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2. Human inherited CCR2 deficiency underlies progressive polycystic lung disease

3. Actin dynamics regulation by TTC7A/PI4KIIIα limits DNA damage and cell death under confinement

4. DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity

5. Tendinopathy

7. Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases

8. The Early Stages of the Magmatic Arc in the Southern Central Andes

9. Clinical replicability of rehabilitation interventions in randomized controlled trials reported in main journals is inadequate

10. A novel pediatric polycystic lung disease caused by CCR2 deficiency

12. Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome

19. Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

20. Rab44 regulates murine mast cell–driven anaphylaxis through kinesin-1–dependent secretory granule translocation

25. Innenrücktitelbild: Small Molecule Inhibitors of Interferon‐Induced JAK‐STAT Signalling (Angew. Chem. 32/2022)

26. Inside Back Cover: Small Molecule Inhibitors of Interferon‐Induced JAK‐STAT Signalling (Angew. Chem. Int. Ed. 32/2022)

27. Small Molecule Inhibitors of Interferon‐Induced JAK‐STAT Signalling

31. Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome

33. Rubella vaccine–induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity

34. Actin dynamics regulation by TTC7A/PI4KIIIα axis limits DNA damage and cell death during leukocyte migration

39. Hemophagocytic Lymphohistiocytosis Gene Mutations in Adult Patients Presenting With CLIPPERS-Like Syndrome

41. HAVCR2 mutations are associated with severe hemophagocytic syndrome in subcutaneous panniculitis-like T-cell lymphoma

43. Clinical replicability of rehabilitation interventions in randomized controlled trials reported in main journals is inadequate

45. Blood monocytes sample MelanA/MART1 antigen for long-lasting cross-presentation to CD8 + T cells after differentiation into dendritic cells

46. Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency

48. Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases

50. Dynamic formation of microvillus inclusions during enterocyte differentiation in Munc18-2–deficient intestinal organoids

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