Eva Richard

Riding the tiger – physiological and pathological effects of superoxide and hydrogen peroxide generated in the mitochondrial matrix

Prolyl peptidases: a serine protease subfamily with high potential for drug discovery

Management of Helicobacter pylori infection—the Maastricht V/Florence Consensus Report

The neuroinvasive potential of SARS‐CoV2 may play a role in the respiratory failure of COVID‐19 patients

Regulatory T cells in autoimmune kidney diseases and transplantation

Transcriptional and epigenetic basis of Treg cell development and function: its genetic anomalies or variations in autoimmune diseases

Mass spectrometry‐based metabolomics

Correction of the map location for the phr gene in Escherichia coli K12

Diagnosis and monitoring of inborn errors of metabolism using urease-pretreatment of urine, isotope dilution, and gas chromatography–mass spectrometry

Nucleotide- and nucleoside-converting ectoenzymes: Important modulators of purinergic signalling cascade

Parkinson disease

Regulation of the Voltage Gated K⁺ Channel K_v1.3 by Recombinant Human Klotho Protein

Cholesterol Catabolism by Mycobacterium tuberculosis Requires Transcriptional and Metabolic Adaptations

CD26: A Multifunctional Integral Membrane and Secreted Protein of Activated Lymphocytes

Recent advances in atherosclerosis-based proteomics: new biomarkers and a future perspective

Combined Immunodeficiencies with Nonfunctional T Lymphocytes

Gas chromatographic–mass spectrometric urinary metabolome analysis to study mutations of inborn errors of metabolism

Targeting RNA splicing for disease therapy

New insights into nNOS regulation of vascular homeostasis

Upregulation of Na⁺,Cl^--Coupled Betaine/ γ-Amino-Butyric Acid Transporter BGT1 by Tau Tubulin Kinase 2

Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences11Accession numbers and URLs for data in this article are as follows: Online Mendelian Inheritance in Man: http://www.ncbi.nlm.nih.gov/omim. For TSC1 (MIM 191100) and TSC2 (MIM 191092). The Human Gene Mutation Data Base, Cardiff (HGMD): http://www.uwcm.acuk/uwcm/mg. For TSC1 120735 and for TSC2 120466. TSC Variation Database: http://www.expmed.bwh.harvard.edu/projects/tsc_database. GenBank: http://www.ncbi.nlm.nih.gov/Genbank. For TSC2 cDNA X75621 and TSC2 complete genomic sequence AC005600.

Evolving concepts of rheumatoid arthritis

Modulation of mitochondrial function by the microbiome metabolite propionic acid in autism and control cell lines

Gas chromatography/flame ionisation detection mass spectrometry for the detection of endogenous urine metabolites for metabonomic studies and its use as a complementary tool to nuclear magnetic resonance spectroscopy

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

Small-molecule inhibitors of protein–protein interactions: progressing towards the dream

Adenosine Deaminase Deficiency: Metabolic Basis of Immune Deficiency and Pulmonary Inflammation

Cystic fibrosis genetics: from molecular understanding to clinical application

Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC

Genotype is an important determinant of phenotype in adenosine deaminase deficiency

Inherited and SomaticCD3ζ Mutations in a Patient with T-Cell Deficiency

Defining roles of specific reactive oxygen species (ROS) in cell biology and physiology

Survey of the year 2003 commercial optical biosensor literature

A survey of the year 2002 commercial optical biosensor literature

The multifunctional or moonlighting protein CD26/DPPIV

Vitamin B12 deficiency

TACI-ligand interactions are required for T cell activation and collagen-induced arthritis in mice

Dipeptidyl-Peptidase IV from Bench to Bedside: An Update on Structural Properties, Functions, and Clinical Aspects of the Enzyme DPP IV

Current linkage map of Escherichia coli

Extracellular vesicles: Exosomes, microvesicles, and friends

Overview of Extracellular Vesicles, Their Origin, Composition, Purpose, and Methods for Exosome Isolation and Analysis

T‐cell receptor signaling and the pathogenesis of autoimmune arthritis: insights from mouse and man

E. coli K-12 pel mutants, which block phage λ DNA injection, coincide with ptsM, which determines a component of a sugar transport system

Regulatory T Cells and Human Disease

Genetic and enzymatic characterization of a conditional lethal mutant of Escherichia coli K12 with a temperature-sensitive DNA ligase

Membrane phospholipid synthesis in Escherichia coli. Cloning of a structural gene (plsB) of the sn-glycerol-3-phosphate acyl/transferase.

Site-specific properties of Tn7 transposition into the E. coli Chromosome

Nitrate respiration in relation to facultative metabolism in enterobacteria

Chromosomal genetics of Pseudomonas

Contributions of Amino Acid Side Chains to the Kinetics and Thermodynamics of the Bivalent Binding of Protein L to Ig κ Light Chain

The Mononuclear Molybdenum Enzymes

Surface Plasmon Resonance Sensors for Detection of Chemical and Biological Species

The Controversial Role of Human Gut Lachnospiraceae

Genetics of ribosomal protein methylation in Escherichia coli

The Mononuclear Molybdenum Enzymes

Escherichia coli K-12 clones that overproduce dam methylase are hypermutable.

Chemistry and Biology Of Multicomponent Reactions

Recalibrated linkage map of Escherichia coli K-12

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Unique insertion site of Tn7 in the E. coli chromosome

In Salmonella enterica , 2-Methylcitrate Blocks Gluconeogenesis

DNA Glycosylases, Endonucleases for Apurinic/Apyrimidinic Sites, and Base Excision-Repair

Clustered Charged Amino Acids of Human Adenosine Deaminase Comprise a Functional Epitope for Binding the Adenosine Deaminase Complexing Protein CD26/Dipeptidyl Peptidase IV

Defining the pathogenicity of creatine deficiency syndrome

Three novel splice mutations in the PCCA gene causing identical exon skipping in propionic acidemia patients

Overview of mutations in thePCCA andPCCB genes causing propionic acidemia

Treatment with antioxidants ameliorates oxidative damage in a mouse model of propionic acidemia

An unusual late-onset case of propionic acidaemia: biochemical investigations, neuroradiological findings and mutation analysis

Oxidative stress and apoptosis in homocystinuria patients with genetic remethylation defects

[Genetic study of mutants of the chl A region in Escherichia coli k12].

Pseudoexon exclusion by antisense therapy in methylmalonic aciduria (MMAuria)

Adenosine deaminase deficiency with mosaicism for a “second-site suppressor” of a splicing mutation: decline in revertant T lymphocytes during enzyme replacement therapy

The Binding Site of Human Adenosine Deaminase for Cd26/Dipeptidyl Peptidase IV

Quantitative Analysis of Mitochondrial Protein Expression in Methylmalonic Acidemia by Two-Dimensional Difference Gel Electrophoresis

Functional characterization of novel genotypes and cellular oxidative stress studies in propionic acidemia