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S Avigad

Showing results (51-60 of 67) with videos related to

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Cancer Genetics and Cytogenetics|March 8, 2000
High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumorR Steinberg, E Freud, M Zer, et al.
Leukemia Research|July 25, 1998
Molecular analysis of childhood acute lymphoblastic leukemia in IsraelO Blau, S Avigad, A Frisch, et al.
Cancer Detection and Prevention|April 28, 2006
Quantitation of alpha-fetoprotein messenger RNA for early detection of recurrent hepatocellular carcinoma: a prospective pilot studyH Schmilovitz-Weiss, S M Stemmer, E Liberzon, et al.
Cancer Genetics and Cytogenetics|March 21, 2003
Molecular cytogenetic parameters in Ewing sarcomaA Amiel, A Ohali, M Fejgin, et al.
Human Genetics|February 1, 1993
A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in north African Jews with phenylketonuriaM Weinstein, R C Eisensmith, V Abadie, et al.
Leukemia Research|June 1, 1995
A distinct subtype of M4/M5 acute myeloblastic leukemia (AML) associated with t(8:16)(p11:p13), in a patient with the variant t(8:19)(p11:q13)--case report and review of the literatureB Stark, P Resnitzky, M Jeison, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 11, 2003
Association between telomerase activity and outcome in patients with nonmetastatic Ewing family of tumorsA Ohali, S Avigad, I J Cohen, et al.
Cancer Letters|July 9, 1999
Mutations of the adenomatous polyposis coli and p53 genes in a child with Turcot's syndromeD Barel, I J Cohen, C Mor, et al.
Pediatric Blood & Cancer|March 30, 2004
Tumor cells are present in stem cell harvests of Ewings sarcoma patients and their persistence following transplantation is associated with relapseI Yaniv, I J Cohen, J Stein, et al.
Oncogene|April 3, 1997
A novel germ line p53 mutation in intron 6 in diverse childhood malignanciesS Avigad, D Barel, O Blau, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Cancer Genetics and Cytogenetics|March 8, 2000
High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumorR Steinberg, E Freud, M Zer, et al.
Leukemia Research|July 25, 1998
Molecular analysis of childhood acute lymphoblastic leukemia in IsraelO Blau, S Avigad, A Frisch, et al.
Cancer Detection and Prevention|April 28, 2006
Quantitation of alpha-fetoprotein messenger RNA for early detection of recurrent hepatocellular carcinoma: a prospective pilot studyH Schmilovitz-Weiss, S M Stemmer, E Liberzon, et al.
Cancer Genetics and Cytogenetics|March 21, 2003
Molecular cytogenetic parameters in Ewing sarcomaA Amiel, A Ohali, M Fejgin, et al.
Human Genetics|February 1, 1993
A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in north African Jews with phenylketonuriaM Weinstein, R C Eisensmith, V Abadie, et al.
Leukemia Research|June 1, 1995
A distinct subtype of M4/M5 acute myeloblastic leukemia (AML) associated with t(8:16)(p11:p13), in a patient with the variant t(8:19)(p11:q13)--case report and review of the literatureB Stark, P Resnitzky, M Jeison, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 11, 2003
Association between telomerase activity and outcome in patients with nonmetastatic Ewing family of tumorsA Ohali, S Avigad, I J Cohen, et al.
Cancer Letters|July 9, 1999
Mutations of the adenomatous polyposis coli and p53 genes in a child with Turcot's syndromeD Barel, I J Cohen, C Mor, et al.
Pediatric Blood & Cancer|March 30, 2004
Tumor cells are present in stem cell harvests of Ewings sarcoma patients and their persistence following transplantation is associated with relapseI Yaniv, I J Cohen, J Stein, et al.
Oncogene|April 3, 1997
A novel germ line p53 mutation in intron 6 in diverse childhood malignanciesS Avigad, D Barel, O Blau, et al.
Pageof 7