Lista de obras - Ellen Heitzer - Dominio Público Uruguay

A Multi-Analyte Approach for Improved Sensitivity of Liquid Biopsies in Prostate Cancer

artículo científico publicado en 2020

A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients. Results from the regorafenib's liquid biopsy (RELAIS) translational biomarker phase II pilot study

artículo científico publicado en 2020

Adipocyte p53 coordinates the response to intermittent fasting by regulating adipose tissue immune cell landscape

artículo científico publicado en 2024

Changes in colorectal carcinoma genomes under anti-EGFR therapy identified by whole-genome plasma DNA sequencing.

artículo científico publicado en 2014

Circulating tumor DNA as a liquid biopsy for cancer

artículo científico publicado en 2014

Circulating tumor cells and DNA as liquid biopsies.

artículo científico publicado en 2013

Co-occurrence of MYC amplification and TP53 mutations in human cancer

artículo científico publicado en 2016

Comparison of three commercial decision support platforms for matching of next-generation sequencing results with therapies in patients with cancer

scientific article published on 01 September 2020

Complex tumor genomes inferred from single circulating tumor cells by array-CGH and next-generation sequencing

artículo científico publicado en 2013

Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors

scientific article published on 28 February 2020

Computer-based symptom assessment is feasible in patients with advanced cancer: results from an international multicenter study, the EPCRC-CSA.

artículo científico publicado en 2012

Depressed patients with incurable cancer: which depressive symptoms do they experience?

artículo científico publicado en 2013

Detection of Circulating Tumor DNA in the Blood of Cancer Patients: An Important Tool in Cancer Chemoprevention.

artículo científico publicado en 2016

Differential survival trends of stage II colorectal cancer patients relate to promoter methylation status of PCDH10, SPARC, and UCHL1.

artículo científico publicado en 2013

Establishment of clival chordoma cell line MUG-CC1 and lymphoblastoid cells as a model for potential new treatment strategies

artículo científico publicado en 2016

Establishment of tumor-specific copy number alterations from plasma DNA of patients with cancer.

artículo científico publicado en 2013

Expanded molecular profiling of myxofibrosarcoma reveals potentially actionable targets

artículo científico publicado en 2017

Exploring chromosomal abnormalities and genetic changes in uterine smooth muscle tumors

artículo científico publicado en 2016

Expression of the cancer-associated DNA polymerase ε P286R in fission yeast leads to translesion synthesis polymerase dependent hypermutation and defective DNA replication

artículo científico publicado en 2021

Extra phenotypic features in a girl with Miller syndrome

scientific article published on 01 April 2011

Facial dysmorphism associated with distinctive spine abnormalities in a girl and her mother

scientific article published on 01 October 2011

Functional Classification of TP53 Mutations in Acute Myeloid Leukemia

scientific article published on 10 March 2020

Genetic and epigenetic analysis of putative breast cancer stem cell models.

artículo científico publicado en 2013

Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X.

artículo científico publicado en 2014

Hematogenous dissemination of glioblastoma multiforme.

artículo científico publicado en 2014

High quality assessment of DNA methylation in archival tissues from colorectal cancer patients using quantitative high-resolution melting analysis

artículo científico publicado en 2009

Human melanoma brain metastases cell line MUG-Mel1, isolated clones and their detailed characterization

artículo científico publicado en 2019

Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection

scientific article published on 11 October 2019

Infrequent p53 gene mutation but UV gradient-like p53 protein positivity in keloids.

artículo científico publicado en 2012

Interviews with patients with advanced cancer--another step towards an international cancer pain classification system

artículo científico publicado en 2012

Lysyl oxidase-like 2 promoter hypermethylation in mid-dermal elastolysis

artículo científico publicado en 2016

Multiplex genetic cancer testing identifies pathogenic mutations in TP53 and CDH1 in a patient with bilateral breast and endometrial adenocarcinoma

artículo científico publicado en 2013

Neuropathic cancer pain: prevalence, severity, analgesics and impact from the European Palliative Care Research Collaborative-Computerised Symptom Assessment study

artículo científico publicado en 2012

Non-invasive detection of genome-wide somatic copy number alterations by liquid biopsies

artículo científico publicado en 2015

POLE mutations in families predisposed to cutaneous melanoma

artículo científico publicado en 2015

Polyclonality of multiple sporadic basal cell carcinomas.

artículo científico publicado en 2009

Preexisting TP53 mutation in therapy-related acute myeloid leukemia

artículo científico publicado en 2014

Primary patient-derived lung adenocarcinoma cell culture challenges the association of cancer stem cells with epithelial-to-mesenchymal transition.

artículo científico publicado en 2017

Publisher Correction: Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection

artículo científico publicado en 2020

Rapid Identification of Plasma DNA Samples with Increased ctDNA Levels by a Modified FAST-SeqS Approach.

artículo científico publicado en 2015

Rapid and reliable detection of LINE-1 hypomethylation using high-resolution melting analysis.

artículo científico

Shallow Whole-Genome Sequencing from Plasma Identifies FGFR1 Amplified Breast Cancers and Predicts Overall Survival

artículo científico publicado en 2020

Single circulating tumor cell sequencing for monitoring.

artículo científico publicado en 2013

Somatic TP53 mutations characterize preleukemic stem cells in acute myeloid leukemia.

artículo científico publicado en 2017

T1799A BRAF Mutation is Common in PUVA Lentigines

artículo científico publicado en 2006

TP53 mutated AML subclones exhibit engraftment in a humanized bone marrow ossicle mouse model

scientific article published on 30 January 2020

Technical Evaluation of Commercial Mutation Analysis Platforms and Reference Materials for Liquid Biopsy Profiling

scientific article published on 16 June 2020

The BRAF V600K mutation is more frequent than the BRAF V600E mutation in melanoma in situ of lentigo maligna type

artículo científico publicado en 2013

The dynamic range of circulating tumor DNA in metastatic breast cancer

artículo científico publicado en 2014

Tubuloids derived from human adult kidney and urine for personalized disease modeling

artículo científico publicado en 2019

Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing.

artículo científico publicado en 2013

Untargeted Assessment of Tumor Fractions in Plasma for Monitoring and Prognostication from Metastatic Breast Cancer Patients Undergoing Systemic Treatment

scientific article published on 14 August 2019

Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer.

artículo científico publicado en 2016

p14ARF Hypermethylation Is Common but INK4a-ARF Locus or p53 Mutations Are Rare in Merkel Cell Carcinoma

artículo científico publicado en 2008

Lista de obras de Ellen Heitzer

A Multi-Analyte Approach for Improved Sensitivity of Liquid Biopsies in Prostate Cancer

A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients. Results from the regorafenib's liquid biopsy (RELAIS) translational biomarker phase II pilot study

Adipocyte p53 coordinates the response to intermittent fasting by regulating adipose tissue immune cell landscape

Changes in colorectal carcinoma genomes under anti-EGFR therapy identified by whole-genome plasma DNA sequencing.

Circulating tumor DNA as a liquid biopsy for cancer

Circulating tumor cells and DNA as liquid biopsies.

Co-occurrence of MYC amplification and TP53 mutations in human cancer

Comparison of three commercial decision support platforms for matching of next-generation sequencing results with therapies in patients with cancer

Complex tumor genomes inferred from single circulating tumor cells by array-CGH and next-generation sequencing

Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors

Computer-based symptom assessment is feasible in patients with advanced cancer: results from an international multicenter study, the EPCRC-CSA.

Depressed patients with incurable cancer: which depressive symptoms do they experience?

Detection of Circulating Tumor DNA in the Blood of Cancer Patients: An Important Tool in Cancer Chemoprevention.

Differential survival trends of stage II colorectal cancer patients relate to promoter methylation status of PCDH10, SPARC, and UCHL1.

Establishment of clival chordoma cell line MUG-CC1 and lymphoblastoid cells as a model for potential new treatment strategies

Establishment of tumor-specific copy number alterations from plasma DNA of patients with cancer.

Expanded molecular profiling of myxofibrosarcoma reveals potentially actionable targets

Exploring chromosomal abnormalities and genetic changes in uterine smooth muscle tumors

Expression of the cancer-associated DNA polymerase ε P286R in fission yeast leads to translesion synthesis polymerase dependent hypermutation and defective DNA replication

Extra phenotypic features in a girl with Miller syndrome

Facial dysmorphism associated with distinctive spine abnormalities in a girl and her mother

Functional Classification of TP53 Mutations in Acute Myeloid Leukemia

Genetic and epigenetic analysis of putative breast cancer stem cell models.

Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X.

Hematogenous dissemination of glioblastoma multiforme.

High quality assessment of DNA methylation in archival tissues from colorectal cancer patients using quantitative high-resolution melting analysis

Human melanoma brain metastases cell line MUG-Mel1, isolated clones and their detailed characterization

Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection

Infrequent p53 gene mutation but UV gradient-like p53 protein positivity in keloids.

Interviews with patients with advanced cancer--another step towards an international cancer pain classification system

Lysyl oxidase-like 2 promoter hypermethylation in mid-dermal elastolysis

Multiplex genetic cancer testing identifies pathogenic mutations in TP53 and CDH1 in a patient with bilateral breast and endometrial adenocarcinoma

Neuropathic cancer pain: prevalence, severity, analgesics and impact from the European Palliative Care Research Collaborative-Computerised Symptom Assessment study

Non-invasive detection of genome-wide somatic copy number alterations by liquid biopsies

POLE mutations in families predisposed to cutaneous melanoma

Polyclonality of multiple sporadic basal cell carcinomas.

Preexisting TP53 mutation in therapy-related acute myeloid leukemia

Primary patient-derived lung adenocarcinoma cell culture challenges the association of cancer stem cells with epithelial-to-mesenchymal transition.

Publisher Correction: Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection

Rapid Identification of Plasma DNA Samples with Increased ctDNA Levels by a Modified FAST-SeqS Approach.

Rapid and reliable detection of LINE-1 hypomethylation using high-resolution melting analysis.

Shallow Whole-Genome Sequencing from Plasma Identifies FGFR1 Amplified Breast Cancers and Predicts Overall Survival

Single circulating tumor cell sequencing for monitoring.

Somatic TP53 mutations characterize preleukemic stem cells in acute myeloid leukemia.

T1799A BRAF Mutation is Common in PUVA Lentigines

TP53 mutated AML subclones exhibit engraftment in a humanized bone marrow ossicle mouse model

Technical Evaluation of Commercial Mutation Analysis Platforms and Reference Materials for Liquid Biopsy Profiling

The BRAF V600K mutation is more frequent than the BRAF V600E mutation in melanoma in situ of lentigo maligna type

The dynamic range of circulating tumor DNA in metastatic breast cancer

Tubuloids derived from human adult kidney and urine for personalized disease modeling

Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing.

Untargeted Assessment of Tumor Fractions in Plasma for Monitoring and Prognostication from Metastatic Breast Cancer Patients Undergoing Systemic Treatment

Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer.

p14ARF Hypermethylation Is Common but INK4a-ARF Locus or p53 Mutations Are Rare in Merkel Cell Carcinoma