Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Comparison of PRPF4 knockdown in HEK293T cells compared to scrambled shRNA control

ABSTRACT: Comparison of PRPF4 knockdown in HEK293T cells compared to scrambled shRNA control

PROVIDER: PRJNA481964 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Similar Datasets

Comparison of PPWD1 knockdown in HEK293T cells compared to scrambled shRNA control

Project description:Comparison of PPWD1 knockdown in HEK293T cells compared to scrambled shRNA control

| PRJNA481942 | ENA

Comparison of CWC27 knockdown in HEK293T cells compared to scrambled shRNA control

Project description:Comparison of CWC27 knockdown in HEK293T cells compared to scrambled shRNA control

| PRJNA481269 | ENA

Comparison of PPIE knockdown in HEK293T cells compared to scrambled shRNA control

Project description:Comparison of PPIE knockdown in HEK293T cells compared to scrambled shRNA control

| PRJNA481351 | ENA

Comparison of PPIL1 knockdown in HEK293T cells compared to scrambled shRNA control

Project description:Comparison of PPIL1 knockdown in HEK293T cells compared to scrambled shRNA control

| PRJNA481959 | ENA

Comparison of PPIG knockdown in HEK293T cells compared to scrambled shRNA control

Project description:Comparison of PPIG knockdown in HEK293T cells compared to scrambled shRNA control

| PRJNA481506 | ENA

Comparison of PPIL3 knockdown in HEK293T cells compared to scrambled shRNA control

Project description:Comparison of PPIL3 knockdown in HEK293T cells compared to scrambled shRNA control

| PRJNA481800 | ENA

Comparison of PPIL2 knockdown in HEK293T cells compared to scrambled shRNA control

Project description:Comparison of PPIL2 knockdown in HEK293T cells compared to scrambled shRNA control

| PRJNA481939 | ENA

Comparison of PPIL1 knockdown in HEK293T cells compared to scrambled shRNA control

Project description:HEK293T cells transduced with shRNA from MISSION library TRCN0000420470 using lentiviral delivery system. HEK293T cells transduced with scrambled shRNA, gifted from Dr. Mauricio Reginato. Tara L Davis, S. RaElle Jackson, Beth Adams, Anh Trinh, Jenna Marinock, Peter Naranjo, NIcholas Fox, and Gueil Wong-Shing performed primary experimental contributions to cell lines, RNA/cDNA preparation, and validation, all Drexel University College of Medicine, Philadelphia, PA. Hetty Rodriguez and John Tobias performed Bioanalyzer and microarray expreriments, and initial data processing. Affiliation: Molecular Profiling Facility and Genomic Analysis Core Bioinformatics Group, University of Pennsylvania, Philadelphia, PA. Human PPIL1 is a cyclophilin, an enzyme that interconverts cis and trans isomers of proline. PPIL1 associates with the human spliceosome, the complex and dynamic machinery that removes intronic sequence from pre-messenger RNA (pre-mRNA). Nothing is known about the function of PPIL1 in regulating transcription or alternative splicing events. To understand the nuclear function of PPIL1, we knocked down PPIL1 in human cells. We characterized a set of alternative splicing and transcriptional events that are PPIL1-responsive. We used these splicing and transcriptional bioassays to show that PPIL1-responsive events are largely specific, even within the cyclophilin family.

2018-10-01 | GSE117381 | GEO

Comparison of PPIL3 knockdown in HEK293T cells compared to scrambled shRNA control

Project description:HEK293T cells transduced with shRNA from MISSION library TRCN0000000185 using lentiviral delivery system. HEK293T cells transduced with scrambled shRNA, gifted from Dr. Mauricio Reginato. Tara L Davis, S. RaElle Jackson, Beth Adams, Anh Trinh, Jonathan Amora, Peter Naranjo, Gueil Wong-Shing, and Nii Martey performed primary experimental contributions to cell lines, RNA/cDNA preparation, and validation, all Drexel University College of Medicine, Philadelphia, PA. Hetty Rodriguez and John Tobias performed Bioanalyzer and microarray expreriments, and initial data processing. Affiliation: Molecular Profiling Facility and Genomic Analysis Core Bioinformatics Group, University of Pennsylvania, Philadelphia, PA. Human PPIL3 is a cyclophilin, an enzyme that interconverts cis and trans isomers of proline. PPIL3 associates with the human spliceosome, the complex and dynamic machinery that removes intronic sequence from pre-messenger RNA (pre-mRNA). Nothing is known about the function of PPIL3 in the nucleus. To understand the function of PPIL3, we knocked down PPIL3 in human cells. We characterized a set of alternative splicing and transcriptional events that are PPIL3-responsive. We used these splicing and transcriptional bioassays to show that PPIL3-responsive events are largely specific, even within the cyclophilin family.

2018-10-01 | GSE117302 | GEO

Comparison of PPIG knockdown in HEK293T cells compared to scrambled shRNA control

Project description:HEK293T cells transduced with shRNA from MISSION library TRCN0000049326 using lentiviral delivery system. HEK293T cells transduced with scrambled shRNA, gifted from Dr. Mauricio Reginato. Tara L Davis, S. RaElle Jackson, Beth Adams, Anh Trinh performed primary experimental contributions to cell lines, RNA/cDNA preparation, and validations, all Drexel University College of Medicine, Philadelphia, PA. Hetty Rodriguez and John Tobias performed Bioanalyzer and microarray expreriments, and initial data processing. Affiliation: Molecular Profiling Facility and Genomic Analysis Core Bioinformatics Group, University of Pennsylvania, Philadelphia, PA. Human PPIG (alias: SR-Cyp, CARS) is a cyclophilin, an enzyme that interconverts cis and trans isomers of proline. The PPIG gene, in addition to the cyclophilin domain, encodes for a multiple C-terminal SR motifs. PPIG associates with the human spliceosome, the complex and dynamic machinery that removes intronic sequence from pre-messenger RNA (pre-mRNA). Nothing is known about the function of PPIG in regulation of alternative splicing. To understand the function of PPIG, we knocked down PPIG in human cells. We characterized a set of alternative splicing and transcriptional events that are PPIG-responsive. We used these splicing and transcriptional bioassays to show that PPIG-responsive events are largely specific, even within the cyclophilin family.

2018-10-01 | GSE117234 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data