunia hybrida: Effect of the hydroxylation gene Hf1 on dihydroflavonol intermediates.

Planta·2013

Hydroxylation of cinnamic acids and flavonoids during biosynthesis of anthocyanins in Petunia hybrida Hort.

Planta·2013

Cell wall localization of dihydroflavonol-glucoside β-glucosidase in flowers of Petunia hybrida.

Planta·2013

A gene controlling rate of anthocyanin synthesis and mutation frequency of the gene An1 in Petunia hybrida.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2013

Revisiting Inherited Metabolic Diseases (IMDs) Through the Lens of Selective Autophagy.

Journal of inherited metabolic disease·2026

Tailored Amino Acid Treatment for Pediatric Patients With Mitochondrial Aminoacyl-tRNA Synthetase Deficiencies.

Journal of inherited metabolic disease·2026

Dichloroacetate Improves Animal Survival, Growth, Neuromuscular Activity, Mitochondrial Stress and Physiology, and Elevated Lactate in C. elegans pdha-1 and dld-1 RNAi Models of Pyruvate Dehydrogenase Complex Deficiency (PDCD).

Journal of inherited metabolic disease·2026

Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency.

Journal of inherited metabolic disease·2026

Essential Oral Single Nutritional Therapy Products for Inherited Metabolic Diseases: Evidence and Consensus Assessment Using a Modified Delphi Method.

Journal of inherited metabolic disease·2026

Congenital Disorders of Glycosylation (CDG): State of the Art in 2026.

Journal of inherited metabolic disease·2026

Lipid droplet-mitochondria crosstalk in osteoarthritis: linking lipid routing to metabolic mismatch.

Frontiers in molecular biosciences·2026

S-HPABA, a marine fungal-derived bioactive compound, exhibits potent lipid-lowering efficacy and safety in modulating lipid dysregulation revealed by integrative lipidomics and molecular biology approaches.

Frontiers in nutrition·2026

Abnormal lipid profiles are associated with markers of impaired fibrinolysis in patients with cirrhosis.

Research and practice in thrombosis and haemostasis·2026

Excess Liver Fat in Type 2 Diabetes Stratified by Intrapancreatic Fat Deposition: A Meta-Analysis of Dual-Organ MRI Studies.

Liver international : official journal of the International Association for the Study of the Liver·2026

Diagnostic value of CT-quantified abdominal fat parameters for metabolic dysfunction-associated fatty liver disease.

BMC gastroenterology·2026

[L-lactylation regulatory network in orthopedic degenerative diseases].

Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery·2026

Related Experiment Videos

Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation

Related Concept Videos

Competitive intramolecular C-C vs. C-O bond coupling reactions toward C6 ring-fused 2-pyridone synthesis.

Glucosylation of flavonoids in petals of Petunia hybrida.

Modification of the B-ring during flavonoid synthesis in Petunia hybrida: Effect of the hydroxylation gene Hf1 on dihydroflavonol intermediates.

Hydroxylation of cinnamic acids and flavonoids during biosynthesis of anthocyanins in Petunia hybrida Hort.

Cell wall localization of dihydroflavonol-glucoside β-glucosidase in flowers of Petunia hybrida.

A gene controlling rate of anthocyanin synthesis and mutation frequency of the gene An1 in Petunia hybrida.

Revisiting Inherited Metabolic Diseases (IMDs) Through the Lens of Selective Autophagy.

Tailored Amino Acid Treatment for Pediatric Patients With Mitochondrial Aminoacyl-tRNA Synthetase Deficiencies.

Dichloroacetate Improves Animal Survival, Growth, Neuromuscular Activity, Mitochondrial Stress and Physiology, and Elevated Lactate in C. elegans pdha-1 and dld-1 RNAi Models of Pyruvate Dehydrogenase Complex Deficiency (PDCD).

Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency.

Essential Oral Single Nutritional Therapy Products for Inherited Metabolic Diseases: Evidence and Consensus Assessment Using a Modified Delphi Method.

Congenital Disorders of Glycosylation (CDG): State of the Art in 2026.

Lipid droplet-mitochondria crosstalk in osteoarthritis: linking lipid routing to metabolic mismatch.

S-HPABA, a marine fungal-derived bioactive compound, exhibits potent lipid-lowering efficacy and safety in modulating lipid dysregulation revealed by integrative lipidomics and molecular biology approaches.

Abnormal lipid profiles are associated with markers of impaired fibrinolysis in patients with cirrhosis.

Excess Liver Fat in Type 2 Diabetes Stratified by Intrapancreatic Fat Deposition: A Meta-Analysis of Dual-Organ MRI Studies.

Diagnostic value of CT-quantified abdominal fat parameters for metabolic dysfunction-associated fatty liver disease.

[L-lactylation regulatory network in orthopedic degenerative diseases].

Related Experiment Videos

Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation

Related Concept Videos

Related Articles