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Low iron availability modulates the course of Chlamydia pneumoniae infection
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Epithelial cells infected with Chlamydophila pneumoniae (Chlamydia pneumoniae) are resistant to apoptosis
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Persistent preswitch clonotypic myeloma cells correlate with decreased survival: evidence for isotype switching within the myeloma clone
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In multiple myeloma, circulating hyperdiploid B cells have clonotypic immunoglobulin heavy chain rearrangements and may mediate spread of disease
CLINICAL CANCER RESEARCH
A HIGH-FREQUENCY OF CIRCULATING B-CELLS SHARE CLONOTYPIC IG HEAVY-CHAIN VDJ REARRANGEMENTS WITH AUTOLOGOUS BONE-MARROW PLASMA-CELLS IN MULTIPLE-MYELOMA, AS MEASURED BY SINGLE-CELL AND IN-SITU REVERSE-TRANSCRIPTASE POLYMERASE-CHAIN-REACTION
Blood
DEFICIENT DRUG TRANSPORTER FUNCTION OF BONE MARROW-LOCALIZED AND LEUKEMIC PLASMA-CELLS IN MULTIPLE-MYELOMA
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CRYPTIC EXPRESSION OF THE CD19 EPITOPE DETECTED BY MAB LEU12 DISTINGUISHES MALIGNANT FROM RESIDUAL POLYCLONAL B-CELLS IN THE BLOOD OF MYELOMA PATIENTS
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AUTOCRINE GROWTH-REGULATION OF CIRCULATING CLONOTYPIC B-CELLS IN HUMAN MULTIPLE-MYELOMA - INTERLEUKIN-6 AND INTERLEUKIN-6 RECEPTOR EXPRESSION
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DRUG-RESISTANT MALIGNANT B-CELLS IN MULTIPLE-MYELOMA EXPRESS CD11B AND CLONOTYPIC TRANSCRIPTS
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CD34(-MYELOMA EXPRESS CD19 AND IGH MESSENGER-RNA AND HAVE PATIENT-SPECIFIC IGH VDJ GENE REARRANGEMENTS() CELLS IN THE BLOOD OF PATIENTS WITH MULTIPLE)
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IN MULTIPLE-MYELOMA, 10-90-PERCENT OF BLOOD B-CELLS HAVE AN IGH CDR3 IDENTICAL TO THAT OF AUTOLOGOUS PLASMA-CELLS, QUANTITATED USING SINGLE-CELL PCR, RT-PCR AND IN-SITU RT-PCR
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CD34(-CELLS IN MULTIPLE-MYELOMA HAVE A REARRANGED IGH VDJ IDENTICAL TO THAT OF AUTOLOGOUS PLASMA-CELLS AS QUANTITATED BY IN-SITU RT-PCR() CIRCULATING B)
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ABNORMAL CYTOKINE EXPRESSION PROFILE IN B-LYMPHOCYTE AND T-LYMPHOCYTEFRESHLY ISOLATED FROM PERIPHERAL-BLOOD OF MULTIPLE-MYELOMA PATIENTS
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