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The relationship between nuclear envelope-derived annulate lamellae and the asymmetric division of primary spermatocytes in aphids
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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/cm.970110404openalex-snapshot
Microtubules are required for centrosome expansion and positioning while microfilaments are required for centrosome separation in sea urchin eggs during fertilization and mitosis
inferredcites →https://doi.org/10.1002/jez.1400190303openalex-snapshot
The predetermination of sex in phylloxerans and aphids
inferredcites →https://doi.org/10.1002/jez.1400900207openalex-snapshot
A cytological and experimental analysis of the meiotic behavior of the univalent X chromosome in the bearberry aphid Tamalia (Phyllaphis) coweni (Ckll.)
inferredcites →https://doi.org/10.1002/jez.1401760309openalex-snapshot
Polar granules of Drosophila. IV. Cytochemical studies showing loss of RNA from polar granules during early stages of embryogenesis
inferredcites →https://doi.org/10.1002/jmor.1051710210openalex-snapshot
Differentiation of Acmaea digitalis oocytes with special reference to lipid‐endoplasmic reticulum‐annulate lamellae‐polyribosome relationships
inferredcites →https://doi.org/10.1002/jmor.1051760206openalex-snapshot
Fibrogranular bodies, annulate lamellae, and polyribosomes in the dragonfly oocyte
inferredcites →https://doi.org/10.1007/bf00123229openalex-snapshot
Characterization of the diffuse stage in the male meiotic prophase and karyotype of Scapteriscus borellii (Orthoptera: Grylloidea)
inferredcites →https://doi.org/10.1007/bf00284937openalex-snapshot
Holocentric chromosomes in Oncopeltus: kinetochore plates are present in mitosis but absent in meiosis
inferredcites →https://doi.org/10.1007/bf00286920openalex-snapshot
Stability of a multiple X chromosome system and associated B chromosomes in birch aphids (Euceraphis spp.; Homoptera: Aphididae)
inferredcites →https://doi.org/10.1007/bf00292958openalex-snapshot
Cytogenetics of two species of Euceraphis (Homoptera, Aphididae)
inferredcites →https://doi.org/10.1007/bf00327316openalex-snapshot
The chromosomes of Schoutedenia lutea (homoptera, aphidoidea, greenideinae), with an account of meiosis in the male
inferredcites →https://doi.org/10.1007/bf00327317openalex-snapshot
Transmission of three radiation-induced translations in the Syrian hamster
inferredcites →https://doi.org/10.1007/bf00327467openalex-snapshot
Spermatogenesis in the aphid Amphorophora tuberculata (Homoptera, Aphididae)
inferredcites →https://doi.org/10.1007/bf00344022openalex-snapshot
Spindel und kinetochoren in der Mitose und Meiose der Baumwollwanze Dysdercus intermedius (Heteroptera)
inferredcites →https://doi.org/10.1007/bf00411809openalex-snapshot
Die symbiontischen einrichtungen im rahmen des generationswechsels monözischer und heterözischer pemphiginen der schwarz- und pyramidenpappel
inferredcites →https://doi.org/10.1007/bf00585855openalex-snapshot
Der Chromosomenzyklus von Tetraneura ulmi de Geer
inferredcites →https://doi.org/10.1007/bf00627210openalex-snapshot
Zur Funktion des ?Flemming-K�rpers? bei der Teilung tierischer Zellen
inferredcites →https://doi.org/10.1007/bf01114903openalex-snapshot
‘De novo’ centrioles originate at sites associated with annulate lamellae in sea-urchin eggs
inferredcites →https://doi.org/10.1007/bf01276994openalex-snapshot
Ultrastructure of the kinetochore inGraphosoma italicum (Hemiptera: Heteroptera)
inferredcites →https://doi.org/10.1007/bf01740773openalex-snapshot
Ribosomal bodies and annulate lamellae in the oocytes of the lizardPodarcis sicula
inferredcites →https://doi.org/10.1016/0014-4827(84)90442-7openalex-snapshot
Centrosomes and mitotic poles
inferredcites →https://doi.org/10.1016/0040-8166(89)90049-9openalex-snapshot
Annulate lamellae: An organelle in search of a function
inferredcites →https://doi.org/10.1016/0309-1651(81)90001-1openalex-snapshot
Membranes in the mitotic apparatus
inferredcites →https://doi.org/10.1016/0892-0354(89)90003-8openalex-snapshot
The annulate lamellae—From obscurity to spotlight
inferredcites →https://doi.org/10.1016/b978-0-12-622590-7.50013-xopenalex-snapshot
The Fine Structure of the Formation of Mitotic Poles in Fertilized Eggs
inferredcites →https://doi.org/10.1016/s0022-5320(68)80056-5openalex-snapshot
Origin and fate of annulate lamellae in arbacia punctulata eggs
inferredcites →https://doi.org/10.1016/s0065-2660(08)60513-1openalex-snapshot
Y Chromosome Function and Spermatogenesis in Drosophila hydei
inferredcites →https://doi.org/10.1038/345263a0openalex-snapshot
Cytoplasmic dynein is localized to kinetochores during mitosis
inferredcites →https://doi.org/10.1038/345266a0openalex-snapshot
Localization of cytoplasmic dynein to mitotic spindles and kinetochores
inferredcites →https://doi.org/10.1080/00222938500770171openalex-snapshot
A new species ofAmphorophora(Homoptera: Aphididae) onGeranium macrorrhizumin Britain
inferredcites →https://doi.org/10.1080/01688170.1987.10510275openalex-snapshot
The Mode of Sex Determination inDinophilus gyrociliatue(Archiannelida)
inferredcites →https://doi.org/10.1083/jcb.103.2.581openalex-snapshot
Oscillatory movements of monooriented chromosomes and their position relative to the spindle pole result from the ejection properties of the aster and half-spindle.
inferredcites →https://doi.org/10.1083/jcb.109.5.2245openalex-snapshot
The motor for poleward chromosome movement in anaphase is in or near the kinetochore.
inferredcites →https://doi.org/10.1083/jcb.110.2.391openalex-snapshot
Poleward force at the kinetochore in metaphase depends on the number of kinetochore microtubules.
inferredcites →https://doi.org/10.1083/jcb.42.1.185openalex-snapshot
ANNULATE LAMELLAE AND "YOLK NUCLEI" IN OOCYTES OF THE DRAGONFLY, LIBELLULA PULCHELLA
inferredcites →https://doi.org/10.1083/jcb.51.3.889openalex-snapshot
EVIDENCE FOR RNA IN THE HEAVY BODIES OF SEA URCHIN EGGS
inferredcites →https://doi.org/10.1083/jcb.88.3.543openalex-snapshot
Chromosome behavior after laser microirradiation of a single kinetochore in mitotic PtK2 cells.
inferredcites →https://doi.org/10.1083/jcb.93.2.374openalex-snapshot
Traction force on a kinetochore at metaphase acts as a linear function of kinetochore fiber length
inferredcites →https://doi.org/10.1111/j.1365-3113.1980.tb00393.xopenalex-snapshot
Chromosome numbers in the Aphididae and their taxonomic significance
inferredcites →https://doi.org/10.1139/g73-093openalex-snapshot
THE ULTRASTRUCTURE OF KINETOCHORES OF UNPAIRED CHROMOSOMES IN A WHEAT HYBRID
inferredcites →https://doi.org/10.1242/jcs.26.1.217openalex-snapshot
Accumulation of gene products in the oocytes of the dragonfly Cordulia Aenea: II. Induction of annulate lamellae within dense masses during diapause
inferredcites →https://doi.org/10.1242/jcs.43.1.177openalex-snapshot
Variations in the distribution and migration of centriole duplexes in mitotic ptk2 cells studied by immunofluorescence microscopy
inferredcites →https://doi.org/10.1242/jcs.91.3.325openalex-snapshot
The prometaphase configuration and chromosome order in early mitosis
inferredcites →https://doi.org/10.2307/1536499openalex-snapshot
SPERMATOGENESIS OF APHIDS; THE FATE OF THE SMALLER SECONDARY SPERMATOCYTE
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.5183.1.4zenodo-depositor-declared
Roger Blackman 1941–2022—an appreciation
inferred← citeshttps://doi.org/10.1002/bies.950160207openalex-snapshot
How meiotic cells deal with non‐exchange chromosomes
inferred← citeshttps://doi.org/10.1007/bf00357059openalex-snapshot
Structure, mitotic and meiotic behaviour, and stability of centromere-like elements devoid of chromosome arms in the fly Megaselia scalaris (Phoridae)
inferred← citeshttps://doi.org/10.1007/bf00710772openalex-snapshot
Synaptonemal polycomplexes in spermatids: a characteristic trait of Orthoptera?
inferred← citeshttps://doi.org/10.1007/s004120000100openalex-snapshot
Inheritance and meiotic behaviour of a de novo chromosome fusion in the aphid Myzus persicae (Sulzer)
inferred← citeshttps://doi.org/10.1016/0020-7322(93)90035-yopenalex-snapshot
Visualization of polyfusomes in gonads of a moth, Ephestia kuehniella Z. (Lepidoptera : Pyralidae), by a microspreading technique and electron microscopy
inferred← citeshttps://doi.org/10.1016/0020-7322(95)00021-6openalex-snapshot
The structure of condensed chromosomes in mitosis and meiosis of insects
inferred← citeshttps://doi.org/10.1016/0968-4328(94)00050-zopenalex-snapshot
Spindle membranes and spindle architecture in invertebrates
inferred← citeshttps://doi.org/10.1016/s0248-4900(02)01191-7openalex-snapshot
The mitotic spindle and associated membranes in the closed mitosis of trichomonads
inferred← citeshttps://doi.org/10.1023/a:1009203500012openalex-snapshot
Orientation of the 'stretched' univalent X chromosome during the unequal first meiotic division in male aphids
inferred← citeshttps://doi.org/10.1034/j.1601-5223.2003.01661.xopenalex-snapshot
Analysis of insect holocentric chromosomes by atomic force microscopy
inferred← citeshttps://doi.org/10.1080/11250009309355818openalex-snapshot
Cytogenetic mechanisms in aphids
inferred← citeshttps://doi.org/10.1111/j.1463-6395.1995.tb00999.xopenalex-snapshot
Spermatogenesis in Tenebrio molitor (Tenebrionidae, Coleoptera): A Fine Structure and Anti‐tubulin Immunofluorescence Study
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