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Case Report: Alpha6 Integrin Disorder Presenting in Childhood with Nail Dysplasia and Onycholysis But No History of Fragile or Bullous Skin Changes
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The Role of CRISPR/Cas9 in Revolutionizing Duchenne's Muscular Dystrophy Treatment: Opportunities and Obstacles
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The Role of the Plasminogen Activator Inhibitor 1 (PAI1) in Ovarian Cancer: Mechanisms and Therapeutic Implications
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Mesenchymal Stem Cells in Clinical Trials for Immune Disorders
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The Alarming Situation of Highly Pathogenic Avian Influenza Viruses in 2019–2023
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Recurrent Cerebral Venous Sinus Thrombosis Occurred in an Acute Lymphoblastic Leukemia Child with Mutated Lipoprotein Lipase Gene during Asparaginase Therapy
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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
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Bridging Innovation Research with Clinical Application: Clinical Trials at the Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences
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ABO Blood Type and Urinary Bladder Cancer: Phenotype, Genotype, Allelic Association with a Clinical or Histological Stage and Recurrence Rate
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Analyzing Cell-free Genomic DNA in Spent Culture Media: Noninvasive Insight into the Blastocysts
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AQP4-AS1 Can Regulate the Expression of Ferroptosis-Related Regulator ALOX15 through Competitive Binding with miR-4476 in Lung Adenocarcinoma
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Gene Mutations in Gastrointestinal Stromal Tumors: Advances in Treatment and Mechanism Research
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16S rRNA Sequencing Reveals Alterations of Gut Bacteria in Hirschsprung-Associated Enterocolitis
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Genetically Predicted Iron Status Is a Causal Risk of Rheumatoid Arthritis: A Mendelian Randomization Study
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Potential Mechanism and Perspectives of Mesenchymal Stem Cell Therapy for Ischemic Stroke: A Review
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Human Viral Oncoproteins and Ubiquitin–Proteasome System
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Phenotypic Heterogeneity in ORAI-1-Associated Congenital Myopathy
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Role of Noncoding RNAs in Modulating Microglial Phenotype
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Mechanism of Genome Editing Tools and Their Application on Genetic Inheritance Disorders
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Expert Consensus on the Diagnosis and Treatment of FGFR Gene-Altered Solid Tumors
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Genomic Landscape Features of Minimally Invasive Adenocarcinoma and Invasive Lung Adenocarcinoma
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Genetic Modifications of Developmental Dyslexia and Its Representation Using In Vivo, In Vitro Model
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Expert Consensus on the Diagnosis and Treatment of NRG1/2 Gene Fusion Solid Tumors
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The Relationship between VDR Gene Polymorphisms Bsm1 and Apa1 with Breast Cancer Risk
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Maternal Uniparental Isodisomy of Chromosome 2 Leading to Homozygous Variants in SPR and ZNF142: A Case Report and Review of the UPD2 Literature
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CRISPR–Cas9 Gene Editing: Curing Genetic Diseases by Inherited Epigenetic Modifications
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Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages
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Laboratory-developed Droplet Digital PCR Assay for Quantification of the JAK2V617F Mutation
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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
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Prevalence and Associations of Co-occurrence of NFE2L2 Mutations and Chromosome 3q26 Amplification in Lung Cancer
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