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Psychoneuroendocrinology|May 1, 1992
Hippocampal type I and type II corticosteroid receptors are modulated by central noradrenergic systemsS Maccari, P Mormède, P V Piazza, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 1, 2003
Patterning of the hyoid cartilage depends upon signals arising from the ventral foregut endodermBlandine Ruhin, Sophie Creuzet, Christine Vincent, et al.Drug Development and Industrial Pharmacy|August 6, 1999
Development of a "continuous-flow adhesion cell" for the assessment of hydrogel adhesionA M Le Ray, P Iooss, A Gouyette, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 9, 2000
Bone mineral density in sixty adult patients with Marfan syndromeJ M Le Parc, P Plantin, G Jondeau, et al.European Urology|November 30, 2000
Cytotoxicity assessment of latex urinary catheters on cultured human urothelial cellsJ L Pariente, L Bordenave, F Jacob, et al.Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|July 13, 2001
Neuroendocrine features of pubertal development in females with mental retardationR M Cento, M Ciampelli, C Proto, et al.The Veterinary Record|March 29, 2001
Correlations of measurements of subclinical claw horn lesions in dairy cattleA M Le Fevre, D N Logue, J E Offer, et al.Biochimie|January 1, 1980
Cofactor regeneration in immobilized enzyme systems: chemical grafting of functional NAD in the active site of dehydrogenasesM D Legoy, V L Garde, J M Le Moullec, et al.British Journal of Anaesthesia|October 26, 2007
Minimum alveolar concentration of halogenated volatile anaesthetics in left ventricular hypertrophy and congestive heart failure in ratsT Barbry, M Le Guen, V De Castro, et al.Journal of Medical Genetics|February 9, 1999
Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutationE Lajeunie, V El Ghouzzi, M Le Merrer, et al.Pageof 392