I L Andrulis - JoVE Visualize

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American Journal of Human Genetics|March 31, 2000

Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 geneM D Taylor, N Gokgoz, I L Andrulis, et al.

Journal of Cellular Physiology|September 1, 1991

CD10 and CD44 genes of leukemic cells and malignant cell lines show no evidence of transformation-related alterationsB L Kee, H K Dadi, R Tran-Paterson, et al.

British Journal of Cancer|June 13, 2001

p53 missense but not truncation mutations are associated with low levels of p21(CIP1/WAF1) mRNA expression in primary human sarcomasS Mousses, N Gokgoz, J S Wunder, et al.

Genomics|April 1, 1989

Molecular structure of the human asparagine synthetase geneY P Zhang, M A Lambert, A E Cairney, et al.

Oncogene|February 16, 1999

Co-amplification and overexpression of CDK4, SAS and MDM2 occurs frequently in human parosteal osteosarcomasJ S Wunder, K Eppert, S R Burrow, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 1, 1995

Expression of the multiple drug resistance gene in human renal cell carcinoma depends on tumor histology, grade, and stageS W Tobe, S E Noble-Topham, I L Andrulis, et al.

Journal of the National Cancer Institute|March 10, 1999

Frequency of p53 mutations in breast carcinomas from Ashkenazi Jewish carriers of BRCA1 mutationsK A Phillips, K Nichol, H Ozcelik, et al.

Clinical Genetics|June 14, 2000

Perceptions of Ashkenazi Jewish breast cancer patients on genetic testing for mutations in BRCA1 and BRCA2K A Phillips, E Warner, W S Meschino, et al.

Oncogene|November 7, 1996

Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of METJ C Lin, S W Scherer, L Tougas, et al.

Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|September 1, 1996

SAS is amplified predominantly in surface osteosarcomaS E Noble-Topham, S R Burrow, K Eppert, et al.

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Showing results (41-50 of 75) with videos related to

Sort By:

Pageof 8

American Journal of Human Genetics|March 31, 2000

Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 geneM D Taylor, N Gokgoz, I L Andrulis, et al.

Journal of Cellular Physiology|September 1, 1991

CD10 and CD44 genes of leukemic cells and malignant cell lines show no evidence of transformation-related alterationsB L Kee, H K Dadi, R Tran-Paterson, et al.

British Journal of Cancer|June 13, 2001

p53 missense but not truncation mutations are associated with low levels of p21(CIP1/WAF1) mRNA expression in primary human sarcomasS Mousses, N Gokgoz, J S Wunder, et al.

Genomics|April 1, 1989

Molecular structure of the human asparagine synthetase geneY P Zhang, M A Lambert, A E Cairney, et al.

Oncogene|February 16, 1999

Co-amplification and overexpression of CDK4, SAS and MDM2 occurs frequently in human parosteal osteosarcomasJ S Wunder, K Eppert, S R Burrow, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 1, 1995

Expression of the multiple drug resistance gene in human renal cell carcinoma depends on tumor histology, grade, and stageS W Tobe, S E Noble-Topham, I L Andrulis, et al.

Journal of the National Cancer Institute|March 10, 1999

Frequency of p53 mutations in breast carcinomas from Ashkenazi Jewish carriers of BRCA1 mutationsK A Phillips, K Nichol, H Ozcelik, et al.

Clinical Genetics|June 14, 2000

Perceptions of Ashkenazi Jewish breast cancer patients on genetic testing for mutations in BRCA1 and BRCA2K A Phillips, E Warner, W S Meschino, et al.

Oncogene|November 7, 1996

Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of METJ C Lin, S W Scherer, L Tougas, et al.

Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|September 1, 1996

SAS is amplified predominantly in surface osteosarcomaS E Noble-Topham, S R Burrow, K Eppert, et al.

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