Role of Noncoding RNAs in Modulating Microglial Phenotype

2024-9-9

Phenotypic Heterogeneity in ORAI-1-Associated Congenital Myopathy

2024-9-5

Potential Mechanism and Perspectives of Mesenchymal Stem Cell Therapy for Ischemic Stroke: A Review

2024-9-2

Human Viral Oncoproteins and Ubiquitin–Proteasome System

2024-9-2

Genetically Predicted Iron Status Is a Causal Risk of Rheumatoid Arthritis: A Mendelian Randomization Study

2024-8-29

16S rRNA Sequencing Reveals Alterations of Gut Bacteria in Hirschsprung-Associated Enterocolitis

2024-8-22

Gene Mutations in Gastrointestinal Stromal Tumors: Advances in Treatment and Mechanism Research

2024-8-22

AQP4-AS1 Can Regulate the Expression of Ferroptosis-Related Regulator ALOX15 through Competitive Binding with miR-4476 in Lung Adenocarcinoma

2024-8-16

Analyzing Cell-free Genomic DNA in Spent Culture Media: Noninvasive Insight into the Blastocysts

2024-7-23

ABO Blood Type and Urinary Bladder Cancer: Phenotype, Genotype, Allelic Association with a Clinical or Histological Stage and Recurrence Rate

2024-7-22

Bridging Innovation Research with Clinical Application: Clinical Trials at the Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences

2024-7-12

46 XX Ovotesticular Disorder of Sex Development with Gonadotropin-Releasing Hormone Receptor, Autosomal Recessive Heterozygous Missense Mutation and Autosomal Dominant Heterozygous Missense Mutation of the PROKR2 Gene: A Case Report

2024-7-9

Recurrent Cerebral Venous Sinus Thrombosis Occurred in an Acute Lymphoblastic Leukemia Child with Mutated Lipoprotein Lipase Gene during Asparaginase Therapy

2024-7-5

The Alarming Situation of Highly Pathogenic Avian Influenza Viruses in 2019–2023

2024-6-28

Mesenchymal Stem Cells in Clinical Trials for Immune Disorders

2024-6-27

Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome

2024-6-1

Comparing Genomic Profiles of ALK Fusion-Positive and ALK Fusion-Negative Nonsmall Cell Lung Cancer Patients

2024-6-1

Identification of a Novel Intronic Mutation in VMA21 Associated with a Classical Form of X-Linked Myopathy with Autophagy

2024-5-10

Analysis of Factors Affecting Hematopoietic Stem Cell Mobilization Efficiency and Early Hematopoietic Reconstruction Indicators during Autologous Peripheral Blood Hematopoietic Stem Cell Transplantation

2024-4-18

Prevalence and Associations of Co-occurrence of NFE2L2 Mutations and Chromosome 3q26 Amplification in Lung Cancer

2024-4-15

Association between Serum Lactate Dehydrogenase Level and 30-day Mortality in Patients with Intracranial Hemorrhage with Acute Leukemia in the Induction Phase: A Cohort Study

2024-4-10

Laboratory-developed Droplet Digital PCR Assay for Quantification of the JAK2V617F Mutation

2024-4-4

The Relationship between VDR Gene Polymorphisms Bsm1 and Apa1 with Breast Cancer Risk

2024-1-1

Identification of Two Variants c.2697A > C and c.3305A > C in USP7 by Analysis of Whole-Exome Sequencing in Chinese Patients with Hao-Fountain Syndrome

2024-1-1

Novel Variants of CEP152 in a Case of Compound-Heterozygous Inheritance of Epilepsy

2024-1-1

Orchestration of Genetic Alterations in PSEN1 and PSEN2 Genes in Development of Alzheimer's Disease through Computational Analysis

2024-1-1

Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives

2024-1-1

Genetic Modifications of Developmental Dyslexia and Its Representation Using In Vivo, In Vitro Model

2024-1-1

CRISPR–Cas9 Gene Editing: Curing Genetic Diseases by Inherited Epigenetic Modifications

2024-1-1

Association of Cytogenetics Aberrations and IGHV Mutations with Outcome in Chronic Lymphocytic Leukemia Patients in a Real-World Clinical Setting

2024-1-1

Identification of Novel Risk Variants of Inflammatory Factors Related to Myeloproliferative Neoplasm: A Bidirectional Mendelian Randomization Study

2024-1-1

A Pair of Compound Heterozygous IARS2 Variants Manifesting West Syndrome and Electrolyte Disorders in a Chinese Patient

2024-1-1

Expert Consensus on the Diagnosis and Treatment of NRG1/2 Gene Fusion Solid Tumors

2024-1-1

Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages

2024-1-1

The Multifaceted Role of Oxytocinergic System and OXTR Gene

2024-1-1

Maternal Uniparental Isodisomy of Chromosome 2 Leading to Homozygous Variants in SPR and ZNF142: A Case Report and Review of the UPD2 Literature

2024-1-1

On the Pentapeptide as the Measurement Unit in Immunology

2024-1-1

Screening for Mutations in Hereditary Cancer Susceptibility Genes in a Region with High Endogamy in Brazil

2023-12-1

Study on Screening Core Biomarkers of Noise and Drug-Induced Hearing Loss Based on Transcriptomics

2023-12-1

Spleen-Derived CCL9 Recruits MDSC to Facilitate Tumor Growth in Orthotopic Hepatoma Mice

2023-12-1

Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype–Phenotype Correlation

2023-12-1

Integrative Analysis of PAIP2B to Identify a Novel Biomarker for Pancreatic Ductal Adenocarcinoma

2023-12-1

Mesenchymal Stem Cells Applications in Alzheimer's Disease

2023-12-1

Early is Better: Report of a Cowden Syndrome

2023-11-27

The Clinical Significance of MicroRNAs in Colorectal Cancer Signaling Pathways: A Review

2023-11-22

The Epigenetic Regulation of Quiescent in Stem Cells

2023-11-22