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Genomics
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September 24, 1999
Cryptic exons as a source of increased diversity of Ewing tumor-associated EWS-FLI1 chimeric products
H Kovar, D Jugovic, T Melot, et al.
Human Molecular Genetics
|
December 1, 1995
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocation
Y Labelle, J Zucman, G Stenman, et al.
The EMBO Journal
|
December 1, 1993
Combinatorial generation of variable fusion proteins in the Ewing family of tumours
J Zucman, T Melot, C Desmaze, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1988
Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12)
C Turc-Carel, A Aurias, F Mugneret, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 1, 1992
In vitro karyotypic and immunophenotypic characterisation of primitive neuroectodermal tumours: similarities to malignant gliomas
M T Jennings, D L Jennings, S A Ebrahim, et al.
Cancer Genetics and Cytogenetics
|
April 1, 1993
Chromosome 12 origin in rings and giant markers in well-differentiated liposarcoma
F Pedeutour, R F Suijkerbuijk, J Van Gaal, et al.
The New England Journal of Medicine
|
August 4, 1994
The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts
O Delattre, J Zucman, T Melot, et al.
Genes, Chromosomes & Cancer
|
April 3, 2001
ALK probe rearrangement in a t(2;11;2)(p23;p15;q31) translocation found in a prenatal myofibroblastic fibrous lesion: toward a molecular definition of an inflammatory myofibroblastic tumor family?
N Sirvent, A L Hawkins, D Moeglin, et al.
Genes, Chromosomes & Cancer
|
April 1, 1994
Comparative genomic hybridization as a tool to define two distinct chromosome 12-derived amplification units in well-differentiated liposarcomas
R F Suijkerbuijk, D E Olde Weghuis, M Van den Berg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1987
Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma
C Turc-Carel, P Dal Cin, J Limon, et al.
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of 12
Search research articles
Search
Showing results (101-110 of 119) with videos related to
Sort By:
Page
of 12
Genomics
|
September 24, 1999
Cryptic exons as a source of increased diversity of Ewing tumor-associated EWS-FLI1 chimeric products
H Kovar, D Jugovic, T Melot, et al.
Human Molecular Genetics
|
December 1, 1995
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocation
Y Labelle, J Zucman, G Stenman, et al.
The EMBO Journal
|
December 1, 1993
Combinatorial generation of variable fusion proteins in the Ewing family of tumours
J Zucman, T Melot, C Desmaze, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1988
Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12)
C Turc-Carel, A Aurias, F Mugneret, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 1, 1992
In vitro karyotypic and immunophenotypic characterisation of primitive neuroectodermal tumours: similarities to malignant gliomas
M T Jennings, D L Jennings, S A Ebrahim, et al.
Cancer Genetics and Cytogenetics
|
April 1, 1993
Chromosome 12 origin in rings and giant markers in well-differentiated liposarcoma
F Pedeutour, R F Suijkerbuijk, J Van Gaal, et al.
The New England Journal of Medicine
|
August 4, 1994
The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts
O Delattre, J Zucman, T Melot, et al.
Genes, Chromosomes & Cancer
|
April 3, 2001
ALK probe rearrangement in a t(2;11;2)(p23;p15;q31) translocation found in a prenatal myofibroblastic fibrous lesion: toward a molecular definition of an inflammatory myofibroblastic tumor family?
N Sirvent, A L Hawkins, D Moeglin, et al.
Genes, Chromosomes & Cancer
|
April 1, 1994
Comparative genomic hybridization as a tool to define two distinct chromosome 12-derived amplification units in well-differentiated liposarcomas
R F Suijkerbuijk, D E Olde Weghuis, M Van den Berg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1987
Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma
C Turc-Carel, P Dal Cin, J Limon, et al.
Page
of 12