Results 51 to 60 of about 5,255 (182)

Marker-free transgenic plants through genetically programmed auto-excision [PDF]

open access: yes, 2007
We present here a vector system to obtain homozygous marker-free transgenic plants without the need of extra handling and within the same time frame as compared to transformation methods in which the marker is not removed.
Verweire, Dimitri   +4 more
core   +2 more sources

An improved protocol for carrot haploid and doubled haploid plant production using induced parthenogenesis and ovule excision in vitro [PDF]

open access: yes, 2014
In this work, we describe an improved protocol for induced parthenogenesis and ovule culture of carrot (Daucus carota L.). The effects of pollination with parsley pollen and/or 2,4-dichlorophenoxyacetic acid (2,4-D) treatment on the stimulation of ...
Adela Adamus   +2 more
core   +1 more source

Androgenesis of Red Cabbage in Isolated Microspore Culture In Vitro. [PDF]

open access: yesPlants (Basel), 2021
Mineykina A   +3 more
europepmc   +1 more source

Changes in plastid biogenesis leading to the formation of albino regenerants in barley microspore culture. [PDF]

open access: yesBMC Plant Biol, 2021
Gajecka M   +5 more
europepmc   +1 more source

Persiapan Tanaman Donor Kultur Mikrospora Brokoli Kultivar BL 10001 [PDF]

open access: yes, 2017
Persiapan tanaman kultur mikrospora penting dilakukan untuk menghasilkan tahapan perkembangan mikrospora yang layak digunakan sebagai tanaman donor mikrospora.
anitasari, S. D. (septarini)
core  

Avoid Contamination in Soybean (Glycine Max, L. [Merrill]) Microspores Culture [PDF]

open access: yes, 2014
Microspore culture is done to obtain pure strains. The purpose of soybean microspore culture to obtainquality seeds. Two important step that must be done is isolation of microspores in starvation medium andsubculture into embryogenesis medium.
Sumarmi, S. (Sumarmi)
core  

The improvement in regenerated doubled haploids from anther culture of wheat by anther transfer [PDF]

open access: yes, 2018
This study was conducted to determine the most suitable method of regeneration by comparing two approaches: transfer of anthers (with and without embryo-like structures) to regeneration conditions after a period of two to four weeks on induction medium (=
Büter, B.   +4 more
core  

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