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Genomic analysis of racial differences in triple negative breast cancer

Genomics (San Diego, Calif.), 2019-12, Vol.111 (6), p.1529-1542

2019

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miR-339 Promotes Development of Stem Cell Leukemia/Lymphoma Syndrome via Downregulation of the BCL2L11 and BAX Proapoptotic Genes

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13), p.3522-3531

2018

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RHOA-regulated IGFBP2 promotes invasion and drives progression of BCR-ABL1 chronic myeloid leukemia

Haematologica (Roma), 2023-01, Vol.108 (1), p.122-134

2023

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Fluoride Alters Gene Expression via Histone H3K27 Acetylation in Ameloblast-like LS8 Cells

International journal of molecular sciences, 2024-09, Vol.25 (17), p.9600

2024

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Analysis of tissue-specific differentially methylated regions (TDMs) in humans

Genomics (San Diego, Calif.), 2007-03, Vol.89 (3), p.326-337

2007

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Quantitative analysis of human tissue-specific differences in methylation

Biochemical and biophysical research communications, 2008-11, Vol.376 (4), p.658-664

2008

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Tissue-specific differentially methylated regions of the human VASA gene are potentially associated with maturation arrest phenotype in the testis

Journal of human genetics, 2009-08, Vol.54 (8), p.450-456

2009

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Regulation of retinoschisin secretion in Weri-Rb1 cells by the F-actin and microtubule cytoskeleton

PloS one, 2011-06, Vol.6 (6), p.e20707-e20707

2011

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A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2)

Journal of human genetics, 2009-12, Vol.54 (12), p.746-748

2009

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Novel Wide-Range Quantitative Nested Real-Time PCR Assay for Mycobacterium tuberculosis DNA: Development and Methodology

Journal of Clinical Microbiology, 2008-05, Vol.46 (5), p.1708-1715

2008

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Novel Wide-Range Quantitative Nested Real-Time PCR Assay for Mycobacterium tuberculosis DNA: Clinical Application for Diagnosis of Tuberculous Meningitis

Journal of Clinical Microbiology, 2008-05, Vol.46 (5), p.1698-1707

2008

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Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells

Genomics data, 2014-12, Vol.2 (C), p.50-52

2014

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The miR-17/92 cluster is involved in the molecular etiology of the SCLL syndrome driven by the BCR-FGFR1 chimeric kinase

Oncogene, 2018-04, Vol.37 (14), p.1926-1938

2018

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Variant profiles of genes mapping to chromosome 16q loss in Wilms tumors reveals link to cilia-related genes and pathways

Genes & cancer, 2020-12, Vol.11 (3-4), p.137-153

2020

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Dysregulated signaling pathways in the development of CNTRL-FGFR1–induced myeloid and lymphoid malignancies associated with FGFR1 in human and mouse models

Blood, 2013-08, Vol.122 (6), p.1007-1016

2013

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Distinct signaling programs associated with progression of FGFR1 driven leukemia in a mouse model of stem cell leukemia lymphoma syndrome

Genomics (San Diego, Calif.), 2019-12, Vol.111 (6), p.1566-1573

2019

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A model of BCR‐FGFR1 driven human AML in immunocompromised mice

British journal of haematology, 2016-11, Vol.175 (3), p.542-545

2016

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A model of BCR ‐ FGFR 1 driven human AML in immunocompromised mice

British journal of haematology, 2016-11, Vol.175 (3), p.542-545

2016

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MicroRNA 339 promotes development of Stem Cell Leukemia/Lymphoma syndrome via downregulation of the BCL2L11 and BAX pro-apoptotic genes

Cancer research (Chicago, Ill.), 2018-05, Vol.78 (13), p.3522-3531

2018

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PI3K mutation and effect of aspirin use in breast cancer

Journal of clinical oncology, 2017-05, Vol.35 (15_suppl), p.e23209-e23209

2017

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A transcription map of the minimally deleted region from 13q14 in B-cell chronic lymphocytic leukemia as defined by large scale sequencing of the 650 kb critical region

Oncogene, 2000-11, Vol.19 (50), p.5772-5780

2000

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The Partner Gene of AML1 in t(16;21) Myeloid Malignancies Is a Novel Member of the MTG8(ETO) Family

Blood, 1998-06, Vol.91 (11), p.4028-4037

1998

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Indoleamine 2,3-dioxygenase inhibition alters the non-coding RNA transcriptome following renal ischemia-reperfusion injury

Transplant immunology, 2014-05, Vol.30 (4), p.140-144

2014

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Acidic-phospholipid Deficiency Represses the Flagellar Master Operon through a Novel Regulatory Region in Escherichia coli

Bioscience, biotechnology, and biochemistry, 1994, Vol.58 (12), p.2305-2307

1994

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Disruption of the gene encoding the β1-subunit of transducin in the Rd4/+ mouse

Investigative ophthalmology & visual science, 2006-04, Vol.47 (4), p.1293-1301

2006

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Genomic analysis of racial differences in triple negative breast cancer

miR-339 Promotes Development of Stem Cell Leukemia/Lymphoma Syndrome via Downregulation of the BCL2L11 and BAX Proapoptotic Genes

RHOA-regulated IGFBP2 promotes invasion and drives progression of BCR-ABL1 chronic myeloid leukemia

Fluoride Alters Gene Expression via Histone H3K27 Acetylation in Ameloblast-like LS8 Cells

Analysis of tissue-specific differentially methylated regions (TDMs) in humans

Quantitative analysis of human tissue-specific differences in methylation

Tissue-specific differentially methylated regions of the human VASA gene are potentially associated with maturation arrest phenotype in the testis

Regulation of retinoschisin secretion in Weri-Rb1 cells by the F-actin and microtubule cytoskeleton

A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2)

Novel Wide-Range Quantitative Nested Real-Time PCR Assay for Mycobacterium tuberculosis DNA: Development and Methodology

Novel Wide-Range Quantitative Nested Real-Time PCR Assay for Mycobacterium tuberculosis DNA: Clinical Application for Diagnosis of Tuberculous Meningitis

Genome-wide analysis of HOXC9-induced neuronal differentiation of neuroblastoma cells

The miR-17/92 cluster is involved in the molecular etiology of the SCLL syndrome driven by the BCR-FGFR1 chimeric kinase

Variant profiles of genes mapping to chromosome 16q loss in Wilms tumors reveals link to cilia-related genes and pathways

Dysregulated signaling pathways in the development of CNTRL-FGFR1–induced myeloid and lymphoid malignancies associated with FGFR1 in human and mouse models

Distinct signaling programs associated with progression of FGFR1 driven leukemia in a mouse model of stem cell leukemia lymphoma syndrome

A model of BCR‐FGFR1 driven human AML in immunocompromised mice

A model of BCR ‐ FGFR 1 driven human AML in immunocompromised mice

MicroRNA 339 promotes development of Stem Cell Leukemia/Lymphoma syndrome via downregulation of the BCL2L11 and BAX pro-apoptotic genes

PI3K mutation and effect of aspirin use in breast cancer

A transcription map of the minimally deleted region from 13q14 in B-cell chronic lymphocytic leukemia as defined by large scale sequencing of the 650 kb critical region

The Partner Gene of AML1 in t(16;21) Myeloid Malignancies Is a Novel Member of the MTG8(ETO) Family

Indoleamine 2,3-dioxygenase inhibition alters the non-coding RNA transcriptome following renal ischemia-reperfusion injury

Acidic-phospholipid Deficiency Represses the Flagellar Master Operon through a Novel Regulatory Region in Escherichia coli

Disruption of the gene encoding the β1-subunit of transducin in the Rd4/+ mouse

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