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- 2000
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Mark
Structural basis of Wiskott-Aldrich syndrome causing mutations in the WH1 domain
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- Contribution to journal › Article
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Mark
Identification of a novel transcription factor-like gene repressed during TGF-beta induced human intestinal epithelial cell differentiation.
(
- Contribution to journal › Published meeting abstract
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Mark
Bruton tyrosine kinase (Btk) in X-linked agammaglobulinemia (XLA)
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- Contribution to journal › Scientific review
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Mark
The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding protein
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- Contribution to journal › Article
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Mark
Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family
(
- Contribution to journal › Article
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Mark
Structural basis for SH2D1A mutations in X-linked lymphoproliferative disease
(
- Contribution to journal › Article
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Mark
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
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- Contribution to journal › Scientific review
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Mark
Identification of novel transcription factor-like gene from human intestinal cells
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- Contribution to journal › Article
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Mark
Molecular modeling of the Jak3 kinase domains and structural basis for severe combined immunodeficiency
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- Contribution to journal › Article
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Mark
Six X-linked agammaglobulinemia-causing missense mutations in the src homology 2 domain of Bruton's tyrosine kinase: Phosphotyrosine-binding and circular dichroism analysis
(
- Contribution to journal › Article