Lista de obras - Lise Lotte Hansen - Dominio Público Uruguay

A nine-nucleotide deletion and splice variation in the coding region of the interferon induced ISG12 gene

artículo científico publicado en 2003

A role for immunohistochemical detection of BRAF V600E prior to BRAF-inhibitor treatment of malignant melanoma?

artículo científico publicado en 2013

Allelic imbalance in selected chromosomal regions in ovarian cancer

scientific article published on 01 November 2002

Allelic loss of 16q23.2-24.2 is an independent marker of good prognosis in primary breast cancer

artículo científico publicado en 1998

Assignment of the human translation termination factor 1 (ETF1) to 5q31.1 and of the proximal marker D5S1995 by radiation hybrid mapping

artículo científico publicado en 1999

Atheroprotective immunization with malondialdehyde-modified LDL is hapten specific and dependent on advanced MDA adducts: implications for development of an atheroprotective vaccine

artículo científico publicado en 2014

Author's reply: To PMID 23159593.

artículo científico publicado en 2013

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.

artículo científico publicado en 2012

Competitive amplification of differentially melting amplicons (CADMA) enables sensitive and direct detection of all mutation types by high-resolution melting analysis.

artículo científico publicado en 2011

Competitive amplification of differentially melting amplicons (CADMA) improves KRAS hotspot mutation testing in colorectal cancer

artículo científico publicado en 2012

Comprehensive Genome Methylation Analysis in Bladder Cancer: Identification and Validation of Novel Methylated Genes and Application of These as Urinary Tumor Markers

article

Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors

artículo científico publicado en 2015

ELMO3: a direct driver of cancer metastasis?

artículo científico publicado en 2014

Effect 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 follicles

article

Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations

artículo científico publicado en 2017

Evaluation of BRAF Mutation Testing Methodologies in Formalin-Fixed, Paraffin-Embedded Cutaneous Melanomas ⬇️

artículo científico publicado el 14 de noviembre de 2012

Familial cancer associated with a polymorphism in ARLTS1

artículo científico publicado en 2005

Genotyping common FSHR polymorphisms based on competitive amplification of differentially melting amplicons (CADMA)

artículo científico publicado en 2014

Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer

artículo científico publicado en 2008

Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients

artículo científico publicado en 2000

High-Resolution Melting Analysis for Mutation Screening of RGSL1, RGS16, and RGS8 in Breast Cancer

article

Hypomethylation and increased expression of the putative oncogene ELMO3 are associated with lung cancer development and metastases formation.

artículo científico publicado en 2014

IGHV1-69-encoded antibodies expressed in chronic lymphocytic leukemia react with malondialdehyde-acetaldehyde adduct, an immunodominant oxidation-specific epitope

artículo científico publicado en 2013

Identification and characterization of locus-specific methylation patterns within novel loci undergoing hypermethylation during breast cancer pathogenesis.

artículo científico publicado en 2014

Identification and validation of highly frequent CpG island hypermethylation in colorectal adenomas and carcinomas

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Improved reproducibility in genome-wide DNA methylation analysis for PAXgene-fixed samples compared with restored formalin-fixed and paraffin-embedded DNA.

artículo científico publicado en 2014

Increased sensitivity of KRAS mutation detection by high-resolution melting analysis of COLD-PCR products

artículo científico publicado en 2010

LOH rather than genotypes ofTP53codon 72 is associated with disease-free survival in primary breast cancer

artículo científico publicado en 2006

Methylation of cancer related genes in tumor and peripheral blood DNA from the same breast cancer patient as two independent events

artículo científico publicado en 2011

Molecular genetic analysis of easily accessible breast tumour DNA, purified from tissue left over from hormone receptor measurement

article

Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene

artículo científico publicado el 1 de enero de 1992

No difference in the frequency of locus-specific methylation in the peripheral blood DNA of women diagnosed with breast cancer and age-matched controls.

artículo científico publicado en 2011

Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha gene

artículo científico publicado en 1991

Publisher Correction: Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations

scientific article published in Scientific Reports

Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1 alpha subunit.

artículo científico publicado en 1994

Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit

scientific article published on 01 June 1993

Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysis

article

Sensitive and fast mutation detection by solid phase chemical cleavage

artículo científico publicado en 1996

Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu.

artículo científico publicado en 2015

TP53 mutation is an independent prognostic marker for poor outcome in both node-negative and node-positive breast cancer

artículo científico publicado en 2000

The influence of DNA degradation in formalin-fixed, paraffin-embedded (FFPE) tissue on locus-specific methylation assessment by MS-HRM

artículo científico publicado en 2015

The role of innate immunity in atherogenesis

artículo científico publicado en 2008

X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation

artículo científico publicado el 1 de enero de 1992

Lista de obras de Lise Lotte Hansen

A nine-nucleotide deletion and splice variation in the coding region of the interferon induced ISG12 gene

A role for immunohistochemical detection of BRAF V600E prior to BRAF-inhibitor treatment of malignant melanoma?

Allelic imbalance in selected chromosomal regions in ovarian cancer

Allelic loss of 16q23.2-24.2 is an independent marker of good prognosis in primary breast cancer

Assignment of the human translation termination factor 1 (ETF1) to 5q31.1 and of the proximal marker D5S1995 by radiation hybrid mapping

Atheroprotective immunization with malondialdehyde-modified LDL is hapten specific and dependent on advanced MDA adducts: implications for development of an atheroprotective vaccine

Author's reply: To PMID 23159593.

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.

Competitive amplification of differentially melting amplicons (CADMA) enables sensitive and direct detection of all mutation types by high-resolution melting analysis.

Competitive amplification of differentially melting amplicons (CADMA) improves KRAS hotspot mutation testing in colorectal cancer

Comprehensive Genome Methylation Analysis in Bladder Cancer: Identification and Validation of Novel Methylated Genes and Application of These as Urinary Tumor Markers

Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors

ELMO3: a direct driver of cancer metastasis?

Effect 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 follicles

Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations

Evaluation of BRAF Mutation Testing Methodologies in Formalin-Fixed, Paraffin-Embedded Cutaneous Melanomas ⬇️

Familial cancer associated with a polymorphism in ARLTS1

Genotyping common FSHR polymorphisms based on competitive amplification of differentially melting amplicons (CADMA)

Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer

Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients

High-Resolution Melting Analysis for Mutation Screening of RGSL1, RGS16, and RGS8 in Breast Cancer

Hypomethylation and increased expression of the putative oncogene ELMO3 are associated with lung cancer development and metastases formation.

IGHV1-69-encoded antibodies expressed in chronic lymphocytic leukemia react with malondialdehyde-acetaldehyde adduct, an immunodominant oxidation-specific epitope

Identification and characterization of locus-specific methylation patterns within novel loci undergoing hypermethylation during breast cancer pathogenesis.

Identification and validation of highly frequent CpG island hypermethylation in colorectal adenomas and carcinomas

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

Improved reproducibility in genome-wide DNA methylation analysis for PAXgene-fixed samples compared with restored formalin-fixed and paraffin-embedded DNA.

Increased sensitivity of KRAS mutation detection by high-resolution melting analysis of COLD-PCR products

LOH rather than genotypes ofTP53codon 72 is associated with disease-free survival in primary breast cancer

Methylation of cancer related genes in tumor and peripheral blood DNA from the same breast cancer patient as two independent events

Molecular genetic analysis of easily accessible breast tumour DNA, purified from tissue left over from hormone receptor measurement

Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene

No difference in the frequency of locus-specific methylation in the peripheral blood DNA of women diagnosed with breast cancer and age-matched controls.

Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha gene

Publisher Correction: Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations

Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1 alpha subunit.

Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit

Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysis

Sensitive and fast mutation detection by solid phase chemical cleavage

Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu.

TP53 mutation is an independent prognostic marker for poor outcome in both node-negative and node-positive breast cancer

The influence of DNA degradation in formalin-fixed, paraffin-embedded (FFPE) tissue on locus-specific methylation assessment by MS-HRM

The role of innate immunity in atherogenesis

X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation