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Genomics
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May 23, 2006
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH
Cecilia de Bustos, Teresita Díaz de Ståhl, Arkadiusz Piotrowski, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2010
Chromosomal and microRNA expression patterns reveal biologically distinct subgroups of 11q- neuroblastoma
Patrick G Buckley, Leah Alcock, Kenneth Bryan, et al.
Cell Reports
|
December 30, 2023
ATM-deficiency-induced microglial activation promotes neurodegeneration in ataxia-telangiectasia
Jenny Lai, Didem Demirbas, Junho Kim, et al.
Cell Reports
|
February 20, 2024
Proteogenomic characterization of primary colorectal cancer and metastatic progression identifies proteome-based subtypes and signatures
Atsushi Tanaka, Makiko Ogawa, Yihua Zhou, et al.
Genes, Chromosomes & Cancer
|
April 1, 2006
Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer
Arkadiusz Piotrowski, Magdalena Benetkiewicz, Uwe Menzel, et al.
International Journal of Oncology
|
February 13, 2003
High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH
Kiran K Mantripragada, Patrick G Buckley, Magdalena Benetkiewicz, et al.
JCO Precision Oncology
|
September 11, 2020
Postmortem Examination of an Aggressive Case of Medullary Thyroid Carcinoma Characterized by Catastrophic Genomic Abnormalities
Sudipto Das, Deirdre Kelly, Bruce Moran, et al.
Plos One
|
November 20, 2009
Widespread dysregulation of MiRNAs by MYCN amplification and chromosomal imbalances in neuroblastoma: association of miRNA expression with survival
Isabella Bray, Kenneth Bryan, Suzanne Prenter, et al.
International Journal of Cancer
|
September 15, 2005
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH
Caroline Jarbo, Patrick G Buckley, Arkadiusz Piotrowski, et al.
International Journal of Cancer
|
July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas
Annelies Fieuw, Candy Kumps, Alexander Schramm, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 49) with videos related to
Sort By:
Page
of 5
Genomics
|
May 23, 2006
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH
Cecilia de Bustos, Teresita Díaz de Ståhl, Arkadiusz Piotrowski, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2010
Chromosomal and microRNA expression patterns reveal biologically distinct subgroups of 11q- neuroblastoma
Patrick G Buckley, Leah Alcock, Kenneth Bryan, et al.
Cell Reports
|
December 30, 2023
ATM-deficiency-induced microglial activation promotes neurodegeneration in ataxia-telangiectasia
Jenny Lai, Didem Demirbas, Junho Kim, et al.
Cell Reports
|
February 20, 2024
Proteogenomic characterization of primary colorectal cancer and metastatic progression identifies proteome-based subtypes and signatures
Atsushi Tanaka, Makiko Ogawa, Yihua Zhou, et al.
Genes, Chromosomes & Cancer
|
April 1, 2006
Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer
Arkadiusz Piotrowski, Magdalena Benetkiewicz, Uwe Menzel, et al.
International Journal of Oncology
|
February 13, 2003
High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH
Kiran K Mantripragada, Patrick G Buckley, Magdalena Benetkiewicz, et al.
JCO Precision Oncology
|
September 11, 2020
Postmortem Examination of an Aggressive Case of Medullary Thyroid Carcinoma Characterized by Catastrophic Genomic Abnormalities
Sudipto Das, Deirdre Kelly, Bruce Moran, et al.
Plos One
|
November 20, 2009
Widespread dysregulation of MiRNAs by MYCN amplification and chromosomal imbalances in neuroblastoma: association of miRNA expression with survival
Isabella Bray, Kenneth Bryan, Suzanne Prenter, et al.
International Journal of Cancer
|
September 15, 2005
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH
Caroline Jarbo, Patrick G Buckley, Arkadiusz Piotrowski, et al.
International Journal of Cancer
|
July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas
Annelies Fieuw, Candy Kumps, Alexander Schramm, et al.
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of 5