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Ethanol tolerance and withdrawal severity in high drinking in the dark selectively bred mice.

BACKGROUNDMouse lines are being selectively bred in replicate for high blood ethanol concentrations (BECs) achieved after limited access of ethanol (EtOH) drinking early in the circadian dark phase. High Drinking in the Dark-1 (HDID-1) mice are in selected generation S21, and the replicate HDID-2 li... Full description

Journal Title: Alcoholism clinical and experimental research, July 2012, Vol.36(7), pp.1152-1161
Main Author: Crabbe, John C
Other Authors: Colville, Alexandre M , Kruse, Lauren C , Cameron, Andy J , Spence, Stephanie E , Schlumbohm, Jason P , Huang, Lawrence C , Metten, Pamela
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: E-ISSN: 1530-0277 ; DOI: 10.1111/j.1530-0277.2011.01715.x
Link: http://search.proquest.com/docview/1024643196/?pq-origsite=primo
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recordid: proquest1024643196
title: Ethanol tolerance and withdrawal severity in high drinking in the dark selectively bred mice.
format: Article
creator:
  • Crabbe, John C
  • Colville, Alexandre M
  • Kruse, Lauren C
  • Cameron, Andy J
  • Spence, Stephanie E
  • Schlumbohm, Jason P
  • Huang, Lawrence C
  • Metten, Pamela
subjects:
  • Alcohol Drinking–Genetics
  • Animals–Pathology
  • Breeding–Drug Effects
  • Circadian Rhythm–Genetics
  • Drug Tolerance–Genetics
  • Ethanol–Administration & Dosage
  • Female–Adverse Effects
  • Male–Genetics
  • Mice–Pathology
  • Mice, Mutant Strains–Pathology
  • Mice, Transgenic–Pathology
  • Severity of Illness Index–Pathology
  • Species Specificity–Pathology
  • Substance Withdrawal Syndrome–Pathology
  • Ethanol
ispartof: Alcoholism, clinical and experimental research, July 2012, Vol.36(7), pp.1152-1161
description: BACKGROUNDMouse lines are being selectively bred in replicate for high blood ethanol concentrations (BECs) achieved after limited access of ethanol (EtOH) drinking early in the circadian dark phase. High Drinking in the Dark-1 (HDID-1) mice are in selected generation S21, and the replicate HDID-2 line...
language: eng
source:
identifier: E-ISSN: 1530-0277 ; DOI: 10.1111/j.1530-0277.2011.01715.x
fulltext: fulltext
issn:
  • 15300277
  • 1530-0277
url: Link


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titleEthanol tolerance and withdrawal severity in high drinking in the dark selectively bred mice.
creatorCrabbe, John C ; Colville, Alexandre M ; Kruse, Lauren C ; Cameron, Andy J ; Spence, Stephanie E ; Schlumbohm, Jason P ; Huang, Lawrence C ; Metten, Pamela
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identifierE-ISSN: 1530-0277 ; DOI: 10.1111/j.1530-0277.2011.01715.x
subjectAlcohol Drinking–Genetics ; Animals–Pathology ; Breeding–Drug Effects ; Circadian Rhythm–Genetics ; Drug Tolerance–Genetics ; Ethanol–Administration & Dosage ; Female–Adverse Effects ; Male–Genetics ; Mice–Pathology ; Mice, Mutant Strains–Pathology ; Mice, Transgenic–Pathology ; Severity of Illness Index–Pathology ; Species Specificity–Pathology ; Substance Withdrawal Syndrome–Pathology ; Ethanol
descriptionBACKGROUNDMouse lines are being selectively bred in replicate for high blood ethanol concentrations (BECs) achieved after limited access of ethanol (EtOH) drinking early in the circadian dark phase. High Drinking in the Dark-1 (HDID-1) mice are in selected generation S21, and the replicate HDID-2 line...
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titleEthanol tolerance and withdrawal severity in high drinking in the dark selectively bred mice.
descriptionBACKGROUNDMouse lines are being selectively bred in replicate for high blood ethanol concentrations (BECs) achieved after limited access of ethanol (EtOH) drinking early in the circadian dark phase. High Drinking in the Dark-1 (HDID-1) mice are in selected generation S21, and the replicate HDID-2 line...
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abstractBACKGROUNDMouse lines are being selectively bred in replicate for high blood ethanol concentrations (BECs) achieved after limited access of ethanol (EtOH) drinking early in the circadian dark phase. High Drinking in the Dark-1 (HDID-1) mice are in selected generation S21, and the replicate HDID-2 line...
doi10.1111/j.1530-0277.2011.01715.x
urlhttp://search.proquest.com/docview/1024643196/
issn01456008
date2012-07-01