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Cell Differentiation|October 1, 1975
The effects of sodium, potassium and ATP on a developmental puff sequence in Drosophila salivary glands in vitroL Rensing, M FischerMammalian Genome : Official Journal of the International Mammalian Genome Society|March 1, 1997
Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouseS R Schmidt, A Gehrig, M R Koehler, et al.Human Heredity|January 1, 1989
X-chromosomal DNA polymorphisms in two ethnic groups from IndiaP K Seth, C Meissner, W Kress, et al.Archives of Dermatology|July 1, 1996
Olmsted syndrome. Case report and identification of a keratin abnormalityD W Kress, M P Seraly, L Falo, et al.European Journal of Pediatrics|June 1, 1994
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative diseaseV Schuster, S Seidenspinner, T Grimm, et al.Brain Research|January 4, 1991
A vasoactive peptide, endothelin-3, is produced by and specifically binds to primary astrocytesH Ehrenreich, J H Kehrl, R W Anderson, et al.Journal of Neuroimmunology|June 4, 2005
Impact of the Asp299Gly polymorphism in the toll-like receptor 4 (tlr-4) gene on disease course of multiple sclerosisA Kroner, F Vogel, A Kolb-Mäurer, et al.Annals of Neurology|January 1, 1995
Tumor necrosis factor-alpha messenger RNA expression in patients with relapsing-remitting multiple sclerosis is associated with disease activityP Rieckmann, M Albrecht, B Kitze, et al.Muscle & Nerve|July 1, 1995
Neurological multisystem manifestation in multiple symmetric lipomatosis: a clinical and electrophysiological studyM Naumann, B Schalke, T Klopstock, et al.Journal of Neurology|January 12, 2011
Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutationsF Hanisch, T Müller, A Dietz, et al.Pageof 289