John C. Crabbe

ORCID: 0000-0001-7111-7204
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Neurotransmitter Receptor Influence on Behavior
  • Neuroscience and Neuropharmacology Research
  • Adipose Tissue and Metabolism
  • Genetic Mapping and Diversity in Plants and Animals
  • Receptor Mechanisms and Signaling
  • Peroxisome Proliferator-Activated Receptors
  • Memory and Neural Mechanisms
  • Stress Responses and Cortisol
  • Biochemical Analysis and Sensing Techniques
  • Alcohol Consumption and Health Effects
  • Neuroendocrine regulation and behavior
  • Epilepsy research and treatment
  • Pharmacological Effects and Toxicity Studies
  • Alcoholism and Thiamine Deficiency
  • Metabolism and Genetic Disorders
  • Diet and metabolism studies
  • Zebrafish Biomedical Research Applications
  • Pharmaceutical studies and practices
  • Neuropeptides and Animal Physiology
  • Electroconvulsive Therapy Studies
  • Sleep and Wakefulness Research
  • Tryptophan and brain disorders
  • Schizophrenia research and treatment
  • Genetic and phenotypic traits in livestock
  • Amino Acid Enzymes and Metabolism

Oregon Health & Science University
2015-2024

VA Portland Health Care System
2016-2024

Portland VA Medical Center
2009-2020

University of California, San Diego
2017

Alcohol Research Group
2001-2016

Veterans Health Administration
1996-2013

University College Cork
2010

Indiana University – Purdue University Indianapolis
2001-2010

McLean Hospital
2010

Harvard University
2010

Strains of mice that show characteristic patterns behavior are critical for research in neurobehavioral genetics. Possible confounding influences the laboratory environment were studied several inbred strains and one null mutant by simultaneous testing three laboratories on a battery six behaviors. Apparatus, test protocols, many environmental variables rigorously equated. differed markedly all behaviors, despite standardization, there systematic differences across labs. For some tests,...

10.1126/science.284.5420.1670 article EN Science 1999-06-04
Gary A. Churchill David Airey Hooman Allayee Joe M. Angel Alan Attie and 95 more J. Thomas Beatty William D. Beavis John K. Belknap Beth Bennett Wade H. Berrettini André Bleich Molly A. Bogue Karl W. Broman Kari J. Buck Edward S. Buckler Margit Burmeister Elissa J. Chesler James M. Cheverud Steven J. Clapcote Melloni N. Cook Roger Cox John C. Crabbe Wim E. Crusio Ariel Darvasi Christian F. Deschepper R. W. Doerge Charles R. Farber Jiřı́ Forejt Daniel P. Gaile Steven J. Garlow Hartmut Geiger Howard K. Gershenfeld Terry Gordon Jing Gu Weikuan Gu Gerald de Haan Nancy L. Hayes Craig Heller Heinz Himmelbauer Robert Hitzemann Kent W. Hunter Hui-Chen Hsu Fuad A. Iraqi Boris Ivandic Howard J. Jacob Ritsert C. Jansen Karl J. Jepsen Dabney K. Johnson Thomas E. Johnson Gerd Kempermann Christina Kendziorski Malak Kotb R. Frank Kooy Bastien Llamas Frank Lammert Jean‐Michel Lassalle Pedro R. Löwenstein Lu Lu Aldons J. Lusis Kenneth F. Manly Ralph Marcucio Doug Matthews Juan F. Medrano Darla R. Miller Guy Mittleman Beverly A. Mock Jeffrey S. Mogil Xavier Montagutelli Grant Morahan D.G. Morris Richard Mott Joseph H. Nadeau Hiroki Nagase Richard S. Nowakowski Bruce F. O’Hara А. В. Осадчук Grier P. Page Beverly Paigen Kenneth Paigen Abraham A. Palmer Huei-Ju Pan Leena Peltonen-Palotie Jeremy L. Peirce Daniel Pomp Michal Pravenec Daniel R. Prows Zhonghua Qi Roger H. Reeves John Roder Glenn D. Rosen Eric E. Schadt Leonard C. Schalkwyk Ze’ev Seltzer Kazuhiro Shimomura Siming Shou Mikko J. Sillanpää Linda D. Siracusa Hans-Willem Snoeck Jimmy L. Spearow Karen L. Svenson

10.1038/ng1104-1133 article EN Nature Genetics 2004-10-28

Recently, we described a simple procedure, Drinking in the Dark (DID), which C57BL/6J mice self-administer ethanol to blood concentration (BEC) above 1 mg/ml. The test consists of replacing water with 20% home cage for 4 h early during dark phase light/dark cycle. Three experiments were conducted explore this high drinking model further. In experiment 1, microanalysis behavior showed that pattern was different from routine intake. 2, impaired performance on accelerating rotarod and balance...

10.1111/j.1601-183x.2006.00210.x article EN Genes Brain & Behavior 2006-02-13

Treatment options for alcohol use disorders (AUDs) have minimally advanced since 2004, while the annual deaths and economic toll increased alarmingly. Phosphodiesterase type 4 (PDE4) is associated with nicotine dependence. PDE4 inhibitors were identified as a potential AUD treatment using bioinformatics approach. We prioritized newer inhibitor, apremilast, ideal repurposing (i.e., FDA approved psoriasis, low incidence of adverse events, excellent safety profile) tested it multiple animal...

10.1172/jci159103 article EN cc-by Journal of Clinical Investigation 2023-01-19

There is increasing interest in determining the extent to which multiple characters related drug sensitivity are influenced by common genes. The principal method for testing existence of such genetic correlations has been examination pairs mouse or rat lines selectively bred resistance a single behavioral effect drug. When pair selected found differ significantly on some trait other than one they were selected, it commonly concluded that significant correlation between traits exists,...

10.1111/j.1530-0277.1990.tb00461.x article EN Alcoholism Clinical and Experimental Research 1990-04-01

The genomic map locations of specific genes controlling behaviors can be identified by studying a panel recombinant inbred (RI) mouse strains. progenitor C57BL/6J (B6) and DBA/2J (D2) strains, 19 the BXD RI strains derived from an F2 cross these progenitors, were tested for 3% 10% ethanol (EtOH) intake. test sequence began with two‐bottle free choice between tap water unsweetened ethanol, ended saccharin‐sweetened ethanol. Saccharin preference was also measured. Correlational analyses...

10.1111/j.1530-0277.1994.tb00062.x article EN Alcoholism Clinical and Experimental Research 1994-08-01

If we conduct the same experiment in two laboratories or repeat a classical study many years later, will obtain results? Recent research with mice neural and behavioral genetics yielded different results for certain phenotypes, these findings suggested to some researchers that behavior may be too unstable fine-scale genetic analysis. Here expand range of data on this question additional and, first time field, formally compare recent experiments conducted 30–50 ago. For ethanol preference...

10.1073/pnas.0605342103 article EN Proceedings of the National Academy of Sciences 2006-10-20

Alcohol dependence (alcoholism) is accompanied by evidence of tolerance, withdrawal (physiological dependence), or compulsive behavior related to alcohol use. Studies strain and individual differences using animal models for acute physiological liability are useful means identify potential genetic determinants in humans. Behavioral quantitative trait analyses were conducted high risk versus resistance dependence. Using a two-step mapping strategy, loci on mouse chromosomes 1, 4, 11 mapped...

10.1523/jneurosci.17-10-03946.1997 article EN cc-by-nc-sa Journal of Neuroscience 1997-05-15

Studies in rodents have determined that intermittent exposure to alcohol vapor can increase subsequent ethanol self-administration, measured with operant and 2-bottle choice procedures. Two key procedural factors demonstrating increased intake are the establishment of stable self-administration before number bouts exposure. The present studies provide additional behavioral validation initial pharmacological this withdrawal-associated drinking procedure.Studies at 2 different sites (Portland...

10.1111/j.1530-0277.2007.00379.x article EN Alcoholism Clinical and Experimental Research 2007-04-18
Coming Soon ...