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F P Li

Showing results (181-190 of 211) with videos related to

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Cancer Research|May 15, 1997
Evidence for genetic heterogeneity in familial Wilms' tumorV Huff, C I Amos, E C Douglass, et al.
Molecular and Cellular Biology|January 29, 2000
Human keratinocytes that express hTERT and also bypass a p16(INK4a)-enforced mechanism that limits life span become immortal yet retain normal growth and differentiation characteristicsM A Dickson, W C Hahn, Y Ino, et al.
Cancer Treatment Reports|November 1, 1979
Phase I trial of bruceantinM B Garnick, R H Blum, G P Canellos, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 1998
Carcinoembryonic antigen in breast nipple aspirate fluidL Foretova, J E Garber, N L Sadowsky, et al.
Medical and Pediatric Oncology|November 1, 1996
Germline WT1 mutations in Wilms' tumor patients: preliminary resultsF P Li, N E Breslow, J M Morgan, et al.
Cancer Research|November 1, 1992
Nonlinkage of 16q markers to familial predisposition to Wilms' tumorV Huff, A E Reeve, M Leppert, et al.
Journal of the National Cancer Institute|August 15, 1992
Recommendations on predictive testing for germ line p53 mutations among cancer-prone individualsF P Li, J E Garber, S H Friend, et al.
Cancer|December 15, 1980
Bone sarcoma as a second malignant neoplasm in children: influence of radiation and genetic predisposition for the Late Effects Study GroupA T Meadows, L C Strong, F P Li, et al.
American Journal of Human Genetics|December 1, 1994
Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinomaJ M Whaley, J Naglich, L Gelbert, et al.
The New England Journal of Medicine|May 14, 1992
Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasmsD Malkin, K W Jolly, N Barbier, et al.
Pageof 22

Showing results (181-190 of 211) with videos related to

Sort By:
Pageof 22
Cancer Research|May 15, 1997
Evidence for genetic heterogeneity in familial Wilms' tumorV Huff, C I Amos, E C Douglass, et al.
Molecular and Cellular Biology|January 29, 2000
Human keratinocytes that express hTERT and also bypass a p16(INK4a)-enforced mechanism that limits life span become immortal yet retain normal growth and differentiation characteristicsM A Dickson, W C Hahn, Y Ino, et al.
Cancer Treatment Reports|November 1, 1979
Phase I trial of bruceantinM B Garnick, R H Blum, G P Canellos, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 1998
Carcinoembryonic antigen in breast nipple aspirate fluidL Foretova, J E Garber, N L Sadowsky, et al.
Medical and Pediatric Oncology|November 1, 1996
Germline WT1 mutations in Wilms' tumor patients: preliminary resultsF P Li, N E Breslow, J M Morgan, et al.
Cancer Research|November 1, 1992
Nonlinkage of 16q markers to familial predisposition to Wilms' tumorV Huff, A E Reeve, M Leppert, et al.
Journal of the National Cancer Institute|August 15, 1992
Recommendations on predictive testing for germ line p53 mutations among cancer-prone individualsF P Li, J E Garber, S H Friend, et al.
Cancer|December 15, 1980
Bone sarcoma as a second malignant neoplasm in children: influence of radiation and genetic predisposition for the Late Effects Study GroupA T Meadows, L C Strong, F P Li, et al.
American Journal of Human Genetics|December 1, 1994
Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinomaJ M Whaley, J Naglich, L Gelbert, et al.
The New England Journal of Medicine|May 14, 1992
Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasmsD Malkin, K W Jolly, N Barbier, et al.
Pageof 22