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Expression of Bruton's tyrosine kinase in B lymphoblastoid cell lines from X‐linked agammaglobulinaemia patients

Clinical and experimental immunology, 1997-02, Vol.107 (2), p.235-240

1997

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B-cell antigen receptor stimulation activates the human Bruton's tyrosine kinase, which is deficient in X-linked agammaglobulinemia

The Journal of biological chemistry, 1994-09, Vol.269 (39), p.23857-23860

1994

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Genetics of human X‐linked immunodeficiency diseases

Clinical and experimental immunology, 1991-08, Vol.85 (2), p.182-192

1991

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Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia

Human genetics, 1989-10, Vol.83 (3), p.267-270

1989

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Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity

Human genetics, 1986-08, Vol.73 (4), p.327-332

1986

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Restricted utilization of germ‐line VH3 genes and short diverse third complementarity‐determining regions (CDR3) in human fetal B lymphocyte immunoglobulin heavy chain rearrangements

European journal of immunology, 1992-01, Vol.22 (1), p.247-251

1992

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VH gene usage in humans: biased usage of the VH6 gene in immature B lymphoid cells

European journal of immunology, 1991-05, Vol.21 (5), p.1311-1314

1991

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Inheritance of a Large Deletion within the Human Immunoglobulin Heavy Chain Constant Region Gene Complex and Immunological Implications

Scandinavian journal of immunology, 1989-05, Vol.29 (5), p.535-541

1989

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Evidence that in X‐linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact

European journal of immunology, 1990-12, Vol.20 (12), p.2603-2608

1990

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Polyclonal hyper-immunoglobulin G1(A1) syndrome: evidence for a dominant immunoglobulin production regulator within the human immunoglobulin heavy chain gene complex

Human genetics, 1989-05, Vol.82 (2), p.194-196

1989

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An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene

Human molecular genetics, 1992-06, Vol.1 (3), p.187-194

1992

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Immunodeficiency disease genes on the X chromosome

Disease markers, 1987-09, Vol.5 (3), p.129

1987

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X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked

Human genetics, 1984-01, Vol.68 (4), p.303-309

1984

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Early diagnosis in X-linked agammaglobulinaemia

European journal of pediatrics, 1988, Vol.147 (1), p.93-95

1988

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The thymus in "bare lymphocyte" syndrome

Advances in experimental medicine and biology, 1985, Vol.186, p.921

1985

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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

European journal of immunology, 1993-12, Vol.23 (12), p.3109-3114

1993

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Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia M

Clinical genetics, 1995-07, Vol.48 (1), p.46-48

1995

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Diversity of immunoglobulin heavy chain gene segment rearrangement in B lymphoblastoid cell lines from X‐linked agammaglobulinemia patients

European journal of immunology, 1991-10, Vol.21 (10), p.2355-2363

1991

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Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus

Human genetics, 1991-11, Vol.88 (1), p.105-111

1991

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Three dinucleotide repeat polymorphisms at the DXS178 locus

Human molecular genetics, 1992-10, Vol.1 (8), p.653-653

1992

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Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid mice

Human molecular genetics, 1994-01, Vol.3 (1), p.161-166

1994

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X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus

Human genetics, 1987-05, Vol.76 (1), p.96-99

1987

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Immunoglobulin heavy chain gene rearrangements in X‐linked agammaglobulinemia

European journal of immunology, 1986, Vol.16 (8), p.963-967

1986

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X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus

Clinical genetics, 1992-09, Vol.42 (3), p.114-121

1992

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Severe combined immunodeficiency in man with an absence of immunoglobulin gene rearrangements but normal T cell receptor assembly

European journal of immunology, 1990-09, Vol.20 (9), p.2051-2056

1990

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Expression of Bruton's tyrosine kinase in B lymphoblastoid cell lines from X‐linked agammaglobulinaemia patients

B-cell antigen receptor stimulation activates the human Bruton's tyrosine kinase, which is deficient in X-linked agammaglobulinemia

Genetics of human X‐linked immunodeficiency diseases

Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia

Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity

Restricted utilization of germ‐line VH3 genes and short diverse third complementarity‐determining regions (CDR3) in human fetal B lymphocyte immunoglobulin heavy chain rearrangements

VH gene usage in humans: biased usage of the VH6 gene in immature B lymphoid cells

Inheritance of a Large Deletion within the Human Immunoglobulin Heavy Chain Constant Region Gene Complex and Immunological Implications

Evidence that in X‐linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact

Polyclonal hyper-immunoglobulin G1(A1) syndrome: evidence for a dominant immunoglobulin production regulator within the human immunoglobulin heavy chain gene complex

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene

Immunodeficiency disease genes on the X chromosome

X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked

Early diagnosis in X-linked agammaglobulinaemia

The thymus in "bare lymphocyte" syndrome

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

Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia M

Diversity of immunoglobulin heavy chain gene segment rearrangement in B lymphoblastoid cell lines from X‐linked agammaglobulinemia patients

Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus

Three dinucleotide repeat polymorphisms at the DXS178 locus

Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid mice

X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus

Immunoglobulin heavy chain gene rearrangements in X‐linked agammaglobulinemia

X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus

Severe combined immunodeficiency in man with an absence of immunoglobulin gene rearrangements but normal T cell receptor assembly

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