Search Results - (Author, Cooperation:J. F. Jia)

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  1. 1
    C. L. Song ; Y. L. Wang ; P. Cheng ; Y. P. Jiang ; W. Li ; T. Zhang ; Z. Li ; K. He ; L. Wang ; J. F. Jia ; H. H. Hung ; C. Wu ; X. Ma ; X. Chen ; Q. K. Xue
    American Association for the Advancement of Science (AAAS)
    Published 2011
    Staff View
    Publication Date:
    2011-06-18
    Publisher:
    American Association for the Advancement of Science (AAAS)
    Print ISSN:
    0036-8075
    Electronic ISSN:
    1095-9203
    Topics:
    Biology
    Chemistry and Pharmacology
    Computer Science
    Medicine
    Natural Sciences in General
    Physics
    Published by:
    http://www.aaas.org/

    Latest Papers from Table of Contents or Articles in Press
  2. 2
    M. X. Wang ; C. Liu ; J. P. Xu ; F. Yang ; L. Miao ; M. Y. Yao ; C. L. Gao ; C. Shen ; X. Ma ; X. Chen ; Z. A. Xu ; Y. Liu ; S. C. Zhang ; D. Qian ; J. F. Jia ; Q. K. Xue
    American Association for the Advancement of Science (AAAS)
    Published 2012
    Staff View
    Publication Date:
    2012-03-17
    Publisher:
    American Association for the Advancement of Science (AAAS)
    Print ISSN:
    0036-8075
    Electronic ISSN:
    1095-9203
    Topics:
    Biology
    Chemistry and Pharmacology
    Computer Science
    Medicine
    Natural Sciences in General
    Physics
    Published by:
    http://www.aaas.org/

    Latest Papers from Table of Contents or Articles in Press
  3. 3
    Wu, S.-C. ; Jia, J.-F. ; Wu, K. ; Lu, S.-H. ; Zhao, R.-G. ; Wang, D.-Z.

    Amsterdam : Elsevier
    Staff View
    ISSN:
    0039-6028
    Source:
    Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics:
    Physics
    Type of Medium:
    Electronic Resource
    URL:
    http://linkinghub.elsevier.com/retrieve/pii/0039-6028(94)90814-1

    Articles: DFG German National Licenses
  4. 4
    Luo, J.-P. ; Jia, J.-F.
    Springer
    Published 1998
    Staff View
    ISSN:
    1432-203X
    Keywords:
    Key wordsAstragalus adsurgens ; Protoplast culture ; Plant regeneration ; Embryogenesis
    Source:
    Springer Online Journal Archives 1860-2000
    Topics:
    Biology
    Notes:
    Abstract A reproducible release of viable protoplasts was obtained from friable calli of Astragalus adsurgens. Protoplasts underwent sustained divisions and formed cell colonies when cultured in either liquid or agarose-solidified Kao and Michayluk (1975) protoplast medium (KM8P) supplemented with 1.5 mg/l 2,4-D, 0.5 mg/l BA and 0.5 M glucose. Compared to liquid culture, agarose bead culture improved division frequency effectively, the two culture systems showing a plating efficiency of 0.8±0.5% and 6.5±0.7%, respectively. Upon transfer to Murashige and Skoog (1962) medium (MS) with 1–2 mg/l BA, alone or in combination with NAA or 2,4-D at 0.1 mg/l, the protoplast-derived calli produced complete plantlets through somatic embryogenesis. The maximum percentage of calli producing somatic embryos (52.5± 2.2%) occurred on MS medium containing 0.1 mg/l NAA and 1 mg/l BA, whereas the maximum number of calli regenerating plantlets (64.7±6.2) was obtained on MS medium with 0.1 mg/l NAA and 2 mg/l BA.
    Type of Medium:
    Electronic Resource
    URL:
    http://dx.doi.org/10.1007/s002990050399

    Articles: DFG German National Licenses
  5. 5
    Luo, J.-P. ; Jia, J.-F.
    Springer
    Published 1998
    Staff View
    ISSN:
    1432-203X
    Keywords:
    Key words Callus induction ; Plant regeneration ; Astragalus adsurgens
    Source:
    Springer Online Journal Archives 1860-2000
    Topics:
    Biology
    Notes:
    Abstract An efficient procedure was developed for inducing callus and plant regeneration using hypocotyl segments of Astragalus adsurgens. The combinations and concentrations of different growth regulators were shown to be critical factors for both the frequency and the type of callus formation as well as for the potential of callus differentiation. Of the four morphologically distinct types of calli that were induced, a friable, yellow callus, i.e. type I, induced on MS medium supplemented with 9.0 µM 2,4-dichlorophenoxyacetic acid and 2.2 µM N6-benzylaminopurine (BA), and then transferred to MS medium containing 0.5 µM α-naphthaleneacetic acid and 8.9 µM BA, exhibited the maximum frequency of shoot regeneration (75%). After regenerated shoots were transferred onto half-strength MS medium without growth regulators, they rooted and complete plants were obtained. Plantlet regeneration from callus cultures required 7–8 weeks.
    Type of Medium:
    Electronic Resource
    URL:
    http://dx.doi.org/10.1007/s002990050443

    Articles: DFG German National Licenses