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UCSF School of Medicine | Department of Pediatrics UCSF Medical Center

Proteinarium: Multi-sample protein-protein interaction analysis and visualization tool.

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Pathway-based genetic analysis of preterm birth.

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Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22.

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Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene.

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Localization and analysis of the principal promoter for human tenascin-X.

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IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease.

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Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.

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A microsatellite-based multipoint index map of human chromosome 22.

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Twelve new polymorphic microsatellites on human chromosome 22.

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The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22.

  • Read more about The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22.
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