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Infertility in the hyperplasic ovary of freshwater planarians: the role of programmed cell death
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/dbio.2000.0120openalex-snapshot
Comparative Aspects of Animal Oogenesis
inferredcites →https://doi.org/10.1007/bf00174615openalex-snapshot
Developmental cell death: morphological diversity and multiple mechanisms
inferredcites →https://doi.org/10.1007/bf01056205openalex-snapshot
Oocyte atresia and reproductive success in fathead minnows (Pimephales promelas) exposed to acidified hardwater environments
inferredcites →https://doi.org/10.1007/s00427-007-0146-3openalex-snapshot
The planarian nanos-like gene Smednos is expressed in germline and eye precursor cells during development and regeneration
inferredcites →https://doi.org/10.1007/s00441-006-0298-xopenalex-snapshot
Mechanisms of programmed cell death during oogenesis in Drosophila virilis
inferredcites →https://doi.org/10.1016/j.bbamcr.2009.02.009openalex-snapshot
Autophagy in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.cellsig.2013.11.028openalex-snapshot
The role of cell signalling in the crosstalk between autophagy and apoptosis
inferredcites →https://doi.org/10.1016/j.crvi.2011.03.009openalex-snapshot
Étude ultrastructurale de l’ovogenèse chez la planaire Schmidtea mediterranea (Plathelminthe, Paludicole)
inferredcites →https://doi.org/10.1016/j.crvi.2011.11.005openalex-snapshot
Ultrastructure of spermatogenesis and mature spermatozoon of the freshwater planarian Schmidtea mediterranea (Platyhelminthes, Paludicola)
inferredcites →https://doi.org/10.1016/j.cub.2006.10.053openalex-snapshot
Direct Induction of Autophagy by Atg1 Inhibits Cell Growth and Induces Apoptotic Cell Death
inferredcites →https://doi.org/10.1016/j.ejsobi.2007.08.034openalex-snapshot
Changes in the ovary cells structure in the earthworm Dendrobaena veneta (Rosa) in neurosecretion deficiency and after exposure to cadmium
inferredcites →https://doi.org/10.1016/j.femsyr.2004.07.006openalex-snapshot
Multiple cell death programs: Charon’s lifts to Hades
inferredcites →https://doi.org/10.1016/j.gyobfe.2005.06.016openalex-snapshot
L'apoptose des cellules folliculaires : son implication dans les protocoles de stimulation ovarienne
inferredcites →https://doi.org/10.1016/j.jhazmat.2013.02.055openalex-snapshot
Singlet oxygen mediated apoptosis by anthrone involving lysosomes and mitochondria at ambient UV exposure
inferredcites →https://doi.org/10.1016/j.taap.2004.11.024openalex-snapshot
Gentamicin-induced apoptosis in LLC-PK1 cells: Involvement of lysosomes and mitochondria
inferredcites →https://doi.org/10.1016/j.tcb.2011.03.007openalex-snapshot
Autophagy and apoptosis: what is the connection?
inferredcites →https://doi.org/10.1016/j.tice.2012.09.003openalex-snapshot
An ultrastructural study of oogenesis and cell dynamics during cocoon shell secretion in the subterranean freshwater planarian Dendrocoelum constrictum (Platyhelminthes, Tricladida)
inferredcites →https://doi.org/10.1016/j.ydbio.2009.01.043openalex-snapshot
Spoltud-1 is a chromatoid body component required for planarian long-term stem cell self-renewal
inferredcites →https://doi.org/10.1016/s0074-7696(08)62312-8openalex-snapshot
Cell Death: The Significance of Apoptosis
inferredcites →https://doi.org/10.1016/s0092-8674(03)00422-7openalex-snapshot
Apoptotic Cells Induce Migration of Phagocytes via Caspase-3-Mediated Release of a Lipid Attraction Signal
inferredcites →https://doi.org/10.1016/s0928-4680(98)80586-5openalex-snapshot
Lysosomal involvement in apoptosis
inferredcites →https://doi.org/10.1016/s1472-6483(10)62052-4openalex-snapshot
Apoptosis in the human ovary
inferredcites →https://doi.org/10.1023/a:1003413627495openalex-snapshot
Characters of the female gonad and the phylogeny of Platyhelminthes
inferredcites →https://doi.org/10.1038/cdd.2011.96openalex-snapshot
Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012
inferredcites →https://doi.org/10.1038/cddis.2013.321openalex-snapshot
ING1 induces apoptosis through direct effects at the mitochondria
inferredcites →https://doi.org/10.1038/cddis.2013.398openalex-snapshot
Erratum: ING1 induces apoptosis through direct effects at the mitochondria
inferredcites →https://doi.org/10.1038/ncomms2811openalex-snapshot
A sex-specific transcription factor controls male identity in a simultaneous hermaphrodite
inferredcites →https://doi.org/10.1038/nrm2239openalex-snapshot
Self-eating and self-killing: crosstalk between autophagy and apoptosis
inferredcites →https://doi.org/10.1038/nrm2312openalex-snapshot
Apoptosis: controlled demolition at the cellular level
inferredcites →https://doi.org/10.1073/pnas.0609708104openalex-snapshot
nanos function is essential for development and regeneration of planarian germ cells
inferredcites →https://doi.org/10.1073/pnas.0703588104openalex-snapshot
Gtdap-1 promotes autophagy and is required for planarian remodeling during regeneration and starvation
inferredcites →https://doi.org/10.1073/pnas.93.25.14559openalex-snapshot
BAX-induced cell death may not require interleukin 1β-converting enzyme-like proteases
inferredcites →https://doi.org/10.1074/jbc.m308347200openalex-snapshot
Selective Disruption of Lysosomes in HeLa Cells Triggers Apoptosis Mediated by Cleavage of Bid by Multiple Papain-like Lysosomal Cathepsins
inferredcites →https://doi.org/10.1078/0171-9335-00359openalex-snapshot
Autophagic and apoptotic features during programmed cell death in the fat body of the tobacco hornworm (Manduca sexta)
inferredcites →https://doi.org/10.1083/jcb.139.1.205openalex-snapshot
Bax Deletion Further Orders the Cell Death Pathway in Cerebellar Granule Cells and Suggests a Caspase-independent Pathway to Cell Death
inferredcites →https://doi.org/10.1083/jcb.153.6.1265openalex-snapshot
Bax and Bak Coalesce into Novel Mitochondria-Associated Clusters during Apoptosis
inferredcites →https://doi.org/10.1111/j.1440-169x.2006.00897.xopenalex-snapshot
Identification and origin of the germline stem cells as revealed by the expression of nanos‐related gene in planarians
inferredcites →https://doi.org/10.1111/j.1463-6409.1974.tb00820.xopenalex-snapshot
Morpho‐karyological Types of Dugesia (Turbellaria, Tricladida) in Israel and Their Distribution Patterns
inferredcites →https://doi.org/10.1146/annurev.ph.28.030166.002251openalex-snapshot
Functions of Lysosomes
inferredcites →https://doi.org/10.1152/physiolgenomics.00073.2009openalex-snapshot
Transcriptome analysis reveals an unexpected role of a collagen tyrosine kinase receptor gene,Ddr2,as a regulator of ovarian function
inferredcites →https://doi.org/10.11646/zootaxa.3551.1.3openalex-snapshot
A new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from the Afromontane forest in South Africa, with an overview of freshwater planarians from the African continent
inferredcites →https://doi.org/10.1172/jci9914openalex-snapshot
Cathepsin B contributes to TNF-α–mediated hepatocyte apoptosis by promoting mitochondrial release of cytochrome c
inferredcites →https://doi.org/10.1186/ar422openalex-snapshot
Fragmentation of Golgi complex and Golgi autoantigens during apoptosis and necrosis
inferredcites →https://doi.org/10.1210/jc.81.7.2702openalex-snapshot
Immunological evidence for the expression of the Fas antigen in the infant and adult human ovary during follicular regression and atresia
inferredcites →https://doi.org/10.1242/dev.01785openalex-snapshot
DjPum, a homologue ofDrosophila Pumilio,is essential to planarian stem cell maintenance
inferredcites →https://doi.org/10.1242/dev.129.13.3255openalex-snapshot
daughterlesscoordinates somatic cell proliferation, differentiation and germline cyst survival during follicle formation inDrosophila
inferredcites →https://doi.org/10.1242/dev.30.2.317openalex-snapshot
Genetic and physiologic control of fissioning and sexuality in planarians
inferredcites →https://doi.org/10.1242/jcs.113.7.1189openalex-snapshot
Autophagic and apoptotic types of programmed cell death exhibit different fates of cytoskeletal filaments
inferredcites →https://doi.org/10.1371/journal.pbio.1000509openalex-snapshot
Genome-Wide Analyses Reveal a Role for Peptide Hormones in Planarian Germline Development
inferredcites →https://doi.org/10.2108/zsj.30.502openalex-snapshot
Reproductive Strategies, Karyology, Parasites, and Taxonomic Status ofDugesiaPopulations from Yemen (Platyhelminthes: Tricladida: Dugesiidae)
inferredcites →https://doi.org/10.4161/auto.3582openalex-snapshot
Apoptosis and Autophagy Function Cooperatively for the Efficacious Execution of Programmed Nurse Cell Death DuringDrosophila virilisOogenesis
inferredcites →https://doi.org/10.4161/auto.4735openalex-snapshot
Autophagy and Apoptosis Coordinate Physiological Cell Death in Larval Salivary Glands ofApis mellifera(Hymenoptera: Apidae)
inferredcites →https://doi.org/10.4161/auto.4934openalex-snapshot
Gtdap-1and the Role of Autophagy During Planarian Regeneration and Starvation
inferredcites →https://doi.org/10.4161/auto.5205openalex-snapshot
Different modes of programmed cell death during oogenesis of the silkmothBombyx mori
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1163/18759866-20191406zenodo-depositor-declared
The invasive alien freshwater flatworm Girardia tigrina (Girard, 1850) (Platyhelminthes, Tricladida) in Western Europe: new insights into its morphology, karyology and reproductive biology
inferred← citeshttps://doi.org/10.3897/zookeys.1233.142976zenodo-depositor-declared
Two new species of freshwater planarian from Hainan Island and Leizhou Peninsula, southern China (Platyhelminthes, Tricladida, Dugesiidae)
inferred← citeshttps://doi.org/10.5281/zenodo.15177339zenodo-depositor-declared
Dugesia saccata Chen & Dong 2025, sp. nov.
inferred← citeshttps://doi.org/10.1007/978-4-431-56609-0_9openalex-snapshot
Reproductive Strategies in Planarians: Insights Gained from the Bioassay System for Sexual Induction in Asexual Dugesia ryukyuensis Worms
inferred← citeshttps://doi.org/10.1007/s10646-021-02439-wopenalex-snapshot
The negative effect of the PI3K inhibitor 3-methyladenine on planarian regeneration via the autophagy signalling pathway
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.131117openalex-snapshot
When treatment increases the contaminant's ecotoxicity: A study of the Fenton process in the degradation of methylene blue
inferred← citeshttps://doi.org/10.1016/j.jcz.2016.01.005openalex-snapshot
Ultrastructural study of oogenesis in the acotylean Echinoplana celerrima, (Platyhelminthes, Polycladida)
inferred← citeshttps://doi.org/10.1016/j.jip.2023.107935openalex-snapshot
Using autophagy, apoptosis, cytoskeleton, and epigenetics markers to investigate the origin of infertility in ex-fissiparous freshwater planarian individuals (nomen nudum species) with hyperplasic ovaries
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2015.11.024openalex-snapshot
Relationship between bcl-2, bax, beclin-1, and cathepsin-D proteins during postovulatory follicular regression in fish ovary
inferred← citeshttps://doi.org/10.1086/691408openalex-snapshot
Dynamics of Cytokine-like Activity in the Hyperplasic Ovary of Ex-fissiparous Planarians
inferred← citeshttps://doi.org/10.1111/zoj.12430openalex-snapshot
A molecular analysis of the phylogenetic position of the suborder Cavernicola within the Tricladida (Platyhelminthes), with the description of a new species of stygobiont flatworm from Benin
inferred← citeshttps://doi.org/10.1155/2024/8299436openalex-snapshot
Two New Species of Freshwater Planarian (Platyhelminthes, Tricladida, Dugesiidae, Dugesia) from Southern China Exhibit Unusual Karyotypes, with a Discussion on Reproduction in Aneuploid Species
inferred← citeshttps://doi.org/10.1242/bio.045013openalex-snapshot
Autophagy-related Djatg8 is required for remodeling in planarians Dugesia japonica
inferred← citeshttps://doi.org/10.18632/aging.204269openalex-snapshot
Fetal programming: in utero exposure to acrylamide leads to intergenerational disrupted ovarian function and accelerated ovarian aging
inferred← citeshttps://doi.org/10.3897/zookeys.1028.60838openalex-snapshot
Integrative descriptions of two new species of Dugesia from Hainan Island, China (Platyhelminthes, Tricladida, Dugesiidae)
inferred← citeshttps://doi.org/10.3897/zookeys.1059.65633openalex-snapshot
Two new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from the tropical monsoon forest in southern China
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