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OMIM - Congenital disorder
L1000 CMAP - Prostate carcinoma VCaP cells treated with ligand perturbagens
L1000 CMAP - Adenocarcinoma of breast MCF7 cells treated with ligand perturbagens
L1000 CMAP - Colorectal cancer HT29 cells treated with ligand perturbagens
L1000 CMAP - Amelanotic malignant melanoma of skin A375 cells treated with ligand perturbagens
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BPOZ-2-deficient mice exhibit aggravated inflammation-associated tissue damage after acute dextran s…
Bioinformatics analysis of the microRNA genes associated with type 2 cardiorenal syndrome.
Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cel…
AAV-based gene editing of type 1 collagen mutation to treat osteogenesis imperfecta.
Frequency of Mutacin Gene Types in Streptococcus mutans Isolated From Oral Potentially Malignant Dis…
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Type 2 Deiodinase Gene Polymorphism and the Treatment of Hypothyroidism Caused by Thyroidectomy in T…
First-line mCapOX+Cetuximab vs. mFOLFOX6+Cetuximab for Metastatic Left-sided CRC With Wild-type RAS/…
The Role of FTO Gene Polymorphism and Insulin Preparation in Obesity in Children With Type 1 Diabete…
Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (…
Mapping Genes for Type 2 (Non-Insulin Dependent) Diabetes Mellitus
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