Add to ORKGComparative genomic hybridization was applied for a comprehensive screening of under- and overrepresentation of genetic material in 13 autoptic small cell lung cancer specimens. The most abundant genetic changes include DNA losses of chromosome arms 3p, 5q, 10q, 13q, and 17p and DNA gains of 3q, 5p, 8q, and 17q. Amplification sites in these tumors were mapped to 22 chromosome bands. The most frequently involved band was 19q13.1 (4 cases). Bands 1p32, 2p23, 7q11.2, 8q24, and 13q33–34 were involved in two cases each
We have sequenced the genomes of 110 small cell lung cancers (SCLC), one of the deadliest human canc...
Genetic alterations such as deletions, amplifications, and translocations occurring on human chromos...
AbstractTo investigate the genomic aberrations that are involved in lung tumorigenesis and therefore...
Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepres...
Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepres...
Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepres...
grantor: University of TorontoComparative Genomic Hybridization (CGH) was used to screen 2...
grantor: University of TorontoComparative Genomic Hybridization (CGH) was used to screen 2...
Lung cancer is the leading cause of cancer-related deaths in North America and Europe for both men ...
Lung cancer is the leading cause of cancer-related deaths in North America and Europe for both men ...
To improve the survival rate in lung cancer, novel molecular targets that facilitate early detectio...
To improve the survival rate in lung cancer, novel molecular targets that facilitate early detectio...
AbstractTo investigate the genomic aberrations that are involved in lung tumorigenesis and therefore...
Lung cancer is a leading cause of cancer deaths throughout the world. Non-small cell lung cancer (NS...
To investigate the genomic aberrations that are involved in lung tumorigenesis and therefore may be ...
We have sequenced the genomes of 110 small cell lung cancers (SCLC), one of the deadliest human canc...
Genetic alterations such as deletions, amplifications, and translocations occurring on human chromos...
AbstractTo investigate the genomic aberrations that are involved in lung tumorigenesis and therefore...
Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepres...
Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepres...
Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepres...
grantor: University of TorontoComparative Genomic Hybridization (CGH) was used to screen 2...
grantor: University of TorontoComparative Genomic Hybridization (CGH) was used to screen 2...
Lung cancer is the leading cause of cancer-related deaths in North America and Europe for both men ...
Lung cancer is the leading cause of cancer-related deaths in North America and Europe for both men ...
To improve the survival rate in lung cancer, novel molecular targets that facilitate early detectio...
To improve the survival rate in lung cancer, novel molecular targets that facilitate early detectio...
AbstractTo investigate the genomic aberrations that are involved in lung tumorigenesis and therefore...
Lung cancer is a leading cause of cancer deaths throughout the world. Non-small cell lung cancer (NS...
To investigate the genomic aberrations that are involved in lung tumorigenesis and therefore may be ...
We have sequenced the genomes of 110 small cell lung cancers (SCLC), one of the deadliest human canc...
Genetic alterations such as deletions, amplifications, and translocations occurring on human chromos...
AbstractTo investigate the genomic aberrations that are involved in lung tumorigenesis and therefore...
