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Ephrin-B3 is the midline barrier that prevents corticospinal tract axons from recrossing, allowing for unilateral motor control.

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Ephrin-B2 selectively marks arterial vessels and neovascularization sites in the adult, with expression in both endothelial and smooth-muscle cells.

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Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.

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Related Experiment Videos

Procedures for in vitro DNA mutagenesis of human leukocyte interferon sequences

Related Concept Videos

Identification of ubiquitin ligases required for skeletal muscle atrophy.

Ephrin-B3 is the midline barrier that prevents corticospinal tract axons from recrossing, allowing for unilateral motor control.

Ephrin-B2 selectively marks arterial vessels and neovascularization sites in the adult, with expression in both endothelial and smooth-muscle cells.

Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.

Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development.

Distinct phenotypes of mutant mice lacking agrin, MuSK, or rapsyn.

Zinc-finger ubiquitin-binding domain of histone deacetylase 6 modulates Tau structure and function.

Chromatin immunoprecipitation assay for analyzing histone H3-mediated regulation of copper homeostasis.

Experimental techniques to evaluate IA-MSCs-mediated alleviation of vasogenic edema following ischemic stroke.

Histone Decatylase 6 and Tau-induced microglial chemotaxis by trans-well migration and wound-scratch assay.

ChIPmentation-based mapping of histone modifications in aging: Experimental design and analytical considerations.

Synthesis and functional characterisation of small molecule activator of p300/CBP lysine acetyltransferase activity: Implications in spinal injury repair.

A Cost-Effective Workflow for Mono- and Multiplex Immunofluorescence in Adherent Two-Dimensional Cell Cultures on Glass Coverslips.

Planar Immunological Synapses Formed by Human CD4 T Cells as In Vitro System to Study Actin and Tubulin Dynamics Through TIRF Microscopy.

Unicentric Castleman disease presenting as hyperenhancing mediastinal mass: A case series diagnosed by linear endobronchial ultrasound guided mediastinal nodal biopsy.

Pretransfusion testing interference profile of IMC-002: A novel anti-CD47 monoclonal antibody engineered for minimized red cell binding.

Investigation of IgM Monoclonal Paraprotein in Bone Marrow Aspiration: The Role of Immunophenotyping by Flow Cytometry in Selecting Cases for Molecular Testing for the p.MYD88 L265P Point Mutation.

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Procedures for in vitro DNA mutagenesis of human leukocyte interferon sequences

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