HTLV-I p24 antigen in circulating immune complexes associated with acute T-lymphoblastic leukemia

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Rhomboid family gene expression profiling in breast normal tissue and tumor samples.

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HTLV-I p24 antigen in circulating immune complexes associated with acute T-lymphoblastic leukemia

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Breast cancer cutaneous metastases are associated to uMUC1 and sialyl Lewis x and to highly malignant primary tumors.

Temporal and spatial expression of Muc2 and Muc5ac mucins during rat respiratory and digestive tracts development.

Spatiotemporal expression of Rhomboid domain containing 2 (Rhbdd2) during rat development.

Muc5ac mucin expression during rat skin development.

IDO is highly expressed in breast cancer and breast cancer-derived circulating microvesicles and associated to aggressive types of tumors by in silico analysis.

Rhomboid family gene expression profiling in breast normal tissue and tumor samples.

The use of MYD88 and IGH polymerase chain reaction in the diagnosis and follow-up of Bing-Neel syndrome.

CD19 antigen: from tumor target to safety switch in CAR-T cell therapy.

Adult-onset activated PI3Kδ syndrome presenting with HLH-like hyperinflammation, autoimmunity, and thrombosis: an underrecognized inborn error of immunity.

Divergent roles of interleukin-12p40 and interleukin-18 in severe fibrosing chronic graft-versus-host-disease, immunity, and post-transplant outcomes.

Response to comment on: "Ligature-induced periodontitis promotes Dnmt3aR878H-driven clonal hematopoiesis".

Optimizing exposure: the case for dose-dense CAR T-cell administration.

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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