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P G Rothberg

Showing results (31-40 of 52) with videos related to

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American Journal of Medical Genetics|October 26, 1999
Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL geneJ F Bradley, D L Collins, R N Schimke, et al.
Cell|August 1, 1980
The genome-linked protein of picornaviruses. VII. Genetic mapping of poliovirus VPg by protein and RNA sequence studiesN Kitamura, C J Adler, P G Rothberg, et al.
Molecular and Cellular Biology|June 1, 1984
Structure and expression of the oncogene c-myc in fresh tumor material from patients with hematopoietic malignanciesP G Rothberg, M D Erisman, R E Diehl, et al.
Archives of Oral Biology|July 22, 1999
Cytokine-mediated stimulation of laminin expression and cell-growth arrest in a human submandibular gland duct-cell line (HSG)P J Daniels, C P McArthur, D P Heruth, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1981
Poliovirus replication proteins: RNA sequence encoding P3-1b and the sites of proteolytic processingB L Semler, C W Anderson, N Kitamura, et al.
Molecular and Cellular Biochemistry|January 12, 2000
Diminished energy metabolism and enhanced apoptosis in livers of B6C3F1 mice treated with the antihepatocarcinogen rotenoneC Wang, J Youssef, B Saran, et al.
Cancer Research|December 1, 1986
Enhanced expression of the c-myc gene in bovine leukemia virus-induced bovine tumorsP Gupta, S V Kashmiri, M D Erisman, et al.
The Journal of Pediatrics|January 15, 2000
Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancyH A Ishmael, L M Pasztor, P G Rothberg, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2001
Von Hippel-Lindau disease masquerading as autosomal dominant polycystic kidney diseaseR K Chatha, A M Johnson, P G Rothberg, et al.
Blood|February 1, 1994
Clonal, nonconstitutional rearrangements of the MLL gene in infant twins with acute lymphoblastic leukemia: in utero chromosome rearrangement of 11q23H J Gill Super, P G Rothberg, H Kobayashi, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|October 26, 1999
Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL geneJ F Bradley, D L Collins, R N Schimke, et al.
Cell|August 1, 1980
The genome-linked protein of picornaviruses. VII. Genetic mapping of poliovirus VPg by protein and RNA sequence studiesN Kitamura, C J Adler, P G Rothberg, et al.
Molecular and Cellular Biology|June 1, 1984
Structure and expression of the oncogene c-myc in fresh tumor material from patients with hematopoietic malignanciesP G Rothberg, M D Erisman, R E Diehl, et al.
Archives of Oral Biology|July 22, 1999
Cytokine-mediated stimulation of laminin expression and cell-growth arrest in a human submandibular gland duct-cell line (HSG)P J Daniels, C P McArthur, D P Heruth, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1981
Poliovirus replication proteins: RNA sequence encoding P3-1b and the sites of proteolytic processingB L Semler, C W Anderson, N Kitamura, et al.
Molecular and Cellular Biochemistry|January 12, 2000
Diminished energy metabolism and enhanced apoptosis in livers of B6C3F1 mice treated with the antihepatocarcinogen rotenoneC Wang, J Youssef, B Saran, et al.
Cancer Research|December 1, 1986
Enhanced expression of the c-myc gene in bovine leukemia virus-induced bovine tumorsP Gupta, S V Kashmiri, M D Erisman, et al.
The Journal of Pediatrics|January 15, 2000
Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancyH A Ishmael, L M Pasztor, P G Rothberg, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2001
Von Hippel-Lindau disease masquerading as autosomal dominant polycystic kidney diseaseR K Chatha, A M Johnson, P G Rothberg, et al.
Blood|February 1, 1994
Clonal, nonconstitutional rearrangements of the MLL gene in infant twins with acute lymphoblastic leukemia: in utero chromosome rearrangement of 11q23H J Gill Super, P G Rothberg, H Kobayashi, et al.
Pageof 6