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TranscriptomicsFFPE study using MIP copy number platform - breast cancer II
A major challenge to the study of tumor DNA copy number (CN) in clinical specimens is the lack of appropriate fresh frozen samples and thus a dependence on Formalin-Fixed Paraffin Embedded (FFPE) banked samples, which typically have more extensive clinical follow up information. However, on most hig...
ORGANISM(S): Homo sapiens 
2010-05-06 | E-GEOD-14744 | biostudies-arrayexpress
TranscriptomicsFFPE study using MIP copy number platform - kidney
A major challenge to the study of tumor DNA copy number (CN) in clinical specimens is the lack of appropriate fresh frozen samples and thus a dependence on Formalin-Fixed Paraffin Embedded (FFPE) banked samples, which typically have more extensive clinical follow up information. However, on most hig...
ORGANISM(S): Homo sapiens 
2010-05-05 | E-GEOD-14740 | biostudies-arrayexpress
TranscriptomicsFFPE study using MIP copy number platform - colorectal
A major challenge to the study of tumor DNA copy number (CN) in clinical specimens is the lack of appropriate fresh frozen samples and thus a dependence on Formalin-Fixed Paraffin Embedded (FFPE) banked samples, which typically have more extensive clinical follow up information. However, on most hig...
ORGANISM(S): Homo sapiens 
2010-05-06 | E-GEOD-14742 | biostudies-arrayexpress
TranscriptomicsFFPE study using MIP copy number platform - liver
: A major challenge to the study of tumor DNA copy number (CN) in clinical specimens is the lack of appropriate fresh frozen samples and thus a dependence on Formalin-Fixed Paraffin Embedded (FFPE) banked samples, which typically have more extensive clinical follow up information. However, o...
ORGANISM(S): Homo sapiens 
2010-05-05 | E-GEOD-14745 | biostudies-arrayexpress
TranscriptomicsFFPE study using MIP copy number platform - bladder/colorectal/kidney/liver
A major challenge to the study of tumor DNA copy number (CN) in clinical specimens is the lack of appropriate fresh frozen samples and thus a dependence on Formalin-Fixed Paraffin Embedded (FFPE) banked samples, which typically have more extensive clinical follow up information. However, on most hig...
ORGANISM(S): Homo sapiens 
2009-02-17 | E-GEOD-14741 | biostudies-arrayexpress
TranscriptomicsLiver tumor/normal pairs
A major challenge to the study of tumor DNA copy number (CN) in clinical specimens is the lack of appropriate fresh frozen samples and thus a dependence on Formalin-Fixed Paraffin Embedded (FFPE) banked samples, which typically have more extensive clinical follow up information. However, on most hi...
ORGANISM(S): Homo sapiens 
2009-01-22 | E-GEOD-14353 | biostudies-arrayexpress
TranscriptomicsFFPE study using MIP copy number platform - breast cancer I
A major challenge to the study of tumor DNA copy number (CN) in clinical specimens is the lack of appropriate fresh frozen samples and thus a dependence on Formalin-Fixed Paraffin Embedded (FFPE) banked samples, which typically have more extensive clinical follow up information. However, on most hig...
ORGANISM(S): Homo sapiens 
2010-05-05 | E-GEOD-14743 | biostudies-arrayexpress
ProteomicsCombining affinity purification and mass spectrometry to define the network of the nuclear proteins interacting with the N-terminal region of FMRP
We identified a nuclear interactome of FMRP by combining subcellular fractionation of rat brains at the post-natal day 14 with pull down affinity purification and mass spectrometry analysis. By this approach, we have listed 55 candidate nuclear partners.
ORGANISM(S): Rattus norvegicus (Rat) 
2022-08-14 | PXD034157 | Pride
Nuclear protein network Mrna metabolism Proteomics Nuclear fractionation Fmrp 
TranscriptomicsFFPE study using MIP copy number platform
This SuperSeries is composed of the following subset Series: GSE14740: FFPE study using MIP copy number platform - kidney GSE14741: FFPE study using MIP copy number platform - bladder/colorectal/kidney/liver GSE14742: FFPE study using MIP copy number platform - colorectal GSE14743: FFPE study using ...
ORGANISM(S): Homo sapiens 
2010-05-06 | E-GEOD-14856 | biostudies-arrayexpress
GenomicsA SNF2 protein targets variable copy number repeats and thereby influences allele-specific expression
ATRX is an X-linked gene of the SWI/SNF family whose role in vivo is currently unknown. Mutations in ATRX cause syndromal mental retardation. ATRX binds to tandem repeat (TR) sequences both in heterochromatin (e.g. telomeres) and euchromatin. Genes associated with these TRs can be dysregulated when ...
ORGANISM(S): Homo sapiens 
2010-11-02 | E-GEOD-22162 | biostudies-arrayexpress
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