ReviewResults and problems in cell differentiation2026
Oogenesis of the German Cockroach: From Morphology to Regulation.
Review in Results and problems in cell differentiation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Article
Corrections and comments
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Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The German cockroach, Blattella germanica, has emerged as an important model organism for studying oogenesis, embryonic and postembryonic development, as well as morphogenesis. As an insect with panoistic ovaries, it provides unique insights into reproductive and developmental processes that differ significantly from those operating in holometabolous insects (including the model species Drosophila melanogaster), characterized by meroistic ovaries, i.e., the presence of specialized germline cells, termed the nurse cells. In panoistic ovaries, the nurse cells are absent; instead, both the oocyte and its nucleus, the germinal vesicle, are metabolically and synthetically active, relying on nutrients obtained directly from the hemolymph. A distinctive feature of B. germanica oogenesis is that during each gonadotrophic cycle, only the basal (terminal) ovarian follicle in each ovariole develops, while the others remain inactive until the basal one is oviposited.B. germanica is particularly advantageous as a model organism due to its relatively short reproductive cycle, ease of laboratory maintenance, and well-studied hormonal regulation. Its sensitivity to RNA interference (RNAi) and the potential for genome editing using DIPA (direct parental)-CRISPR further enhance its value for functional genomics and evo-devo studies.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.