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Search Results to Olufunmilayo Olopade

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One or more keywords matched the following items that are connected to Olopade, Olufunmilayo

Item TypeName
Concept Chromosome Banding
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 2
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 8
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 3
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 14
Concept Chromosome Deletion
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 7
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 9
Concept Chromosome Breakpoints
Concept Chromosome Disorders
Concept Chromosome Aberrations
Concept Chromosomes, Human, Pair 16
Concept Chromosomes, Human, Pair 18
Concept Physical Chromosome Mapping
Academic Article Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia.
Academic Article Clinical, morphologic, and cytogenetic characteristics of 26 patients with acute erythroblastic leukemia.
Academic Article Generation of small insert genomic FISH probes with high signal intensity suitable for deletion mapping.
Academic Article Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer.
Academic Article The 9p21 region in bladder cancer cell lines: large homozygous deletion inactivate the CDKN2, CDKN2B and MTAP genes.
Academic Article Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996.
Academic Article Familial myeloid leukemia associated with loss of the long arm of chromosome 5.
Academic Article Scaffold-associated regions in the human type I interferon gene cluster on the short arm of chromosome 9.
Academic Article Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q.
Academic Article Alterations of the 9p21 and 9q33 chromosomal bands in clinical bladder cancer specimens by fluorescence in situ hybridization.
Academic Article Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas.
Academic Article Molecular-cytogenetic analysis of HER-2/neu gene in BRCA1-associated breast cancers.
Academic Article EDD, the human orthologue of the hyperplastic discs tumour suppressor gene, is amplified and overexpressed in cancer.
Academic Article Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types.
Academic Article BRCA1 promoter methylation in sporadic breast cancer is associated with reduced BRCA1 copy number and chromosome 17 aneusomy.
Academic Article Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer.
Academic Article No evidence for core-binding factor CBFbeta as a leukemia predisposing factor in chromosome 16q22-linked familial AML.
Academic Article Clinical, morphologic, and cytogenetic characteristics of patients with lymphoid malignancies characterized by both t(14;18)(q32;q21) and t(8;14)(q24;q32) or t(8;22)(q24;q11).
Academic Article Chromosome band 16q22-linked familial AML: exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphisms.
Academic Article Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.
Academic Article Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma.
Academic Article Refined mapping of genomic rearrangements involving the short arm of chromosome 9 in acute lymphoblastic leukemias and other hematologic malignancies.
Academic Article Construction of a 2.8-megabase yeast artificial chromosome contig and cloning of the human methylthioadenosine phosphorylase gene from the tumor suppressor region on 9p21.
Academic Article Detection of 9p deletions in leukemia cell lines by interphase fluorescence in situ hybridization with YAC-derived probes.
Academic Article p16 alterations and deletion mapping of 9p21-p22 in malignant mesothelioma.
Academic Article Breakpoint junctions of chromosome 9p deletions in two human glioma cell lines.
Academic Article Analysis of tumor suppressor gene on human chromosome 9 in mouse x human somatic cell hybrids.
Academic Article Detection of CDKN2 deletions in tumor cell lines and primary glioma by interphase fluorescence in situ hybridization.
Academic Article Homozygous loss of the interferon genes defines the critical region on 9p that is deleted in lung cancers.
Academic Article Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo-astrocytomas.
Academic Article Structure of the human type-I interferon gene cluster determined from a YAC clone contig.
Academic Article Genetic variation in IGFBP2 and IGFBP5 is associated with breast cancer in populations of African descent.
Academic Article Homozygous deletions within chromosomal bands 9p21-22 in bladder cancer.
Academic Article Mapping a putative tumor suppressor gene on chromosome 9 bands p21-p22 with microdissection probes.
Academic Article Searching for large genomic rearrangements of the BRCA1 gene in a Nigerian population.
Academic Article Increased p16 levels correlate with pRb alterations in human urothelial cells.
Academic Article Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia.
Academic Article Genomewide scan for loss of heterozygosity and chromosomal amplification in breast carcinoma using single-nucleotide polymorphism arrays.
Academic Article Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers.
Academic Article Tumor genome analysis includes germline genome: are we ready for surprises?
Academic Article Obituary: Janet Davison Rowley 1925-2013.
Academic Article Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Academic Article Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
Academic Article Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
Academic Article Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
Academic Article Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
Academic Article Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
Academic Article Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer.
Academic Article Characterizing Genetic Susceptibility to Breast Cancer in Women of African Ancestry.
Academic Article Identification of novel common breast cancer risk variants at the 6q25 locusĀ among Latinas.
Academic Article Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.

Search Criteria
  • Chromosomes Human Pair 7