Found: 27
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Novel causative variants in Legius syndrome: SPRED1 Genotype spectrum expansion.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 12, p. 1, doi. 10.1002/ajmg.a.63824
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- Article
Genomic Analysis Made It Possible to Identify Gene-Driver Alterations Covering the Time Window between Diagnosis of Neuroblastoma 4S and the Progression to Stage 4.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 12, p. 6513, doi. 10.3390/ijms23126513
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- Article
Exosomes from Plasma of Neuroblastoma Patients Contain Doublestranded DNA Reflecting the Mutational Status of Parental Tumor Cells.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3667, doi. 10.3390/ijms22073667
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- Article
Role of GOLPH3 and TPX2 in Neuroblastoma DNA Damage Response and Cell Resistance to Chemotherapy.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 19, p. 4764, doi. 10.3390/ijms20194764
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- Article
Genomic coamplification of CDK4/MDM2/FRS2 is associated with very poor prognosis and atypical clinical features in neuroblastoma patients.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 5, p. 277, doi. 10.1002/gcc.22827
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- Article
Induction of Epithelial Mesenchimal Transition and Vasculogenesis in the Lenses of Dbl Oncogene Transgenic Mice.
- Published in:
- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0007058
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- Article
High frequency of development of B cell lymphoproliferation and diffuse large B cell lymphoma in Dbl knock-in mice.
- Published in:
- Journal of Molecular Medicine, 2011, v. 89, n. 5, p. 493, doi. 10.1007/s00109-010-0712-4
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- Article
19p loss is significantly enriched in older age neuroblastoma patients and correlates with poor prognosis.
- Published in:
- NPJ Genomic Medicine, 2020, v. 5, n. 1, p. 1, doi. 10.1038/s41525-020-0125-4
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- Publication type:
- Article
Multiple Genes with Potential Tumor Suppressive Activity Are Present on Chromosome 10q Loss in Neuroblastoma and Are Associated with Poor Prognosis.
- Published in:
- Cancers, 2023, v. 15, n. 7, p. 2035, doi. 10.3390/cancers15072035
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- Article
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213.
- Published in:
- Cancers, 2023, v. 15, n. 6, p. 1916, doi. 10.3390/cancers15061916
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- Article
A Simple, Test-Based Method to Control the Overestimation Bias in the Analysis of Potential Prognostic Tumour Markers.
- Published in:
- Cancers, 2023, v. 15, n. 4, p. 1188, doi. 10.3390/cancers15041188
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- Publication type:
- Article
High Grade of Amplification of Six Regions on Chromosome 2p in a Neuroblastoma Patient with Very Poor Outcome: The Putative New Oncogene TSSC1.
- Published in:
- Cancers, 2021, v. 13, n. 22, p. 5792, doi. 10.3390/cancers13225792
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- Publication type:
- Article
Enhancement of Neuroblastoma NK-Cell-Mediated Lysis through NF-kB p65 Subunit-Induced Expression of FAS and PVR, the Loss of Which Is Associated with Poor Patient Outcome.
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- Cancers, 2021, v. 13, n. 17, p. 4368, doi. 10.3390/cancers13174368
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- Article
Ezrin interacts with the tumor suppressor CHL1 and promotes neuronal differentiation of human neuroblastoma.
- Published in:
- PLoS ONE, 2020, v. 15, n. 12, p. 1, doi. 10.1371/journal.pone.0244069
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- Article
Molecular Genetics in Neuroblastoma Prognosis.
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- Children, 2021, v. 8, n. 6, p. 1, doi. 10.3390/children8060456
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- Article
Clinical and genetic analysis of patients with segmental overgrowth features and somatic mammalian target of rapamycin (mTOR) pathway disruption: Possible novel clinical issues.
- Published in:
- Birth Defects Research, 2022, v. 114, n. 20, p. 1440, doi. 10.1002/bdr2.2113
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- Article
The first case of mosaic MNX1 mutation in an adult female with features of Currarino syndrome.
- Published in:
- Birth Defects Research, 2021, v. 113, n. 15, p. 1161, doi. 10.1002/bdr2.1936
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- Publication type:
- Article
Abdominal rhabdoid tumor presenting with symptomatic spinal epidural compression in a newborn. A case report.
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- Frontiers in Pediatrics, 2024, p. 1, doi. 10.3389/fped.2023.1337760
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- Article
Neuroblastoma Cell Lines Are Refractory to Genotoxic Drug-Mediated Induction of Ligands for NK Cell-Activating Receptors.
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- 2018
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- Publication type:
- journal article
Roniciclib down-regulates stemness and inhibits cell growth by inducing nucleolar stress in neuroblastoma.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-69499-6
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- Article
Overexpression of H2AFX gene in neuroblastoma is associated with worse prognosis.
- Published in:
- Pediatric Blood & Cancer, 2024, v. 71, n. 9, p. 1, doi. 10.1002/pbc.31146
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- Publication type:
- Article
E2F3 gene expression is a potential negative prognostic marker for localised and MYCN not‐amplified neuroblastoma: Results of in silico analysis of 786 samples.
- Published in:
- Pediatric Blood & Cancer, 2022, v. 69, n. 10, p. 1, doi. 10.1002/pbc.29800
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- Article
Loss of whole chromosome X predicts prognosis of neuroblastoma patients with numerical genomic profile.
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- 2019
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- Publication type:
- journal article
The Over-Expression of E2F3 Might Serve as Prognostic Marker for Neuroblastoma Patients with Stage 4S Disease.
- Published in:
- Diagnostics (2075-4418), 2020, v. 10, n. 5, p. 315, doi. 10.3390/diagnostics10050315
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- Publication type:
- Article
Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity.
- Published in:
- Human Mutation, 2023, p. 1, doi. 10.1155/2023/3160653
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- Article
Neuroblastoma Patients' Outcome and Chromosomal Instability.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 21, p. 15514, doi. 10.3390/ijms242115514
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- Publication type:
- Article
Immunohistochemical analysis of PDK1, PHD3 and HIF-1α expression defines the hypoxic status of neuroblastoma tumors.
- Published in:
- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0187206
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- Publication type:
- Article