about
Alterations of E-cadherin and beta-catenin in gastric cancerMutation analysis of the CHK2 gene in breast carcinoma and other cancersChromosomal assignment of retinoic acid receptor (RAR) genes in the human, mouse, and rat genomesIdentification of miRNAs in a liver of a human fetus by a modified method.Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinomaDrosophila homolog of the murine Int-1 protooncogene.Quantitative analysis of miRNA expression in several developmental stages of human livers.Molecular genetics of breast cancer progression.The Brca1 and Brca2 proteins and tumor pathogenesis.Quantitative analysis of miRNA expression in seven human foetal and adult organsSimilar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) mice.Multiple chromosomal rearrangements in a spontaneously arising t(6;7) rat immunocytoma juxtapose c-myc and immunoglobulin heavy chain sequences.Demethylation of the region around exon 2 of MLH1 gene in gastrointestinal cancer.Differences in c-myc and pvt-1 amplification in SEWA sarcoma sublines selected for adherent or non-adherent growth.High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancer.Loss of heterozygosity at the FHIT gene in different solid human tumours and its association with survival in colorectal cancer patients.Chromosome localization and expression pattern of Lmyc and Bmyc in murine embryonal carcinoma cells.Germline mutations in DNA repair and cell cycle checkpoint genes: consequential somatic gene alterations and genome instability.Analysis of chromosome alterations and the E-cadherin and FHIT genes in lobular breast cancer.Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2.High frequency of LOH at chromosome 18q in human breast cancer: association with high S-phase fraction and low progesterone receptor content.MicroRNA-451 suppresses tumor cell growth by down-regulating IL6R gene expression.Specific polypeptide differences in normal versus malignant human breast tissues by two-dimensional electrophoresis.Catabolite repressive effects of 5-thio-D-glucose on Saccharomyces cerevisiae.Deletions at the chromosome 3 common eliminated region 1 on 3p21.3 in human breast tumors.Isoenzyme pattern and subcellular localization of hexokinases in human breast cancer and nonpathological breast tissueThe effect of mismatch repair deficiency on tumourigenesis; microsatellite instability affecting genes containing short repeated sequencesReplication error in colorectal carcinoma: association with loss of heterozygosity at mismatch repair loci and clinicopathological variablesIdentification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: screening reveals low frequency in Icelandic breast cancer patientsHigh prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patientsLoss of heterozygosity on chromosome 9 in human breast cancer: Association with clinical variables and genetic changes at other chromosome regionsDifferent tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non-polyposis colon cancer traitMapping of chromosome-3 alterations in human breast-cancer using microsatellite PCR markers - correlation with clinical-variablesAltered expression of E-cadherin in breast cancerAmplification of c-myc and pvt-1 homologous sequences in acute nonlymphatic leukemiaReduced Fhit expression in sporadic and BRCA2-linked breast carcinomasSimilarities and differences in the regulation of N-myc and c-myc genes in murine embryonal carcinoma cellsRat c-raf oncogene is located on chromosome 4 and may be activated by sequences from chromosome 13
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P50
description
researcher, ORCID id # 0000-0003-4125-1714
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wetenschapper
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name
S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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prefLabel
S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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S Ingvarsson
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P214
P906
P106
P1153
7005702890
P214
P31
P496
0000-0003-4125-1714
P7859
viaf-63978094