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UCSF School of Medicine | Department of Pediatrics UCSF Medical Center

Multidimensional, integrative profiling identifies BCL2L1 methylation as a predictor of MCL1 dependency in pediatric malignancies.

  • Read more about Multidimensional, integrative profiling identifies BCL2L1 methylation as a predictor of MCL1 dependency in pediatric malignancies.

Noise induces Ca2+ signaling waves and Chop/S-Xbp1 expression in the hearing cochlea.

  • Read more about Noise induces Ca2+ signaling waves and Chop/S-Xbp1 expression in the hearing cochlea.

DRA involvement in linaclotide stimulated bicarbonate secretion during loss of CFTR function.

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Coordinated immune dysregulation in juvenile dermatomyositis revealed by single-cell genomics.

  • Read more about Coordinated immune dysregulation in juvenile dermatomyositis revealed by single-cell genomics.

TMTC4 is a hair-cell-specific human deafness gene.

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Human hepatic organoids for the analysis of human genetic diseases.

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Homeostatic cytokines reciprocally modulate the emergence of prenatal effector PLZF+CD4+ T cells in humans.

  • Read more about Homeostatic cytokines reciprocally modulate the emergence of prenatal effector PLZF+CD4+ T cells in humans.

Structural and functional analyses of a germline KRAS T50I mutation provide insights into Raf activation.

  • Read more about Structural and functional analyses of a germline KRAS T50I mutation provide insights into Raf activation.

Autoantigen profiling reveals a shared post-COVID signature in fully recovered and long COVID patients.

  • Read more about Autoantigen profiling reveals a shared post-COVID signature in fully recovered and long COVID patients.

Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition.

  • Read more about Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition.

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