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Nature|January 3, 1985
Isolation and structure of a novel C-terminally amidated opioid peptide, amidorphin, from bovine adrenal medullaB R Seizinger, D C Liebisch, C Gramsch, et al.Acta Neuropathologica|January 1, 1993
Deletions on the long arm of chromosome 17 in pilocytic astrocytomaA von Deimling, D N Louis, A G Menon, et al.Cancer Genetics and Cytogenetics|October 1, 1992
Cytogenetic and molecular studies of a familial renal cell carcinomaH J Decker, B Wullich, J M Whaley, et al.Science (New York, N.Y.)|April 17, 1987
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosisB R Seizinger, G Rouleau, L J Ozelius, et al.Proceedings of the National Academy of Sciences of the United States of America|July 22, 1997
The p53 tumor suppressor targets a novel regulator of G protein signalingL Buckbinder, S Velasco-Miguel, Y Chen, et al.Journal of Medical Genetics|September 1, 1987
DNA linkage analysis in Von Recklinghausen neurofibromatosisB R Seizinger, G Rouleau, A H Lane, et al.Oncogene|May 18, 1995
Farnesyltransferase inhibitors are inhibitors of Ras but not R-Ras2/TC21, transformationJ M Carboni, N Yan, A D Cox, et al.Genomics|May 1, 1991
Parental origin of chromosome 22 loss in sporadic and NF2 neuromasB Fontaine, M Sanson, O Delattre, et al.The Journal of Investigative Dermatology|March 1, 1996
Chromosome 17 allelic loss and NF1-GRD mutations do not play a significant role as molecular mechanisms leading to melanoma tumorigenesisL Gómez, M P Rubio, M T Martin, et al.Nature Genetics|February 1, 1994
Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour typesA B Bianchi, T Hara, V Ramesh, et al.Pageof 8