Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Homeobox genes in the developing mouse brain

J Y Vollmer1, R G Clerc

  • 1CNS Research Laboratories, Roche Ltd., Basel, Switzerland.

Journal of Neurochemistry
|July 2, 1998
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Dalcetrapib: no off-target toxicity on blood pressure or on genes related to the renin-angiotensin-aldosterone system in rats.

British journal of pharmacology·2009
Same author

Subcellular compartmentalization of activation and desensitization of responses mediated by NK2 neurokinin receptors.

The Journal of biological chemistry·1999
Same author

Pharmacological characterisation of the recombinant human CRF binding protein using a simple assay.

Journal of neuroscience methods·1998
Same author

Labelling of CRF1 and CRF2 receptors using the novel radioligand, [3H]-urocortin.

Neuropharmacology·1998
Same author

The high-mobility group protein T160 binds to both linear and cruciform DNA and mediates DNA bending as determined by ring closure.

Experimental cell research·1997
Same author

Expression of a novel murine homeobox gene in the developing cerebellar external granular layer during its proliferation.

Developmental dynamics : an official publication of the American Association of Anatomists·1996
Same journal

From Synapses to Circuits, the Role of KIBRA and the WWC Family in Adaptive Brain Function.

Journal of neurochemistry·2026
Same journal

The Golgi as a Microtubule Organiser in Neurons.

Journal of neurochemistry·2026
Same journal

A PARK9 iPSC-Derived Dopaminergic Neuron Model Enables Drug Screening Targeting Autophagy-Lysosome Pathway Dysfunction in Parkinson's Disease.

Journal of neurochemistry·2026
Same journal

Opposing Estrous Cycle-Dependent Norepinephrine and Dopamine Regulation in Response to Methamphetamine.

Journal of neurochemistry·2026
Same journal

Exercise Snacking in Alzheimer's Disease: A Mechanistic Rationale Based on Repeated Exerkine Signaling.

Journal of neurochemistry·2026
Same journal

The Converging Effects of Different Categories of Antidepressants on the Brain: A Systematic Meta-Analysis of Public Transcriptional Profiling Data From the Hippocampus and Cortex.

Journal of neurochemistry·2026
See all related articles

Homeobox genes are crucial for vertebrate brain development. Mutations in these genes are linked to developmental disorders, highlighting their essential role in embryogenesis and neuronal function.

Area of Science:

  • Developmental Biology
  • Genetics
  • Neuroscience

Background:

  • Homeobox genes encode homeodomain proteins, acting as master regulatory elements in embryonic development.
  • These genes are fundamental to understanding ontogenesis and the intricate processes of embryo development.
  • The role of homeobox genes in vertebrate brain development is well-established, with implications for congenital disorders.

Purpose of the Study:

  • To review the expression patterns of mouse homeobox genes during brain embryogenesis.
  • To examine the phenotypes associated with mutations in these genes.
  • To elucidate the role of homeobox genes in specifying neuronal functions in the developing brain.

Main Methods:

  • Review of existing literature on homeobox gene expression.

Related Experiment Videos

  • Analysis of data from mouse developmental mutants.
  • Correlation of genetic mutations with observed phenotypes in vertebrate brain development.
  • Main Results:

    • A wide array of mouse homeobox genes are implicated in brain embryogenesis.
    • Specific expression patterns of these genes are crucial for neuronal development.
    • Mutations in homeobox genes lead to observable developmental defects.

    Conclusions:

    • Homeobox genes are indispensable for proper vertebrate brain development.
    • Understanding their roles is key to deciphering developmental abnormalities and neurological disorders.
    • Further research into homeobox gene function can inform therapeutic strategies for related syndromes.