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Concomitant inhibition of B7-H3 and PD-L1 expression by a novel and synthetic microRNA delivers potent antitumor activities in colorectal tumor models

Investigational new drugs, 2021-10, Vol.39 (5), p.1267-1274

2021

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Single-cell Sequencing Reveals Variants in ARID1A , GPRC5A and MLL2 Driving Self-renewal of Human Bladder Cancer Stem Cells

European urology, 2017-01, Vol.71 (1), p.8-12

2017

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A genome‐wide study of the relationship between chromosomal abnormalities and gene expression in colorectal tumors

Genes chromosomes & cancer, 2021-04, Vol.60 (4), p.250-262

2021

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Detection of DNA copy number alterations by matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of single nucleotide polymorphisms

Clinical chemistry and laboratory medicine, 2022-09, Vol.60 (10), p.1543-1550

2022

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Molecular alterations in colorectal adenomas and intramucosal adenocarcinomas defined by high-density single-nucleotide polymorphism arrays

Journal of gastroenterology, 2017-11, Vol.52 (11), p.1158-1168

2017

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Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer

The Journal of pathology, 2022-05, Vol.257 (1), p.68-81

2022

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Holocene population expansion of a tropical bee coincides with early human colonization of Fiji rather than climate change

Molecular ecology, 2021-08, Vol.30 (16), p.4005-4022

2021

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Conjunctival melanoma copy number alterations and correlation with mutation status, tumor features, and clinical outcome

Pigment cell and melanoma research, 2019-07, Vol.32 (4), p.564-575

2019

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Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing

Experimental and molecular pathology, 2017-02, Vol.102 (1), p.156-161

2017

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Kasumi leukemia cell lines: characterization of tumor genomes with ethnic origin and scales of genomic alterations

Human cell : official journal of Human Cell Research Society, 2020-07, Vol.33 (3), p.868-876

2020

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Identification of genetic alterations in extramammary Paget disease using whole exome analysis

Journal of dermatological science, 2019-04, Vol.94 (1), p.229-235

2019

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Steroidogenic factor-1 (SF-1, NR5A1) and human disease

Molecular and cellular endocrinology, 2011-04, Vol.336 (1-2), p.198-205

2011

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Copy number alteration analysis for neuroblastoma using droplet digital polymerase chain reaction

Pediatrics international, 2021-10, Vol.63 (10), p.1192-1197

2021

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SNP in Chalcone Synthase gene is associated with variation of 6-gingerol content in contrasting landraces of Zingiber officinale.Roscoe

Gene, 2015-07, Vol.566 (2), p.184-188

2015

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Somatic copy number alterations predict response to platinum therapy in epithelial ovarian cancer

Gynecologic oncology, 2014-12, Vol.135 (3), p.415-422

2014

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Genome-wide single-nucleotide polymorphism array-based karyotyping in myelodysplastic syndrome and chronic myelomonocytic leukemia and its impact on treatment outcomes following decitabine treatment

Annals of hematology, 2013-04, Vol.92 (4), p.459-469

2013

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A strong association between VEGF-A rs28357093 and amyotrophic lateral sclerosis: a brazilian genetic study

Molecular biology reports, 2022-09, Vol.49 (9), p.9129-9133

2022

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Comprehensive analysis of somatic copy number alterations in clear cell renal cell carcinoma

Molecular carcinogenesis, 2020-04, Vol.59 (4), p.412-424

2020

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Prognostic gene alterations and clonal changes in childhood B-ALL

Leukemia research, 2019-08, Vol.83, p.106159-106159, Article 106159

2019

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Profiling Numerical and Structural Chromosomal Instability in Different Cancer Types

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2825, p.345

2024

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Overexpression of NAD(P)H:quinone oxidoreductase 1 (NQO1) and genomic gain of the NQO1 locus modulates breast cancer cell sensitivity to quinones

Life sciences (1973), 2016-01, Vol.145, p.57-65

2016

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Fluorescence detection of single-nucleotide differences using aptamer-forming binary DNA probes

Analyst (London), 2016-10, Vol.141 (21), p.6087-6092

2016

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Genetic and Epigenetic Alteration in Gastric Carcinogenesis

Helicobacter (Cambridge, Mass.), 2010-09, Vol.15 (s1), p.34-39

2010

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Combining targeted sequencing and ultra-low-pass whole-genome sequencing for accurate somatic copy number alteration detection

Functional & integrative genomics, 2021-03, Vol.21 (2), p.161-169

2021

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Mapping chromosomal instability induced by small-molecular therapeutics in a yeast model

Applied microbiology and biotechnology, 2019-06, Vol.103 (12), p.4869-4880

2019

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Concomitant inhibition of B7-H3 and PD-L1 expression by a novel and synthetic microRNA delivers potent antitumor activities in colorectal tumor models

Single-cell Sequencing Reveals Variants in ARID1A , GPRC5A and MLL2 Driving Self-renewal of Human Bladder Cancer Stem Cells

A genome‐wide study of the relationship between chromosomal abnormalities and gene expression in colorectal tumors

Detection of DNA copy number alterations by matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of single nucleotide polymorphisms

Molecular alterations in colorectal adenomas and intramucosal adenocarcinomas defined by high-density single-nucleotide polymorphism arrays

Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer

Holocene population expansion of a tropical bee coincides with early human colonization of Fiji rather than climate change

Conjunctival melanoma copy number alterations and correlation with mutation status, tumor features, and clinical outcome

Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing

Kasumi leukemia cell lines: characterization of tumor genomes with ethnic origin and scales of genomic alterations

Identification of genetic alterations in extramammary Paget disease using whole exome analysis

Steroidogenic factor-1 (SF-1, NR5A1) and human disease

Copy number alteration analysis for neuroblastoma using droplet digital polymerase chain reaction

SNP in Chalcone Synthase gene is associated with variation of 6-gingerol content in contrasting landraces of Zingiber officinale.Roscoe

Somatic copy number alterations predict response to platinum therapy in epithelial ovarian cancer

Genome-wide single-nucleotide polymorphism array-based karyotyping in myelodysplastic syndrome and chronic myelomonocytic leukemia and its impact on treatment outcomes following decitabine treatment

A strong association between VEGF-A rs28357093 and amyotrophic lateral sclerosis: a brazilian genetic study

Comprehensive analysis of somatic copy number alterations in clear cell renal cell carcinoma

Prognostic gene alterations and clonal changes in childhood B-ALL

Profiling Numerical and Structural Chromosomal Instability in Different Cancer Types

Overexpression of NAD(P)H:quinone oxidoreductase 1 (NQO1) and genomic gain of the NQO1 locus modulates breast cancer cell sensitivity to quinones

Fluorescence detection of single-nucleotide differences using aptamer-forming binary DNA probes

Genetic and Epigenetic Alteration in Gastric Carcinogenesis

Combining targeted sequencing and ultra-low-pass whole-genome sequencing for accurate somatic copy number alteration detection

Mapping chromosomal instability induced by small-molecular therapeutics in a yeast model

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