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Origin of facultative heterochromatin in the endosperm ofGagea lutea (Liliaceae)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-642-76395-3openalex-snapshot
Comparative Embryology of Angiosperms
inferredcites →https://doi.org/10.1007/978-3-642-94689-9_1openalex-snapshot
Morphologie und Entwicklungsgeschichte der Zelle
inferredcites →https://doi.org/10.1007/978-3-7091-5473-1_1openalex-snapshot
Strukturtypen der Ruhekerne von Pflanzen und Tieren
inferredcites →https://doi.org/10.1007/978-3-7091-8222-2openalex-snapshot
Embryologie und Fortpflanzungsbiologie der Angiospermen
inferredcites →https://doi.org/10.1007/bf00223672openalex-snapshot
Flow cytometric and Feulgen densitometric analysis of genome size variation in Pisum
inferredcites →https://doi.org/10.1007/bf00319480openalex-snapshot
Notizen zur endomitotlschen Polyploidisierung in Trichocyten und Elaiosomen sowie �ber Kernstrukturen bei Gagea lutea
inferredcites →https://doi.org/10.1007/bf00936335openalex-snapshot
?Self-tanning??a new and important source of stoichiometric error in cytophotometric determination of nuclear DNA content in plants
inferredcites →https://doi.org/10.1007/bf00984369openalex-snapshot
Karyotype constancy and genome size variation in BulgarianCrepis foetida s. l. (Asteraceae)
inferredcites →https://doi.org/10.1007/bf01322281openalex-snapshot
Double fertilization inEphedra trifurca, a non-flowering seed plant: The relationship between fertilization events and the cell cycle
inferredcites →https://doi.org/10.1007/bf01373367openalex-snapshot
�ber die Entwicklung des Embryosacks vonMelampyrum undParentucellia latifolia (Scrophulariaceae, Pedicularieae)
inferredcites →https://doi.org/10.1007/bf01909727openalex-snapshot
Die Embryosackentwicklung in der Gattung Gagea Salisb
inferredcites →https://doi.org/10.1007/bf02281863openalex-snapshot
Differential underacetylation of histones H2A, H3 and H4 on the inactive X chromosome in human female cells
inferredcites →https://doi.org/10.1007/bf02344352openalex-snapshot
Microtubular organization during asymmetrical division of the generative cell inGagea lutea
inferredcites →https://doi.org/10.1007/s004250050285openalex-snapshot
Structure and DNA methylation pattern of partially heterochromatinised endosperm nuclei in Gagea lutea (Liliaceae)
inferredcites →https://doi.org/10.1016/0092-8674(93)90419-qopenalex-snapshot
The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression
inferredcites →https://doi.org/10.1038/163676a0openalex-snapshot
A Morphological Distinction between Neurones of the Male and Female, and the Behaviour of the Nucleolar Satellite during Accelerated Nucleoprotein Synthesis
inferredcites →https://doi.org/10.1038/190372a0openalex-snapshot
Gene Action in the X-chromosome of the Mouse (Mus musculus L.)
inferredcites →https://doi.org/10.1083/jcb.2.6.765openalex-snapshot
DNA IN GAMETOGENESIS AND EMBRYOGENY IN TRADESCANTIA
inferredcites →https://doi.org/10.1105/tpc.7.12.1975openalex-snapshot
Double Fertilization in Gnetum gnemon: The Relationship between the Cell Cycle and Sexual Reproduction.
inferredcites →https://doi.org/10.1111/j.1438-8677.1998.tb00716.xopenalex-snapshot
Genome Size in Sphagnum (Peat Moss)
inferredcites →https://doi.org/10.1126/science.145.3628.130openalex-snapshot
Heterochromatic Chromosomes in the Coccids
inferredcites →https://doi.org/10.1139/g87-085openalex-snapshot
A DNA cytophotometric and chromosome banding study in Hedera helix (Araliaceae), with reference to differential DNA replication associated with juvenile–adult phase change
inferredcites →https://doi.org/10.1139/g94-092openalex-snapshot
Genome size variation in Pisum sativum
inferredcites →https://doi.org/10.1242/dev.126.5.1065openalex-snapshot
Expression of the cell cycle in sperm of Arabidopsis: implications for understanding patterns of gametogenesis and fertilization in plants and other eukaryotes
inferredcites →https://doi.org/10.1515/bchm.1998.379.10.1235openalex-snapshot
Histone H4 Underacetylation in Plant Facultative Heterochromatin
inferredcites →https://doi.org/10.2307/2441475openalex-snapshot
A NEW CLEARING‐SQUASH TECHNIQUE FOR THE STUDY OF OVULE DEVELOPMENT IN ANGIOSPERMS
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.714.3.1zenodo-depositor-declared
Significance of basal-most leaf anatomy in taxonomy of Gagea (Liliaceae): a study of species from Kurdistan, Iraq
inferred← citeshttps://doi.org/10.1007/s00606-008-0081-4openalex-snapshot
Phylogenetic relationships of Gagea Salisb. (Liliaceae) in Italy, inferred from molecular and morphological data matrices
inferred← citeshttps://doi.org/10.1016/b978-012301463-4/50004-8openalex-snapshot
Genome Size Evolution in Plants
inferred← citeshttps://doi.org/10.1017/s0960258520000148openalex-snapshot
Endosperm variability: from endoreduplication within a seed to higher ploidy across species, and its competence
inferred← citeshttps://doi.org/10.1080/00087114.2008.10589615openalex-snapshot
Contribution to the cytotaxonomical knowledge of the genusGageaSalisb. (Liliaceae). III. New karyological data from the central Mediterranean area
inferred← citeshttps://doi.org/10.1080/00087114.2015.1109923openalex-snapshot
Genome size estimates for nine species ofGageaSalisb. (Liliaceae) from the Mediterranean region
inferred← citeshttps://doi.org/10.1080/11263500600756090openalex-snapshot
A comparative analysis of embryo-sac development in three closely-related Gagea species (Liliaceae), with some considerations on their reproductive strategies
inferred← citeshttps://doi.org/10.1093/aob/mci003openalex-snapshot
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects
inferred← citeshttps://doi.org/10.1105/tpc.114.122655openalex-snapshot
Translocations of Chromosome End-Segments and Facultative Heterochromatin Promote Meiotic Ring Formation in Evening Primroses
inferred← citeshttps://doi.org/10.1111/j.1756-1051.2011.01187.xopenalex-snapshot
New light on phylogeny and taxonomy of the Eurasian Gagea villosa – G. fragifera complex (Liliaceae)
inferred← citeshttps://doi.org/10.1186/s40064-015-1167-4openalex-snapshot
Genome sizes of 227 accessions of Gagea (Liliaceae) discriminate between the species from the Netherlands and reveal new ploidies in Gagea
inferred← citeshttps://doi.org/10.1186/s40529-017-0194-6openalex-snapshot
Studies of life history of Gagea graeca (Liliaceae) based on morphological and molecular methods
inferred← citeshttps://doi.org/10.1186/s40529-023-00405-9openalex-snapshot
Taxonomic implications of leaf morphology and epidermal anatomy for 14 species of Gagea (Liliaceae) from Xinjiang, China
inferred← citeshttps://doi.org/10.1508/cytologia.79.69openalex-snapshot
Development of Female Gametophyte in Gagea villosa
inferred← citeshttps://doi.org/10.2478/s11756-014-0439-8openalex-snapshot
Microsporogenesis, pollen mitosis and pollen tube growth in Gagea villosa (Liliaceae)
inferred← citeshttps://doi.org/10.3389/fevo.2020.516640openalex-snapshot
Poles Apart: Monosporic, Bisporic, and Tetrasporic Embryo Sacs Revisited
inferred← citeshttps://doi.org/10.5603/4614openalex-snapshot
Rumex acetosa Y chromosomes: constitutive or facultative heterochromatin?
inferred← citeshttps://doi.org/10.6084/m9.figshare.26646676openalex-snapshot
Additional file 1 of Taxonomic implications of leaf morphology and epidermal anatomy for 14 species of Gagea (Liliaceae) from Xinjiang, China
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