User profiles for Michael J. Gambello

Michael Gambello

Professor of Human Genetics, Emory University
Verified email at emory.edu
Cited by 8242

Expression of Pseudomonas aeruginosa Virulence Genes Requires Cell-to-Cell Communication

L Passador, JM Cook, MJ Gambello, L Rust… - Science, 1993 - science.org
Pseudomonas aeruginosa is an opportunistic human pathogen that causes a variety of
infections in immunocompromised hosts and individuals with cystic fibrosis. Expression of …

Cloning and characterization of the Pseudomonas aeruginosa lasR gene, a transcriptional activator of elastase expression

MJ Gambello, BH Iglewski - Journal of bacteriology, 1991 - Am Soc Microbiol
We report the discovery of the lasR gene, which positively regulates elastase expression in
Pseudomonas aeruginosa PAO1. The lasR gene was cloned by its ability to restore a …

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

S Hirotsune, MW Fleck, MJ Gambello, GJ Bix, A Chen… - Nature …, 1998 - nature.com
Heterozygous mutation or deletion of the ß subunit of platelet-activating factor acetylhydrolase
(PAFAH1B1, also known as LIS1) in humans is associated with type I lissencephaly, a …

[HTML][HTML] A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system

…, A Shionoya, M Ishida, MJ Gambello, J Yingling… - Neuron, 2000 - cell.com
Mutations in mammalian Lis1 (Pafah1b1) result in neuronal migration defects. Several lines
of evidence suggest that LIS1 participates in pathways regulating microtubule function, but …

LasR of Pseudomonas aeruginosa is a transcriptional activator of the alkaline protease gene (apr) and an enhancer of exotoxin A expression

MJ Gambello, S Kaye, BH Iglewski - Infection and immunity, 1993 - Am Soc Microbiol
The lasR gene of Pseudomonas aeruginosa is required for transcription of the genes for
elastase (lasB) and LasA protease (lasA), two proteases associated with virulence. We report …

Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration

T Tanaka, FF Serneo, C Higgins, MJ Gambello… - The Journal of cell …, 2004 - rupress.org
Humans with mutations in either DCX or LIS1 display nearly identical neuronal migration
defects, known as lissencephaly. To define subcellular mechanisms, we have combined in vitro …

14-3-3ε is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller–Dieker syndrome

K Toyo-Oka, A Shionoya, MJ Gambello, C Cardoso… - Nature …, 2003 - nature.com
Heterozygous deletions of 17p13.3 result in the human neuronal migration disorders
isolated lissencephaly sequence (ILS) and the more severe Miller–Dieker syndrome (MDS). …

Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1

…, M Niethammer, R Ayala, Y Zhou, MJ Gambello… - Nature cell …, 2000 - nature.com
Whereas total loss of Lis1 is lethal, disruption of one allele of the Lis1 gene results in brain
abnormalities, indicating that developing neurons are particularly sensitive to a reduction in …

[HTML][HTML] Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

GM Enns, V Shashi, M Bainbridge, MJ Gambello… - Genetics in …, 2014 - nature.com
Purpose: The endoplasmic reticulum–associated degradation pathway is responsible for
the translocation of misfolded proteins across the endoplasmic reticulum membrane into the …

[HTML][HTML] Mammalian target of rapamycin (mTOR) activation increases axonal growth capacity of injured peripheral nerves

N Abe, SH Borson, MJ Gambello, F Wang… - Journal of Biological …, 2010 - ASBMB
Unlike neurons in the central nervous system (CNS), injured neurons in the peripheral
nervous system (PNS) can regenerate their axons and reinnervate their targets. However, …