| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0165-4608(96)00404-9 |
| P698 | PubMed publication ID | 9283596 |
| P50 | author | Henry Seth Friedman | Q73422966 |
| P2093 | author name string | McLendon RE | |
| McKeever PE | |||
| Bigner SH | |||
| Fuchs H | |||
| P2860 | cites work | Allelic status of chromosome 1 in neoplasms of the nervous system. | Q55480525 |
| Cytogenetic analysis of 109 pediatric central nervous system tumors. | Q55482615 | ||
| Ring chromosome 12 resulting from nonrandom telomeric associations with the short arm of chromosome 15 in a cerebellar astrocytoma. | Q55482696 | ||
| Chromosomes in the genesis and progression of ependymomas. | Q55482716 | ||
| Isochromosome 17q in primitive neuroectodermal tumors of the central nervous system. | Q55485038 | ||
| A cytogenetic study of 53 human gliomas. | Q55485308 | ||
| Trisomy 7 and sex chromosome loss in human brain tissue | Q69456029 | ||
| Prognostic implications of chromosome 17p deletions in human medulloblastomas | Q70790944 | ||
| Microsatellite analysis of childhood brain tumors | Q71574842 | ||
| Cytogenetics of malignant gliomas: I. The autosomes with reference to rearrangements | Q71581364 | ||
| Cytogenetics of malignant gliomas. II. The sex chromosomes with reference to X isodisomy and the role of numerical X/Y changes | Q71581412 | ||
| Chromosome analysis of brain tumors in childhood | Q71678473 | ||
| Chromosomal abnormalities in 47 pediatric brain tumors | Q71916756 | ||
| Correlation of cytogenetic and fluorescence in situ hybridization (FISH) studies in normal and gliotic brain | Q72182693 | ||
| Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood | Q28270587 | ||
| Functional evidence for a second tumor suppressor gene on human chromosome 17. | Q36643971 | ||
| The new WHO classification of brain tumours | Q40807273 | ||
| Chromosome aberrations in four ependymomas | Q41464560 | ||
| Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas | Q41489842 | ||
| Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma | Q42060909 | ||
| Cytogenetic studies in 45 pediatric brain tumors | Q42130694 | ||
| Chromosome abnormalities in low-grade central nervous system tumors | Q43421068 | ||
| Cytogenetic Studies of Pediatric Brain and Spinal Cord Tumors | Q43917961 | ||
| Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas | Q43960135 | ||
| Chromosomal patterns in human malignant astrocytomas | Q44760395 | ||
| N-myc and c-myc oncogenes amplification in medulloblastomas. Evidence of particularly aggressive behavior of a tumor with c-myc amplification. | Q45118490 | ||
| Deletion of chromosome arm 17p DNA sequences in pediatric high-grade and juvenile pilocytic astrocytomas. | Q45970212 | ||
| Cytogenetic analysis of 39 pediatric central nervous system tumors | Q46144100 | ||
| Deletion mapping of the medulloblastoma locus on chromosome 17p. | Q46677766 | ||
| Structural chromosomal abnormalities in human medulloblastoma | Q48125276 | ||
| Chromosomal composition of a series of 22 human low-grade gliomas | Q48173952 | ||
| Gliosis specimens contain clonal cytogenetic abnormalities | Q48288638 | ||
| Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors | Q48415494 | ||
| Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo‐astrocytomas | Q48417497 | ||
| Telomeric associations evolving to ring chromosomes in a recurrent pleomorphic xanthoastrocytoma | Q48473092 | ||
| Karyotypes in 90 human gliomas | Q48538978 | ||
| Trisomy 7 and sex chromosome loss need not be representative of tumor parenchyma cells in malignant glioma | Q48636527 | ||
| Monosomy 22 in rhabdoid or atypical tumors of the brain | Q48868477 | ||
| Loss of genetic information in central nervous system tumors common to children and young adults | Q48946826 | ||
| Accumulation of chromosomal changes in human glioma progression. A cytogenetic study of 50 cases. | Q51047176 | ||
| Involvement of chromosome 22 in ependymomas. | Q53012981 | ||
| Cytogenetic abnormalities in human ependymomas. | Q53512892 | ||
| P4510 | describes a project that uses | D721 Med | Q54817251 |
| P433 | issue | 2 | |
| P921 | main subject | cell line | Q21014462 |
| P304 | page(s) | 125-134 | |
| P577 | publication date | 1997-09-01 | |
| P1433 | published in | Cancer Genetics and Cytogenetics | Q15753061 |
| P1476 | title | Chromosomal characteristics of childhood brain tumors | |
| P478 | volume | 97 |
| Q34457479 | A review of the cytogenetics of 58 pediatric brain tumors |
| Q55467648 | An update on mouse brain tumor models in cancer drug discovery. |
| Q37143958 | Antiangiogenic strategies in medulloblastoma: reality or mystery. |
| Q36532504 | BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas |
| Q24658389 | Biological background of pediatric medulloblastoma and ependymoma: a review from a translational research perspective |
| Q35576526 | Brain tumours: classification and genes |
| Q55475143 | Chemosensitivity in childhood brain tumours in vitro: evidence of differential sensitivity to lomustine (CCNU) and vincristine. |
| Q48264502 | Chromosomal aberrations detected by comparative genomic hybridization (CGH) in human astrocytic tumors |
| Q36477098 | Chromosomal variation in mammalian neuronal cells: known facts and attractive hypotheses |
| Q33871385 | Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma |
| Q34783428 | Classifying the medulloblastoma: insights from morphology and molecular genetics |
| Q49090427 | Clinicopathological features and global genomic copy number alterations of pilomyxoid astrocytoma in the hypothalamus/optic pathway: comparative analysis with pilocytic astrocytoma using array-based comparative genomic hybridization |
| Q36620330 | Comparative genomic hybridization and histological variation in primitive neuroectodermal tumours |
| Q48484979 | Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas. |
| Q48353225 | Constitutional t(16;22)(p13.3;q11.2 approximately 12) in a primitive neuroectodermal tumor of the pineal region |
| Q48355116 | Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation. |
| Q33433941 | Cytogenetic findings in a rare pediatric mixed glioneuronal tumor and review of the literature |
| Q30454402 | Detection of human neurotropic JC virus DNA sequence and expression of the viral oncogenic protein in pediatric medulloblastomas |
| Q38089818 | Diagnosis of childhood astrocytomas |
| Q33772206 | Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion gene |
| Q28360514 | Expression of a human polyomavirus oncoprotein and tumour suppressor proteins in medulloblastomas |
| Q34085362 | Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma |
| Q55475253 | Gains and losses of DNA sequences in childhood brain tumors analyzed by comparative genomic hybridization. |
| Q55476452 | Genetic alterations in pediatric high-grade astrocytomas. |
| Q48112393 | Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability. |
| Q35133413 | Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma |
| Q84475591 | Genomic aberrations in pediatric gliomas and embryonal tumors |
| Q37386688 | Genomic analysis of pilocytic astrocytomas at 0.97 Mb resolution shows an increasing tendency toward chromosomal copy number change with age. |
| Q52144741 | Glioblastoma in long-term survivors of acute lymphoblastic leukemia: Report of two cases. |
| Q42520955 | Histological features and expression of enzymes implicated in melatonin synthesis in pineal parenchymal tumours and in cultured tumoural pineal cells |
| Q48623214 | Human medulloblastomas lack point mutations and homozygous deletions of the hSNF5/INI1 tumour suppressor gene |
| Q55474476 | Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults. |
| Q38462467 | Imbalances of chromosome 17 in medulloblastomas determined by comparative genomic hybridisation and fluorescence in situ hybridisation |
| Q26738711 | In vitro models of medulloblastoma: Choosing the right tool for the job |
| Q39938042 | Integrated molecular analysis suggests a three-class model for low-grade gliomas: a proof-of-concept study |
| Q55473638 | Interphase fluorescence in situ hybridization and DNA flow cytometry analysis of medulloblastomas with a normal karyotype. |
| Q35751428 | KIAA1549: BRAF Gene Fusion and FGFR1 Hotspot Mutations Are Prognostic Factors in Pilocytic Astrocytomas |
| Q55472199 | Karyotypic evolution pathways in medulloblastoma/primitive neuroectodermal tumor determined with a combination of spectral karyotyping, G-banding, and fluorescence in situ hybridization. |
| Q38569310 | Low Grade Gliomas in Children. |
| Q48494872 | Low-grade astrocytoma in a child with encephalocraniocutaneous lipomatosis. |
| Q24683906 | Microarray analysis of pediatric ependymoma identifies a cluster of 112 candidate genes including four transcripts at 22q12.1-q13.3 |
| Q56673183 | Microarray analysis of pediatric ependymoma identifies a cluster of 112 candidate genes including four transcripts at 22q12.1-q13.3 |
| Q35104265 | Molecular abnormalities and correlations with tumor response and outcome in glioma patients |
| Q34478051 | Molecular genetics of pineal region neoplasms |
| Q36021558 | Molecular pathogenesis of astrocytic tumours |
| Q36021571 | Molecular pathogenesis of childhood brain tumors |
| Q34578601 | Paediatric embryonic brain tumours. biological and clinical relevance of molecular genetic abnormalities |
| Q37533670 | Pediatric brain tumors: current treatment strategies and future therapeutic approaches |
| Q35842014 | Pediatric high-grade astrocytomas show chromosomal imbalances distinct from adult cases |
| Q34051368 | Pediatric low-grade gliomas |
| Q33847771 | Pediatric low-grade gliomas: how modern biology reshapes the clinical field |
| Q49150021 | Pilocytic astrocytomas do not show most of the genetic changes commonly seen in diffuse astrocytomas |
| Q34802431 | Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13. |
| Q36025403 | Recent advances in embryonal tumours of the central nervous system |
| Q55465502 | Subtelomeric analysis of pediatric astrocytoma: subchromosomal instability is a distinctive feature of pleomorphic xanthoastrocytoma. |
| Q34977333 | Survival following treatment for intracranial ependymoma: a review |
| Q35212566 | The Wnt signaling pathway in solid childhood tumors |
| Q37523394 | The genetic and epigenetic basis of ependymoma. |
Search more.