Metabolomics and hormonomics to crack the code of filbert growth

[1]  J. Hernández-Ruiz,et al.  Role of Melatonin to Enhance Phytoremediation Capacity , 2019, Applied Sciences.

[2]  E. Mudge,et al.  The Terroir of Cannabis: Terpene Metabolomics as a Tool to Understand Cannabis sativa Selections , 2019, Planta Medica.

[3]  Jianguo Xia,et al.  MetaboAnalystR 2.0: From Raw Spectra to Biological Insights , 2019, Metabolites.

[4]  W. Islam,et al.  Melatonin Mediates Enhancement of Stress Tolerance in Plants , 2019, International journal of molecular sciences.

[5]  L. A. Erland,et al.  Serotonin in Plants , 2019, Serotonin.

[6]  M. B. Arnao,et al.  Melatonin: A New Plant Hormone and/or a Plant Master Regulator? , 2019, Trends in plant science.

[7]  B. Matysiak,et al.  In vitro propagation of Rosa ‘Konstancin’ (R. rugosa × R. beggeriana), a plant with high nutritional and pro-health value , 2018, Folia Horticulturae.

[8]  Vahid Tavallali EFFECT OF IRON NANO CHELATE ON ANTIOXIDANT ACTIVITY, POLYPHENOLIC CONTENTS AND ESSENTIAL OIL COMPOSITION OF Portulaca oleracea L. , 2018, Acta Scientiarum Polonorum Hortorum Cultus.

[9]  Jasmine Chong,et al.  MetaboAnalystR: an R package for flexible and reproducible analysis of metabolomics data , 2018, Bioinform..

[10]  David S. Wishart,et al.  MetaboAnalyst 4.0: towards more transparent and integrative metabolomics analysis , 2018, Nucleic Acids Res..

[11]  K. Ljung,et al.  Plant Hormonomics: Multiple Phytohormone Profiling by Targeted Metabolomics1[OPEN] , 2018, Plant Physiology.

[12]  L. A. Erland,et al.  Indoleamines and phenylpropanoids modify development in the bryophyte Plagiomnium cuspidatum (Hedw.) T.J. Kop , 2018, In Vitro Cellular & Developmental Biology - Plant.

[13]  L. A. Erland,et al.  Melatonin and serotonin: Mediators in the symphony of plant morphogenesis , 2018, Journal of pineal research.

[14]  M. B. Arnao,et al.  Melatonin and its relationship to plant hormones , 2018, Annals of botany.

[15]  L. A. Erland,et al.  Melatonin in plant signalling and behaviour. , 2018, Functional plant biology : FPB.

[16]  L. A. Erland,et al.  Bark and wood tissues of American elm exhibit distinct responses to Dutch elm disease , 2017, Scientific Reports.

[17]  R. Niedz,et al.  Developing hazelnut tissue culture medium free of ion confounding , 2017, Plant Cell, Tissue and Organ Culture (PCTOC).

[18]  B. Pawłowska,et al.  Biochemical and morphometric analysis of Rosa tomentosa and Rosa rubiginosa during application of liquid culture systems for in vitro shoot production , 2017 .

[19]  P. Saxena,et al.  Plant signals during beetle (Scolytus multistriatus) feeding in American elm (Ulmus americana Planch) , 2017, Plant signaling & behavior.

[20]  M. Fischer,et al.  Food Targeting: Geographical Origin Determination of Hazelnuts (Corylus avellana) by LC-QqQ-MS/MS-Based Targeted Metabolomics Application. , 2017, Journal of agricultural and food chemistry.

[21]  J. A. Sullivan,et al.  Iron supplementation promotes in vitro shoot induction and multiplication of Baptisia australis , 2017, Plant Cell, Tissue and Organ Culture (PCTOC).

[22]  L. A. Erland,et al.  Serotonin: An ancient molecule and an important regulator of plant processes. , 2016, Biotechnology advances.

[23]  L. Ruíz-Herrera,et al.  Serotonin modulates Arabidopsis root growth via changes in reactive oxygen species and jasmonic acid-ethylene signaling. , 2016, Physiologia plantarum.

[24]  P. Saxena,et al.  An efficient temporary immersion system for micropropagation of hybrid hazelnut , 2016 .

[25]  P. Saxena,et al.  Identification and characterization of serotonin as an anti-browning compound of apple and pear , 2015 .

[26]  R. Reiter,et al.  A new balancing act: The many roles of melatonin and serotonin in plant growth and development , 2015, Plant signaling & behavior.

[27]  Á. Contreras,et al.  Improved walnut mass micropropagation through the combined use of phloroglucinol and FeEDDHA , 2015, Plant Cell, Tissue and Organ Culture (PCTOC).

[28]  L. Fuentes-Broto,et al.  Phytomelatonin: Assisting Plants to Survive and Thrive , 2015, Molecules.

[29]  P. Brown,et al.  Metabolomics for phytochemical discovery: development of statistical approaches using a cranberry model system. , 2015, Journal of natural products.

[30]  L. Strader,et al.  Auxin activity: Past, present, and future. , 2015, American journal of botany.

[31]  R. Hardeland Melatonin in plants and other phototrophs: advances and gaps concerning the diversity of functions. , 2015, Journal of experimental botany.

[32]  F. Baluška,et al.  Salt stress-induced seedling growth inhibition coincides with differential distribution of serotonin and melatonin in sunflower seedling roots and cotyledons. , 2014, Physiologia plantarum.

[33]  B. Reed,et al.  Minor nutrients are critical for the improved growth of Corylus avellana shoot cultures , 2014, Plant Cell, Tissue and Organ Culture (PCTOC).

[34]  S. Maki,et al.  Modeling optimal mineral nutrition for hazelnut micropropagation , 2014, Plant Cell, Tissue and Organ Culture (PCTOC).

[35]  P. Saxena,et al.  Galanthamine, an anti-cholinesterase drug, effects plant growth and development in Artemisia tridentata Nutt. via modulation of auxin and neurotransmitter signaling , 2014, Plant signaling & behavior.

[36]  S. Murch,et al.  In vitro conservation, phytochemistry, and medicinal activity of Artemisia tridentata Nutt.: metabolomics as a hypothesis-generating tool for plant tissue culture , 2014, Plant Growth Regulation.

[37]  P. Saxena,et al.  Galanthamine, an anticholinesterase drug, effects plant growth and development in Artemisia tridentate Nutt. via modulation of auxin and neutrotransmitter signaling. , 2014, Plant signaling & behavior.

[38]  S. Murch,et al.  Targeted and Untargeted Phytochemistry of Ligusticum canbyi: Indoleamines, Phthalides, Antioxidant Potential, and Use of Metabolomics as a Hypothesis-Generating Technique for Compound Discovery , 2013, Planta Medica.

[39]  C. Turi,et al.  Phytochemistry and Neurological Activity of Ceremonial Smokes Collected from the Native Okanagan Species Artemisia Tridentata Nutt. , 2013 .

[40]  A. Dale,et al.  Improved shoot multiplication and development in hybrid hazelnut nodal cultures by ethylenediamine di-2-hydroxy-phenylacetic acid (Fe-EDDHA) , 2013, Canadian Journal of Plant Science.

[41]  GarrisonWalter,et al.  Improved shoot multiplication and development in hybrid hazelnut nodal cultures by ethylenediamine di-2-hydroxy-phenylacetic acid (Fe-EDDHA) , 2013 .

[42]  R. Reiter,et al.  On the free radical scavenging activities of melatonin's metabolites, AFMK and AMK , 2013, Journal of pineal research.

[43]  A. Pieterse Is flowering in Lemnaceae stress-induced? A review , 2013 .

[44]  Susanne Rasmussen,et al.  REVIEW: PART OF A HIGHLIGHT ON BREEDING STRATEGIES FOR FORAGE AND GRASS IMPROVEMENT Metabolomics of forage plants: a review , 2012 .

[45]  Ramón Pelagio-Flores,et al.  Melatonin regulates Arabidopsis root system architecture likely acting independently of auxin signaling , 2012, Journal of pineal research.

[46]  P. Brown,et al.  Comparisons of large (Vaccinium macrocarpon Ait.) and small (Vaccinium oxycoccos L., Vaccinium vitis-idaea L.) cranberry in British Columbia by phytochemical determination, antioxidant potential, and metabolomic profiling with chemometric analysis. , 2012, Planta medica.

[47]  Kazuki Saito,et al.  KNApSAcK family databases: integrated metabolite-plant species databases for multifaceted plant research. , 2012, Plant & cell physiology.

[48]  L. Zechmeister Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products / Progrès dans la Chimie des Substances Organiques Naturelles , 2012 .

[49]  P. Brown,et al.  Phytochemical diversity of cranberry (Vaccinium macrocarpon Aiton) cultivars by anthocyanin determination and metabolomic profiling with chemometric analysis. , 2012, Journal of agricultural and food chemistry.

[50]  Marco Arlorio,et al.  Chemotype and genotype chemometrical evaluation applied to authentication and traceability of “Tonda Gentile Trilobata” hazelnuts from Piedmont (Italy) , 2011 .

[51]  Gokare A. Ravishankar,et al.  Phytoserotonin , 2011 .

[52]  Jianguo Xia,et al.  Web-based inference of biological patterns, functions and pathways from metabolomic data using MetaboAnalyst , 2011, Nature Protocols.

[53]  L. Macías-Rodríguez,et al.  Serotonin, a tryptophan-derived signal conserved in plants and animals, regulates root system architecture probably acting as a natural auxin inhibitor in Arabidopsis thaliana. , 2011, Plant & cell physiology.

[54]  M. Nurul Islam,et al.  Comparative analysis of bioactive phytochemicals from Scutellaria baicalensis, Scutellaria lateriflora, Scutellaria racemosa, Scutellaria tomentosa and Scutellaria wrightii by LC-DAD-MS , 2011, Metabolomics.

[55]  P. Saxena,et al.  Melatonin and serotonin in flowers and fruits of Datura metel L. , 2009, Journal of pineal research.

[56]  R. Reiter,et al.  Kynuramines, metabolites of melatonin and other indoles: the resurrection of an almost forgotten class of biogenic amines , 2009, Journal of pineal research.

[57]  David S. Wishart,et al.  MetaboAnalyst: a web server for metabolomic data analysis and interpretation , 2009, Nucleic Acids Res..

[58]  J. Friml,et al.  Auxin and other signals on the move in plants. , 2009, Nature chemical biology.

[59]  Jaroslava Dubová,et al.  Cytokinins modulate auxin-induced organogenesis in plants via regulation of the auxin efflux , 2009, Proceedings of the National Academy of Sciences.

[60]  A. Ishihara,et al.  Induction of serotonin accumulation by feeding of rice striped stem borer in rice leaves , 2008, Plant signaling & behavior.

[61]  F. Matsuda,et al.  The tryptophan pathway is involved in the defense responses of rice against pathogenic infection via serotonin production. , 2008, The Plant journal : for cell and molecular biology.

[62]  B. R. Smith,et al.  Fe-EDDHA Alleviates Chlorosis in `Concord' Grapevines Grown at High pH , 2006 .

[63]  D. Nutt,et al.  Tryptophan metabolism in the central nervous system: medical implications , 2006, Expert Reviews in Molecular Medicine.

[64]  B. Bartel,et al.  Auxin: regulation, action, and interaction. , 2005, Annals of botany.

[65]  D. Goodenowe,et al.  A metabolomic analysis of medicinal diversity in Huang-qin (Scutellaria baicalensis Georgi) genotypes: discovery of novel compounds , 2004, Plant Cell Reports.

[66]  B. R. Smith,et al.  CO2 Assimilation, Photosynthetic Enzymes, and Carbohydrates of `Concord' Grape Leaves in Response to Iron Supply , 2004 .

[67]  H. Bienfait,et al.  Distribution and secondary effects of EDDHA in some vegetable species , 2004 .

[68]  S. Sopory,et al.  Evidence for some common signal transduction events for opposite regulation of nitrate reductase and phytochrome-I gene expression by light , 1995, Plant Molecular Biology.

[69]  B. Krajnčič,et al.  Mechanisms of EDDHA effects on the promotion of floral induction in the long-day plant Lemna minor (L.). , 2003, Journal of plant physiology.

[70]  Tanya Parish,et al.  The common aromatic amino acid biosynthesis pathway is essential in Mycobacterium tuberculosis. , 2002, Microbiology.

[71]  P. Saxena,et al.  The role of serotonin and melatonin in plant morphogenesis: Regulation of auxin-induced root organogenesis in in vitro-cultured explants of st. John's Wort (Hypericum perforatum L.) , 2001, In Vitro Cellular & Developmental Biology - Plant.

[72]  O. Fiehn,et al.  Metabolite profiling for plant functional genomics , 2000, Nature Biotechnology.

[73]  P. Saxena,et al.  Melatonin in feverfew and other medicinal plants , 1997, The Lancet.

[74]  R. Reiter,et al.  Identification of melatonin in plants and its effects on plasma melatonin levels and binding to melatonin receptors in vertebrates. , 1995, Biochemistry and molecular biology international.

[75]  Xiaoling Yu,et al.  A micropropagation system for hazelnuts (Corylus species) , 1995 .

[76]  R. Reiter,et al.  Melatonin in edible plants identified by radioimmunoassay and by high performance liquid chromatography‐mass spectrometry , 1995, Journal of pineal research.

[77]  S. Sopory,et al.  5‐Hydroxytryptamine affects turnover of polyphosphoinositides in maize and stimulates nitrate reductase in the absence of light , 1994, FEBS letters.

[78]  S. Sopory,et al.  Evidence of regulation of calcium uptake by phytochrome in maize protoplasts. , 1985, Biochemical and biophysical research communications.

[79]  J. Driver,et al.  In Vitro Propagation of Paradox Walnut Rootstock , 1984, HortScience.

[80]  J. Driver,et al.  In vitro propagation of Paradox walnut rootstock [Juglans hindsii X Juglans regia, tissue culture] , 1984 .

[81]  B. Stowe,et al.  Occurrence and Metabolism of Simple Indoles in Plants , 1959 .

[82]  C. Miller,et al.  Chemical regulation of growth and organ formation in plant tissues cultured in vitro. , 1957, Symposia of the Society for Experimental Biology.

[83]  K. Bowden,et al.  5-Hydroxytryptamine: its Occurrence in Cowhage , 1954, Nature.