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The Biochemical Journal|February 17, 2010
Transglutaminase-2: a new endostatin partner in the extracellular matrix of endothelial cellsClément Faye, Antonio Inforzato, Marine Bignon, et al.Antimicrobial Agents and Chemotherapy|July 22, 2009
Dosing regimens of cotrimoxazole (trimethoprim-sulfamethoxazole) for melioidosisAllen C Cheng, Emma S McBryde, Vanaporn Wuthiekanun, et al.Malaria Journal|September 15, 2009
The role of simple mathematical models in malaria elimination strategy designLisa J White, Richard J Maude, Wirichada Pongtavornpinyo, et al.Veterinary Microbiology|September 5, 2008
Comparison of the value of measurement of serum galactomannan and Aspergillus-specific antibodies in the diagnosis of canine sino-nasal aspergillosisF Billen, D Peeters, I R Peters, et al.The Journal of Biological Chemistry|February 13, 2007
The factor H variant associated with age-related macular degeneration (His-384) and the non-disease-associated form bind differentially to C-reactive protein, fibromodulin, DNA, and necrotic cellsAndreas P Sjöberg, Leendert A Trouw, Simon J Clark, et al.The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Clinical, biochemical, and molecular investigations of a genetic isolate of growth hormone insensitivity (Laron's syndrome)L Baumbach, A Schiavi, R Bartlett, et al.Biochemistry|August 27, 1996
Structure and activity of an active site substitution of ricin A chainP J Day, S R Ernst, A E Frankel, et al.Journal of Comparative Pathology|May 14, 2013
The histopathology of idiopathic pulmonary fibrosis in West Highland white terriers shares features of both non-specific interstitial pneumonia and usual interstitial pneumonia in manP Syrjä, H P Heikkilä, L Lilja-Maula, et al.Transactions of the Royal Society of Tropical Medicine and Hygiene|January 1, 1975
Arbovirus infections in Sarawak, October 1968-February 1970: human serological studies in a land Dyak villageE T Bowen, D I Simpson, G S Platt, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 1998
Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutationF L Mastaglia, N Harker, B A Phillips, et al.Pageof 226