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X-linked agammaglobulinemia

Known as: AGMX1, Bruton's Agammaglobulinemia, BRUTON-TYPE AGAMMAGLOBULINEMIA 
X-linked agammaglobulinemia. An immunodeficiency state characterized (usually) by profoundly low concentrations of serum immunoglobulins of all… Expand
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
More than 50 years after Ogdeon Bruton's discovery of congenital agammaglobulinemia, human primary immunodeficiencies (PIDs… Expand
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Review
2006
Review
2006
X‐linked agammaglobulinemia (XLA) is a hereditary immunodeficiency caused by mutations in the gene encoding Bruton tyrosine… Expand
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Highly Cited
2005
Highly Cited
2005
H igher education is a business: it produces and sells educational services to customers for a price and it buys inputs with… Expand
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Highly Cited
2001
Highly Cited
2001
Recombinant vectors based on adeno-associated virus (AAV) or human immunodeficiency 1 (lentivirus) are promising tools for long… Expand
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Review
1996
Review
1996
X-linked agammaglobulinemia (XLA), characterized by a profound deficiency of B lymphocytes due to an arrest in B lymphocyte… Expand
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Highly Cited
1994
Highly Cited
1994
The gene mutated in the human disease, X-linked agammaglobulinemia (XLA), is related to the Src gene family of cytoplasmic… Expand
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Highly Cited
1993
Highly Cited
1993
Mice that bear the X-linked immunodeficiency (xid) mutation have a B lymphocyte-specific defect resulting in an inability to make… Expand
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Review
1991
Review
1991
X-linked agammaglobulinemia (XLA) patients manifest a very low production of immunoglobulins (Ig) of all classes and plasma cells… Expand
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Highly Cited
1986
Highly Cited
1986
Although X-linked agammaglobulinemia was one of the first immunodeficiencies described,1 the genetic defect responsible for this… Expand
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Highly Cited
1985
Highly Cited
1985
  • M. Conley
  • Journal of immunology
  • 1985
  • Corpus ID: 9371093
X-linked agammaglobulinemia (XLA) has been described as a disorder in which pre-B cells fail to differentiate into B cells… Expand
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