Results 171 to 180 of about 4,601 (219)

Lignin biosynthesis pathway repressors in gymnosperms: differential repressor domains as compared to angiosperms. [PDF]

For Res (Fayettev)
Ranade SS, García-Gil MR.
europepmc   +1 more source

Chemometric analysis of monoterpenes and sesquiterpenes of conifers. [PDF]

Front Plant Sci
Bakó E, Böszörményi A, Vargáné Szabó B, Engh MA, Hegyi P, Ványolós A, Csupor D.   +6 more
europepmc   +1 more source

Pyrolysis-assisted catalytic conversion of wood in hot-compressed water for the production of aromatic monomers and syngas without external hydrogen addition. [PDF]

RSC Adv
Ikeda-Francisco A, Wang J, Minami E, Kawamoto H.   +3 more
europepmc   +1 more source

Harnessing Molecular Phylogeny and Chemometrics for Taxonomic Validation of Korean Aromatic Plants: Integrating Genomics with Practical Applications. [PDF]

Plants (Basel)
Amin A, Park S.
europepmc   +1 more source

Morphological Ambiguity between <i>Chambersiella</i> Cobb, 1920, and <i>Geraldius Sanwal</i>, 1971: A Taxonomic Dilemma Solved through a Note from N. A. Cobb. [PDF]

J Nematol
Eisenback JD, Vieira P.
europepmc   +1 more source

Population Genetic Diversity and Structure of Ancient Tree Populations of Cryptomeria japonica var. sinensis Based on RAD-seq Data

Forests, 2020
Research highlights: Our study is the first to explore the genetic composition of ancient Cryptomeria trees across a distribution range in China. Background and objectives: Cryptomeria japonica var.
Yafeng Wen, Kentaro Uchiyama, Yoshihiko Tsumura   +2 more
exaly   +2 more sources

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Labdanes from Cryptomeria japonica

Phytochemistry, 1994
Abstract Twenty-seven labdanes were isolated from the leaves of Cryptomeria japonica . The new compounds include 15-(2-oxopropylidene)labd-8(17)-en-19-oic acid, 15-oxolabda-8(17),13 E -dien-19-oic acid, 7β-acetoxy-15-hydroxy-labda-8(17),13 E -dien-19-oic acid methyl ester, 14-hydroxy-15-norlabd-8(17)-en-19-oic acid methyl ester, 15-hydroxy-labda-8 ...
Su, W. C., Cheng, Y. S., Fang, Jim-Min
openaire   +1 more source

A diterpene quinone from the bark of Cryptomeria japonica

Phytochemistry, 2002
A diterpene, cryptoquinone, was isolated from the bark of Cryptomeria japonica, the structure, 7,11,14-trioxoabieta-8,12-diene, was established by spectral analyses and X-ray crystallography. This diterpene quinone showed moderate antifungal activities against Pyricularia orizae and Alternaria alternata, and cytotoxic activity against mouse lymphoid ...
Hisayoshi, Kofujita, Michikazu, Ota, Kouetsu, Takahashi, Yasushi, Kawai, Yoshiki, Hayashi   +4 more
openaire   +2 more sources

The Suspensor of Cryptomeria japonica

Botanical Gazette, 1932
The outstanding features found in the embryogeny of Cryptomeria are cleavage polyembryony, the absence of typical primary suspensors, and the apical cell method of growth in the early embryo.
openaire   +1 more source