 Rats, Sprague-Dawley
"Rats, Sprague-Dawley" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A strain of albino rat used widely for experimental purposes because of its calmness and ease of handling. It was developed by the Sprague-Dawley Animal Company.
| Descriptor ID |
D017207
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| MeSH Number(s) |
B01.050.150.900.649.865.635.505.700.750
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Rats, Sprague-Dawley".
Below are MeSH descriptors whose meaning is more specific than "Rats, Sprague-Dawley".
This graph shows the total number of publications written about "Rats, Sprague-Dawley" by people in this website by year, and whether "Rats, Sprague-Dawley" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1992 | 0 | 1 | 1 | | 1993 | 0 | 8 | 8 | | 1994 | 0 | 4 | 4 | | 1995 | 1 | 5 | 6 | | 1996 | 0 | 9 | 9 | | 1997 | 0 | 4 | 4 | | 1998 | 0 | 5 | 5 | | 1999 | 0 | 8 | 8 | | 2000 | 0 | 6 | 6 | | 2001 | 0 | 9 | 9 | | 2002 | 0 | 10 | 10 | | 2003 | 0 | 18 | 18 | | 2004 | 0 | 16 | 16 | | 2005 | 0 | 17 | 17 | | 2006 | 0 | 23 | 23 | | 2007 | 0 | 10 | 10 | | 2008 | 0 | 16 | 16 | | 2009 | 0 | 16 | 16 | | 2010 | 0 | 18 | 18 | | 2011 | 0 | 16 | 16 | | 2012 | 0 | 19 | 19 | | 2013 | 0 | 21 | 21 | | 2014 | 0 | 20 | 20 | | 2015 | 0 | 20 | 20 | | 2016 | 0 | 8 | 8 | | 2017 | 0 | 8 | 8 | | 2018 | 0 | 21 | 21 | | 2019 | 0 | 9 | 9 | | 2020 | 0 | 9 | 9 | | 2021 | 0 | 3 | 3 |
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Below are the most recent publications written about "Rats, Sprague-Dawley" by people in Profiles.
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Akazawa Y, Fujioka T, Ide H, Yazaki K, Honjo O, Sun M, Friedberg MK. Impaired right and left ventricular function and relaxation induced by pulmonary regurgitation are not reversed by tardive antifibrosis treatment. Am J Physiol Heart Circ Physiol. 2021 07 01; 321(1):H38-H51.
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Friedlander Y, Zanette B, Lindenmaier AA, Fliss J, Li D, Emami K, Jankov RP, Kassner A, Santyr G. Effect of inhaled oxygen concentration on 129 Xe chemical shift of red blood cells in rat lungs. Magn Reson Med. 2021 09; 86(3):1187-1193.
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Shama S, Unger S, Pouliot Y, Doyen A, Suwal S, Pencharz P, Pitino MA, Sergius M, Aufreiter S, Stone D, O'Connor DL. A Human Milk-Based Protein Concentrate Developed for Preterm Infants Retains Bioactive Proteins and Supports Growth of Weanling Rats. J Nutr. 2021 04 08; 151(4):840-847.
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Berg EL, Ching TM, Bruun DA, Rivera JK, Careaga M, Ellegood J, Lerch JP, Wöhr M, Lein PJ, Silverman JL. Translational outcomes relevant to neurodevelopmental disorders following early life exposure of rats to chlorpyrifos. J Neurodev Disord. 2020 12 16; 12(1):40.
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Ishii R, Okumura K, Akazawa Y, Malhi M, Ebata R, Sun M, Fujioka T, Kato H, Honjo O, Kabir G, Kuebler WM, Connelly K, Maynes JT, Friedberg MK. Heart Rate Reduction Improves Right Ventricular Function and Fibrosis in Pulmonary Hypertension. Am J Respir Cell Mol Biol. 2020 12; 63(6):843-855.
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Miyake H, Koike Y, Seo S, Lee C, Li B, Ganji N, Pierro A. The effect of pre- and post-remote ischemic conditioning reduces the injury associated with intestinal ischemia/reperfusion. Pediatr Surg Int. 2020 Dec; 36(12):1437-1442.
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Ivanovska J, Kang NC, Ivanovski N, Nagy A, Belik J, Gauda EB. Recombinant adiponectin protects the newborn rat lung from lipopolysaccharide-induced inflammatory injury. Physiol Rep. 2020 09; 8(17):e14553.
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Mühlig AK, Keir LS, Abt JC, Heidelbach HS, Horton R, Welsh GI, Meyer-Schwesinger C, Licht C, Coward RJ, Fester L, Saleem MA, Oh J. Podocytes Produce and Secrete Functional Complement C3 and Complement Factor H. Front Immunol. 2020; 11:1833.
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Harding EK, Boivin B, Salter MW. Intracellular Calcium Responses Encode Action Potential Firing in Spinal Cord Lamina I Neurons. J Neurosci. 2020 06 03; 40(23):4439-4456.
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Koike Y, Li B, Lee C, Alganabi M, Zhu H, Chusilp S, Lee D, Cheng S, Li Q, Pierro A. The intestinal injury caused by ischemia-reperfusion is attenuated by amniotic fluid stem cells via the release of tumor necrosis factor-stimulated gene 6 protein. FASEB J. 2020 05; 34(5):6824-6836.
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