FGFR1 gene
Evidence from:
primary |
all sources
Related entities (73)
Mentioned in (60)
Papers in which this entity is mentioned.
- Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models. (2026)
- Whole-genome landscapes of 1,364 breast cancers. (2026)
- Stratified Medicine Pediatrics: Cell-Free DNA and Serial Tumor Sequencing Identifies Subtype-Specific Cancer Evolution and Epigenetic States. (2025)
- Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
- Three-dimensional genome landscape of primary human cancers. (2025)
- Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (2024)
- The landscape of drug sensitivity and resistance in sarcoma. (2024)
- Towards understandings of serine/arginine-rich splicing factors. (2023)
- RNA splicing dysregulation and the hallmarks of cancer. (2023)
- Chronic oligodendrocyte injury in central nervous system pathologies. (2022)
- Single-cell genomic variation induced by mutational processes in cancer. (2022)
- Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
- Biologically informed deep neural network for prostate cancer discovery. (2021)
- Effects of chronic intermittent ethanol exposure and withdrawal on neuroblastoma cell transcriptome. (2020)
- Exploring the landscape of focal amplifications in cancer using AmpliconArchitect. (2019)
- CYP2A6 is associated with obesity: studies in human samples and a high fat diet mouse model. (2019)
- Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors. (2018)
- The Role of the Endocannabinoid System and Genetic Variation in Adolescent Brain Development. (2018)
- Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
- Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
- Cerebral organoids reveal early cortical maldevelopment in schizophrenia-computational anatomy and genomics, role of FGFR1. (2017)
- Statistical algorithms improve accuracy of gene fusion detection. (2017)
- The Reactome pathway Knowledgebase. (2016)
- An Fgf-Shh signaling hierarchy regulates early specification of the zebrafish skull. (2016)
- Development and clinical application of an integrative genomic approach to personalized cancer therapy. (2016)
- Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets. (2015)
- The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS. (2015)
- Mechanisms of retinoic acid signalling and its roles in organ and limb development. (2015)
- Impact of prenatal environmental stress on cortical development. (2015)
- Comprehensive genomic profiles of small cell lung cancer. (2015)
- Activation of the FGFR-STAT3 pathway in breast cancer cells induces a hyaluronan-rich microenvironment that licenses tumor formation. (2014)
- Programming of neural cells by (endo)cannabinoids: from physiological rules to emerging therapies. (2014)
- SRF regulates craniofacial development through selective recruitment of MRTF cofactors by PDGF signaling. (2014)
- Low-dose maternal alcohol consumption: effects in the hearts of offspring in early life and adulthood. (2014)
- Fetal alcohol spectrum disorders and their transmission through genetic and epigenetic mechanisms. (2014)
- Direct functional consequences of ZRS enhancer mutation combine with secondary long range SHH signalling effects to cause preaxial polydactyly. (2014)
- Stressed Liver and Muscle Call on Adipocytes with FGF21. (2013)
- Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
- Hand in glove: brain and skull in development and dysmorphogenesis. (2013)
- Suppression and epigenetic regulation of MiR-9 contributes to ethanol teratology: evidence from zebrafish and murine fetal neural stem cell models. (2013)
- Pan-cancer patterns of somatic copy number alteration. (2013)
- Zebrafish models of human liver development and disease. (2013)
- High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
- FGF21 promotes metabolic homeostasis via white adipose and leptin in mice. (2012)
- Cleft lip and palate: understanding genetic and environmental influences. (2011)
- "CRASH"ing with the worm: insights into L1CAM functions and mechanisms. (2010)
- Primary contribution to zebrafish heart regeneration by gata4(+) cardiomyocytes. (2010)
- A random cell motility gradient downstream of FGF controls elongation of an amniote embryo. (2010)
- TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction. (2009)
- Pathogenesis of holoprosencephaly. (2009)
- Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. (2008)
- Molecular specification and patterning of progenitor cells in the lateral and medial ganglionic eminences. (2008)
- Perlecan controls neurogenesis in the developing telencephalon. (2007)
- Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans. (2006)
- Ethanol inhibits L1 cell adhesion molecule activation of mitogen-activated protein kinases. (2006)
- Growth-associated protein GAP-43 and L1 act synergistically to promote regenerative growth of Purkinje cell axons in vivo. (2005)
- Macrophage-derived tumor necrosis factor alpha, an early developmental signal for motoneuron death. (2004)
- Evolutionary divergence of platelet-derived growth factor alpha receptor signaling mechanisms. (2003)
- Myelination is altered in insulin-like growth factor-I null mutant mice. (2002)
- Concurrent stimulation of cannabinoid CB1 and dopamine D2 receptors augments cAMP accumulation in striatal neurons: evidence for a Gs linkage to the CB1 receptor. (1997)
Merged raw entities (9)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| fgfr1 | gene | 51 | 188 |
| fgfr | gene | 18 | 49 |
| fgfr1c | gene | 1 | 1 |
| nfgfr1 | gene | 1 | 4 |
| fgfr1(sp-/nls) | gene | — | — |
| fgfr1(sp-/nls)(tk-) | gene | — | — |
| fgf receptor 1 | gene | — | — |
| fibroblast growth factor receptor 1 | gene | — | — |
| nuclear fgfr1 | gene | — | — |