ADAR1-mediated RNA editing links ganglioside catabolism to glioblastoma stem cell maintenance is a research paper published in Journal of Clinical Investigation (2022). On theSindex it has a DataRank of 0. It has been cited 83 times.
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National Cancer Institute
Grant: CA217066,CA217065,CA238662,CA197718,CA154130,CA169117,CA171652
National Institute of General Medical Sciences
Grant: GM04936,GM052872
National Human Genome Research Institute
Grant: HG004659
National Institute of Neurological Disorders and Stroke
Grant: NS087913,NS089272,NS103434
National Cancer Institute
Grant: CA047904
NHGRI NIH HHS
Grant: R01 HG004659
NIGMS NIH HHS
Grant: T32 GM007250
NCI NIH HHS
Grant: F30 CA217066
NCI NIH HHS
Grant: R01 CA169117
NINDS NIH HHS
Grant: R01 NS087913
NCI NIH HHS
Grant: R01 CA171652
NINDS NIH HHS
Grant: R01 NS089272
NCI NIH HHS
Grant: R01 CA154130
NIGMS NIH HHS
Grant: R01 GM052872
NINDS NIH HHS
Grant: R01 NS103434
NCI NIH HHS
Grant: R35 CA197718
NCI NIH HHS
Grant: F30 CA217065
NCI NIH HHS
Grant: P30 CA047904
NCI NIH HHS
Grant: R01 CA238662
NIGMS NIH HHS
Grant: R01 GM049369
National Institutes of Health
Grant: 5F30CA217065-05
Epigenetic Regulation of Lipid Metabolism in Glioma Stem Cells
National Institutes of Health
Grant: 5F30CA217066-05
The Unfolded Protein Response in Glioblastoma
National Institutes of Health
Grant: 5R01NS087913-04
Metabolism Informs Intertumoral & Intratumoral Heterogeneity
National Institutes of Health
Grant: 5R01GM052872-14
Regulation of RNA metabolism and cell growth control by SR protein kinases
National Institutes of Health
Grant: 2R01GM049369-18
Function and regulation of the human splicing factor SC35
National Institutes of Health
Grant: 5R01HG004659-08
Functional RNA elements in the human genome
National Institutes of Health
Grant: 3P30CA047904-07S1
CANCER CENTER SUPPORT GRANT
FWCI
5.88
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Additional file 6 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 6 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 7 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 7 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 8 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 8 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 1 of Exosome-transmitted circCABIN1 promotes temozolomide resistance in glioblastoma via sustaining ErbB downstream signaling
Additional file 1 of Exosome-transmitted circCABIN1 promotes temozolomide resistance in glioblastoma via sustaining ErbB downstream signaling
Additional file 4 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 5 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 2 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 3 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 1 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 1 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 4 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 2 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 3 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses
Additional file 5 of The anterior gradient homologue 2 (AGR2) co-localises with the glucose-regulated protein 78 (GRP78) in cancer stem cells, and is critical for the survival and drug resistance of recurrent glioblastoma: in situ and in vitro analyses