2003

Aubertot J.-N., Reau R., Dupeuble F., Grippon S., Penaud A., Pinochet X., Taverne M. Developing integrated protection of rapeseed: The Leptosphaeria maculans Phoma | [Mise au point de la protection intégre´e du colza: Exemple du Phoma (Leptosphaeria maculans)]. OCL - Oleagineux Corps Gras Lipides 10 (3) , 202-207.
Borges A.A., Cools H.J., Lucas J.A. Menadione sodium bisulphite: A novel plant defence activator which enhances local and systemic resistance to infection by Leptosphaeria maculans in oilseed rape. Plant Pathology 52 (4) , 429-436.
Cozijnsen A.J., Howlett B.J. Characterisation of the mating-type locus of the plant pathogenic ascomycete Leptosphaeria maculans. Current Genetics 43 (5) , 351-357.
Dejoux J.-F., Meynard J.-M., Reau R., Roche R., Saulas P. Evaluation of environmentally-friendly crop management systems based on very early sowing dates for winter oilseed rape in France. Agronomie 23 (8) , 725-736.
Evans N., Fitt B., van den Bosch F., Eckert M., Huang Y-J., Pietravalle S., Karolewski Z., Rouxel T., Balesdent M-H., Ross S., Gout L., Brun H., Andrivon D., Bousset L., Gladders P., Pinochet X., Penaud A., Jedryczka M., Kachlicki P., Stachowiak A., Olechnowicz J., Podlesna A., Happstadius I., Meyer J., Renard M. (2003). Stem canker of oilseed rape: molecular tools and mathematical modelling to deploy durable resistance. Proceedings 11 International Rapeseed Congress, Copenhagen: 36-38.
Granér G., Hamberg M., Meijer J. Screening of oxylipins for control of oilseed rape (Brassica napus) fungal pathogens. Phytochemistry 63 (1) , 89-95.
Griffiths K.M., Bacic A., Howlett B.J. Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans. Phytochemistry 62 (2) , 147-153.
Huang Y.J., Fitt B.D.L., Hall A.M. Survival of A-group and B-group Leptosphaeria maculans (Phoma stem canker) ascospores in air and mycelium on oilseed rape stem debris. Annals of Applied Biology 143 (3) , 359-369.
Huang Y.J., Toscano-Underwood, C., Fitt B.D.L., Hu X.J., Hall A.M. Effects of temperature on ascospore germination and penetration of oilseed rape (Brassica napus) leaves by A- or B-group Leptosphaeria maculans (Phoma stem canker). Plant Pathology 52 (2) , 245-255.
Idnurm A., Howlett B.J. Analysis of loss of pathogenicity mutants reveals that repeat-induced point mutations can occur in the Dothideomycete Leptosphaeria maculans. Fungal Genetics and Biology 39 (1) , 31-37.
Idnurm A., Taylor J.L., Pedras M.S.C., Howlett, B.J. Small scale functional genomics of the blackleg fungus, Leptosphaeria maculans: Analysis of a 38 kb region. Australasian Plant Pathology 32 (4) , 511-519.
Idnurm A., Warnecke D.C., Heinz E., Howlett B.J. Characterisation of neutral trehalase and UDP-glucose:sterol glucosyltransferase genes from the plant pathogenic fungus Leptosphaeria maculans. Physiological and Molecular Plant Pathology 62 (5) , 305-313.
Li C.-X., Cowling W.A.. Identification of a single dominant allele for resistance to blackleg in Brassica napus 'Surpass 400'. Plant Breeding 122 (6) , 485-488.
Malhi S.S., Raza M., Schoenau J.J., Mermut A.R., Kutcher R., Johnston A.M., Gill K.S. Feasibility of boron fertilization for yield, seed quality and B uptake of canola in northeastern Saskatchewan. Canadian Journal of Soil Science 83 (1) , 99-108.
Marcroft S.J., Sprague S.J., Pymer S.J., Salisbury P.A., Howlett B.J.. Factors affecting production of inoculum of the blackleg fungus (Leptosphaeria maculans) in south-eastern Australia. Australian Journal of Experimental Agriculture 43 (10) , 1231-1236.
Mendes-Pereira E., Balesdent M.-H., Brun H., Rouxel T. Molecular phylogeny of the Leptosphaeria maculans-L. biglobosa species complex. Mycological Research 107 (11) , 1287-1304.
Pedras M.S.C., Chumala P.B., Suchy M. Phytoalexins from Thlaspi arvense, a wild crucifer resistant to virulent Leptosphaeria maculans: Structures, syntheses and antifungal activity. Phytochemistry 64 (5) , 949-956.
Pedras M.S.C., Ismaila N., Quail J.W., Boyetchko S.M. Structure, chemistry, and biological activity of pseudophomins A and B, new cyclic lipodepsipeptides isolated from the biocontrol bacterium Pseudomonas fluorescens. Phytochemistry 62 (7) , 1105-1114.
Pedras M.S.C., Montaut S. Probing crucial metabolic pathways in fungal pathogens of crucifers: Biotransformation of indole-3-acetaldoxime, 4-hydroxyphenylacetaldoxime, and their metabolites. Bioorganic and Medicinal Chemistry 11 (14) , 3115-3120.
Pedras M.S.C., Montaut S., Zaharia I.L., Gai Y., Ward, D.E. Transformation of the host-selective toxin destruxin B by wild crucifers: Probing a detoxification pathway. Phytochemistry 64 (5) , 957-963.
Pinochet X. , Mestries E. , Penaud A. , Delourme R. , Chevre A.-M. , Renard M. , Brun H. , Bousset L. , Balesdent, M.-H. , Rouxel, T. , Aubertot, J.-N. Towards a durable management of genetic resistances to Leptosphaeria maculans. OCL - Oleagineux Corps Gras Lipides 10 (3) , 208-211.
Rouxel T., Penaud A., Pinochet X., Brun H., Gout L., Delourme R., Schmit J., Balesdent M.-H. A 10-year survey of populations of Leptosphaeria maculans in France indicates a rapid adaptation towards the Rlm1 resistance gene of oilseed rape. European Journal of Plant Pathology 109 (8) , 871-881.
Rouxel T., Willner E., Coudard L., Balesdent M.-H. Screening and identification of resistance to Leptosphaeria maculans (stem canker) in Brassica napus accessions. Euphytica 133 (2) , 219-231.
Salam M.U., Khangura R.K., Diggle A.J., Barbetti M.J. Blackleg sporacle: A model for predicting onset of pseudothecia maturity and seasonal ascospore showers in relation to blackleg of canola. Phytopathology 93 (9) , 1073-1081.
Scholze P., Krämer R., Marthe F., Ryschka U., Klocke E., Schumann G. Improvement of disease resistance in cabbage: 2. Clubroot, Alternaria- and Phoma-leaf spot diseases | [Verbesserung der Krankheitsresistenz von Kohlgemüse: 2. Kohlhernie, Atlernaria- und Phoma -Blattfleckenkrankheit]. Gesunde Pflanzen 55 (7) , 199-204.
Singh B., Rajan, Bhalla, S., Chalam V.C., PandeyB.M., Singh S.K., Kumar N., Khetarpal R.K. Quarantine processing of imported transgenic planting material. Indian Journal of Agricultural Sciences 73 (2) , 97-100.
Szlávik S Z; Jędryczka M; Kiss I; Lewartowska E; Nagy G. Population structure and pathogenicity grouping of L. maculans isolates from Hungary. Blackleg News, 3-4.
Toscano-Underwood C., Huang Y.J., Fitt B.D.L., Hall A.M. Effects of temperature on maturation of pseudothecia of Leptosphaeria maculans and L. biglobosa on oilseed rape stem debris. Plant Pathology 52 (6) , 726-736.
Useh N.M., Nok A.J., Esievo K.A. Pathogenesis and pathology of blackleg in ruminants: the role of toxins and neuraminidase. A short review. The Veterinary quarterly 25 (4) , 155-159.
Wherrett A.D., Sivasithamparam K., Barbetti M.J. Chemical manipulation of Leptosphaeria maculans (blackleg disease) pseudothecial development and timing of ascospore discharge from canola (Brassica napus) residues. Australian Journal of Agricultural Research 54 (9) , 837-848.
Wretblad S., Bohman S., Dixelius C. Overexpression of a Brassica nigra cDNA gives enhanced resistance to Leptosphaeria maculans in B. napus. Molecular Plant-Microbe Interactions 16 (6) , 477-484.
Zhu B., Rimmer S.R. Inheritance of resistance to Leptosphaeria maculans in two accessions of Brassica napus Canadian Journal of Plant Pathology 25 (1) , 98-103.