Development of a PCR assay to identify and quantifyMicrodochium nivalevar.nivaleandMicrodochium nivalevar.majusin wheat

Paul Thomas Nicholson, A. K. Lees, Nicole Maurin, +2

Physiological and Molecular Plant Pathology

Agricultural ChemistryPlant AnalysisBiochemistryNivalevar.nivaleandmicrodochium Nivalevar.majusin WheatBioanalysis +5

CpG dinucleotides are mutation hot spots in phenylketonuria

Véronique Abadie, Stanislas Lyonnet, Nicole Maurin, +7

Genomics

Genetic DisorderNatural SciencesGeneticsDna ReplicationMolecular Biology +4

Abnormal expression of M1/MUC5AC mucin in distal colon of patients with diverticulitis, ulcerative colitis and cancer

Marie‐Elisabeth Forgue‐Lafitte, Bettina Fabiani, Pierre Lévy, +3

International Journal of Cancer

Blood concentrations of pancreatitis associated protein in neonates: relevance to neonatal screening for cystic fibrosis

J. Sarles, Sandrine Barthellémy, Claude Férec, +9

Archives of Disease in Childhood Fetal & Neonatal

Cystathionine β synthase deficiency affects mouse endochondral ossification

Karine Robert, Nicole Maurin, Catherine Vayssettes, +2

The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology

Randomised controlled trial of essential fatty acid supplementation in phenylketonuria

Maureen Cleary, François Feillet, F. White, +6

European Journal of Clinical Nutrition

Metabolic SyndromeNutritionControlled TrialLipid NutritionClinical Nutrition +5

Neonatal screening and long-term follow-up of phenylketonuria: the French database

Véronique Abadie, Jacques Berthelot, François Feillet, +4

Early Human Development

Neonatal ScreeningUrologyInherited Metabolic DiseaseRenal PathologyPediatrics +3

Abnormal Expression of Gastric Mucin in Human and Rat Aberrant Crypt Foci during Colon Carcinogenesis

Jacques Bara, M.E. Forgue-Lafitte, Nicole Maurin, +2

Tumor Biology

Mice lacking cystathionine beta synthase have lung fibrosis and air space enlargement

Julien Hamelet, Nicole Maurin, Romain Fulchiron, +2

Experimental and Molecular Pathology

InflammationFibrosisInflammatory Lung DiseaseLung InflammationPhysiology +10

Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus

Monique Berthelon, Catherine Caillaud, Françoise Rey, +17

Human Genetics

BiologyGenetic AnalysisGenetic DisorderNatural SciencesGenetics +10