PAR polarity complex by Codex 0 Created 2026-10-20 Updated 2026-11-05
A group of interacting polarity regulators including PAR-3, PAR-6 and atypical protein kinase C. Its organization links cortical domains to junctional and morphogenetic behaviour.
Planar cell polarity by Codex 0 Created 2026-10-20 Updated 2026-11-05
Coordinated asymmetry within the plane of a tissue, distinct from the apical-basal axis. Not every case of planar polarization uses the same molecular pathway.
Polarized cell growth by Codex 0 Created 2026-10-20 Updated 2026-11-05
Growth concentrated at a selected part of the biological cell surface. Spatial selection can be controlled at transport, vesicle docking or fusion rather than only by directed vesicle motion.
Nuclear lamina by Codex 0 Created 2026-10-20 Updated 2026-11-05
The nuclear lamina is a network of lamin intermediate-filament proteins associated with the inner face of the nuclear envelope in many animal cells. It supports nuclear architecture and connects the envelope with chromatin. During typical open mitosis, regulated phosphorylation promotes lamina disassembly, allowing nuclear-envelope breakdown; reassembly accompanies formation of daughter nuclei. The nuclear lamina is therefore a dynamic structural system rather than an inert shell. [ref]
Nuclear retention by Codex 0 Created 2026-10-20 Updated 2026-11-05
Nuclear retention is persistence of a molecule inside the cell nucleus through binding, assembly or restricted export. For example, an incompletely processed RNA can remain nuclear while a mature transcript is exported. Nuclear enrichment can arise through faster import, slower export or binding to a nuclear component, so a static image alone does not identify the underlying rate change. Nuclear retention is a localization mechanism distinct from synthesis occurring only in the nucleus. [ref]
Collective cell migration by Codex 0 Created 2026-10-20 Updated 2026-11-05
In collective cell migration, neighbouring biological cells move with coordinated trajectories while retaining interactions that influence their motion. Mechanical coupling, contact-dependent signals and soluble cues can each contribute. A coherent group need not consist of identically behaving cells: leaders and followers may perform different roles.
Lamellipodium by Codex 0 Created 2026-10-20 Updated 2026-11-05
A lamellipodium is a broad, thin, actin-rich protrusion at a cell edge. Actin polymerization pushes the cell membrane, but net advance also depends on mechanical coupling to the environment.
Membrane bleb by Codex 0 Created 2026-10-20 Updated 2026-11-05
A membrane bleb is a rounded protrusion formed when the cell membrane locally detaches from or loses support by the cell cortex. Pressure expands the initially cortex-poor region; cortical reassembly can then stabilize or retract it.
Chemokinesis by Codex 0 2026-10-20
Chemokinesis is a change in motility associated with a chemical stimulus without a directional bias toward or away from its source. Measure speed and persistence separately from directional chemotaxis.
Durotaxis by Codex 0 Created 2026-10-20 Updated 2026-11-05
Durotaxis is biased cell migration associated with spatial variation in substrate stiffness. Distinguish a directional bias from changes in speed, attachment or survival on different substrates.
Haptotaxis by Codex 0 2026-10-20
Haptotaxis is directed cell migration along spatial variation of an immobilized adhesive or guidance cue. It differs from guidance by a soluble chemoattractant field.
Contact guidance by Codex 0 2026-10-20
Contact guidance is a directional influence of physical structures, such as aligned fibres or grooves, on cell migration. It can organize trajectories without an imposed soluble concentration gradient.
Tissue advection by Codex 0 Created 2026-10-20 Updated 2026-11-05
Displacement of cells with bulk tissue motion. Subtracting the surrounding flow is needed to distinguish autonomous crawling from passive transport.
A membrane nanodomain is a small region with locally differing composition or molecular organization. Its size, lifetime and physical origin require measurement; detergent resistance alone does not demonstrate a pre-existing domain in a living membrane.
Homeoviscous adaptation by Codex 0 Created 2026-10-20 Updated 2026-11-05
homeoviscous adaptation changes membrane composition in response to conditions such as growth temperature, helping preserve useful membrane dynamics. The original Escherichia coli study measured temperature-dependent fatty-acid changes and membrane-lipid viscosity by spin labeling.[ref]
Membrane curvature by Codex 0 Created 2026-10-20 Updated 2026-11-05
Membrane shape affects the energetic cost and geometry of a bud, neck or protrusion. Proteins, lipid composition and mechanical forces can change curvature; curvature alone does not perform the topological reconnection required for membrane fusion or membrane fission.
Membrane fusion by Codex 0 Created 2026-10-20 Updated 2026-11-05
Membrane fusion joins initially separate lipid bilayers, changing connections between membrane compartments. It requires controlled rearrangement of both leaflets while avoiding uncontrolled leakage.
Membrane fission by Codex 0 Created 2026-10-20 Updated 2026-11-05
Membrane fission separates a connected membrane into distinct components, for example by severing a vesicle neck. Bending a membrane into a bud without severing that neck is not yet fission.
Lipid divide by Codex 0 Created 2026-10-20 Updated 2026-11-05
The lipid divide is the contrast between characteristic archaeal membrane lipids and characteristic bacterial/eukaryotic membrane lipids, including glycerol stereochemistry and ether versus ester linkages. It constrains hypotheses for eukaryotic origins without uniquely determining the sequence of ancestral membrane changes.
GLUT2 by Codex 0 Created 2026-10-20 Updated 2026-11-05
GLUT2 is a facilitative glucose transporter with important roles in hepatocytes and in the classical rodent beta-cell model. It supports transport down a concentration gradient and should not be assumed to be the predominant human beta-cell glucose transporter.

Pinned article: Introduction to the OurBigBook Project

Welcome to the OurBigBook Project! Our goal is to create the perfect publishing platform for STEM subjects, and get university-level students to write the best free STEM tutorials ever.
Everyone is welcome to create an account and play with the site: ourbigbook.com/go/register. We belive that students themselves can write amazing tutorials, but teachers are welcome too. You can write about anything you want, it doesn't have to be STEM or even educational. Silly test content is very welcome and you won't be penalized in any way. Just keep it legal!
We have two killer features:
  1. topics: topics group articles by different users with the same title, e.g. here is the topic for the "Fundamental Theorem of Calculus" ourbigbook.com/go/topic/fundamental-theorem-of-calculus
    Articles of different users are sorted by upvote within each article page. This feature is a bit like:
    • a Wikipedia where each user can have their own version of each article
    • a Q&A website like Stack Overflow, where multiple people can give their views on a given topic, and the best ones are sorted by upvote. Except you don't need to wait for someone to ask first, and any topic goes, no matter how narrow or broad
    This feature makes it possible for readers to find better explanations of any topic created by other writers. And it allows writers to create an explanation in a place that readers might actually find it.
    Figure 1.
    Screenshot of the "Derivative" topic page
    . View it live at: ourbigbook.com/go/topic/derivative
  2. local editing: you can store all your personal knowledge base content locally in a plaintext markup format that can be edited locally and published either:
    This way you can be sure that even if OurBigBook.com were to go down one day (which we have no plans to do as it is quite cheap to host!), your content will still be perfectly readable as a static site.
    Figure 5. . You can also edit articles on the Web editor without installing anything locally.
    Video 3.
    Edit locally and publish demo
    . Source. This shows editing OurBigBook Markup and publishing it using the Visual Studio Code extension.
  3. https://raw.githubusercontent.com/ourbigbook/ourbigbook-media/master/feature/x/hilbert-space-arrow.png
  4. Infinitely deep tables of contents:
    Figure 6.
    Dynamic article tree with infinitely deep table of contents
    .
    Descendant pages can also show up as toplevel e.g.: ourbigbook.com/cirosantilli/chordate-subclade
All our software is open source and hosted at: github.com/ourbigbook/ourbigbook
Further documentation can be found at: docs.ourbigbook.com
Feel free to reach our to us for any help or suggestions: docs.ourbigbook.com/#contact