Works matching DE "ASCLEPIADOIDEAE"
Results: 276
Cynanchum (Apocynaceae: Asclepiadoideae): A pantropical Asclepiadoid genus revisited.
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- Taxon, 2016, v. 65, n. 3, p. 467, doi. 10.12705/653.3
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(2421-2422) Proposals to conserve the names Forsteronia and Pinochia (Apocynaceae), the former with a conserved type.
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- Taxon, 2016, v. 65, n. 1, p. 189, doi. 10.12705/651.21
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(2333) Proposal to conserve the name Tweedia (Apocynaceae: Asclepiadoideae) with a conserved type.
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- Taxon, 2014, v. 63, n. 6, p. 1375, doi. 10.12705/636.24
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Is the southern South American genus Tweedia (Apocynaceae: Asclepiadoideae) monophyletic? Molecular phylogenies, distribution and taxonomy.
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- Taxon, 2014, v. 63, n. 6, p. 1265, doi. 10.12705/636.35
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(1929-1930) Proposals to conserve Macbridea Elliott (Lamiaceae) and Seutera (Asclepiadaceae) against Macbridea Raf. (Asclepiadaceae).
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- Taxon, 2010, v. 59, n. 2, p. 646, doi. 10.1002/tax.592035
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Pollinaria of Hoya (Marsdenieae, Apocynaceae)—shedding light on molecular phylogenetics.
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- Taxon, 2007, v. 56, n. 2, p. 465, doi. 10.1002/tax.562017
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Subtribal division of Ceropegieae (Apocynaceae-Asclepiadoideae).
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- Taxon, 2004, v. 53, n. 1, p. 61, doi. 10.2307/4135489
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Enhanced rooting in in vitro derived shootlets of Jasminanthes tuyetanhiae T.B. Tran & Rodda (Apocynaceae, Asclepiadoideae) through microponic system.
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- Plant Cell, Tissue & Organ Culture, 2024, v. 157, n. 2, p. 1, doi. 10.1007/s11240-024-02753-1
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A New C<sub>21</sub>-steroidal Cynansteroid O from Roots of Cynanchum auriculatum.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 3, p. 512, doi. 10.1007/s10600-023-04038-z
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Lupane and Ursane-Type Triterpenoids from Pergularia tomentosa.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 4, p. 790, doi. 10.1007/s10600-018-2477-x
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A New Steroid from Dregea sinensis.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 5, p. 862, doi. 10.1007/s10600-014-1101-y
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Radical scavenging activity of decalpoline, a novel compound characterized from Decalepis hamiltonii.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 2, p. 225, doi. 10.1007/s10600-012-0210-8
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Callus culture and in vitro biosynthesis of cardiac glycosides from Calotropis gigantea (L.) Ait.
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- In Vitro Cellular & Developmental Biology Plant, 2013, v. 49, n. 4, p. 455, doi. 10.1007/s11627-012-9481-9
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Soil type does not affect seed ageing when soil water potential and temperature are controlled.
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- Plant & Soil, 2009, v. 320, n. 1/2, p. 131, doi. 10.1007/s11104-008-9878-8
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Andromonoecious sex expression of flowers and pollinia delivery by insects in a Japanese milkweed Metaplexis japonica (Asclepiadaceae), with special reference to its floral morphology.
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- Plant Species Biology, 2006, v. 21, n. 3, p. 193, doi. 10.1111/j.1442-1984.2006.00165.x
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Pollen-mediated Gene Flow in a Population of <em>Cynanchum grandifolium</em> var. <em>nikoense</em> (Asclepiadaceae).
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- Plant Species Biology, 1993, v. 8, n. 1, p. 45, doi. 10.1111/j.1442-1984.1993.tb00233.x
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In deep shade, elevated CO<sub>2</sub> increases the vigor of tropical climbing plants.
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- Global Change Biology, 2002, v. 8, n. 11, p. 1109, doi. 10.1046/j.1365-2486.2002.00533.x
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Associations of plant fitness, leaf chemistry, and damage suggest. selection mosaic in plant-herbivore interactions.
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- Ecology, 2010, v. 91, n. 9, p. 2650, doi. 10.1890/09-0589.1
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A Revised Classification of the Apocynaceae s.l.
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- Botanical Review, 2000, v. 66, n. 1, p. 1, doi. 10.1007/BF02857781
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Ruehssia quirinopolensis (Apocynaceae), a new species from the Cerrado Domain, Brazil.
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- Rodriguésia, 2021, v. 72, p. 1, doi. 10.1590/2175-7860202172068
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Flora of Ceará, Brazil: subtribe Gonolobinae (Asclepiadoideae/Apocynaceae).
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- Rodriguésia, 2021, v. 72, p. 1, doi. 10.1590/2175-7860202172069
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Flora of Ceará, Brazil: Ditassa (Asclepiadoideae/Apocynaceae).
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- Rodriguésia, 2021, v. 72, p. 1, doi. 10.1590/2175-7860202172070
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Apocynaceae in the Atlantic Forest of Rio Grande do Norte, Brazil.
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- Rodriguésia, 2021, v. 72, p. 1, doi. 10.1590/2175-7860202172082
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Novelties in Oxypetalum (Apocynaceae: Asclepiadoideae): a new species and revalidation of the name O. megapotamicum.
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- Rodriguésia, 2021, v. 72, p. 1, doi. 10.1590/2175-7860202172014
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Reproductive phenology of Ditassa burchellii (Apocynaceae, Asclepiadoideae), a herbaceous vine, in a semi-deciduous forest from Brazil.
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- Rodriguésia, 2019, v. 70, n. 1, p. 1, doi. 10.1590/2175-7860201970006
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Analgesic, anti-inflammatory and antipyretic activities of Pergularia daemia and Carissa carandas.
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- DARU: Journal of Pharmaceutical Sciences, 2009, v. 17, n. 3, p. 168
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Alternate host ranges of Cronartium flaccidum and Cronartium ribicola in northern Europe.
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- Botany, 2012, v. 90, n. 8, p. 694, doi. 10.1139/b2012-039
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Matelea decipiens (Asclepiadaceae): A New County Record from Illinois.
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- Castanea, 2013, v. 78, n. 1, p. 79, doi. 10.2179/12-032
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Noteworthy Collections: ALABAMA.
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- Castanea, 2009, v. 74, n. 2, p. 185, doi. 10.2179/08-055.1
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In vitro propagation of Huernia hystrix : an endangered medicinal and ornamental succulent.
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- Plant Cell, Tissue & Organ Culture, 2009, v. 96, n. 3, p. 273, doi. 10.1007/s11240-008-9484-8
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Phylogenetic positions of Thai members of Gymnema, Gymnemopsis and Sarcolobus (Apocynaceae, Asclepiadoideae, Marsdenieae), and two new Sarcolobus species uncovered by morpho-molecular evidence.
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- Journal of Plant Research, 2024, v. 137, n. 6, p. 951, doi. 10.1007/s10265-024-01562-z
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Molecular phylogeny of Vincetoxicum (Apocynaceae, Asclepiadoideae) from Thailand and integrative taxonomy corroborating a new cryptic species within Vincetoxicum kerrii.
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- Journal of Plant Research, 2024, v. 137, n. 1, p. 21, doi. 10.1007/s10265-023-01501-4
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Moth pollination of Metaplexis japonica (Apocynaceae): pollinaria transfer on the tip of the proboscis.
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- Journal of Plant Research, 2005, v. 118, n. 4, p. 257, doi. 10.1007/s10265-005-0216-4
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EXPERIMENTAL ANALYSIS ON CHLOROPHYLL, AMINO ACID AND NITRATE CONTENTS OF APOCYNACEAE AND ASCLEPIADACEAE.
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- Plant Archives (09725210), 2020, v. 20, n. 2, p. 2238
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EXPERIMENTAL ANALYSIS ON CHLOROPHYLL, AMINO ACID AND NITRATE CONTENTS OF APOCYNACEAE AND ASCLEPIADACEAE.
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- Plant Archives (09725210), 2020, v. 20, n. 1, p. 2238
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Antimicrobial activity of Gymnema sylvestre (Asclepiadaceae).
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- Journal of Acute Disease, 2013, v. 2, n. 3, p. 222, doi. 10.1016/S2221-6189(13)60131-6
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Development of quality control parameters for the standardization of gymnema sylvestre.
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- Journal of Acute Disease, 2012, v. 1, n. 2, p. 141, doi. 10.1016/S2221-6189(13)60032-3
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PROXIMATE, MINERALS AND ANTINUTRIENT ASSESSMENT OF THE LEAVES AND TENDERSTEM OF Leptadeniahastata (PERS.) DECNE.
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- Bayero Journal of Pure & Applied Sciences, 2016, v. 9, n. 2, p. 43, doi. 10.4314/bajopas.v9i2.9
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Sedative and anxiolytic effects of ethanolic extract of Calotropis gigantea (Asclepiadaceae) leaves.
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- Asian Pacific Journal of Tropical Biomedicine, 2014, v. 4, p. S400, doi. 10.12980/APJTB.4.2014C1147
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Enhancement of erectile function of sexually naïve rats by β–sitosterol and α–β–amyrin acetate isolated from the hexane extract of Mondia whitei
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- Asian Pacific Journal of Tropical Biomedicine, 2012, v. 2, n. s3, p. S1266, doi. 10.1016/S2221-1691(12)60397-9
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Gymnema sylvestre R. Br. suspension cell extract show antidiabetic potential in Alloxan induced diabetic albino male rats
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- Asian Pacific Journal of Tropical Biomedicine, 2012, v. 2, n. s2, p. S930, doi. 10.1016/S2221-1691(12)60339-6
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The protective role of Gongronema latifolium in acetaminophen induced hepatic toxicity in Wistar rats
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- Asian Pacific Journal of Tropical Biomedicine, 2011, v. 1, n. S2, p. S151, doi. 10.1016/S2221-1691(11)60145-7
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POLLINIA MORPHOLOGY OF SOME PLANTS OF ASCLEPIADACEAE IN LOWER COASTAL PLAIN OF WEST BENGAL: A SYSTEMATIC APPROACH.
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- Journal of Advanced Scientific Research, 2019, v. 10, n. 1, p. 32
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PHYTOCHEMICAL EVALUATION OF AERIAL PART OF LEPTADENIA RETICULATA (Retz) FOR POLYPHENOLIC COMPOUND AND FREE RADICAL SCAVENGING ACTIVITY.
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- Pharma Science Monitor, 2013, v. 4, n. 1, p. 3418
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A REVIEW ON PHYTOCHEMICAL AND PHARMACOLOGICAL PROPERTIES OF LEPTADENIA RETICULATA (RETZ).
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- Pharma Science Monitor, 2013, v. 4, n. 1, p. 3408
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GYMNEMA SYLVESTRE: A COMPREHENSIVE REVIEW.
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- Pharma Science Monitor, 2012, v. 3, n. 4, p. 2402
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Micromorphology studies of three important medicinal plants of Asclepiadaceae family.
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- Notulae Scientia Biologicae, 2020, v. 12, n. 1, p. 22, doi. 10.15835/nsb12110528
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Pollination and seedling ecology of Decalepis hamiltonii Wight & Arn. (Periplocaceae), a commercially important, endemic and endangered species.
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- Journal of Threatened Taxa, 2009, v. 1, n. 10, p. 497, doi. 10.11609/JoTT.o2168.497-506
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Origin and early evolution of Ceropegieae (Apocynaceae-Asclepiadoideae).
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- Systematics & Biodiversity, 2017, v. 15, n. 2, p. 143, doi. 10.1080/14772000.2016.1238019
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A large-scale inventory of liana diversity in tropical forests of South Eastern Ghats, India.
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- Systematics & Biodiversity, 2010, v. 8, n. 2, p. 289, doi. 10.1080/14772001003723546
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