Pages that link to "Q21144984"
Jump to navigation
Jump to search
The following pages link to U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line (Q21144984):
Displaying 50 items.
- U-87MG ATCC (Q7863603) (← links)
- Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome (Q24336742) (← links)
- NCG 4.0: the network of cancer genes in the era of massive mutational screenings of cancer genomes (Q24596715) (← links)
- Network of Cancer Genes (NCG 3.0): integration and analysis of genetic and network properties of cancer genes (Q24619351) (← links)
- Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens (Q24622594) (← links)
- In vivo models of primary brain tumors: pitfalls and perspectives (Q26862847) (← links)
- Contemporary murine models in preclinical astrocytoma drug development (Q27026937) (← links)
- Sensitive Tumorigenic Potential Evaluation of Adult Human Multipotent Neural Cells Immortalized by hTERT Gene Transduction (Q27335199) (← links)
- Analysis of next-generation genomic data in cancer: accomplishments and challenges (Q28293359) (← links)
- Exosomes reflect the hypoxic status of glioma cells and mediate hypoxia-dependent activation of vascular cells during tumor development (Q28397739) (← links)
- Engineered drug resistant γδ T cells kill glioblastoma cell lines during a chemotherapy challenge: a strategy for combining chemo- and immunotherapy (Q28485036) (← links)
- High-resolution mutational profiling suggests the genetic validity of glioblastoma patient-derived pre-clinical models (Q28486219) (← links)
- Doxycycline alters metabolism and proliferation of human cell lines (Q28533505) (← links)
- Distinct patterns of somatic alterations in a lymphoblastoid and a tumor genome derived from the same individual (Q28741663) (← links)
- Modulation of HJURP (Holliday Junction-Recognizing Protein) levels is correlated with glioblastoma cells survival (Q30419684) (← links)
- Characterization of a setup to test the impact of high-amplitude pressure waves on living cells. (Q30444140) (← links)
- Cooperativity between MAPK and PI3K signaling activation is required for glioblastoma pathogenesis (Q30545759) (← links)
- ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data (Q30561080) (← links)
- Fastbreak: a tool for analysis and visualization of structural variations in genomic data (Q30572597) (← links)
- Linking proteomic and transcriptional data through the interactome and epigenome reveals a map of oncogene-induced signaling (Q30588679) (← links)
- Secondary Data Analytics of Aquaporin Expression Levels in Glioblastoma Stem-Like Cells (Q30987653) (← links)
- Challenges of sequencing human genomes (Q33592630) (← links)
- Local alignment of generalized k-base encoded DNA sequence (Q33615417) (← links)
- The (r)evolution of cancer genetics (Q33622812) (← links)
- Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA (Q33713232) (← links)
- Integrated analysis of recurrent properties of cancer genes to identify novel drivers (Q33742981) (← links)
- Silencing of protein kinase D2 induces glioma cell senescence via p53-dependent and -independent pathways. (Q33753441) (← links)
- SeqWare Query Engine: storing and searching sequence data in the cloud (Q33787339) (← links)
- A murine model of targeted infusion for intracranial tumors (Q33848111) (← links)
- Modulation of the inwardly rectifying potassium channel Kir4.1 by the pro-invasive miR-5096 in glioblastoma cells (Q33914091) (← links)
- Comprehensive genomic analysis of a BRCA2 deficient human pancreatic cancer (Q33959327) (← links)
- Myc inhibition is effective against glioma and reveals a role for Myc in proficient mitosis. (Q34086373) (← links)
- Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing (Q34189262) (← links)
- Current review of in vivo GBM rodent models: emphasis on the CNS-1 tumour model (Q34198939) (← links)
- Next-generation sequencing of colorectal cancers in chinese: identification of a recurrent frame-shift and gain-of-function Indel mutation in the TFDP1 gene (Q34247927) (← links)
- Recurrent somatic mutation of FAT1 in multiple human cancers leads to aberrant Wnt activation. (Q34324645) (← links)
- Multiplexed detection and label-free quantitation of microRNAs using arrays of silicon photonic microring resonators (Q34363395) (← links)
- Long span DNA paired-end-tag (DNA-PET) sequencing strategy for the interrogation of genomic structural mutations and fusion-point-guided reconstruction of amplicons. (Q34430902) (← links)
- Next-generation sequencing of endoscopic biopsies identifies ARID1A as a tumor-suppressor gene in Barrett's esophagus (Q34547790) (← links)
- OASIS/CREB3L1 is induced by endoplasmic reticulum stress in human glioma cell lines and contributes to the unfolded protein response, extracellular matrix production and cell migration (Q34555813) (← links)
- CMV-independent lysis of glioblastoma by ex vivo expanded/activated Vδ1+ γδ T cells (Q34946005) (← links)
- N-methylpurine DNA glycosylase and DNA polymerase beta modulate BER inhibitor potentiation of glioma cells to temozolomide (Q34977358) (← links)
- High CD49f expression is associated with osteosarcoma tumor progression: a study using patient-derived primary cell cultures (Q35000400) (← links)
- MiR-21 in the extracellular vesicles (EVs) of cerebrospinal fluid (CSF): a platform for glioblastoma biomarker development (Q35036059) (← links)
- Cell-type-specific regulation of raft-associated Akt signaling (Q35064848) (← links)
- FRA2 is a STAT5 target gene regulated by IL-2 in human CD4 T cells. (Q35109000) (← links)
- Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV (Q35231005) (← links)
- Genome sequence-independent identification of RNA editing sites (Q35243317) (← links)
- The polyamine catabolic enzyme SAT1 modulates tumorigenesis and radiation response in GBM (Q35296657) (← links)
- Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers (Q35345680) (← links)