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Genes, Chromosomes & Cancer
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November 1, 1994
Cytogenetic analysis of 63 non-small cell lung carcinomas: recurrent chromosome alterations amid frequent and widespread genomic upheaval
J R Testa, J M Siegfried, Z Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 15, 1993
Universal mapping probes and the origin of human chromosome 3
O Hino, J R Testa, K H Buetow, et al.
Human Molecular Genetics
|
August 1, 1997
Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice
K B Avraham, T Hasson, T Sobe, et al.
Oncogene
|
March 1, 1993
Structure, expression and chromosomal mapping of c-akt: relationship to v-akt and its implications
A Bellacosa, T F Franke, M E Gonzalez-Portal, et al.
International Journal of Cancer
|
April 22, 1997
Detection of low-fraction K-ras mutations in primary lung tumors using a sensitive method
P Keohavong, D Zhu, A C Melacrinos, et al.
The Journal of Biological Chemistry
|
March 8, 1996
Cloning of a putative ligand for the T1/ST2 receptor
M A Gayle, J L Slack, T P Bonnert, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Chromosomal localization of the Ox-44 (CD53) leukocyte antigen gene in man and rodents
T Taguchi, A Bellacosa, J Y Zhou, et al.
Genomics
|
October 13, 2001
Cloning and chromosomal localization of a gene encoding a novel serine/threonine kinase belonging to the subfamily of testis-specific kinases
P E Visconti, Z Hao, M A Purdon, et al.
Oncogene
|
February 3, 2000
Expression of GPC3, an X-linked recessive overgrowth gene, is silenced in malignant mesothelioma
S S Murthy, T Shen, A De Rienzo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 1995
High frequency of inactivating mutations in the neurofibromatosis type 2 gene (NF2) in primary malignant mesotheliomas
A B Bianchi, S I Mitsunaga, J Q Cheng, et al.
Page
of 22
Search research articles
Search
Showing results (191-200 of 217) with videos related to
Sort By:
Page
of 22
Genes, Chromosomes & Cancer
|
November 1, 1994
Cytogenetic analysis of 63 non-small cell lung carcinomas: recurrent chromosome alterations amid frequent and widespread genomic upheaval
J R Testa, J M Siegfried, Z Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 15, 1993
Universal mapping probes and the origin of human chromosome 3
O Hino, J R Testa, K H Buetow, et al.
Human Molecular Genetics
|
August 1, 1997
Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice
K B Avraham, T Hasson, T Sobe, et al.
Oncogene
|
March 1, 1993
Structure, expression and chromosomal mapping of c-akt: relationship to v-akt and its implications
A Bellacosa, T F Franke, M E Gonzalez-Portal, et al.
International Journal of Cancer
|
April 22, 1997
Detection of low-fraction K-ras mutations in primary lung tumors using a sensitive method
P Keohavong, D Zhu, A C Melacrinos, et al.
The Journal of Biological Chemistry
|
March 8, 1996
Cloning of a putative ligand for the T1/ST2 receptor
M A Gayle, J L Slack, T P Bonnert, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Chromosomal localization of the Ox-44 (CD53) leukocyte antigen gene in man and rodents
T Taguchi, A Bellacosa, J Y Zhou, et al.
Genomics
|
October 13, 2001
Cloning and chromosomal localization of a gene encoding a novel serine/threonine kinase belonging to the subfamily of testis-specific kinases
P E Visconti, Z Hao, M A Purdon, et al.
Oncogene
|
February 3, 2000
Expression of GPC3, an X-linked recessive overgrowth gene, is silenced in malignant mesothelioma
S S Murthy, T Shen, A De Rienzo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 1995
High frequency of inactivating mutations in the neurofibromatosis type 2 gene (NF2) in primary malignant mesotheliomas
A B Bianchi, S I Mitsunaga, J Q Cheng, et al.
Page
of 22