Pages that link to "Q55485308"
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The following pages link to A cytogenetic study of 53 human gliomas. (Q55485308):
Displaying 50 items.
- Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 (Q24313491) (← links)
- Molecular cloning and functional analysis of the adenovirus E1A-associated 300-kD protein (p300) reveals a protein with properties of a transcriptional adaptor (Q28286827) (← links)
- Chromosome studies of solid tumours (Q30499067) (← links)
- Non‐isotopic molecular cytogenetics in neuro‐oncology (Q32126669) (← links)
- Oligodendroglial tumors: diagnostic and molecular pathology (Q33699159) (← links)
- Karyotype studies in 18 ependymomas with literature review of 107 cases (Q33718650) (← links)
- Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma (Q33871385) (← links)
- Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma (Q34085362) (← links)
- A review of the cytogenetics of 58 pediatric brain tumors (Q34457479) (← links)
- Genetic imbalances in pleomorphic xanthoastrocytoma detected by comparative genomic hybridization and literature review (Q34500804) (← links)
- Cellular mechanisms targeted during astrocytoma progression (Q34983621) (← links)
- Cytogenetic and FISH studies in myelodysplasia, acute myeloid leukemia, chronic lymphocytic leukemia and lymphoma (Q34996228) (← links)
- Near-haploid clones in a malignant fibrous histiocytoma (Q35229187) (← links)
- Brain tumours: classification and genes (Q35576526) (← links)
- Genetic profile of gliosarcomas (Q35745419) (← links)
- Near-haploidy and subsequent polyploidization characterize the progression of peripheral chondrosarcoma. (Q35829605) (← links)
- Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p (Q35834029) (← links)
- Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses (Q35834190) (← links)
- Molecular pathogenesis of astrocytic tumours (Q36021558) (← links)
- Purine and pyrimidine metabolism in human gliomas: relation to chromosomal aberrations (Q36079980) (← links)
- Medulloblastoma: II. A pathobiologic overview (Q36340011) (← links)
- Cytogenetics and Molecular Genetics of Malignant Gliomas and Medulloblastoma (Q36476788) (← links)
- BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas (Q36532504) (← links)
- Genetic alterations in glioma and medulloblastoma (Q36941609) (← links)
- Genomic analysis of pilocytic astrocytomas at 0.97 Mb resolution shows an increasing tendency toward chromosomal copy number change with age. (Q37386688) (← links)
- A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature. (Q37672406) (← links)
- The potential of carboxypeptidase M as a therapeutic target in cancer (Q38072098) (← links)
- Coamplification on chromosomes 7p12-13 and 9q12-13 identified by reverse chromosome painting in a glioblastoma multiforme (Q38511330) (← links)
- High-resolution, dual-platform aCGH analysis reveals frequent HIPK2 amplification and increased expression in pilocytic astrocytomas. (Q39992412) (← links)
- Genetics of primary brain tumors: a review (Q40686977) (← links)
- Identification of uncommon chromosomal aberrations in the neuroglioma cell line H4 by spectral karyotyping (Q40785730) (← links)
- Genomic changes in glioblastoma cell lines detected by comparative genomic hybridization (Q40864844) (← links)
- The molecular biology of ependymomas (Q40898736) (← links)
- Deletion mapping of the long arm of chromosome 10 in glioblastoma multiforme (Q41075821) (← links)
- Molecular biology of pediatric gliomas (Q41131665) (← links)
- Interphase cytogenetic analysis of solid tumors by non-isotopic DNA in situ hybridization (Q41236837) (← links)
- Morphologic, immunologic, biochemical, and cytogenetic characteristics of the human glioblastoma-derived cell line, SNB-19. (Q41300723) (← links)
- Enhanced MYCN expression and isochromosome 17q in pineoblastoma cell lines (Q41492646) (← links)
- Karyotype analyses of 20 human glioma cell lines (Q41499235) (← links)
- Changes in glial fibrillary acidic protein and karyotype during culturing of two cell lines established from human glioblastoma multiforme (Q41678069) (← links)
- Near Haploidy in Breast Cancer: A Particular Pathway of Chromosome Evolution (Q41733205) (← links)
- Investigation of genetic alterations associated with the grade of astrocytic tumor by comparative genomic hybridization (Q41749107) (← links)
- Multiple deleted regions on the long arm of chromosome 6 in astrocytic tumours (Q41903586) (← links)
- Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma (Q42060909) (← links)
- Cytogenetic studies in 45 pediatric brain tumors (Q42130694) (← links)
- Chromosomal characteristics of childhood brain tumors (Q42815862) (← links)
- A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines (Q42820697) (← links)
- Interphase cytogenetics of brain tumors (Q43537352) (← links)
- Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas (Q43960135) (← links)
- Detection of multiple gains and losses of genetic material in ten glioma cell lines by comparative genomic hybridization. (Q46416397) (← links)