Discover open access scientific publications

Search, annotate, share and cite publications

Publications by S Meshinchi

NUP98/JARID1A Is a Novel Recurrent Abnormality in Pediatric Acute Megakaryoblastic Leukemia With a Distinct HOX Gene Expression Pattern

Leukemia

English

Copy-Neutral Loss of Heterozygosity Is Prevalent and a Late Event in the Pathogenesis of FLT3/ITD AML

English

Related publications

Coagulation FXIII-A Protein Expression Defines Three Novel Sub-Populations in Pediatric B-Cell Progenitor Acute Lymphoblastic Leukemia Characterized by Distinct Gene Expression Signatures

Frontiers in Oncology

Cancer Research

Oncology

2019

English

Genomic 5-Hydroxymethylcytosine Levels Correlate With TET2 Mutations and a Distinct Global Gene Expression Pattern in Secondary Acute Myeloid Leukemia

English

Overexpression of CDX2 Perturbs HOX Gene Expression in Murine Progenitors Depending on Its N-Terminal Domain and Is Closely Correlated With Deregulated HOX Gene Expression in Human Acute Myeloid Leukemia

English

A Novel Spliced Fusion of MLL With CT45A2in a Pediatric Biphenotypic Acute Leukemia

English

Recurrent Deletions of IKZF1 in Pediatric Acute Myeloid Leukemia

Haematologica

Hematology

2015

English

PAX5-KIAA1549L: A Novel Fusion Gene in a Case of Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia

Molecular Cytogenetics

English

HOX Gene Regulation in Acute Myeloid Leukemia: CDX Marks the Spot?

Cell Cycle

Medicine

Developmental Biology

Cell Biology

Molecular Biology

2007

English

Mediastinal Germ Cell Tumor Associated With Acute Megakaryoblastic Leukemia.

Japanese Journal of Lung Cancer

English

A Novel Mechanism of NPM1 Cytoplasmic Localization in Acute Myeloid Leukemia: The Recurrent Gene Fusion NPM1-HAUS1

Haematologica

Hematology

2016

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by S Meshinchi

NUP98/JARID1A Is a Novel Recurrent Abnormality in Pediatric Acute Megakaryoblastic Leukemia With a Distinct HOX Gene Expression Pattern

Copy-Neutral Loss of Heterozygosity Is Prevalent and a Late Event in the Pathogenesis of FLT3/ITD AML

Related publications

Coagulation FXIII-A Protein Expression Defines Three Novel Sub-Populations in Pediatric B-Cell Progenitor Acute Lymphoblastic Leukemia Characterized by Distinct Gene Expression Signatures

Genomic 5-Hydroxymethylcytosine Levels Correlate With TET2 Mutations and a Distinct Global Gene Expression Pattern in Secondary Acute Myeloid Leukemia

Overexpression of CDX2 Perturbs HOX Gene Expression in Murine Progenitors Depending on Its N-Terminal Domain and Is Closely Correlated With Deregulated HOX Gene Expression in Human Acute Myeloid Leukemia

A Novel Spliced Fusion of MLL With CT45A2in a Pediatric Biphenotypic Acute Leukemia

Recurrent Deletions of IKZF1 in Pediatric Acute Myeloid Leukemia

PAX5-KIAA1549L: A Novel Fusion Gene in a Case of Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia

HOX Gene Regulation in Acute Myeloid Leukemia: CDX Marks the Spot?

Mediastinal Germ Cell Tumor Associated With Acute Megakaryoblastic Leukemia.

A Novel Mechanism of NPM1 Cytoplasmic Localization in Acute Myeloid Leukemia: The Recurrent Gene Fusion NPM1-HAUS1