Search research articles
Contact Us
Filters
Showing results (111-120 of 201) with videos related to
Page
of 21
Sort By:
Cancer Research
|
June 15, 1994
A common region of homozygous deletion in malignant human gliomas lies between the IFN alpha/omega gene cluster and the D9S171 locus
K Ichimura, E E Schmidt, N Yamaguchi, et al.
British Journal of Cancer
|
March 29, 2000
Analysis of pilocytic astrocytoma by comparative genomic hybridization
D Sanoudou, O Tingby, M A Ferguson-Smith, et al.
Genes, Chromosomes & Cancer
|
May 20, 1998
Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades
K Ichimura, E E Schmidt, A Miyakawa, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1989
Mitotic recombination of chromosome 17 in astrocytomas
C D James, E Carlbom, M Nordenskjold, et al.
Journal of Medical Genetics
|
January 7, 2005
A PDGFRA promoter polymorphism, which disrupts the binding of ZNF148, is associated with primitive neuroectodermal tumours and ependymomas
C De Bustos, A Smits, B Strömberg, et al.
Neuropathology and Applied Neurobiology
|
September 14, 2010
CpG island hypermethylation of the neurofibromatosis type 2 (NF2) gene is rare in sporadic vestibular schwannomas
P J Kullar, D M Pearson, D S Malley, et al.
The American Journal of Pathology
|
November 1, 1994
Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p
J Reifenberger, G Reifenberger, L Liu, et al.
Brain Pathology (Zurich, Switzerland)
|
July 23, 1999
Amplification and expression of cyclin D genes (CCND1, CCND2 and CCND3) in human malignant gliomas
R Büschges, R G Weber, B Actor, et al.
The American Journal of Pathology
|
July 1, 1996
Epidermal growth factor receptor expression in oligodendroglial tumors
J Reifenberger, G Reifenberger, K Ichimura, et al.
British Journal of Cancer
|
January 1, 1997
Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumours
E E Schmidt, K Ichimura, K R Messerle, et al.
Page
of 21
Search research articles
Search
Showing results (111-120 of 201) with videos related to
Sort By:
Page
of 21
Cancer Research
|
June 15, 1994
A common region of homozygous deletion in malignant human gliomas lies between the IFN alpha/omega gene cluster and the D9S171 locus
K Ichimura, E E Schmidt, N Yamaguchi, et al.
British Journal of Cancer
|
March 29, 2000
Analysis of pilocytic astrocytoma by comparative genomic hybridization
D Sanoudou, O Tingby, M A Ferguson-Smith, et al.
Genes, Chromosomes & Cancer
|
May 20, 1998
Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades
K Ichimura, E E Schmidt, A Miyakawa, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1989
Mitotic recombination of chromosome 17 in astrocytomas
C D James, E Carlbom, M Nordenskjold, et al.
Journal of Medical Genetics
|
January 7, 2005
A PDGFRA promoter polymorphism, which disrupts the binding of ZNF148, is associated with primitive neuroectodermal tumours and ependymomas
C De Bustos, A Smits, B Strömberg, et al.
Neuropathology and Applied Neurobiology
|
September 14, 2010
CpG island hypermethylation of the neurofibromatosis type 2 (NF2) gene is rare in sporadic vestibular schwannomas
P J Kullar, D M Pearson, D S Malley, et al.
The American Journal of Pathology
|
November 1, 1994
Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p
J Reifenberger, G Reifenberger, L Liu, et al.
Brain Pathology (Zurich, Switzerland)
|
July 23, 1999
Amplification and expression of cyclin D genes (CCND1, CCND2 and CCND3) in human malignant gliomas
R Büschges, R G Weber, B Actor, et al.
The American Journal of Pathology
|
July 1, 1996
Epidermal growth factor receptor expression in oligodendroglial tumors
J Reifenberger, G Reifenberger, K Ichimura, et al.
British Journal of Cancer
|
January 1, 1997
Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumours
E E Schmidt, K Ichimura, K R Messerle, et al.
Page
of 21