Showing results (961-970 of 984) with videos related to

Sort By:
Pageof 99
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 1, 1984
Calcitonin gene-related peptide immunoreactivity in the spinal cord of man and of eight other speciesS J Gibson, J M Polak, S R Bloom, et al.
Histochemistry|January 1, 1982
Mapping, quantitative distribution and origin of substance p- and VIP-containing nerves in the uvea of guinea pig eyeG Terenghi, J M Polak, L Probert, et al.
Tissue Engineering|September 8, 2005
Repopulation of human pulmonary epithelium by bone marrow cells: a potential means to promote repairC Albera, J M Polak, S Janes, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 31, 2014
Effects of changes in neonatal thyroid status on the development of neuropeptide systems in the rat brainP L Woodhams, J McGovern, G P McGregor, et al.
The Journal of Pathology|June 6, 1998
Lack of inducible nitric oxide synthase in bronchial epithelium: a possible mechanism of susceptibility to infection in cystic fibrosisQ H Meng, D R Springall, A E Bishop, et al.
Circulation|September 25, 2001
Quantitative myocardial cytokine expression and activation of the apoptotic pathway in patients who require left ventricular assist devicesE J Birks, N Latif, V Owen, et al.
The American Journal of Gastroenterology|June 23, 2001
Pantoprazole therapy in the long-term management of severe acid peptic disease: clinical efficacy, safety, serum gastrin, gastric histology, and endocrine cell studiesK D Bardhan, P Cherian, A E Bishop, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delayM Balasubramanian, J P H Shield, C L Acerini, et al.
Human Pathology|February 17, 2007
Neonatal hyperinsulinism: clinicopathologic correlationP Delonlay, A Simon, L Galmiche-Rolland, et al.
European Journal of Endocrinology|September 13, 2014
Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutationsH E Ramos, A Carré, L Chevrier, et al.
Pageof 99