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Rituximab resistance in ITP and beyond
Zhengrui Xiao
,
Irina Murakhovskaya
Oncology
Research output
:
Contribution to journal
›
Review article
›
peer-review
17
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Keyphrases
Adaptive Immune Response
50%
Added Benefit
50%
B Cells
100%
Cell-to-cell
100%
FcRn
50%
Immune Thrombocytopenia
100%
Inducing Treatment
50%
Innate Immune Response
50%
Megakaryocytes
50%
Novel Therapeutics
100%
Novel Therapies
50%
Over 50
50%
Pathogenic Mechanism
50%
Plasma Cells
100%
Potential Therapeutics
50%
Resistance Development
50%
Rituximab
50%
Rituximab Resistance
100%
Splenectomy
50%
T Cells
100%
Therapeutic Interventions
50%
Treatment-free Remission
50%
Immunology and Microbiology
Adaptive Immune System
33%
B Cell
66%
Idiopathic Thrombocytopenic Purpura
100%
Immunoglobulin Producing Cell
66%
Innate Immune System
33%
Megakaryocyte
33%
Rituximab
100%
T Cell
66%
Pharmacology, Toxicology and Pharmaceutical Science
Idiopathic Thrombocytopenic Purpura
100%
Pathophysiology
33%
Remission
33%
Rituximab
100%