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Curcumin modulates DNA methylation in colorectal cancer cells

PloS one, 2013-02, Vol.8 (2), p.e57709

2013

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Recursive SVM feature selection and sample classification for mass-spectrometry and microarray data

BMC bioinformatics, 2006-04, Vol.7 (1), p.197-197, Article 197

2006

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De novo constitutional MLH1 epimutations confer early‐onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one

International journal of cancer, 2011-02, Vol.128 (4), p.869-878

2011

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Genome-wide analysis of DNA copy number alterations and loss of heterozygosity in intracranial germ cell tumors

Pediatric blood & cancer, 2014-04, Vol.61 (4), p.593-600

2014

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Histone induced platelet aggregation is inhibited by normal albumin

Thrombosis research, 2013-07, Vol.132 (1), p.69-76

2013

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Boswellic acid induces epigenetic alterations by modulating DNA methylation in colorectal cancer cells

Cancer biology & therapy, 2012-05, Vol.13 (7), p.542-552

2012

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Immunodepletion Plasma Proteomics by TripleTOF 5600 and Orbitrap Elite/LTQ-Orbitrap Velos/Q Exactive Mass Spectrometers

Journal of proteome research, 2013-10, Vol.12 (10), p.4351-4365

2013

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M1182 Novel Evidence for Curcumin-Induced DNA Methylation Changes in Colon Cancer Cells

Gastroenterology (New York, N.Y. 1943), 2010, Vol.138 (5), p.S-349-S-349

2010

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S1965 Novel Evidence for Soma-Wide MLH1 Hypermethylation and a Global Methylation Defect in Non-Familial Early-Onset Colorectal Cancer

Gastroenterology (New York, N.Y. 1943), 2009, Vol.136 (5), p.A-303-A-303

2009

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Abstract 2614: CCAR2 acetylation establishes a BET/BRD9 acetyl switch in response to combined deacetylase and bromodomain inhibition

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.2614-2614

2019

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Cell-Specific Gene Expression in Langerhans Cell Histiocytosis Lesions Reveals a Distinct Profile Compared with Epidermal Langerhans Cells

The Journal of immunology (1950), 2010-04, Vol.184 (8), p.4557-4567

2010

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A clinically relevant orthotopic xenograft model of ependymoma that maintains the genomic signature of the primary tumor and preserves cancer stem cells in vivo

Neuro-oncology (Charlottesville, Va.), 2010-06, Vol.12 (6), p.580-594

2010

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Characterization of broadly pleiotropic phenotypes caused by an hfq insertion mutation in Escherichia coli K‐12

Molecular microbiology, 1994-07, Vol.13 (1), p.35-49

1994

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Analysis of Human Proteome Organization Plasma Proteome Project (HUPO PPP) reference specimens using surface enhanced laser desorption/ionization-time of flight (SELDI-TOF) mass spectrometry: Multi-institution correlation of spectra and identification of biomarkers

Proteomics (Weinheim), 2005-08, Vol.5 (13), p.3467-3474

2005

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Genome-Wide High-Density SNP Linkage Search for Glioma Susceptibility Loci: Results from the Gliogene Consortium

Cancer research (Chicago, Ill.), 2011-12, Vol.71 (24), p.7568-7575

2011

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Identification of the miaB gene, involved in methylthiolation of isopentenylated A37 derivatives in the tRNA of Salmonella typhimurium and Escherichia coli

Journal of bacteriology, 1999-12, Vol.181 (23), p.7256-7265

1999

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Host heterogeneous ribonucleoprotein K (hnRNP K) as a potential target to suppress hepatitis B virus replication

PLoS medicine, 2005-07, Vol.2 (7), p.e163-e163

2005

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Regulation of substrate recognition by the MiaA tRNA prenyltransferase modification enzyme of Escherichia coli K-12

The Journal of biological chemistry, 1997-05, Vol.272 (20), p.13073-13083

1997

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The miaA mutator phenotype of Escherichia coli K-12 requires recombination functions

Journal of bacteriology, 2001-03, Vol.183 (5), p.1796-1800

2001

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Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles

Leukemia, 2011-10, Vol.25 (10), p.1555-1563

2011

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Regulation of Substrate Recognition by the MiaA tRNA Prenyltransferase Modification Enzyme of Escherichia coliK-12

The Journal of biological chemistry, 1997-05, Vol.272 (20), p.13073-13083

1997

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Cell-Specific Gene Expression in Langerhans Cell Histiocytosis Lesions Reveals a Distinct Profile Compared to Epidermal Langerhans Cells1

The Journal of immunology (1950), 2010-03, Vol.184 (8), p.4557-4567

2010

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The miaA Mutator Phenotype ofEscherichia coli K-12 Requires Recombination Functions

Journal of Bacteriology, 2001-03, Vol.183 (5), p.1796

2001

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Analysis of Human Proteome Organization Plasma Proteome Project (HUPO PPP) reference specimens using surface enhanced laser desorption/ionization-time of flight (SELDI-TOF) mass spectrometry : Multi-institution correlation of spectra and identification of biomarkers: Exploring the Human Plasma Proteome: The HUPO Plasma Proteome Project (HPPP)

Proteomics (Weinheim), 2005, Vol.5 (13), p.3467-3474

2005

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Curcumin modulates DNA methylation in colorectal cancer cells

Recursive SVM feature selection and sample classification for mass-spectrometry and microarray data

De novo constitutional MLH1 epimutations confer early‐onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one

Genome-wide analysis of DNA copy number alterations and loss of heterozygosity in intracranial germ cell tumors

Histone induced platelet aggregation is inhibited by normal albumin

Boswellic acid induces epigenetic alterations by modulating DNA methylation in colorectal cancer cells

Immunodepletion Plasma Proteomics by TripleTOF 5600 and Orbitrap Elite/LTQ-Orbitrap Velos/Q Exactive Mass Spectrometers

M1182 Novel Evidence for Curcumin-Induced DNA Methylation Changes in Colon Cancer Cells

S1965 Novel Evidence for Soma-Wide MLH1 Hypermethylation and a Global Methylation Defect in Non-Familial Early-Onset Colorectal Cancer

Abstract 2614: CCAR2 acetylation establishes a BET/BRD9 acetyl switch in response to combined deacetylase and bromodomain inhibition

Cell-Specific Gene Expression in Langerhans Cell Histiocytosis Lesions Reveals a Distinct Profile Compared with Epidermal Langerhans Cells

A clinically relevant orthotopic xenograft model of ependymoma that maintains the genomic signature of the primary tumor and preserves cancer stem cells in vivo

Characterization of broadly pleiotropic phenotypes caused by an hfq insertion mutation in Escherichia coli K‐12

Analysis of Human Proteome Organization Plasma Proteome Project (HUPO PPP) reference specimens using surface enhanced laser desorption/ionization-time of flight (SELDI-TOF) mass spectrometry: Multi-institution correlation of spectra and identification of biomarkers

Genome-Wide High-Density SNP Linkage Search for Glioma Susceptibility Loci: Results from the Gliogene Consortium

Identification of the miaB gene, involved in methylthiolation of isopentenylated A37 derivatives in the tRNA of Salmonella typhimurium and Escherichia coli

Host heterogeneous ribonucleoprotein K (hnRNP K) as a potential target to suppress hepatitis B virus replication

Regulation of substrate recognition by the MiaA tRNA prenyltransferase modification enzyme of Escherichia coli K-12

The miaA mutator phenotype of Escherichia coli K-12 requires recombination functions

Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles

Regulation of Substrate Recognition by the MiaA tRNA Prenyltransferase Modification Enzyme of Escherichia coliK-12

IKZF1 and 22q11.22 Deletions and PDGFRA Gains Are Associated with Poor Outcome in Down Syndrome Acute Lymphoblastic Leukemia

Cell-Specific Gene Expression in Langerhans Cell Histiocytosis Lesions Reveals a Distinct Profile Compared to Epidermal Langerhans Cells1

The miaA Mutator Phenotype ofEscherichia coli K-12 Requires Recombination Functions

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