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Laser‐induced graphene (LIG) provides a scalable, laser‐direct‐written route to porous graphene architecture with tunable chemistry and defect density. Through heterojunction engineering, catalytic functionalization, and intrinsic self‐heating, LIG achieves highly sensitive and selective detection of NOX, NH3, H2, and humidity, supporting next ...
Nan Jiang +8 more
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This study developed a hierarchical targeting nanoplatform, siTREM2@ETP‐PEOz‐OMVs, against triple‐negative breast cancer (TNBC) bone metastasis. It precisely delivers therapeutic siTREM2 to monocytes/macrophages within the metastatic niche. This intervention dually regulates cell fate: reprogramming immunosuppressive macrophages and inhibiting ...
Fanglu Chen +12 more
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In vitro propagation ofAtractylodes lancea
Plant Cell Reports, 1984Shoot cultures ofAtractylodes lancea DC. (Compositae) have been established by inoculating the flower bud on Linsmaier-Skoog's medium supplemented with 10(-5) M naphthaleneacetic acid and 10(-5) M 6-benzyl-aminopurine. Shoots were multiplied on a medium containing 10(-6) M 6-benzylaminopurine.
N, Hiraoka +3 more
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In vitro propagation of cashewnut
Plant Cell Reports, 1996In vitro plant propagation was developed for seedling shoot tips, leaf axils, and cotyledonary nodes of cashew, Anacardium occidentale. Factors affecting multiplication rate included age of explant source, explant type, medium composition, light requirements, and transfer frequency. Cotyledonary nodes produced more buds than other explant types.
S, Das, T B, Jha, S, Jha
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Acta Horticulturae, 1997
A method for propagation of tulip in vitro is reported. Shoots were regenerated from stem explants placed on medium containing 5/iM zeatin and 5ftM a-naphthaleneacetic acid. However, about 90% of the structures formed under these conditions did not contain a meristem and could not be used for propagation.
Kuijpers, A.M., Langens-Gerrits, M.
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A method for propagation of tulip in vitro is reported. Shoots were regenerated from stem explants placed on medium containing 5/iM zeatin and 5ftM a-naphthaleneacetic acid. However, about 90% of the structures formed under these conditions did not contain a meristem and could not be used for propagation.
Kuijpers, A.M., Langens-Gerrits, M.
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In vitro propagation of Iris pallida
Plant Cell Reports, 1993Plantlets were regenerated from callus of Iris pallida, an important perfume plant. Only the leaf base attached to the rhizome had the ability to generate yellow-colored callus on LS medium supplemented with 1 mg/l 2,4-D and 0.1 mg/l KT in the dark.
Y, Gozu +6 more
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In Vitro Propagation of Jojoba
2012Jojoba (Simmondsia chinensis (Link) Schn.) is a nontraditional crop in arid and semi-arid areas. Vegetative propagation can be achieved by layering, grafting, or rooting semi-hardwood cuttings, but the highest number of possible propagules is limited by the size of the plants and time of the year.
Berta E, Llorente, Nancy M, Apóstolo
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2009
In vitro propagation of rose is an important tool for rapid multiplication and development of new cultivars with desirable traits. However, successful in vitro propagation requires an understanding of specific requirements and precise manipulation of various factors.
Pratap Kumar, Pati +3 more
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In vitro propagation of rose is an important tool for rapid multiplication and development of new cultivars with desirable traits. However, successful in vitro propagation requires an understanding of specific requirements and precise manipulation of various factors.
Pratap Kumar, Pati +3 more
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Propagation of B Lymphocytes in Vitro
1984Several differentiative states of the mature B lymphocyte are well known, including clonal expansion, antibody secretion, heavy chain class switching, and somatic mutation. However, the precise sequence of these differentiative events, and the mechanism by which immunoregulatory cells and mediators influence this sequence remains uncertain. This is due
J, Braun, J M, Kiely, E R, Unanue
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In Vitro Propagation of Hydrangea spp.
2012Hydrangea (Hortensia) is a highly popular ornamental plant for garden decoration, and now it is commercially produced for cut flower branches. For in vitro culture, Murashige and Skoog medium supplemented with BA (0.25 mg/L) and sucrose (30 g/L) was used.
Barbara, Ruffoni +2 more
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