Lista de obras - A Aggerholm - Dominio Público Uruguay

A certified plasmid reference material for the standardisation of BCR-ABL1 mRNA quantification by real-time quantitative PCR

artículo científico publicado en 2014

A pharmacodynamic study of 5-azacytidine in the P39 cell line

artículo científico publicado en 2006

Characterization and prognostic significance of mitochondrial DNA variations in acute myeloid leukemia

artículo científico publicado en 2013

Congenital hypoplastic bone marrow failure associated with a de novo partial deletion of the MECOM gene at 3q26.2.

artículo científico publicado en 2018

Delineation and molecular characterization of acute myeloid leukemia patients with coduplication of FLT3 and MLL.

artículo científico publicado en 2005

Delineation of known and new transcript variants of the SETMAR (Metnase) gene and the expression profile in hematologic neoplasms.

artículo científico publicado en 2014

Detection of mutations in GC-rich DNA by bisulphite denaturing gradient gel electrophoresis.

artículo científico publicado en 1998

Diagnostic and molecular genetic challenges in male incontinentia pigmenti: a case report.

artículo científico publicado en 2013

Differential expression levels and methylation status of ROBO1 in mantle cell lymphoma and chronic lymphocytic leukaemia

artículo científico publicado en 2016

Distinguishing myelofibrosis from polycythemia vera and essential thrombocythemia: The utility of enumerating circulating stem cells with aberrant hMICL expression by flow cytometry

artículo científico publicado en 2018

Extreme hyperleukocytosis in a pediatric T-ALL patient with a rare translocation, t(7;19)(q35;p13), and submicroscopic deletions at 4q25, 7q33 and 10q23.

artículo científico publicado en 2013

Gene expression profiling of Polycomb, Hox and Meis genes in patients with acute myeloid leukaemia

artículo científico publicado en 2008

Genetic and epigenetic similarities and differences between childhood and adult AML

artículo científico publicado en 2011

Maintenance treatment with azacytidine for patients with high-risk myelodysplastic syndromes (MDS) or acute myeloid leukaemia following MDS in complete remission after induction chemotherapy

artículo científico publicado en 2010

Molecular typing of adult acute myeloid leukaemia: significance of translocations, tandem duplications, methylation, and selective gene expression profiling.

artículo científico publicado en 2005

Mutational analysis of the tumour suppressor gene MMAC1/PTEN in malignant myeloid disorders

artículo científico publicado en 2000

Negative effect of DNA hypermethylation on the outcome of intensive chemotherapy in older patients with high-risk myelodysplastic syndromes and acute myeloid leukemia following myelodysplastic syndrome

artículo científico publicado en 2007

Persistence ofDNMT3Amutations at long-term remission in adult patients with AML

artículo científico publicado en 2014

Pre-screening HIV-1 reverse transcriptase resistance mutations in subtype B patients using a novel multiplex primer extension assay.

artículo científico publicado en 2009

Promoter hypermethylation of p15INK4B, HIC1, CDH1, and ER is frequent in myelodysplastic syndrome and predicts poor prognosis in early-stage patients

artículo científico publicado en 2006

Promoter hypermethylation of the retinoic acid receptor beta2 gene is frequent in acute myeloid leukaemia and associated with the presence of CBFbeta-MYH11 fusion transcripts.

artículo científico publicado en 2006

Role of mitogen-activated protein kinases, nuclear factor-kappaB, and interferon regulatory factor 3 in Toll-like receptor 4-mediated activation of HIV long terminal repeat

artículo científico publicado en 2009

Skewed ratio between type 1 and type 2 CALR mutations in Essential Thrombocytosis patients with concomitant JAK2 V617F mutation

artículo científico publicado en 2018

Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing

The combined expression of HOXA4 and MEIS1 is an independent prognostic factor in patients with AML.

artículo científico publicado en 2009

Lista de obras de A Aggerholm

A certified plasmid reference material for the standardisation of BCR-ABL1 mRNA quantification by real-time quantitative PCR

A pharmacodynamic study of 5-azacytidine in the P39 cell line

Characterization and prognostic significance of mitochondrial DNA variations in acute myeloid leukemia

Congenital hypoplastic bone marrow failure associated with a de novo partial deletion of the MECOM gene at 3q26.2.

Delineation and molecular characterization of acute myeloid leukemia patients with coduplication of FLT3 and MLL.

Delineation of known and new transcript variants of the SETMAR (Metnase) gene and the expression profile in hematologic neoplasms.

Detection of mutations in GC-rich DNA by bisulphite denaturing gradient gel electrophoresis.

Diagnostic and molecular genetic challenges in male incontinentia pigmenti: a case report.

Differential expression levels and methylation status of ROBO1 in mantle cell lymphoma and chronic lymphocytic leukaemia

Distinguishing myelofibrosis from polycythemia vera and essential thrombocythemia: The utility of enumerating circulating stem cells with aberrant hMICL expression by flow cytometry

Extreme hyperleukocytosis in a pediatric T-ALL patient with a rare translocation, t(7;19)(q35;p13), and submicroscopic deletions at 4q25, 7q33 and 10q23.

Gene expression profiling of Polycomb, Hox and Meis genes in patients with acute myeloid leukaemia

Genetic and epigenetic similarities and differences between childhood and adult AML

Maintenance treatment with azacytidine for patients with high-risk myelodysplastic syndromes (MDS) or acute myeloid leukaemia following MDS in complete remission after induction chemotherapy

Molecular typing of adult acute myeloid leukaemia: significance of translocations, tandem duplications, methylation, and selective gene expression profiling.

Mutational analysis of the tumour suppressor gene MMAC1/PTEN in malignant myeloid disorders

Negative effect of DNA hypermethylation on the outcome of intensive chemotherapy in older patients with high-risk myelodysplastic syndromes and acute myeloid leukemia following myelodysplastic syndrome

Persistence ofDNMT3Amutations at long-term remission in adult patients with AML

Pre-screening HIV-1 reverse transcriptase resistance mutations in subtype B patients using a novel multiplex primer extension assay.

Promoter hypermethylation of p15INK4B, HIC1, CDH1, and ER is frequent in myelodysplastic syndrome and predicts poor prognosis in early-stage patients

Promoter hypermethylation of the retinoic acid receptor beta2 gene is frequent in acute myeloid leukaemia and associated with the presence of CBFbeta-MYH11 fusion transcripts.

Role of mitogen-activated protein kinases, nuclear factor-kappaB, and interferon regulatory factor 3 in Toll-like receptor 4-mediated activation of HIV long terminal repeat

Skewed ratio between type 1 and type 2 CALR mutations in Essential Thrombocytosis patients with concomitant JAK2 V617F mutation

Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing

The combined expression of HOXA4 and MEIS1 is an independent prognostic factor in patients with AML.