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Somatic Cell and Molecular Genetics|July 14, 1998
Exon trapping and sequence-based methods of gene finding in transcript mapping of human 4p16.3I Pribill, G T Barnes, J Chen, et al.
American Journal of Human Genetics|December 1, 1986
Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11M Farrall, E Watson, G Bates, et al.
Physiological Genomics|September 23, 2010
Molecular signatures and new candidates to target the pathogenesis of rheumatoid arthritisU Ungethuem, T Haeupl, H Witt, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
The Journal of Cell Biology|January 3, 2001
Metaphase to anaphase (mat) transition-defective mutants in Caenorhabditis elegansA Golden, P L Sadler, M R Wallenfang, et al.
Current Biology : CB|March 28, 2023
Molecular encoding of stimulus features in a single sensory neuron type enables neuronal and behavioral plasticityNathan Harris, Samuel G Bates, Zihao Zhuang, et al.
American Journal of Human Genetics|May 1, 1985
Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutationC Ingle, R Williamson, A de la Chapelle, et al.
Diagnostics (Basel, Switzerland)|June 28, 2023
Developing an Artificial Intelligence-Based Representation of a Virtual Patient Model for Real-Time Diagnosis of Acute Respiratory Distress SyndromeChadi S Barakat, Konstantin Sharafutdinov, Josefine Busch, et al.
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