The Barley mlo-gene: an important powdery mildew resistance source
Agronomie, 20 7 (2000) 745-756
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
Clade V MLO Genes Are Negative Modulators of Cucumber Defence Response to Meloidogyne incognita
Xiaoxiao Xie, Jian Ling, Shaoyun Dong, Mingjuan Zhai, Junru Lu, Jianlong Zhao, Xueyong Yang, Xin Dong, Yan Li, Richard G. F. Visser, Yuling Bai, Zhenchuan Mao, Shengping Zhang and Bingyan XieMolecular Plant Pathology 26 (4) (2025)
https://doi.org/10.1111/mpp.70078
Mapping of resistance genes to powdery mildew based on DNA re-sequencing and bulk segregant analysis in Capsicum
Tao Zhang, Paul W. Bosland, Yan Ma, Yuhang Wang, Wei Li, Weifu Kong, Min Wei, Panpan Duan, Gaoyuan Zhang and Bingqiang WeiProtoplasma 262 (3) 489 (2025)
https://doi.org/10.1007/s00709-024-02013-1
Potential of conventional and new breeding technologies to manage soybean diseases
Muhammad Ismail Buzdar, Muhammad Jawad Akbar Awan, Ghulam Raza, Rubab Zahra Naqvi, Shahid Mansoor and Imran AminPhytopathology Research 7 (1) (2025)
https://doi.org/10.1186/s42483-025-00338-0
Allelic value in gene regulation—implications for gene editing
Mazahar Moin, Mayank Rai and Wricha TyagiAnnals of Botany (2025)
https://doi.org/10.1093/aob/mcaf072
54 143 (2024)
https://doi.org/10.1007/978-981-97-8739-5_8
The development of pleiotropic phenotypes in powdery mildew‐resistant barley and Arabidopsis thaliana mlo mutants is linked to nitrogen availability
Matthias Freh, Anja Reinstädler, Kira D. Neumann, Ulla Neumann and Ralph PanstrugaPlant, Cell & Environment 47 (7) 2360 (2024)
https://doi.org/10.1111/pce.14884
CsPM5.2, a phosphate transporter protein‐like gene, promotes powdery mildew resistance in cucumber
Jingxian Sun, Jingtao Nie, Tingting Xiao, Chunli Guo, Duo Lv, Keyan Zhang, Huan‐Le He, Junsong Pan, Run Cai and Gang WangThe Plant Journal 117 (5) 1487 (2024)
https://doi.org/10.1111/tpj.16576
(2023)
https://doi.org/10.1101/2023.01.25.525488
Oligogenic Control of Quantitative Resistance Against Powdery Mildew Revealed in Portuguese Common Bean Germplasm
Susana T. Leitão, Francisco A. Mendes, Diego Rubiales and Maria Carlota Vaz PattoPlant Disease 107 (10) 3113 (2023)
https://doi.org/10.1094/PDIS-02-23-0313-RE
Comprehensive comparative assessment of the Arabidopsis thaliana MLO2–CALMODULIN2 interaction by various in vitro and in vivo protein–protein interaction assays
Kira von Bongartz, Björn Sabelleck, Anežka Baquero Forero, Hannah Kuhn, Franz Leissing and Ralph PanstrugaBiochemical Journal 480 (20) 1615 (2023)
https://doi.org/10.1042/BCJ20230255
Virulence Variability and Genetic Diversity in Blumeria graminis f. sp. hordei in Southeastern and Southwestern China
Yanyu Wang, Guoxin Zhang, Fengtao Wang, Xiaowei Lang, Xiaoqian Zhao, Jinghuan Zhu, Chaoyue Hu, Jinghuang Hu, Yanxia Zhang, Xiaobo Yao, Haifeng Liu, Ting Ma, Yi Niu, Zhaodi Wang, Jing Feng, Wangmu and Ruiming LinPlant Disease 107 (3) 809 (2023)
https://doi.org/10.1094/PDIS-04-22-0944-RE
Identification of Quantitative Trait Loci Associated with Powdery Mildew Resistance in Spring Barley under Conditions of Southeastern Kazakhstan
Yuliya Genievskaya, Alibek Zatybekov, Saule Abugalieva and Yerlan TuruspekovPlants 12 (12) 2375 (2023)
https://doi.org/10.3390/plants12122375
(2023)
https://doi.org/10.21203/rs.3.rs-2962194/v1
Concepts of trait diversity – the key to effective IPM for resilience in arable systems?
Adrian C Newton and Alison J KarleyOutlook on Agriculture 52 (3) 264 (2023)
https://doi.org/10.1177/00307270231179749
NLR- and mlo-Based Resistance Mechanisms against Powdery Mildew in Cannabis sativa
Tiziana M. SirangeloPlants 13 (1) 105 (2023)
https://doi.org/10.3390/plants13010105
Improving sustainable crop protection using population genetics concepts
Méline Saubin, Clémentine Louet, Lydia Bousset, Frédéric Fabre, Pascal Frey, Isabelle Fudal, Frédéric Grognard, Frédéric Hamelin, Ludovic Mailleret, Solenn Stoeckel, Suzanne Touzeau, Benjamin Petre and Fabien HalkettMolecular Ecology 32 (10) 2461 (2023)
https://doi.org/10.1111/mec.16634
Challenges in Ramularia collo-cygni Control
Andres Mäe and Riinu KiikerEncyclopedia 2 (1) 256 (2022)
https://doi.org/10.3390/encyclopedia2010017
Barley Ror1 encodes a class XI myosin required for mlo‐based broad‐spectrum resistance to the fungal powdery mildew pathogen
Johanna Acevedo‐Garcia, Kim Walden, Franz Leissing, Kira Baumgarten, Katarzyna Drwiega, Mark Kwaaitaal, Anja Reinstädler, Matthias Freh, Xue Dong, Geo Velikkakam James, Lisa C. Baus, Martin Mascher, Nils Stein, Korbinian Schneeberger, Nahal Brocke‐Ahmadinejad, Martin Kollmar, Paul Schulze‐Lefert and Ralph PanstrugaThe Plant Journal 112 (1) 84 (2022)
https://doi.org/10.1111/tpj.15930
2523 63 (2022)
https://doi.org/10.1007/978-1-0716-2449-4_5
187 (2022)
https://doi.org/10.1007/978-3-030-87289-2_7
Plant pathology: Precision genome engineering keeps wheat disease at bay
Julian R. Greenwood and John P. RathjenCurrent Biology 32 (8) R382 (2022)
https://doi.org/10.1016/j.cub.2022.03.044
Gene-Based Resistance to Erysiphe Species Causing Powdery Mildew Disease in Peas (Pisum sativum L.)
Jyoti Devi, Gyan P. Mishra, Vidya Sagar, Vineet Kaswan, Rakesh K. Dubey, Prabhakar M. Singh, Shyam K. Sharma and Tusar K. BeheraGenes 13 (2) 316 (2022)
https://doi.org/10.3390/genes13020316
Advances in Durable Resistance to Diseases in Staple Food Crops: A Review
Natalia Kozub, Oksana Sozinova, Igor Sozinov, Anatolii Karelov, Liliya Janse, Lidiya Mishchenko, Oleksandr Borzykh and Yaroslav BlumeThe Open Agriculture Journal 16 (1) (2022)
https://doi.org/10.2174/18743315-v16-e220922-2022-HT14-3623-2
Characterization of lncRNAs and mRNAs involved in powdery mildew resistance in cucumber
Jingtao Nie, Huazen Wang, Wanlu Zhang, et al.Phytopathology® (2021)
https://doi.org/10.1094/PHYTO-11-20-0521-R
79 (2021)
https://doi.org/10.1007/978-981-16-3832-9_5
77 (2021)
https://doi.org/10.1007/978-981-16-1974-8_2
Agrobacterium-Mediated Capsicum annuum Gene Editing in Two Cultivars, Hot Pepper CM334 and Bell Pepper Dempsey
Sung-il Park, Hyun-Bin Kim, Hyun-Ji Jeon and Hyeran KimInternational Journal of Molecular Sciences 22 (8) 3921 (2021)
https://doi.org/10.3390/ijms22083921
Fungal Development and Callose Deposition in Compatible and Incompatible Interactions in Melon Infected with Powdery Mildew
Paola Beraldo-Hoischen, Caroline Hoefle and Ana I. López-SeséPathogens 10 (7) 873 (2021)
https://doi.org/10.3390/pathogens10070873
Food Security and Plant Disease Management
Sopan Ganpatrao Wagh, Manoj Baliram Pohare and Ravindra Ramrao KaleFood Security and Plant Disease Management 171 (2021)
https://doi.org/10.1016/B978-0-12-821843-3.00020-9
(2021)
https://doi.org/10.1101/2021.07.16.452661
The MLO1 powdery mildew susceptibility gene in Lathyrus species: The power of high‐density linkage maps in comparative mapping and synteny analysis
Carmen Santos, Carlos Polanco, Diego Rubiales and Maria Carlota Vaz PattoThe Plant Genome 14 (2) (2021)
https://doi.org/10.1002/tpg2.20090
Traits discovery in Hordeum vulgare sbsp. spontaneum accessions and in lines derived from interspecific crosses with wild Hordeum species for enhancing barley breeding efforts
Sajid Rehman, Mariam Amouzoune, Houda Hiddar, Hafid Aberkane, Rachid Benkirane, Abdelkarim Filali‐Maltouf, Muamar Al‐Jaboobi, Leila Acqbouch, Athanasios Tsivelikas, Ramesh Pal Singh Verma, Zakaria Kehel, Ahmed Birouk and Ahmed AmriCrop Science 61 (1) 219 (2021)
https://doi.org/10.1002/csc2.20360
Analysis of allelic variants of RhMLO genes in rose and functional studies on susceptibility to powdery mildew related to clade V homologs
Peihong Fang, Paul Arens, Xintong Liu, Xin Zhang, Deepika Lakwani, Fabrice Foucher, Jérémy Clotault, Juliane Geike, Helgard Kaufmann, Thomas Debener, Yuling Bai, Zhao Zhang and Marinus J. M. SmuldersTheoretical and Applied Genetics 134 (8) 2495 (2021)
https://doi.org/10.1007/s00122-021-03838-7
Mlo Resistance to Powdery Mildew (Blumeria graminis f. sp. hordei) in Barley Landraces Collected in Yemen
Jerzy H. Czembor and Elżbieta CzemborAgronomy 11 (8) 1582 (2021)
https://doi.org/10.3390/agronomy11081582
Genome-Wide Characterization of the MLO Gene Family in Cannabis sativa Reveals Two Genes as Strong Candidates for Powdery Mildew Susceptibility
Noémi Pépin, Francois Olivier Hebert and David L. JolyFrontiers in Plant Science 12 (2021)
https://doi.org/10.3389/fpls.2021.729261
A Post-Haustorial Defense Mechanism is Mediated by the Powdery Mildew Resistance Gene, PmG3M, Derived from Wild Emmer Wheat
Zhen-Zhen Wei, Valentyna Klymiuk, Valeria Bocharova, Curtis Pozniak and Tzion FahimaPathogens 9 (6) 418 (2020)
https://doi.org/10.3390/pathogens9060418
Mapping Powdery Mildew (Blumeria graminis f. sp. tritici) Resistance in Wild and Cultivated Tetraploid Wheats
Rosanna Simeone, Luciana Piarulli, Domenica Nigro, Massimo Antonio Signorile, Emanuela Blanco, Giacomo Mangini and Antonio BlancoInternational Journal of Molecular Sciences 21 (21) 7910 (2020)
https://doi.org/10.3390/ijms21217910
Evidence for Allele-Specific Levels of Enhanced Susceptibility of Wheat mlo Mutants to the Hemibiotrophic Fungal Pathogen Magnaporthe oryzae pv. Triticum
Katrin Gruner, Tobias Esser, Johanna Acevedo-Garcia, Matthias Freh, Michael Habig, Roxana Strugala, Eva Stukenbrock, Ulrich Schaffrath and Ralph PanstrugaGenes 11 (5) 517 (2020)
https://doi.org/10.3390/genes11050517
390 (2020)
https://doi.org/10.1002/9781119409144.ch49
The Mungbean Genome
Thomas J. Noble, Brett Williams, Thi My Linh Hoang, et al.Compendium of Plant Genomes, The Mungbean Genome 169 (2020)
https://doi.org/10.1007/978-3-030-20008-4_11
Fitopatojenlere Karşı Dayanıklılıkta CRISPR/Cas Teknolojisi
Serap DEMİREL, Mustafa USTA and Fatih DEMİRELEuropean Journal of Science and Technology (2020)
https://doi.org/10.31590/ejosat.765369
ShNPSN11, a vesicle-transport-related gene, confers disease resistance in tomato to Oidium neolycopersici
Qinggui Lian, Yanan Meng, Xinbei Zhao, Yuanliu Xu, Yang Wang, Brad Day and Qing MaBiochemical Journal 477 (19) 3851 (2020)
https://doi.org/10.1042/BCJ20190776
Mechanisms of powdery mildew resistance of wheat – a review of molecular breeding
Yichen Kang, Meixue Zhou, Angela Merry and Karen BarryPlant Pathology 69 (4) 601 (2020)
https://doi.org/10.1111/ppa.13166
MLO Differentially Regulates Barley Root Colonization by Beneficial Endophytic and Mycorrhizal Fungi
Magdalena Hilbert, Mara Novero, Hanna Rovenich, et al.Frontiers in Plant Science 10 (2020)
https://doi.org/10.3389/fpls.2019.01678
Powdery Mildew Disease of Crucifers: Biology, Ecology and Disease Management
Govind Singh Saharan, Naresh K. Mehta and Prabhu Dayal MeenaPowdery Mildew Disease of Crucifers: Biology, Ecology and Disease Management 177 (2019)
https://doi.org/10.1007/978-981-13-9853-7_7
Identification of QTLs for powdery mildew (Podosphaera aphanis; syn. Sphaerotheca macularis f. sp. fragariae) susceptibility in cultivated strawberry (Fragaria ×ananassa)
Daniel J. Sargent, Matteo Buti, Nada Šurbanovski, et al.PLOS ONE 14 (9) e0222829 (2019)
https://doi.org/10.1371/journal.pone.0222829
Control of powdery mildew (Blumeria graminis spp.) in cereals by Serenade®ASO (Bacillus amyloliquefaciens (former subtilis) strain QST 713)
Niels Matzen, Thies Marten Heick and Lise Nistrup JørgensenBiological Control 139 104067 (2019)
https://doi.org/10.1016/j.biocontrol.2019.104067
Genome editing for plant disease resistance: applications and perspectives
Kangquan Yin and Jin-Long QiuPhilosophical Transactions of the Royal Society B: Biological Sciences 374 (1767) 20180322 (2019)
https://doi.org/10.1098/rstb.2018.0322
Arabidopsis MLO2 is a negative regulator of sensitivity to extracellular reactive oxygen species
Fuqiang Cui, Hongpo Wu, Omid Safronov, Panpan Zhang, Rajeev Kumar, Hannes Kollist, Jarkko Salojärvi, Ralph Panstruga and Kirk OvermyerPlant, Cell & Environment 41 (4) 782 (2018)
https://doi.org/10.1111/pce.13144
Tomato disease resistances in the post-genomics era
Yuling Bai, Zhe Yan, E. Moriones and R. Fernández-MuñozActa Horticulturae (1207) 1 (2018)
https://doi.org/10.17660/ActaHortic.2018.1207.1
mlo‐based powdery mildew resistance in hexaploid bread wheat generated by a non‐transgenic TILLING approach
Johanna Acevedo‐Garcia, David Spencer, Hannah Thieron, Anja Reinstädler, Kim Hammond‐Kosack, Andrew L. Phillips and Ralph PanstrugaPlant Biotechnology Journal 15 (3) 367 (2017)
https://doi.org/10.1111/pbi.12631
Signaling Mechanisms Underlying Resistance Responses: What Have We Learned, and How Is It Being Applied?
Aardra Kachroo, Paul Vincelli and Pradeep KachrooPhytopathology® 107 (12) 1452 (2017)
https://doi.org/10.1094/PHYTO-04-17-0130-RVW
Mining the Cicer arietinum genome for the mildew locus O (Mlo) gene family and comparative evolutionary analysis of the Mlo genes from Medicago truncatula and some other plant species
Reena Deshmukh, V. K. Singh and Brahma Deo SinghJournal of Plant Research 130 (2) 239 (2017)
https://doi.org/10.1007/s10265-016-0868-2
Genome-wide Identification, Classification and Expression Analysis of the Mildew Resistance Locus O ( MLO ) Gene Family in Sweet Orange ( Citrus sinensis )
Li-Ping Liu, Jin-Wang Qu, Xiao-Qu Yi and Huan-Huan HuangBrazilian Archives of Biology and Technology 60 (2017)
https://doi.org/10.1590/1678-4324-2017160474
Chemical suppressors of mlo-mediated powdery mildew resistance
Hongpo Wu, Mark Kwaaitaal, Roxana Strugala, Ulrich Schaffrath, Paweł Bednarek and Ralph PanstrugaBioscience Reports 37 (6) (2017)
https://doi.org/10.1042/BSR20171389
The powdery mildew-resistant Arabidopsis mlo2 mlo6 mlo12 triple mutant displays altered infection phenotypes with diverse types of phytopathogens
Johanna Acevedo-Garcia, Katrin Gruner, Anja Reinstädler, Ariane Kemen, Eric Kemen, Lingxue Cao, Frank L. W. Takken, Marco U. Reitz, Patrick Schäfer, Richard J. O’Connell, Stefan Kusch, Hannah Kuhn and Ralph PanstrugaScientific Reports 7 (1) (2017)
https://doi.org/10.1038/s41598-017-07188-7
Genome-wide identification and comparison of legume MLO gene family
Nicolas Rispail and Diego RubialesScientific Reports 6 (1) (2016)
https://doi.org/10.1038/srep32673
Powdery mildew resistance in the Japanese domestic tobacco cultivar Kokubu is associated with aberrant splicing of MLO orthologues
T. Fujimura, S. Sato, T. Tajima and M. AraiPlant Pathology 65 (8) 1358 (2016)
https://doi.org/10.1111/ppa.12498
Fighting Asian Soybean Rust
Caspar Langenbach, Ruth Campe, Sebastian F. Beyer, André N. Mueller and Uwe ConrathFrontiers in Plant Science 7 (2016)
https://doi.org/10.3389/fpls.2016.00797
Down-regulation of Arabidopsis DND1 orthologs in potato and tomato leads to broad-spectrum resistance to late blight and powdery mildew
Kaile Sun, Anne-Marie A. Wolters, Annelies E. H. M. Loonen, et al.Transgenic Research 25 (2) 123 (2016)
https://doi.org/10.1007/s11248-015-9921-5
The knock‐down of the expression of MdMLO19 reduces susceptibility to powdery mildew (Podosphaera leucotricha) in apple (Malus domestica)
Stefano Pessina, Dario Angeli, Stefan Martens, Richard G.F. Visser, Yuling Bai, Francesco Salamini, Riccardo Velasco, Henk J. Schouten and Mickael MalnoyPlant Biotechnology Journal 14 (10) 2033 (2016)
https://doi.org/10.1111/pbi.12562
Knockdown of MLO genes reduces susceptibility to powdery mildew in grapevine
Stefano Pessina, Luisa Lenzi, Michele Perazzolli, et al.Horticulture Research 3 (1) 16016 (2016)
https://doi.org/10.1038/hortres.2016.16
Silencing of six susceptibility genes results in potato late blight resistance
Kaile Sun, Anne-Marie A. Wolters, Jack H. Vossen, et al.Transgenic Research 25 (5) 731 (2016)
https://doi.org/10.1007/s11248-016-9964-2
Structure, evolution and functional inference on the Mildew Locus O (MLO) gene family in three cultivated Cucurbitaceae spp.
Paolo Iovieno, Giuseppe Andolfo, Adalgisa Schiavulli, et al.BMC Genomics 16 (1) (2015)
https://doi.org/10.1186/s12864-015-2325-3
Loss-of-Function Mutations in CsMLO1 Confer Durable Powdery Mildew Resistance in Cucumber (Cucumis sativus L.)
Jingtao Nie, Yunli Wang, Huanle He, et al.Frontiers in Plant Science 6 (2015)
https://doi.org/10.3389/fpls.2015.01155
Identification of candidate MLO powdery mildew susceptibility genes in cultivated Solanaceae and functional characterization of tobacco NtMLO1
Michela Appiano, Stefano Pavan, Domenico Catalano, et al.Transgenic Research 24 (5) 847 (2015)
https://doi.org/10.1007/s11248-015-9878-4
Penetration resistance to Erysiphe pisi in pea mediated by er1 gene is associated with protein cross-linking but not with callose apposition or hypersensitive response
R. Iglesias-García, D. Rubiales and S. FondevillaEuphytica 201 (3) 381 (2015)
https://doi.org/10.1007/s10681-014-1221-2
Hyperspectral phenotyping on the microscopic scale: towards automated characterization of plant-pathogen interactions
Matheus Kuska, Mirwaes Wahabzada, Marlene Leucker, Heinz-Wilhelm Dehne, Kristian Kersting, Erich-Christian Oerke, Ulrike Steiner and Anne-Katrin MahleinPlant Methods 11 (1) (2015)
https://doi.org/10.1186/s13007-015-0073-7
Precision agriculture '15
M. Kuska, M. Wahabzada, S. Thomas, et al.Precision agriculture '15 611 (2015)
https://doi.org/10.3920/978-90-8686-814-8_76
Identification and Genetic Analysis of a Novel Rice Spotted-Leaf Mutant with Broad-Spectrum Resistance to Xanthomonas oryzae pv. oryzae
Hai-chao SHEN, Yong-feng SHI, Bao-hua FENG, et al.Journal of Integrative Agriculture 13 (4) 713 (2014)
https://doi.org/10.1016/S2095-3119(13)60393-7
Magical mystery tour: MLO proteins in plant immunity and beyond
Johanna Acevedo‐Garcia, Stefan Kusch and Ralph PanstrugaNew Phytologist 204 (2) 273 (2014)
https://doi.org/10.1111/nph.12889
Emerging Technologies and Management of Crop Stress Tolerance
Memoona Ilyas, Khola Rafique, Sania Ahmed, et al.Emerging Technologies and Management of Crop Stress Tolerance 193 (2014)
https://doi.org/10.1016/B978-0-12-800875-1.00009-0
When virulence originates from non-agricultural hosts: New insights into plant breeding
Thibault Leroy, Bruno Le Cam and Christophe LemaireInfection, Genetics and Evolution 27 521 (2014)
https://doi.org/10.1016/j.meegid.2013.12.022
Pepper mildew resistance locus O interacts with pepper calmodulin and suppresses Xanthomonas AvrBsT-triggered cell death and defense responses
Dae Sung Kim, Hyong Woo Choi and Byung Kook HwangPlanta 240 (4) 827 (2014)
https://doi.org/10.1007/s00425-014-2134-y
Identification of candidate genes required for susceptibility to powdery or downy mildew in cucumber
Henk J. Schouten, Julian Krauskopf, Richard G. F. Visser and Yuling BaiEuphytica 200 (3) 475 (2014)
https://doi.org/10.1007/s10681-014-1216-z
The peculiarities of genetic structure of the Blumeria graminis f. sp. hordei population in Lithuania
Inese Kokina, Grazina Statkeviciute, Alge Leistrumaite and Isaak RashalZemdirbyste-Agriculture 101 (4) 419 (2014)
https://doi.org/10.13080/z-a.2014.101.053
Pyramiding, alternating or mixing: comparative performances of deployment strategies of nematode resistance genes to promote plant resistance efficiency and durability
Caroline Djian-Caporalino, Alain Palloix, Ariane Fazari, et al.BMC Plant Biology 14 (1) 53 (2014)
https://doi.org/10.1186/1471-2229-14-53
Wheat gene TaS3 contributes to powdery mildew susceptibility
Shaohui Li, Rui Ji, Robert Dudler, et al.Plant Cell Reports 32 (12) 1891 (2013)
https://doi.org/10.1007/s00299-013-1501-7
High diversity, low spatial structure and rapid pathotype evolution in Moroccan populations of Blumeria graminis f.sp. hordei
Helen R. Jensen, Antonín Dreiseitl, Mohammed Sadiki and Daniel J. SchoenEuropean Journal of Plant Pathology 136 (2) 323 (2013)
https://doi.org/10.1007/s10658-013-0166-y
A Recessive Resistance to Rice yellow mottle virus Is Associated with a Rice Homolog of the CPR5 Gene, a Regulator of Active Defense Mechanisms
Julie Orjuela, E. F. Thiémélé Deless, Olufisayo Kolade, Sophie Chéron, Alain Ghesquière and Laurence AlbarMolecular Plant-Microbe Interactions® 26 (12) 1455 (2013)
https://doi.org/10.1094/MPMI-05-13-0127-R
Inheritance of resistance to Fusarium oxysporum f. sp. cubense race 1 in bananas
Reuben Tendo Ssali, Andrew Kiggundu, Jim Lorenzen, Eldad Karamura, Wilberforce Tushemereirwe and Altus ViljoenEuphytica 194 (3) 425 (2013)
https://doi.org/10.1007/s10681-013-0971-6
Cellular and molecular analyses of coffee resistance to Hemileia vastatrix and nonhost resistance to Uromyces vignae in the resistance-donor genotype HDT832/2
Inês Diniz, Pedro Talhinhas, Helena Gil Azinheira, et al.European Journal of Plant Pathology 133 (1) 141 (2012)
https://doi.org/10.1007/s10658-011-9925-9
Regulation of basal resistance by a powdery mildew‐induced cysteine‐rich receptor‐like protein kinase in barley
CBGOWDA RAYAPURAM, MICHAEL K. JENSEN, FABIAN MAISER, JOHANNA VIKGREN SHANIR, HENRIK HORNSHØJ, JESPER H. RUNG, PER L. GREGERSEN, PATRICK SCHWEIZER, DAVID B. COLLINGE and MICHAEL F. LYNGKJÆRMolecular Plant Pathology 13 (2) 135 (2012)
https://doi.org/10.1111/j.1364-3703.2011.00736.x
Pea powdery mildew er1 resistance is associated to loss-of-function mutations at a MLO homologous locus
Stefano Pavan, Adalgisa Schiavulli, Michela Appiano, et al.Theoretical and Applied Genetics 123 (8) 1425 (2011)
https://doi.org/10.1007/s00122-011-1677-6
Durable broad‐spectrum powdery mildew resistance in pea er1 plants is conferred by natural loss‐of‐function mutations in PsMLO1
MATT HUMPHRY, ANJA REINSTÄDLER, SERGEY IVANOV, TON BISSELING and RALPH PANSTRUGAMolecular Plant Pathology 12 (9) 866 (2011)
https://doi.org/10.1111/j.1364-3703.2011.00718.x
Isolation, fine mapping and expression profiling of a lesion mimic genotype, spl NF4050-8 that confers blast resistance in rice
Raman Babu, Chang-Jie Jiang, Xin Xu, et al.Theoretical and Applied Genetics 122 (4) 831 (2011)
https://doi.org/10.1007/s00122-010-1490-7
Novel induced mlo mutant alleles in combination with site-directed mutagenesis reveal functionally important domains in the heptahelical barley Mlo protein
Anja Reinstädler, Judith Müller, Jerzy H Czembor, Pietro Piffanelli and Ralph PanstrugaBMC Plant Biology 10 (1) (2010)
https://doi.org/10.1186/1471-2229-10-31
Integrated G Proteins Signaling in Plants
Justine Lorek, Ralph Panstruga and Ralph HückelhovenSignaling and Communication in Plants, Integrated G Proteins Signaling in Plants 197 (2010)
https://doi.org/10.1007/978-3-642-03524-1_11
Mapping of powdery mildew resistance genes in a newly determined accession of Hordeum vulgare ssp. spontaneum
K. Teturová, J. Řepková, P. Lízal and A. DreiseitlAnnals of Applied Biology 156 (2) 157 (2010)
https://doi.org/10.1111/j.1744-7348.2009.00375.x
Loss of susceptibility as a novel breeding strategy for durable and broad-spectrum resistance
Stefano Pavan, Evert Jacobsen, Richard G. F. Visser and Yuling BaiMolecular Breeding 25 (1) 1 (2010)
https://doi.org/10.1007/s11032-009-9323-6
The barley mutant emr2 shows enhanced resistance against several fungal leaf pathogens
M. Jansen and U. SchaffrathPlant Breeding 128 (2) 124 (2009)
https://doi.org/10.1111/j.1439-0523.2008.01604.x
Naturally Occurring Broad-Spectrum Powdery Mildew Resistance in a Central American Tomato Accession Is Caused by Loss of Mlo Function
Yuling Bai, Stefano Pavan, Zheng Zheng, Nana F. Zappel, Anja Reinstädler, Concetta Lotti, Claudio De Giovanni, Luigi Ricciardi, Pim Lindhout, Richard Visser, Klaus Theres and Ralph PanstrugaMolecular Plant-Microbe Interactions® 21 (1) 30 (2008)
https://doi.org/10.1094/MPMI-21-1-0030
Rice lesion mimic mutants with enhanced resistance to diseases
Changjian Wu, Alicia Bordeos, Ma. Reina Suzette Madamba, et al.Molecular Genetics and Genomics 279 (6) 605 (2008)
https://doi.org/10.1007/s00438-008-0337-2
Identification of grapevineMLOgene candidates involved in susceptibility to powdery mildew
Angela Feechan, Angelica M. Jermakow, Laurent Torregrosa, Ralph Panstruga and Ian B. DryFunctional Plant Biology 35 (12) 1255 (2008)
https://doi.org/10.1071/FP08173
Advances in Agronomy
D.D. Stuthman, K.J. Leonard and J. Miller‐GarvinAdvances in Agronomy 95 319 (2007)
https://doi.org/10.1016/S0065-2113(07)95004-X
The barley mutant emr1 exhibits restored resistance against Magnaporthe oryzae in the hypersusceptible mlo-genetic background
Marcus Jansen, Birgit Jarosch and Ulrich SchaffrathPlanta 225 (6) 1381 (2007)
https://doi.org/10.1007/s00425-006-0447-1
Further isolation of AFLP and LMS markers for the mapping of the Ol-2 locus related to powdery mildew (Oidium neolycopersici) resistance in tomato (Solanum lycopersicum L.)
Luigi Ricciardi, Concetta Lotti, Stefano Pavan, et al.Plant Science 172 (4) 746 (2007)
https://doi.org/10.1016/j.plantsci.2006.12.003
155 (2006)
https://doi.org/10.1007/978-3-540-34389-9_4
Improved Resistance Management for Durable Disease Control: A Case Study of Phoma Stem Canker of Oilseed Rape (Brassica napus)
J. N. Aubertot, J. S. West, L. Bousset-Vaslin, M. U. Salam, M. J. Barbetti and A. J. DiggleEuropean Journal of Plant Pathology 114 (1) 91 (2006)
https://doi.org/10.1007/s10658-005-3628-z
Characterization of resistance to powdery mildew (Erysiphe pisi) in a germplasm collection of Lathyrus sativus
M. C. Vaz Patto, M. Fernández‐Aparicio, A. Moral and D. RubialesPlant Breeding 125 (3) 308 (2006)
https://doi.org/10.1111/j.1439-0523.2006.01220.x