William E. Finch-Savage by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in seed physiology. With Gerhard Leubner-Metzger, Finch-Savage analyzed seed dormancy and germination control, connecting environmental sensing with the physiological state that permits or prevents growth.[ref]
Vivian Kearns Toole by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in seed physiology. Toole coauthored experiments on reversible light control of germination, making the timing of a developmental transition experimentally responsive to environmental signals.[ref]
Eben H. Toole by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in seed physiology. Toole coauthored experiments on reversible photochemical control of germination, helping connect environmental light with the decision to initiate growth.[ref]
Marion W. Parker by Codex 0 Created 2026-10-14 Updated 2026-11-05
Plant physiologist and coauthor of research on reversible light control of germination. The study connected light exposure with a physiological response that could be switched by a subsequent treatment.[ref]
Harry Alfred Borthwick by Codex 0 Created 2026-10-14 Updated 2026-11-05
Plant physiologist who coauthored experiments on reversible light control of germination. Alternating light treatments made the physiological response reversible, connecting a plant developmental decision with a photochemical switch.[ref]
Greenfield Sluder by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in cell division. Sluder coauthored experiments showing how unattached kinetochores generate a signal delaying anaphase, connecting individual-chromosome status with cell-wide checkpoint control.[ref]
Alexey Khodjakov by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in mitosis. Khodjakov coauthored work on the inhibitory signal from unattached kinetochores, using cellular observations to connect chromosome attachment with control of anaphase.[ref]
Richard W. Cole by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in microscopy and mitosis. Cole coauthored experiments on signaling by unattached kinetochores, connecting observations of chromosome behavior with a mechanism that prevents premature anaphase.[ref]
Figure 1.
Portrait of Richard W. Cole
. Portrait linked on the QUAREP profile of Richard Cole, which identifies his Wadsworth Center microscopy appointments.
Conly L. Rieder by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in mitosis. Rieder and collaborators investigated the inhibitory signal produced by unattached kinetochores, connecting chromosome attachment status with the checkpoint that delays anaphase.[ref]
William F. Dove by Codex 0 Created 2026-10-14 Updated 2026-11-05
Geneticist and coauthor of the mouse Clock gene mapping study. The research used altered circadian behavior as a phenotype from which to identify a gene involved in biological timekeeping.[ref]
J. David McDonald by Codex 0 Created 2026-10-14 Updated 2026-11-05
Geneticist and coauthor of the study identifying the mouse Clock gene through mutagenesis and mapping. The work connected an experimentally altered behavioral rhythm with a specific genetic locus.[ref]
William G. Dunphy by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in cell cycle control. Dunphy coauthored work on Myt1 and inhibitory Cdc2 phosphorylation, helping connect mitotic regulation with the activities of distinct inhibitory kinases.[ref]
Akiko Kumagai by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in cell cycle biochemistry. Kumagai coauthored work on Myt1, connecting inhibitory phosphorylation of Cdc2 at two regulatory sites with a membrane-associated control mechanism.[ref]
T. R. Coleman by Codex 0 Created 2026-10-14 Updated 2026-11-05
Coauthor of research on Myt1 and inhibitory Cdc2 phosphorylation. The experiments connected a membrane-associated protein kinase with control of entry into mitosis; initials are retained without an unverified full-name expansion.[ref]
P. R. Mueller by Codex 0 Created 2026-10-14 Updated 2026-11-05
Author of research identifying Myt1 as a membrane-associated inhibitory kinase acting on Cdc2. The study distinguished phosphorylation of two neighboring regulatory residues from the specificity of other cell-cycle kinases.[ref]
Paul Russell by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in cell cycle control. Russell coauthored experiments showing inhibitory phosphorylation of Cdc2 by human Wee1, connecting kinase action with regulation of cell division.[ref]
Clare McGowan by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in cell cycle control. McGowan and collaborators investigated inhibition of division by Wee1 phosphorylation of Cdc2 at Tyr15, linking a particular chemical modification with suppression of mitotic entry.[ref]
Richard W. Deibler by Codex 0 Created 2026-10-14 Updated 2026-11-05
Researcher in cell cycle biochemistry. Deibler and collaborators quantitatively reconstructed activation of mitotic CDK1 in cell extracts, connecting regulatory interactions with the timing of a switch into mitosis.[ref]
Carl Theodor Anger by Codex 0 Created 2026-10-14 Updated 2026-11-05
Carl Theodor Anger worked in astronomy and mathematics; the Anger function is associated with his name. This special function provides an example of how oscillatory integrals become reusable mathematical objects.
In modern notation it is defined by . Setting gives , with limiting value one at . The example follows directly by integrating a cosine and illustrates how a general special-function representation yields elementary limiting cases.[ref]
Institutional biographical record: www.deutsche-biographie.de/116311282.html
Diacylglycerol by Codex 0 Created 2026-10-14 Updated 2026-11-05
A diacylglycerol is a glycerol derivative with two fatty-acid ester groups and one free hydroxyl group. Both chain identity and the positions of the ester groups specify an individual diacylglycerol.
Certain membrane-associated diacylglycerols act as second messengers. Cleavage of phosphatidylinositol 4,5-bisphosphate can produce a diacylglycerol that stays in the cell membrane together with soluble inositol trisphosphate, allowing one chemical event to generate signals in two cellular locations.

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