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2. Respiratory Syncytial Virus Infects Regulatory B Cells in Human Neonates via Chemokine Receptor CX3CR1 and Promotes Lung Disease Severity

10. An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

11. PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator–dependent autoimmunity

12. Public T cell receptors confer high-avidity CD4 responses to HIV controllers

13. Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation

14. Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency

19. Outcomes Following Gene Therapy in Patients With Severe Wiskott-Aldrich Syndrome

20. A recurrent dominant negative E47 mutation causes agammaglobulinemia and BCR- B cells. Lebanese Syrian Associated Charities, grants and research fellow-ships from the National Health and Medical Research Council of Australia, the St. Giles Foundation, the National Center for Research Resources, the National Center for Advancing Sciences (NCATS; grant number 8UL1TR000043 from the NIH), and the Rockefeller University

22. Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections

24. Stable and Functional Lymphoid Reconstitution in Artemis-deficient Mice Following Lentiviral Artemis Gene Transfer Into Hematopoietic Stem Cells

25. A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency

26. Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

28. Inherited and somatic CD3(sym) mutations in a patient with T-cell deficiency

29. Efficacy of Gene Therapy for X-Linked Severe Combined Immunodeficiency

31. Clonal evidence for the transduction of CD34+ cells with lymphomyeloid differentiation potential and self-renewal capacity in the SCID-X1 gene therapy trial

45. Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ('FILS syndrome')

46. Bystander hyperactivation of preimmune CD8+ T cells in chronic HCV patients

47. Author response: Bystander hyperactivation of preimmune CD8+ T cells in chronic HCV patients

48. Cancer-targeted IL-12 controls human rhabdomyosarcoma by senescence induction and myogenic differentiation

49. Hypomorphic RAG1 mutations and CMV infection: a new phenotype of severe combined immunodeficiency

50. Adoptive Transfer of Tumor-Reactive Melan-A-Specific CTL Clones in Melanoma Patients Is Followed by Increased Frequencies of Additional Melan-A-Specific T Cells 1 The Journal of Immunology

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