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The Journal of Clinical Endocrinology and Metabolism|May 7, 2009
Mutation analysis of the muscarinic cholinergic receptor genes in isolated growth hormone deficiency type IBAli Mohamadi, Marco Martari, Cindy D Holladay, et al.
Computer Methods in Biomechanics and Biomedical Engineering|August 14, 2009
Characterisation of a phenomenological model for commercial pneumatic muscle actuatorsJ L Serres, D B Reynolds, C A Phillips, et al.
The Journal of Pediatrics|June 1, 1984
Isolated growth hormone deficiency type 1A in a Japanese familyY Nishi, K Aihara, T Usui, et al.
Journal of Cellular Physiology|January 7, 2000
Short-chain fatty acids reduce expression of specific protein kinase C isoforms in human colonic epithelial cellsK L Rickard, P R Gibson, N J Wilson, et al.
Human Molecular Genetics|April 1, 1995
Localization of craniosynostosis Adelaide type to 4p16G E Hollway, H A Phillips, L C Adès, et al.
Biochimica Et Biophysica Acta|September 19, 1995
Molecular cloning and sequencing of the gene encoding a sheep arginine vasopressin type 1a receptorA M Hutchins, P A Phillips, D J Venter, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1993
Heterogeneous growth hormone (GH) gene mutations in familial GH deficiencyJ D Cogan, J A Phillips, N Sakati, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|December 16, 2016
A validated UPLC-MS/MS method for the analysis of linezolid and a novel oxazolidinone derivative (PH027) in plasma and its application to tissue distribution study in rabbitsMohsen A Hedaya, Vidhya Thomas, Mohamed E Abdel-Hamid, et al.
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