Resultados de búsqueda - "triploid"

  1. Maximum-likelihood method identifies meiotic restitution mechanism from heterozygosity transmission of centromeric loci: application in citrus por Cuenca, José, Aleza, Pablo, Juárez, José, García-Lor, Andrés, Froelicher, Yann, Navarro, Luis, Ollitrault, Patrick

    Publicado 2017
    “…This new method was used to identify the meiotic restitution mechanism in nineteen mandarin genotypes used as female parents in triploid citrus breeding. SDR was identified for 85.3% of 543 triploid hybrids and FDR for 0.6%. …”
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    Artículo
  2. Evaluation of Mchare and Matooke Bananas for Resistance to Fusarium oxysporum f. sp. cubense Race 1 por Ndayihanzamaso, P., Mostert, D., Matthews, M.C., Mahuku, George S., Jomanga, K., Mpanda, H.J., Mduma, H., Brown, A., Uwimana, Brigitte, Swennen, Rony L., Tumuhimbise, Robooni, Viljoen, Altus

    Publicado 2020
    “…Fusarium wilt, caused by the soil-borne fungus Fusarium oxysporum f. sp. cubense (Foc) race 1, is a major disease of bananas in East Africa. Triploid East African Highland (Matooke) bananas are resistant to Foc race 1, but the response of diploid (Mchare and Muraru) bananas to the fungus is largely unknown. …”
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    Journal Article
  3. Development and performance of balck sigatoka-resistant tetraploid hybrids of plantain (Musa spp., AAB group) por Vuylsteke, D.R., Swennen, R.L., Ortiz, R.

    Publicado 1992
    “…Conversely, the 4x progeny of plantain readily expressed black sigatoka resistance when crossed with ‘Calcutta 4’. Progenies of the triploid plantain cvs. ‘Obino l'Ewai’ and ‘Bobby Tannap’ differed in their black sigatoka breeding values, the former producing larger numbers of promising hybrids. …”
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    Journal Article
  4. The banana (Musa acuminata) genome and the evolution of monocotyledonous plants por D’Hont, Angélique, Denoeud, F., Aury, J.M., Baurens, F.C., Guignon, Valentin, Dita, M., Roux, N.

    Publicado 2012
    “…It involved hybridizations between diverse species and subspecies, fostered by human migrations2, and selection of diploid and triploid seedless, parthenocarpic hybrids thereafter widely dispersed by vegetative propagation. …”
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    Journal Article
  5. Musa genetics por Ortíz, R.

    Publicado 1995
    “…The triploid nature of plantain and its pattern of inheritance should have represented a challenge and an incentive for geneticists. …”
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    Capítulo de libro
  6. Traits that define yield and genetic gain in east African highland banana breeding por Batte, M., Swennen, Rony L., Uwimana, Brigitte, Akech, V., Brown, A., Geleta, M., Ortíz, R .

    Publicado 2021
    “…Significant increases of bunch weight and yield potential were noted from the landrace triploid germplasm, their derived primary tetraploid hybrids and secondary triploid bred-germplasm. …”
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    Journal Article
  7. Rare instances of haploid inducer DNA in potato dihaploids and ploidy-dependent genome instability por Amundson, K.R., Ordoñez, B., Santayana, M., Ng'ang'a, M.L., Henry, I.M., Bonierbale, Merideth W., Khan, A., Tan, E.H., Comai, L.

    Publicado 2021
    “…Chromosomal breaks commonly affected the paternal genome in the dihaploid and tetraploid progeny, but not in the triploid progeny, correlating instability to sperm ploidy and to haploid induction. …”
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    Journal Article
  8. Seasonal variation of apparent male fertility and 2n pollen production in plantain and banana por Ortíz, R., Ulburghs, F., Okoro, J.

    Publicado 1998
    “…AAA genomic group) depend on identifying triploid, female-fertile clones and crossing them with male-fertile, diploid wild or cultivated accessions. …”
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    Journal Article
  9. Comparison of PCRbased molecular marker analyses of Musa breeding populations por Crouch, J.H., Crouch, H.K., Constandt, H., Gysel, A. van, Breyne, P., Montagu, M. van, Jarret, Robert L., Ortíz, R.

    Publicado 1999
    “…AFLP analysis of a full-sib tetraploid hybrid population confirmed previous reports based on VNTR analysis, of a high frequency of recombination during 2n (3x) gamete formation by a triploid plantain landrace. In addition, both VNTR and RAPD analyses of a full-sib triploid hybrid population suggested a high frequency of homoeologous recombination during n (2x) gamete formation by tetraploid hybrids. …”
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    Journal Article
  10. Molecular and cytogenetic study of east African highland banana por Nemecková, A., Christelová, P., Cížková, J., Nyine, M., Houwe, Ines van den, Svacina, R., Uwimana, Brigitte, Swennen, Rony L., Doležel, Jaroslav, Hribova, E.

    Publicado 2018
    “…A total of 38 triploid EAHB accessions available in the Musa germplasm collection (International Transit Centre, Leuven, Belgium) were characterized. …”
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    Journal Article
  11. Applications of biotechnology to citrus improvement in Spain por Navarro, Luis, Olivares-Fuster, Oscar, Juárez, José, Aleza, Pablo, Pina, José A., Ballester-Olmos, José F., Cervera, Magdalena, Fagoaga, Carmen, Durán-Vila, Núria, Pena, Leandro

    Publicado 2017
    “…It is used in large programs to recover triploid seedless hybrid varieties from aborted seeds from 2n x 4n and 2n x 2n crosses; c) Protoplast fusion. …”
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    Objeto de conferencia
  12. Embryogenic response from anther culture of cultivars of loquat (Eriobotrya japonica (Thunb.) Lindl.) from different origins por Blasco, Manuel, Badenes, María L., Naval, María M.

    Publicado 2017
    “…Flow cytometry and chromosome counts revealed that the plantlet was triploid. The single triploid plant obtained was unexpected and its origin is obscure. …”
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    Artículo
  13. A rare case of a natural contact zone in Morocco between an autopolyploid and an allopolyploid of Centaurea aspera with sterile tetraploid hybrids por Garmendia, A., Ferriol, M., Juárez, José, Zajac, A., Kaluzny, K., Merle, H.

    Publicado 2017
    “…In Spain, hybrids were triploid (from reduced gametes A and gamete AB), highly sterile and exerted a ‘triploid block’. …”
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    Artículo
  14. Analytical breeding por Ortíz, R.

    Publicado 2003
    “…Triploid Musa hybrids may also occur due to USP among 2x, i.e., one 2x producing 2n gametes. …”
    Enlace del recurso
    Journal Article
  15. Musa germplasm A and B genomic composition differentially affects their susceptibility to banana bunchy top virus and its aphid vector, Pentalonia nigronervosa por Ngatat, S., Hanna, R., Lienou, J., Ghogomu, R., Nguidang, S.P.K., Enoh, A.C., Ndemba, B., Korie, S., Fotso Kuate, A., Nanga, S.N., Fiaboe, K., Kumar, P. Lava

    Publicado 2022
    “…In the field, the highest apterous aphid density per plant (29.2 ± 6.7) occurred on the AAB triploid Batard and the lowest (0.4 ± 0.2) on the AA diploid Pisang Tongat. …”
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    Journal Article
  16. Interspecific introgression patterns reveal the origins of worldwide cultivated bananas in New Guinea por Martin, Guillaume, Cottin, Aurélien, Baurens, Franc-Christophe, Labadie, Karine, Hervouet, Catherine, Salmon, Frédéric, Paulo-de-la-Reberdiere, Nilda, van den Houwe, Ines, Sardos, Julie, Aury, Jean-Marc, D’Hont, Angélique, Yahiaoui, Nabila

    Publicado 2023
    “…Informative alleles for each of these genetic pools were pinpointed and used to obtain genome ancestry mosaics of accessions. Diploid and triploid cultivars had genome mosaics involving three up to possibly seven contributors. …”
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    Journal Article
  17. Pilot study to screen alleles under selection related to drought tolerance in banana por Breton, Catherine, Cenci, Alberto, Roux, Nicolas, Rouard, Mathieu, Carpentier, Sebastien

    Publicado 2020
    “…The present pilot study describes the methodology to analyse and select Single Nucleotide Polymorphism (SNP) alleles in two conditions (drought stressed and control) on triploid Musa acuminata AAA, ABB and AAB genotypes. …”
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    Póster
  18. Next generation sequencing based genotyping, cytometry and phenotyping for understanding diversity and evolution of guinea yams por Girma, G., Hyma, K.E., Asiedu, Robert, Mitchell, S.E., Gedil, Melaku A, Spillane, Charles

    Publicado 2014
    “…Using flow cytometry a single ploidy level was inferred across D. cayenensis (3x, N = 21), D. praehensilis (2x, N = 7), and D. mangenotiana (3x, N = 5) accessions, whereas both diploid and triploid (or aneuploid) accessions were present in D. rotundata (N = 11 and N = 32, respectively). …”
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    Journal Article
  19. Postharvest Behavior of New Mandarin Cultivars Obtained in the IVIA por Sdiri, Sawsen, Navarro, Pilar, Cuenca, José, Pardo, José, Salvador, Alejandra

    Publicado 2017
    “…A triploid breeding program has been carried out in Plant Protection and Biotechnology Center at the Instituto Valenciano de Investigaciones Agrarias (IVIA) based on sexual hybridization, embryo rescue and ploidy analysis by flow cytometry in order to obtain new mandarin cultivars with late harvest. 'Safor' and 'Garbi' mandarins are new triploid hybrids recently released characterized by their high quality and seedless fruits. …”
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