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V P Collins

Showing results (191-200 of 227) with videos related to

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Genes, Chromosomes & Cancer|May 25, 1999
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?C E Bruder, K Ichimura, E Blennow, et al.
Genes, Chromosomes & Cancer|June 1, 1994
Deletions on chromosome 22 in sporadic meningiomaM H Ruttledge, Y G Xie, F Y Han, et al.
American Journal of Ophthalmology|May 15, 1987
Immunohistochemical characterization of human retinoblastomas in situ with multiple markersE Perentes, C P Herbort, L J Rubinstein, et al.
Oncogene|August 1, 1994
Functional characterization of an EGF receptor with a truncated extracellular domain expressed in glioblastomas with EGFR gene amplificationA J Ekstrand, N Longo, M L Hamid, et al.
Human Genetics|February 1, 1990
Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qterJ P Dumanski, A H Geurts van Kessel, M Ruttledge, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Regional localization of the human platelet-derived endothelial cell growth factor (ECGF1) gene to chromosome 22q13G Stenman, P Sahlin, J P Dumanski, et al.
Scandinavian Journal of Urology and Nephrology. Supplementum|January 1, 1994
Cytogenetics of prostate cancer. Consensus Conference on Diagnosis and Prognostic Parameters in Localized Prostate Cancer. Stockholm, Sweden, May 12-13, 1993F M Debruyne, V P Collins, H van Dekken, et al.
Cancer Research|November 15, 1994
CDK4 amplification is an alternative mechanism to p16 gene homozygous deletion in glioma cell linesJ He, J R Allen, V P Collins, et al.
Cancer|July 27, 1999
Comparative genomic hybridization in patients with supratentorial and infratentorial primitive neuroectodermal tumorsC Russo, M Pellarin, O Tingby, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|October 11, 2001
Molecular characterization of DDX26, a human DEAD-box RNA helicase, located on chromosome 7p12A A Camargo, D N Nunes, H B Samaia, et al.
Pageof 23

Showing results (191-200 of 227) with videos related to

Sort By:
Pageof 23
Genes, Chromosomes & Cancer|May 25, 1999
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?C E Bruder, K Ichimura, E Blennow, et al.
Genes, Chromosomes & Cancer|June 1, 1994
Deletions on chromosome 22 in sporadic meningiomaM H Ruttledge, Y G Xie, F Y Han, et al.
American Journal of Ophthalmology|May 15, 1987
Immunohistochemical characterization of human retinoblastomas in situ with multiple markersE Perentes, C P Herbort, L J Rubinstein, et al.
Oncogene|August 1, 1994
Functional characterization of an EGF receptor with a truncated extracellular domain expressed in glioblastomas with EGFR gene amplificationA J Ekstrand, N Longo, M L Hamid, et al.
Human Genetics|February 1, 1990
Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qterJ P Dumanski, A H Geurts van Kessel, M Ruttledge, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Regional localization of the human platelet-derived endothelial cell growth factor (ECGF1) gene to chromosome 22q13G Stenman, P Sahlin, J P Dumanski, et al.
Scandinavian Journal of Urology and Nephrology. Supplementum|January 1, 1994
Cytogenetics of prostate cancer. Consensus Conference on Diagnosis and Prognostic Parameters in Localized Prostate Cancer. Stockholm, Sweden, May 12-13, 1993F M Debruyne, V P Collins, H van Dekken, et al.
Cancer Research|November 15, 1994
CDK4 amplification is an alternative mechanism to p16 gene homozygous deletion in glioma cell linesJ He, J R Allen, V P Collins, et al.
Cancer|July 27, 1999
Comparative genomic hybridization in patients with supratentorial and infratentorial primitive neuroectodermal tumorsC Russo, M Pellarin, O Tingby, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|October 11, 2001
Molecular characterization of DDX26, a human DEAD-box RNA helicase, located on chromosome 7p12A A Camargo, D N Nunes, H B Samaia, et al.
Pageof 23