about
Effects of THBS3, SPARC and SPP1 expression on biological behavior and survival in patients with osteosarcomaChromosomal mapping of the human and murine orphan receptors ERRalpha (ESRRA) and ERRbeta (ESRRB) and identification of a novel human ERRalpha-related pseudogeneThe human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2- N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant proteinCloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13Three-color FISH analysis of TMPRSS2/ERG fusions in prostate cancer indicates that genomic microdeletion of chromosome 21 is associated with rearrangementA method for accurate detection of genomic microdeletions using real-time quantitative PCR.Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for MolecularFISH analysis of 107 prostate cancers shows that PTEN genomic deletion is associated with poor clinical outcome.Identification of human brain tumour initiating cellsMapping of the gene encoding the integrin-linked kinase, ILK, to human chromosome 11p15.5-p15.4Profiling genomic copy number changes in retinoblastoma beyond loss of RB1Structural characterization and mapping of the normal epithelial cell-specific 1 geneLocalization of the interferon-induced, 2-5A-dependent RNase gene (RNS4) to human chromosome 1q25Localization of the human interferon-induced, ds-RNA activated p68 kinase gene (PRKR) to chromosome 2p21-p22Cytosolic phospholipase A2 gene in human and rat: chromosomal localization and polymorphic markersA heat shock gene at 14q22: mapping and expressionSmoking-induced chromosomal segregation anomalies identified by FISH analysis of spermMurine Pif1 interacts with telomerase and is dispensable for telomere function in vivoLats2/Kpm is required for embryonic development, proliferation control and genomic integrityPlk4 is required for cytokinesis and maintenance of chromosomal stability.Identification of a novel zinc finger gene, zf5-3, as a potential mediator of neuroblastoma differentiation.Use of whole genome amplification and comparative genomic hybridisation to detect chromosomal copy number alterations in cell line material and tumour tissue.Resolution of genotypic heterogeneity in prostate tumors using polymerase chain reaction and comparative genomic hybridization on microdissected carcinoma and prostatic intraepithelial neoplasia foci.p53 Alteration and chromosomal instability in prostatic high-grade intraepithelial neoplasia and concurrent carcinoma: analysis by immunohistochemistry, interphase in situ hybridization, and sequencing of laser-captured microdissected specimens.The use of whole genome amplification to study chromosomal changes in prostate cancer: insights into genome-wide signature of preneoplasia associated with cancer progression.Amplification of telomerase (hTERT) gene is a poor prognostic marker in non-small-cell lung cancerLarge scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasiaGenomic alterations in sporadic synchronous primary breast cancer using array and metaphase comparative genomic hybridization.Sister chromatid exchange.In vitro analysis of integrated global high-resolution DNA methylation profiling with genomic imbalance and gene expression in osteosarcoma.Complex Mosaic Ring Chromosome 11 Associated with Hemizygous Loss of 8.6 Mb of 11q24.2qter in Atypical Jacobsen Syndrome.Expression analysis of genes associated with human osteosarcoma tumors shows correlation of RUNX2 overexpression with poor response to chemotherapy.Digital expression profiling identifies RUNX2, CDC5L, MDM2, RECQL4, and CDK4 as potential predictive biomarkers for neo-adjuvant chemotherapy response in paediatric osteosarcoma.Recurrent anomalies of 6q25 in chondromyxoid fibroma.Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia.Role of Pirh2 in mediating the regulation of p53 and c-Myc.Prkar1a is an osteosarcoma tumor suppressor that defines a molecular subclass in miceAssociation of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome.Measles virus replication in lymphatic cells and organs of CD150 (SLAM) transgenic mice.Mutations in SUFU predispose to medulloblastoma.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jeremy A Squire
@nl
Jeremy A Squire
@sl
Jeremy A. Squire
@en
Jeremy A. Squire
@es
type
label
Jeremy A Squire
@nl
Jeremy A Squire
@sl
Jeremy A. Squire
@en
Jeremy A. Squire
@es
altLabel
JA Squire
@en
prefLabel
Jeremy A Squire
@nl
Jeremy A Squire
@sl
Jeremy A. Squire
@en
Jeremy A. Squire
@es
P1053
A-9352-2012
P106
P1153
7102094488
P21
P31
P3829
P496
0000-0002-9863-468X