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American Journal of Physiology. Lung Cellular and Molecular Physiology|August 9, 2005
Gene transfer of CFTR to airway epithelia: low levels of expression are sufficient to correct Cl- transport and overexpression can generate basolateral CFTRSara L Farmen, Philip H Karp, Philip Ng, et al.
Molecular and Cellular Biology|March 10, 2001
Dach1 mutant mice bear no gross abnormalities in eye, limb, and brain development and exhibit postnatal lethalityR J Davis, W Shen, Y I Sandler, et al.
The Journal of Clinical Investigation|May 15, 1996
Role of the intercellular adhesion molecule-1(ICAM-1) in endotoxin-induced pneumonia evaluated using ICAM-1 antisense oligonucleotides, anti-ICAM-1 monoclonal antibodies, and ICAM-1 mutant miceT Kumasaka, W M Quinlan, N A Doyle, et al.
Neuroscience|October 24, 2006
Morphine priming in rats with chronic inflammation reveals a dichotomy between antihyperalgesic and antinociceptive properties of deltorphinL Gendron, M J Esdaile, F Mennicken, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 31, 1997
Mice deficient in the alpha7 neuronal nicotinic acetylcholine receptor lack alpha-bungarotoxin binding sites and hippocampal fast nicotinic currentsA Orr-Urtreger, F M Göldner, M Saeki, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 21, 2003
Central role of fibroblast alpha3 nicotinic acetylcholine receptor in mediating cutaneous effects of nicotineJuan Arredondo, Leon L Hall, Assane Ndoye, et al.
Analytical and Bioanalytical Chemistry|September 21, 2011
Structural characterization of heparins from different commercial sourcesFuming Zhang, Bo Yang, Mellisa Ly, et al.
Behavioural Brain Research|August 15, 2000
Altered baroreflex responses in alpha7 deficient miceD Franceschini, A Orr-Urtreger, W Yu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
Hepatocyte gene therapy in a large animal: a neonatal bovine model of citrullinemiaB Lee, J A Dennis, P J Healy, et al.
Nature Genetics|May 27, 2008
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterTrilochan Sahoo, Daniela del Gaudio, Jennifer R German, et al.
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