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Epilepsy research gets new guidance.
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- Nature Medicine, 2002, v. 8, n. 3, p. 219, doi. 10.1038/nm0302-219
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THE EXPRESSION PATTERN OF WILMS' TUMOUR GENE ( WT1) PRODUCT IN NORMAL TISSUES AND PAEDIATRIC RENAL TUMOURS.
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- Journal of Pathology, 1996, v. 179, n. 2, p. 162, doi. 10.1002/(SICI)1096-9896(199606)179:2<162::AID-PATH545>3.0.CO;2-0
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Aberrant expression of the tumour suppressor gene p53 is very frequent in Wilms' tumours.
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- Journal of Pathology, 1992, v. 168, n. 2, p. 237, doi. 10.1002/path.1711680213
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A model of BCR- FGFR1 driven human AML in immunocompromised mice.
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- British Journal of Haematology, 2016, v. 175, n. 3, p. 542, doi. 10.1111/bjh.13877
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- Article
Selective inactivation of LGI1 in neuronal precursor cells leads to cortical dysplasia in mice.
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- Genesis: The Journal of Genetics & Development, 2019, v. 57, n. 2, p. N.PAG, doi. 10.1002/dvg.23268
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- Article
Acute Progression of BCR-FGFR1 Induced Murine BLympho/Myeloproliferative Disorder Suggests Involvement of Lineages at the Pro-B Cell Stage.
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- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038265
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Loss of Zebrafish lgi1b Leads to Hydrocephalus and Sensitization to Pentylenetetrazol Induced Seizure-Like Behavior.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024596
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Analysis of Wilms Tumors Using SNP Mapping Array-Based Comparative Genomic Hybridization.
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- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018941
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Homozygous inactivation of the LGI1 gene results in hypomyelination in the peripheral and central nervous systems.
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- Journal of Neuroscience Research, 2010, v. 88, n. 15, p. 3328, doi. 10.1002/jnr.22496
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Transgelin increases metastatic potential of colorectal cancer cells in vivo and alters expression of genes involved in cell motility.
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- BMC Cancer, 2016, v. 16, p. 1, doi. 10.1186/s12885-016-2105-8
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A truncated derivative of FGFR1 kinase cooperates with FLT3 and KIT to transform hematopoietic stem cells in syndromic and de novo AML.
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- Molecular Cancer, 2022, v. 21, n. 1, p. 1, doi. 10.1186/s12943-022-01628-3
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IRAK1-regulated IFN-γ signaling induces MDSC to facilitate immune evasion in FGFR1-driven hematological malignancies.
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- Molecular Cancer, 2021, v. 20, n. 1, p. 1, doi. 10.1186/s12943-021-01460-1
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Phosphorylation of the SSBP2 and ABL proteins by the ZNF198-FGFR1 fusion kinase seen in atypical myeloproliferative disorders as revealed by phosphopeptide-specific MS.
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- Proteomics, 2009, v. 9, n. 16, p. 3979, doi. 10.1002/pmic.200800852
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HSPA1A is an important regulator of the stability and function of ZNF198 and its oncogenic derivative, ZNF198-FGFR1.
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- Journal of Cellular Biochemistry, 2007, v. 102, n. 5, p. 1308, doi. 10.1002/jcb.21362
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CLCA2 tumour suppressor gene in 1p31 is epigenetically regulated in breast cancer.
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- Oncogene, 2004, v. 23, n. 7, p. 1474, doi. 10.1038/sj.onc.1207249
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Manipulation of nonsense mediated decay identifies gene mutations in colon cancer Cells with microsatellite instability.
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- Oncogene, 2004, v. 23, n. 3, p. 639, doi. 10.1038/sj.onc.1207178
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Suppression of the cell proliferation and invasion phenotypes in glioma cells by the LGI1 gene.
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- Oncogene, 2003, v. 22, n. 26, p. 3985, doi. 10.1038/sj.onc.1206584
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ZNF198 protein, involved in rearrangement in myeloproliferative disease, forms complexes with the DNA repair-associated HHR6A/6B and RAD18 proteins.
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- Oncogene, 2003, v. 22, n. 22, p. 3417, doi. 10.1038/sj.onc.1206408
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- Article
WAVE3, an actin-polymerization gene, is truncated and inactivated as a result of a constitutional t(1;13)(q21;q12) chromosome translocation in a patient with ganglioneuroblastoma.
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- Oncogene, 2002, v. 21, n. 38, p. 5967, doi. 10.1038/sj.onc.1205734
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A novel member of the WD-repeat gene family, WDR11, maps to the 10q26 region and is disrupted by a chromosome translocation in human glioblastoma cells.
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- Oncogene, 2001, v. 20, n. 38, p. 5378, doi. 10.1038/sj.onc.1204694
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Primary tumor-induced immunity eradicates disseminated tumor cells in syngeneic mouse model.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09015-1
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The temporal and spatial expression pattern of the LGI1 epilepsy predisposition gene during mouse embryonic cranial development.
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- BMC Neuroscience, 2011, v. 12, n. 1, p. 43, doi. 10.1186/1471-2202-12-43
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TTC4, a novel candidate tumor suppressor gene at 1p31 is often mutated in malignant melanoma of the skin.
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- Oncogene, 2000, v. 19, n. 50, p. 5817, doi. 10.1038/sj.onc.1203961
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A transcription map of the minimally deleted region from 13q14 in B-cell chronic lymphocytic leukemia as defined by large scale sequencing of the 650 kb critical region.
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- Oncogene, 2000, v. 19, n. 50, p. 5772, doi. 10.1038/sj.onc.1203978
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Cloning of TACC1, an embryonically expressed, potentially transforming coiled coil containing gene, from the 8p11 breast cancer amplicon.
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- Oncogene, 1999, v. 18, n. 27, p. 4032, doi. 10.1038/sj.onc.1202801
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A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors.
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- Oncogene, 1998, v. 17, n. 22, p. 2873, doi. 10.1038/sj.onc.1202481
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Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.
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- Oncogene, 1998, v. 17, n. 3, p. 395, doi. 10.1038/sj.onc.1201927
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A novel missense mutation in patients from a retinoblastoma pedigree showing only mild expression of the tumor phenotype.
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- Oncogene, 1998, v. 16, n. 24, p. 3211, doi. 10.1038/sj.onc.1201833
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Targeted therapy of human malignant glioma in a mouse model by 2-5A antisense directed against telomerase RNA.
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- Oncogene, 1998, v. 16, n. 25, p. 3323, doi. 10.1038/sj.onc.1201885
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Inhibition of telomerase increases the susceptibility of human malignant glioblastoma cells to cisplatin-induced apoptosis.
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- Oncogene, 1998, v. 16, n. 17, p. 2243, doi. 10.1038/sj.onc.1201754
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Cloning of the human Gfi-1 gene and its mapping to chromosome region 1p22.
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- Oncogene, 1997, v. 14, n. 8, p. 1003, doi. 10.1038/sj.onc.1200910
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- Article
Critical role of the WASF3 gene in JAK2/STAT3 regulation of cancer cell motility.
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- Carcinogenesis, 2013, v. 34, n. 9, p. 1994, doi. 10.1093/carcin/bgt167
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Monocytic and granulocytic myeloid derived suppressor cells differentially regulate spatiotemporal tumour plasticity during metastatic cascade.
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- Nature Communications, 2017, v. 8, n. 4, p. 14979, doi. 10.1038/ncomms14979
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Homozygous Deletion of the LGI1 Gene in Mice Leads to Developmental Abnormalities Resulting in Cortical Dysplasia.
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- Brain Pathology, 2015, v. 25, n. 5, p. 587, doi. 10.1111/bpa.12225
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Genome Wide Copy Number Abnormalities in Pediatric Medulloblastomas as Assessed by Array Comparative Genome Hybridization.
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- Brain Pathology, 2007, v. 17, n. 3, p. 282, doi. 10.1111/j.1750-3639.2007.00072.x
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Critical individual roles of the BCR and FGFR1 kinase domains in BCR‐FGFR1‐driven stem cell leukemia/lymphoma syndrome.
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- International Journal of Cancer, 2020, v. 146, n. 8, p. 2243, doi. 10.1002/ijc.32665
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Mutation in the FGFR1 tyrosine kinase domain or inactivation of PTEN is associated with acquired resistance to FGFR inhibitors in FGFR1-driven leukemia/lymphomas.
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- International Journal of Cancer, 2017, v. 141, n. 9, p. 1822, doi. 10.1002/ijc.30848
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Development of ZMYM2-FGFR1 driven AML in human CD34+ cells in immunocompromised mice.
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- International Journal of Cancer, 2016, v. 139, n. 4, p. 836, doi. 10.1002/ijc.30100
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- Article
HIF1A induces expression of the WASF3 metastasis-associated gene under hypoxic conditions.
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- International Journal of Cancer, 2012, v. 131, n. 6, p. E905, doi. 10.1002/ijc.27631
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Functional interrelationship between the WASF3 and KISS1 metastasis-associated genes in breast cancer cells.
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- International Journal of Cancer, 2011, v. 129, n. 12, p. 2825, doi. 10.1002/ijc.25964
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Promotion of invasion by mutant RAS is dependent on activation of the WASF3 metastasis promoter gene.
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- Genes, Chromosomes & Cancer, 2017, v. 56, n. 6, p. 493, doi. 10.1002/gcc.22453
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Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 2008, v. 47, n. 3, p. 221, doi. 10.1002/gcc.20524
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Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 10, p. 875, doi. 10.1002/gcc.20474
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Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 1, p. 53, doi. 10.1002/gcc.20388
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Array CGH analysis of pediatric medulloblastomas.
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 3, p. 290, doi. 10.1002/gcc.20292
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Novel amplicons on the short arm of chromosome 7 identified using high resolution array CGH contain over expressed genes in addition to EGFR in glioblastoma multiforme.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 4, p. 392, doi. 10.1002/gcc.20256
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Genomic profiling of myeloid sarcoma by array comparative genomic hybridizationA part of this work was presented at Oncogenomics meeting: Dissecting cancer through genome research, San Diego, California, 2005.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 4, p. 373, doi. 10.1002/gcc.20239
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Identification of consistent novel submegabase deletions in low-grade oligodendrogliomas using array-based comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 1, p. 85, doi. 10.1002/gcc.20218
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Molecular characterization of a 7p15-21 homozygous deletion in a Wilms tumor.
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- Genes, Chromosomes & Cancer, 2003, v. 36, n. 1, p. 1, doi. 10.1002/gcc.10133
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Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 160, doi. 10.1002/(SICI)1098-2264(199802)21:2<160::AID-GCC12>3.0.CO;2-V
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