about
A nine-nucleotide deletion and splice variation in the coding region of the interferon induced ISG12 geneFamilial cancer associated with a polymorphism in ARLTS1Identification and characterization of locus-specific methylation patterns within novel loci undergoing hypermethylation during breast cancer pathogenesis.Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer.Identification and validation of highly frequent CpG island hypermethylation in colorectal adenomas and carcinomas.Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1 alpha subunit.Competitive amplification of differentially melting amplicons (CADMA) improves KRAS hotspot mutation testing in colorectal cancerImproved reproducibility in genome-wide DNA methylation analysis for PAXgene-fixed samples compared with restored formalin-fixed and paraffin-embedded DNA.Genotyping common FSHR polymorphisms based on competitive amplification of differentially melting amplicons (CADMA)Methylation of cancer related genes in tumor and peripheral blood DNA from the same breast cancer patient as two independent events.Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors.Identification of accurate reference genes for RT-qPCR analysis of formalin-fixed paraffin-embedded tissue from primary non-small cell lung cancers and brain and lymph node metastases.Competitive amplification of differentially melting amplicons (CADMA) enables sensitive and direct detection of all mutation types by high-resolution melting analysis.Increased sensitivity of KRAS mutation detection by high-resolution melting analysis of COLD-PCR products.No difference in the frequency of locus-specific methylation in the peripheral blood DNA of women diagnosed with breast cancer and age-matched controls.Hypomethylation and increased expression of the putative oncogene ELMO3 are associated with lung cancer development and metastases formation.Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutationsELMO3: a direct driver of cancer metastasis?Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha gene.Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients.Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu.Author's reply: To PMID 23159593.Assignment of the human translation termination factor 1 (ETF1) to 5q31.1 and of the proximal marker D5S1995 by radiation hybrid mapping.Chromosome 1q25.3 copy number alterations in primary breast cancers detected by multiplex ligation-dependent probe amplification and allelic imbalance assays and its comparison with fluorescent in situ hybridization assays.A role for immunohistochemical detection of BRAF V600E prior to BRAF-inhibitor treatment of malignant melanoma?The influence of DNA degradation in formalin-fixed, paraffin-embedded (FFPE) tissue on locus-specific methylation assessment by MS-HRMEffect of the FSH receptor single nucleotide polymorphisms (FSHR 307/680) on the follicular fluid hormone profile and the granulosa cell gene expression in human small antral folliclesComprehensive Genome Methylation Analysis in Bladder Cancer: Identification and Validation of Novel Methylated Genes and Application of These as Urinary Tumor MarkersHigh-Resolution Melting Analysis for Mutation Screening of RGSL1, RGS16, and RGS8 in Breast CancerLOH rather than genotypes ofTP53codon 72 is associated with disease-free survival in primary breast cancerAllelic imbalance in selected chromosomal regions in ovarian cancerTP53 mutation is an independent prognostic marker for poor outcome in both node-negative and node-positive breast cancerAllelic loss of 16q23.2-24.2 is an independent marker of good prognosis in primary breast cancerMolecular genetic analysis of easily accessible breast tumour DNA, purified from tissue left over from hormone receptor measurementRefined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysisPyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunitPublisher Correction: Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutationsSensitive and fast mutation detection by solid phase chemical cleavage
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Lise Lotte Hansen
@ast
Lise Lotte Hansen
@en
Lise Lotte Hansen
@es
Lise Lotte Hansen
@nl
Lise Lotte Hansen
@sl
type
label
Lise Lotte Hansen
@ast
Lise Lotte Hansen
@en
Lise Lotte Hansen
@es
Lise Lotte Hansen
@nl
Lise Lotte Hansen
@sl
prefLabel
Lise Lotte Hansen
@ast
Lise Lotte Hansen
@en
Lise Lotte Hansen
@es
Lise Lotte Hansen
@nl
Lise Lotte Hansen
@sl
P1053
I-3377-2016
P106
P21
P2798
P31
P3829
P496
0000-0001-7915-2506