The reproductive organs of conifers and angiosperms differ in morphology in several fundamental respects. The conifer Norway spruce (Picea abies) form pollen and seed cones from separate meristems whereas angiosperms bear bipartite flowers with sepals and petals surrounding two inner whorls of stamens and carpels. Despite these differences in morphology this thesis present data to suggest that reproductive development in conifers and angiosperms is regulated by a similar molecular mechanism. This implies an evolutionary conservation of the major mechanism for reproductive development since the origin of seed plants. Flower organ identity in angiosperms is determined by regulatory genes belonging to the MADS-box gene family of transcription...
MADS-box genes have been found in all eukaryotes, but their number has greatly expanded in plants, w...
International audienceFlowering plants evolved from an unidentified gymnosperm ancestor. Comparison ...
Flowers sensu lato are short, specialized axes bearing closely aggregated sporophylls. They are typi...
The reproductive organs of conifers and angiosperms differ in morphology in several fundamental resp...
The evolutionary relationships between the angiosperm floral organs and the reproductive organs of o...
This work is focused on the molecular genetic basis for morphological change in evolution. Genes bel...
MADS-box genes are important regulators of reproductive development in seed plants, including both f...
Flower development progress through distinct phases that are controlled by complex genetic networks,...
Evolutionary developmental genetics (evodevotics) is a novel scientific endeavor which assumes that ...
Evolutionary developmental genetics (evodevotics) is a novel scientific endeavor which assumes that ...
This PhD is focused around the deep evolutionary history of floral-organ identity MADS-box genes. MA...
Type II MADS-box genes determine the organ identity in angiosperm reproductive structures. Current k...
This PhD is focused around the deep evolutionary history of floral-organ identity MADS-box genes. MA...
Class B floral homeotic genes specify the identity of petals and stamens during the development of a...
MADS-box genes have been found in all eukaryotes, but their number has greatly expanded in plants, w...
International audienceFlowering plants evolved from an unidentified gymnosperm ancestor. Comparison ...
Flowers sensu lato are short, specialized axes bearing closely aggregated sporophylls. They are typi...
The reproductive organs of conifers and angiosperms differ in morphology in several fundamental resp...
The evolutionary relationships between the angiosperm floral organs and the reproductive organs of o...
This work is focused on the molecular genetic basis for morphological change in evolution. Genes bel...
MADS-box genes are important regulators of reproductive development in seed plants, including both f...
Flower development progress through distinct phases that are controlled by complex genetic networks,...
Evolutionary developmental genetics (evodevotics) is a novel scientific endeavor which assumes that ...
Evolutionary developmental genetics (evodevotics) is a novel scientific endeavor which assumes that ...
This PhD is focused around the deep evolutionary history of floral-organ identity MADS-box genes. MA...
Type II MADS-box genes determine the organ identity in angiosperm reproductive structures. Current k...
This PhD is focused around the deep evolutionary history of floral-organ identity MADS-box genes. MA...
Class B floral homeotic genes specify the identity of petals and stamens during the development of a...
MADS-box genes have been found in all eukaryotes, but their number has greatly expanded in plants, w...
International audienceFlowering plants evolved from an unidentified gymnosperm ancestor. Comparison ...
Flowers sensu lato are short, specialized axes bearing closely aggregated sporophylls. They are typi...