Pages that link to "Q48207079"
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The following pages link to Diversity of immunoglobulin heavy chain gene segment rearrangement in B lymphoblastoid cell lines from X-linked agammaglobulinemia patients (Q48207079):
Displaying 14 items.
- Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire. (Q33896289) (← links)
- X-linked agammaglobulinemia (Q34099457) (← links)
- The human VH repertoire: a restricted set of VH genes may be the target of immune regulation (Q36196150) (← links)
- Diversification, not use, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome (Q36362304) (← links)
- Characterization of immunoglobulin by mass spectrometry with applications for the clinical laboratory (Q38155231) (← links)
- Molecular and cellular aspects of X-linked agammaglobulinemia. (Q40373279) (← links)
- Breakthroughs in the understanding and therapy of primary immunodeficiency. (Q40681331) (← links)
- V(D)J recombination pathology. (Q41134314) (← links)
- The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stages (Q41510794) (← links)
- Immunoglobulin kappa light chain germ-line transcripts in human precursor B lymphocytes (Q41591551) (← links)
- The VDJ repertoire expressed in human preB cells reflects the selection of bona fide heavy chains (Q48067974) (← links)
- Diversity of immunoglobulin kappa light chain gene rearrangements and evidence for somatic mutation in V kappa IV family gene segments in X-linked agammaglobulinemia (Q48130703) (← links)
- Restricted utilization of germ-line VH3 genes and short diverse third complementarity-determining regions (CDR3) in human fetal B lymphocyte immunoglobulin heavy chain rearrangements (Q48190559) (← links)
- B-cell receptor repertoire sequencing in patients with primary immunodeficiency: a review (Q48300362) (← links)