Maria Gallegos

Associate Professor

Department of Biological Sciences

(510) 885-2856
SC-S 351
Photo of Maria Gallegos

Professional Focus

My lab is interested in neurodevelopment. We want to understand how a neuron's complex morphology is not only established but maintained throughout the life of an animal. Our long-term goal is to identify the genes and understand the molecular mechanisms that specifically control late steps in neurodevelopment by exploiting the experimental advantages and anatomical simplicity of the nematode, Caenorhabditis elegans. Conserved molecules required to build this worm’s simple nervous system often function to regulate neurodevelopment in higher eukaryotes. Our hope is that the conserved molecules we identify might function similarly in mammals during development and within the context of injury or disease. For example, genes that act to terminate neurite growth as the nervous system forms might also hinder regrowth in severed axons that fail to regenerate.


  • Ph.D. University of Wisconsin, Madison


Fall Quarter 2015
Course #SecCourse TitleDaysFromToLocationCampusTextbook Info
BIOL 312101Principles of GeneticsMWF10:40AM11:50AMSC-N120Hayward Campus View Books
BIOL 31211APrinciples of GeneticsW12:00PM12:50PMSC-N104Hayward Campus View Books
BIOL 31211BPrinciples of GeneticsF12:00PM12:50PMSC-N104Hayward Campus View Books
BIOL 682101Grad Sem:Cell & Molecular BiolM2:00PM4:30PMSC-S149Hayward Campus View Books
BIOL 691007University ThesisARR ARRHayward Campus View Books


Gallegos, M. and Sanjeev Balakrishnan et al. (Under Final Review for Publication). The C. elegans Rab family: Identification, Classification and Toolkit Construction. (D. Dupuy, Ed.) PloS One.

O'Halloran, D. M., Hamilton, O. S., Lee, J. I., Gallegos, M., & L'Etoile, N. D. (2012). Changes in cGMP Levels Affect the Localization of EGL-4 in AWC in Caenorhabditis elegans. (D. Dupuy, Ed.) PloS One, 7(2), e31614.

Gallegos, M. and Bargmann, C. (2004). Mechanosensory neurite termination and tiling are directed by SAX-2 and the SAX-1 kinase. Neuron 44(2):239-249. 

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