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International Journal of Molecular Medicine|September 22, 2000
Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRsP Seeman, R Mazanec, J Zidar, et al.The Journal of Allergy and Clinical Immunology|May 10, 2001
Idiopathic environmental intolerance: increased prevalence of panic disorder-associated cholecystokinin B receptor allele 7K Binkley, N King, N Poonai, et al.Neurology|August 25, 2004
Hearing loss as the first feature of late-onset axonal CMT disease due to a novel P0 mutationP Seeman, R Mazanec, K Huehne, et al.Vaccine|March 10, 2005
Immunopropylactic approaches against chemical carcinogenesisStefan S De Buck, Claude P MullerPhysical Review. E, Statistical, Nonlinear, and Soft Matter Physics|April 27, 2011
Secondary structure of double-stranded DNA under stretching: elucidation of the stretched formM Maaloum, A-F Beker, P MullerEuropean Cytokine Network|June 12, 2001
Functional characterization of the mouse lymphotoxin-beta receptor promoterP Muller, D N Männel, T HehlgansLancet (London, England)|December 12, 1981
Association of spinocerebellar disorders with cystic fibrosis or chronic childhood cholestasis and very low serum vitamin EE Elias, D P Muller, J ScottCell Biophysics|September 1, 1980
Correlation between cell density, membrane fluidity, and the availability of transferrin receptors in Friend erythroleukemic cellsC P Muller, Z Volloch, M ShinitzkyNeuropathology and Applied Neurobiology|July 1, 1987
Studies on the neurobiology of vitamin E (alpha-tocopherol) and some other antioxidant systems in the ratM A Goss-Sampson, D P MullerAllergie Und Immunologie|January 1, 1976
[Lectin arthritis--a new arthritis model]V K Thoss, G Raabe, P MullerPageof 95