Control in situ of the pyruvate kinase activity of Escherichia coli

Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the ERSD-associated gamma-G284R mutant.

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Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain.

Journal of thrombosis and haemostasis : JTH·2003

Genetic control of manno(fructo)kinase activity in Escherichia coli.

Proceedings of the National Academy of Sciences of the United States of America·2001

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.

Blood·2001

Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms.

Journal of human genetics·2001

Coexistence of a novel homozygous nonsense mutation in exon 13 of the factor V gene with the homozygous Leiden mutation in two unrelated patients with severe factor V deficiency.

British journal of haematology·2001

DNA ligase LigE increases bacterial transformation with damaged extracellular DNA.

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Inhibition of dipeptidyl peptidase 7 impairs lysophagy in LLOMe-treated HepG2 cells.

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FEBS letters·2026

RNA-related functions of BRCA2 in transcription, replication, and genome stability.

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Reactive oxygen species-induced lipid peroxidation mediates Wnt-dependent lipodystrophy and associated skin fibrosis.

FEBS letters·2026

Glis1 regulates metabolic programming by promoting H3K18 lactylation to alleviate neuronal senescence following spinal cord injury.

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Carbon dots in tissue repair: from cell behavior to microenvironment remodeling.

Frontiers in bioengineering and biotechnology·2026

Histidine alleviates copper-induced intestinal inflammation through oxidative stress-mediated mitochondrial damage and the Hif1α-Tnfα/Il1β pathway.

Frontiers in immunology·2026

QQ-Based Oxygen Extraction Fraction (OEF) Mapping in Mouse Brain: Initial Experience.

Magnetic resonance in medicine·2026

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Control in situ of the pyruvate kinase activity of Escherichia coli

Related Concept Videos

Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the ERSD-associated gamma-G284R mutant.

Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain.

Genetic control of manno(fructo)kinase activity in Escherichia coli.

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.

Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms.

Coexistence of a novel homozygous nonsense mutation in exon 13 of the factor V gene with the homozygous Leiden mutation in two unrelated patients with severe factor V deficiency.

DNA ligase LigE increases bacterial transformation with damaged extracellular DNA.

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Inhibition of dipeptidyl peptidase 7 impairs lysophagy in LLOMe-treated HepG2 cells.

Becoming the bull: Structural insights and engineering strategies for ultralong CDR-H3 paratopes from cattle.

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Reactive oxygen species-induced lipid peroxidation mediates Wnt-dependent lipodystrophy and associated skin fibrosis.

Glis1 regulates metabolic programming by promoting H3K18 lactylation to alleviate neuronal senescence following spinal cord injury.

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Control in situ of the pyruvate kinase activity of Escherichia coli

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