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Biological role of endoreplication in the process of spermatogenesis inChara vulgaris L.

https://doi.org/10.1007/bf01322627
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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1537-2197.1982.tb13251.xopenalex-snapshot
DNA CONTENT AND HETEROCHROMATIN VARIATIONS IN VARIOUS TISSUES OF PEANUT (ARACHIS HYPOGAEA)
inferredcites →https://doi.org/10.1007/978-3-642-68347-3openalex-snapshot
Nucleic Acids and Proteins in Plants II
inferredcites →https://doi.org/10.1007/bf00048400openalex-snapshot
Endopolyploidy: Towards an understanding of its biological significance
inferredcites →https://doi.org/10.1007/bf00392780openalex-snapshot
Endomitosis and the effect of gibberellic acid in different Pisum sativum L. cultivars
inferredcites →https://doi.org/10.1007/bf00397384openalex-snapshot
Changes in ultrastructure of plasmodesmata during spermatogenesis in Chara vulgaris L.
inferredcites →https://doi.org/10.1007/bf00495679openalex-snapshot
Autoradiographic and ultrastructural study of Cucurbita pepo root cells during their growth and differentiation
inferredcites →https://doi.org/10.1007/bf00984606openalex-snapshot
Consequences of artificial and natural chromosome doubling on DNA, RNA and protein contents inCochlearia (Brassicaceae)
inferredcites →https://doi.org/10.1007/bf01276594openalex-snapshot
The reserve proteins in the cells of mature cotyledons ofLupinus albus var.Lucky
inferredcites →https://doi.org/10.1007/bf01276998openalex-snapshot
Changes in the occurrence and ultrastructure of plasmodesmata in antheridia ofChara vulgaris L. during different stages of spermatogenesis
inferredcites →https://doi.org/10.1007/bf01287623openalex-snapshot
DNA and protein content relationship in the cells of mature cotyledons ofPisum sativum
inferredcites →https://doi.org/10.1007/bf01290870openalex-snapshot
Symplasmic isolation ofChara vulgaris antheridium and mechanisms regulating the process of spermatogenesis
inferredcites →https://doi.org/10.1007/bf01624003openalex-snapshot
Plasmodesmata between synchronously and asynchronously developing cells of the antheridial filaments ofChara vulgaris L.
inferredcites →https://doi.org/10.1016/0012-1606(72)90047-4openalex-snapshot
Macromolecular synthesis during plant embryogeny: Rates of RNA synthesis in Phaseolus coccineus embryos and suspensors
inferredcites →https://doi.org/10.1016/s0015-3796(87)80067-7openalex-snapshot
Changes in Nuclear, Nucleolar, and Cytoplasmic Protein Contents during Differentiation of Root Parenchyma Cells in Species with Different Dynamics of DNA Endoreplication
inferredcites →https://doi.org/10.1016/s0044-328x(74)80142-xopenalex-snapshot
The Phaseolus suspensor and its polytene chromosomes
inferredcites →https://doi.org/10.1071/bi9680255openalex-snapshot
Ultrastructure and Differentiation In Chara Sp. III. Formation of the Antheridium
inferredcites →https://doi.org/10.1083/jcb.35.2.377openalex-snapshot
MICROSPECTROPHOTOMETRIC ANALYSIS OF NUCLEAR DNA IN CHARA ZEYLANICA
inferredcites →https://doi.org/10.1093/jxb/24.1.216openalex-snapshot
The Formation of Polyploid Cells in Ripening Cotyledons of Pisum sativum L. in Relation to Ribosome and Protein Synthesis
inferredcites →https://doi.org/10.1104/pp.51.6.1005openalex-snapshot
Deoxyribonucleic Acid and Ribonucleic Acid Synthesis during the Cell Expansion Phase of Cotyledon Development in Vicia faba L
inferredcites →https://doi.org/10.2216/i0031-8884-26-4-435.1openalex-snapshot
The quantities of DNA in the vegetative nuclei of Chara vulgaris and Tolypella glomerata (Charophyta)
inferredcites →https://doi.org/10.5586/asbp.1988.052openalex-snapshot
Studies on the role of gibberellins in the regulation of spermatogenesis in Chara vulgaris L.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/oneeco.9.e117655zenodo-depositor-declared
What we really know about the dormancy, reproduction, germination and cultivation of charophytes (Characeae)
inferred← citeshttps://doi.org/10.1006/cbir.1998.0242openalex-snapshot
ANTHERIDIAL CHROMATIN CONDENSATION FACTOR FROM MALE SEX ORGANS OF CHARA TOMENTOSA
inferred← citeshttps://doi.org/10.1007/978-3-642-60035-7_12openalex-snapshot
Plasmodesmal Cou lin p g and Cell Differentiation in Aigae
inferred← citeshttps://doi.org/10.1007/bf00197801openalex-snapshot
Autoradiographic studies on the role of plasmodesmata in the transport of gibberellin
inferred← citeshttps://doi.org/10.1007/bf00937825openalex-snapshot
Endopolyploidization patterns in non-generative antheridial cells in mono- and dioeciousChara spp. (Characeae) with different DNA C-values
inferred← citeshttps://doi.org/10.1007/bf00942143openalex-snapshot
Cell cycle duration in antheridial filaments ofChara spp. (Characeae) with different genome size and heterochromatin content
inferred← citeshttps://doi.org/10.1007/bf02960261openalex-snapshot
The excitability of plant cells: With a special emphasis on characean internodal cells
inferred← citeshttps://doi.org/10.1007/s00299-016-1979-xopenalex-snapshot
PIN2-like proteins may contribute to the regulation of morphogenetic processes during spermatogenesis in Chara vulgaris
inferred← citeshttps://doi.org/10.1007/s00709-003-0001-yopenalex-snapshot
Plasmodesmal changes are related to different developmental stages of antheridia of Chara species
inferred← citeshttps://doi.org/10.1016/j.flora.2023.152421openalex-snapshot
Genome size and DNA endoreplication pattern of non-generative cells in the antheridia of Chara connivens Salzmann ex A. Braun from Northern Morocco
inferred← citeshttps://doi.org/10.1023/b:biop.0000023874.59655.beopenalex-snapshot
Effect of Chilling on DNA Endoreplication in Root Cortex Cells and Root Hairs of Soybean Seedlings
inferred← citeshttps://doi.org/10.1080/09291019509360324openalex-snapshot
Circadian rhythm of protein synthesis in generative and non‐generative antheridial cells ofChara VulgarisL.
inferred← citeshttps://doi.org/10.1093/jxb/erm071openalex-snapshot
Role of DNA endoreduplication, lipotubuloids, and gibberellic acid in epidermal cell growth during fruit development of Ornithogalum umbellatum
inferred← citeshttps://doi.org/10.1093/oxfordjournals.pcp.a029348openalex-snapshot
Effect of GA3 Treatment on the Number of Spermatozoids and Endopolyploidy Levels of Non-Generative Cells in Antheridia of Chara vulgaris L.
inferred← citeshttps://doi.org/10.1111/j.1438-8677.1996.tb00550.xopenalex-snapshot
Different Patterns of Intercellular Transport of Lucifer Yellow in Young and Mature Antheridia of Chara vulgaris L.
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2010.00874.xopenalex-snapshot
WHAT DO WE KNOW ABOUT CHAROPHYTE (STREPTOPHYTA) LIFE CYCLES?1
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