162 results on '"Rohr, Jan"'
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2. A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS.
3. Correction to: Functional Relevance of CTLA4 Variants: an Upgraded Approach to Assess CTLA4‑Dependent Transendocytosis by Flow Cytometry
4. Comprehensive infectious disease screening in a cohort of unaccompanied refugee minors in Germany from 2016 to 2017: A cross-sectional study.
5. Differential trafficking of ligands trogocytosed via CD28 versus CTLA4 promotes collective cellular control of co-stimulation
6. Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity
7. A mouse model that is immunologically tolerant to reporter and modifier proteins
8. Analyzing trogocytosis of T lymphocytes by flow cytometry and confocal microscopy
9. Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome
10. Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency
11. Oncogenic JAK2V617F causes PD-L1 expression, mediating immune escape in myeloproliferative neoplasms
12. Assessing T lymphocyte function and differentiation by genetically encoded reporter systems
13. A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings
14. Single cell behavior in T cell differentiation
15. Genetic Disorders of Immune Regulation
16. Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea
17. Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation
18. Heterogeneous Differentiation Patterns of Individual CD8⁺ T Cells
19. A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings.
20. Cytomegalovirus subverts macrophage identity
21. Inhibition of acid sphingomyelinase increases regulatory T cells in humans
22. Pulmonary granulomatosis of genetic origin
23. Clinical and immunologic consequences of a somatic reversion in a patient with X-linked severe combined immunodeficiency
24. Chronic Inflammatory Bowel Disease as Key Manifestation of Atypical ARTEMIS Deficiency
25. Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11
26. A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS
27. Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations
28. Trigger‐dependent differences determine therapeutic outcome in murine primary hemophagocytic lymphohistiocytosis
29. Quorum Regulation via Nested Antagonistic Feedback Circuits Mediated by the Receptors CD28 and CTLA-4 Confers Robustness to T Cell Population Dynamics
30. The Most Frequent DCLRE1C (ARTEMIS) Mutations are Based on Homologous Recombination Events
31. Pancytopenia in a 4-year-old boy (Discussion and Diagnosis)
32. Pancytopenia in a 4-year-old boy (Case Presentation)
33. Differentiation of EBV-induced post-transplant Hodgkin lymphoma from Hodgkin-like post-transplant lymphoproliferative disease
34. Pulmonary granulomatosis of genetic origin.
35. Proinflammatory cytokine response toward fungi but not bacteria in chronic granulomatous disease
36. Transplantation from a symptomatic carrier sister restores host defenses but does not prevent colitis in NEMO deficiency
37. Oncogenic JAK2 V617F causes PD-L1 expression, mediating immune escape in myeloproliferative neoplasms
38. Additional file 6: of Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
39. Additional file 3: of Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
40. Additional file 4: of Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
41. Additional file 7: of Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
42. Additional file 5: of Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
43. Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome
44. Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
45. Hyperactive mTOR Pathway Promotes Lymphoproliferation and Abnormal Differentiation in Human Autoimmune Lymphoproliferative Syndrome
46. Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases
47. Heterogeneous Differentiation Patterns of Individual CD8 + T Cells
48. The CD8+ T cell response to infection is dominated by the progeny of few naïve T cells (110.12)
49. The most frequentDCLRE1C(ARTEMIS) mutations are based on homologous recombination events
50. Chronic Inflammatory Bowel Disease as Key Manifestation of Atypical ARTEMIS Deficiency
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