Assignment of Na,K-ATPase beta 2-subunit gene (Atpb-2) to mouse chromosome 11

Deep ulcers are associated with increased C-reactive protein in active ulcerative colitis.

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver·2023

Utility of the QuantiFERON-TB Gold In-Tube assay for the diagnosis of tuberculosis in Moroccan children.

The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease·2016

A genome-wide association study of pulmonary tuberculosis in Morocco.

Human genetics·2016

Pott's disease in Moroccan children: clinical features and investigation of the interleukin-12/interferon-γ pathway.

The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease·2015

Survival analysis and microarray profiling identify Cd40 as a candidate for the Salmonella susceptibility locus, Ity5.

Genes and immunity·2015

An ENU-induced splicing mutation reveals a role for Unc93b1 in early immune cell activation following influenza A H1N1 infection.

Genes and immunity·2014

Enhancer-promoter interaction maps in pig implantation tissue identify candidate cis-regulatory elements and regulatory variants.

Genomics·2026

Genomic signatures of the Arctic-adapted North American gray wolf ecotype.

Genomics·2026

HIF-1 signaling contributes to lenvatinib resistance in patient-derived HCC organoids.

Genomics·2026

Unraveling the genomic blueprint of the Indian black soldier fly: From genome assembly to evolutionary insights.

Genomics·2026

Single-cell spatial transcriptomic atlas of the mouse adrenal gland reveals sexual dimorphism in steroidogenic enzyme and hormone receptor expression.

Genomics·2026

Comprehensive analysis of metabolomics and transcriptomics of radiation-induced rectal injury.

Genomics·2026

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Journal of blood medicine·2026

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Journal of molecular neuroscience : MN·2026

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Frontiers in endocrinology·2026

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Frontiers in psychiatry·2026

Compound Heterozygous PCDH15 Variants Associated With Cone-Rod Dystrophy in a Chinese Pedigree.

Molecular genetics & genomic medicine·2026

Genetically Predicted Muscle Mass and Function in Relation to Deep Vein Thrombosis: A Two-step Mendelian Randomization Study Highlighting the Mediating Role of BMI.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis·2026

Related Experiment Videos

Assignment of Na,K-ATPase beta 2-subunit gene (Atpb-2) to mouse chromosome 11

Related Concept Videos

Deep ulcers are associated with increased C-reactive protein in active ulcerative colitis.

Utility of the QuantiFERON-TB Gold In-Tube assay for the diagnosis of tuberculosis in Moroccan children.

A genome-wide association study of pulmonary tuberculosis in Morocco.

Pott's disease in Moroccan children: clinical features and investigation of the interleukin-12/interferon-γ pathway.

Survival analysis and microarray profiling identify Cd40 as a candidate for the Salmonella susceptibility locus, Ity5.

An ENU-induced splicing mutation reveals a role for Unc93b1 in early immune cell activation following influenza A H1N1 infection.

Enhancer-promoter interaction maps in pig implantation tissue identify candidate cis-regulatory elements and regulatory variants.

Genomic signatures of the Arctic-adapted North American gray wolf ecotype.

HIF-1 signaling contributes to lenvatinib resistance in patient-derived HCC organoids.

Unraveling the genomic blueprint of the Indian black soldier fly: From genome assembly to evolutionary insights.

Single-cell spatial transcriptomic atlas of the mouse adrenal gland reveals sexual dimorphism in steroidogenic enzyme and hormone receptor expression.

Comprehensive analysis of metabolomics and transcriptomics of radiation-induced rectal injury.

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Compound Heterozygous PCDH15 Variants Associated With Cone-Rod Dystrophy in a Chinese Pedigree.

Genetically Predicted Muscle Mass and Function in Relation to Deep Vein Thrombosis: A Two-step Mendelian Randomization Study Highlighting the Mediating Role of BMI.

Related Experiment Videos

Assignment of Na,K-ATPase beta 2-subunit gene (Atpb-2) to mouse chromosome 11

Related Concept Videos

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