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The American Journal of Pathology|August 23, 2011
Inclusion body myositis: laser microdissection reveals differential up-regulation of IFN-γ signaling cascade in attacked versus nonattacked myofibersJana Ivanidze, Reinhard Hoffmann, Hanns Lochmüller, et al.British Journal of Cancer|April 7, 1998
Correlation between basic fibroblast growth factor immunostaining of stromal cells and stromelysin-3 mRNA expression in human breast carcinomaC Linder, P Byström, G Engel, et al.The British Journal of Dermatology|June 3, 1999
Predictive value of serum S100B for monitoring patients with metastatic melanoma during chemotherapy and/or immunotherapyA Hauschild, G Engel, W Brenner, et al.International Journal of Oncology|May 17, 2011
Limited invasive capacity of plt plus ras transformed rat fibrosarcoma cells effective in experimental metastasisG Engel, P Popowicz, H Marshall, et al.Neurology|March 10, 2006
Novel congenital myasthenic syndromes associated with defects in quantal releaseM Milone, T Fukuda, X M Shen, et al.Psychiatry Research|August 27, 2018
Dimensional analysis of emotion trajectories before and after disordered eating behaviors in a sample of women with bulimia nervosaKendra R Becker, Sarah Fischer, Ross D Crosby, et al.Human Molecular Genetics|September 23, 2008
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndromeAkio Masuda, Xin-Ming Shen, Mikako Ito, et al.Neurology|February 17, 2017
Congenital myopathy associated with the triadin knockout syndromeAndrew G Engel, Keeley R Redhage, David J Tester, et al.Muscle & Nerve|December 1, 1993
Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptorA G Engel, A Nagel, T J Walls, et al.Neuromuscular Disorders : NMD|August 6, 2019
A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmissionStefan Nicolau, Teerin Liewluck, Xin-Ming Shen, et al.Pageof 63