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Oncogene
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May 2, 1996
A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas
V Shridhar, S Rivard, R Shridhar, et al.
Genomics
|
July 1, 1996
A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints
W Paradee, C M Wilke, L Wang, et al.
Oncogene
|
August 8, 1998
PTEN/MMAC1 mutations identified in small cell, but not in non-small cell lung cancers
A Yokomizo, D J Tindall, H Drabkin, et al.
American Journal of Human Genetics
|
September 1, 1991
Isolation of large numbers of chromosome 3-specific cosmids containing clusters of rare restriction-endonuclease sites
W A Golembieski, S E Smith, F Recchia, et al.
Cancer Research
|
November 21, 2000
Human papillomavirus type 16 integrations in cervical tumors frequently occur in common fragile sites
E C Thorland, S L Myers, D H Persing, et al.
Genomics
|
August 29, 1998
Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions
M Mai, H Huang, C Reed, et al.
Genes, Chromosomes & Cancer
|
January 19, 1999
Frequent deletions within FRA7G at 7q31.2 in invasive epithelial ovarian cancer
H Huang, C P Reed, A Mordi, et al.
Genes, Chromosomes & Cancer
|
April 29, 1998
An FHIT tumor suppressor gene?
M M Le Beau, H Drabkin, T W Glover, et al.
Human Molecular Genetics
|
May 16, 1998
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction
M M Le Beau, F V Rassool, M E Neilly, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 5, 1998
The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8
R M Gemmill, J D West, F Boldog, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 166) with videos related to
Sort By:
Page
of 17
Oncogene
|
May 2, 1996
A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas
V Shridhar, S Rivard, R Shridhar, et al.
Genomics
|
July 1, 1996
A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints
W Paradee, C M Wilke, L Wang, et al.
Oncogene
|
August 8, 1998
PTEN/MMAC1 mutations identified in small cell, but not in non-small cell lung cancers
A Yokomizo, D J Tindall, H Drabkin, et al.
American Journal of Human Genetics
|
September 1, 1991
Isolation of large numbers of chromosome 3-specific cosmids containing clusters of rare restriction-endonuclease sites
W A Golembieski, S E Smith, F Recchia, et al.
Cancer Research
|
November 21, 2000
Human papillomavirus type 16 integrations in cervical tumors frequently occur in common fragile sites
E C Thorland, S L Myers, D H Persing, et al.
Genomics
|
August 29, 1998
Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions
M Mai, H Huang, C Reed, et al.
Genes, Chromosomes & Cancer
|
January 19, 1999
Frequent deletions within FRA7G at 7q31.2 in invasive epithelial ovarian cancer
H Huang, C P Reed, A Mordi, et al.
Genes, Chromosomes & Cancer
|
April 29, 1998
An FHIT tumor suppressor gene?
M M Le Beau, H Drabkin, T W Glover, et al.
Human Molecular Genetics
|
May 16, 1998
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction
M M Le Beau, F V Rassool, M E Neilly, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 5, 1998
The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8
R M Gemmill, J D West, F Boldog, et al.
Page
of 17