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Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein

Stem cell reports, 2021-04, Vol.16 (4), p.985-996

2021

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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 nucleotide alterations in MicroRNAs and human cancer-A not fully explored field

Non-coding RNA research, 2020-03, Vol.5 (1), p.27-31

Zhao, Dan

2020

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Low-density lipoprotein receptor variants are associated with spontaneous and treatment-induced recovery from hepatitis C virus infection

Infection, genetics and evolution, 2009-09, Vol.9 (5), p.847-852

2009

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Evaluation of cell-free DNA approaches for multi-cancer early detection

Cancer cell, 2022-12, Vol.40 (12), p.1537-1549.e12

2022

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Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data

Annals of oncology, 2015-01, Vol.26 (1), p.64-70

2015

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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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Precision Nutrition

2023

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Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

Leukemia, 2010-02, Vol.24 (2), p.438-449

2010

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Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population

Nutrients, 2020-11, Vol.12 (11), p.3389

2020

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The Clinical Utility of Optical Genome Mapping for the Assessment of Genomic Aberrations in Acute Lymphoblastic Leukemia

Cancers, 2021-08, Vol.13 (17), p.4388

2021

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Genetic alterations in hepatocellular carcinoma: An update

World journal of gastroenterology : WJG, 2016-11, Vol.22 (41), p.9069-9095

2016

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Catecholaminergic Gene Polymorphisms Are Associated with GI Symptoms and Morphological Brain Changes in Irritable Bowel Syndrome

PloS one, 2015-08, Vol.10 (8), p.e0135910-e0135910

2015

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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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A clinically applicable molecular classification of oncocytic cell thyroid nodules

Endocrine-related cancer, 2023-09, Vol.30 (9), p.1

2023

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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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Molecular alterations in gastric cancer with special reference to the early-onset subtype

World journal of gastroenterology : WJG, 2016-02, Vol.22 (8), p.2460-2474

2016

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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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A new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing

Briefings in bioinformatics, 2021-11, Vol.22 (6)

2021

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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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Genetic alterations within the DENND1A gene in patients with polycystic ovary syndrome (PCOS)

PloS one, 2013-09, Vol.8 (9), p.e77186-e77186

2013

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Target genes discovery through copy number alteration analysis in human hepatocellular carcinoma

World journal of gastroenterology : WJG, 2013-12, Vol.19 (47), p.8873-8879

2013

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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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Chromosomal Aberrations in Canine Gliomas Define Candidate Genes and Common Pathways in Dogs and Humans

Journal of neuropathology and experimental neurology, 2016-07, Vol.75 (7), p.700-710

2016

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Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein

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

Single nucleotide alterations in MicroRNAs and human cancer-A not fully explored field

Low-density lipoprotein receptor variants are associated with spontaneous and treatment-induced recovery from hepatitis C virus infection

Evaluation of cell-free DNA approaches for multi-cancer early detection

Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data

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

Precision Nutrition

Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population

The Clinical Utility of Optical Genome Mapping for the Assessment of Genomic Aberrations in Acute Lymphoblastic Leukemia

Genetic alterations in hepatocellular carcinoma: An update

Catecholaminergic Gene Polymorphisms Are Associated with GI Symptoms and Morphological Brain Changes in Irritable Bowel Syndrome

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

A clinically applicable molecular classification of oncocytic cell thyroid nodules

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

Molecular alterations in gastric cancer with special reference to the early-onset subtype

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

A new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing

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

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

Genetic alterations within the DENND1A gene in patients with polycystic ovary syndrome (PCOS)

Target genes discovery through copy number alteration analysis in human hepatocellular carcinoma

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

Chromosomal Aberrations in Canine Gliomas Define Candidate Genes and Common Pathways in Dogs and Humans

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