Results 281 to 290 of about 5,782,005 (384)

PROTEINS IN MULTIPLE MYELOMA

open access: yesJournal of Biological Chemistry, 1953
Frank W. Putnam, Bernard Udin
openaire   +3 more sources

A case of visceral leishmaniasis mimicking connective tissue disease

open access: yes
Rheumatology &Autoimmunity, EarlyView.
Yucui Li   +4 more
wiley   +1 more source

Can we identify individuals at risk to develop multiple myeloma? A machine learning‐based predictive model

open access: yesBritish Journal of Haematology, EarlyView.
Individuals who may develop multiple myeloma within 5 years. Stage I (left) identifies patient and control groups and variables that differ between them. Stage II (middle) develops a complex SGBOOST model to predict future MM patients. Stage III (right) develops a simplified model.
Moshe Mittelman   +8 more
wiley   +1 more source

Mapping VEXAS‐associated and rare UBA1 variants in the United Kingdom: Insights from patient cohorts and the general population

open access: yesBritish Journal of Haematology, EarlyView.
VEXAS syndrome is a late‐onset inflammatory disorder with rheumatological and haematological features. Epidemiological studies of VEXAS syndrome so far have been limited. Analysis of various UK cohorts estimates the incidence of VEXAS to be 1.51/100 000, or 171 new cases in the population of men over the age of 50 who are being investigated for myeloid
Ana Martinez Rodriguez   +15 more
wiley   +1 more source

Predictors of frontline doublet or triplet regimen initiation in transplant-ineligible newly diagnosed multiple myeloma. [PDF]

open access: yesFuture Sci OA
Pianko MJ   +6 more
europepmc   +1 more source

Human heat shock protein‐specific cytotoxic T lymphocytes display potent antitumour immunity in multiple myeloma

open access: yesBritish Journal of Haematology, 2014
Rong Li   +10 more
semanticscholar   +1 more source

Daratumumab and isatuximab differentially affect CD38 detection on plasma cells in myeloma: Anti‐CD38 nanobody (clone JK36) and CD319 combination improve flow cytometric identification of plasma cells after targeted therapies

open access: yesBritish Journal of Haematology, EarlyView.
Daratumumab and isatuximab differentially affect plasma cell identification by anti‐CD38 detection antibodies. HB‐7 and JK36 bind to CD38 epitopes E1 and E3, respectively, and co‐staining of plasma cells in the absence of CD38‐directed drugs results in a diagonal staining pattern (top left).
Afshin Shameli   +5 more
wiley   +1 more source

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