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Beth S. Ruben

Researcher at University of California, San Francisco

Publications -  52
Citations -  2232

Beth S. Ruben is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Nail (anatomy) & Nail plate. The author has an hindex of 16, co-authored 52 publications receiving 1857 citations. Previous affiliations of Beth S. Ruben include University of California & Palo Alto Medical Foundation.

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The Genetic Evolution of Melanoma from Precursor Lesions

TL;DR: The succession of genetic alterations during melanoma progression was defined, showing distinct evolutionary trajectories for different melanoma subtypes, and an intermediate category of melanocytic neoplasia was identified, characterized by the presence of more than one pathogenic genetic alteration and distinctive histopathological features.
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Acrodermatitis enteropathica and an overview of zinc metabolism

TL;DR: In this paper, the authors provide an overview of zinc metabolism and a description of inherited and acquired zinc deficiency, which is made by way of clinical presentation together with histopathology and laboratory tests.
Journal Article

Classification, clinical manifestations, and immunopathological mechanisms of the epithelial variant of paraneoplastic autoimmune multiorgan syndrome: a reappraisal of paraneoplastic pemphigus.

TL;DR: The more encompassing term "paraneoplastic autoimmune multiorgan syndrome," or PAMS, is suggested to be applied to classify the diverse mucocutaneous and respiratory presentations of PNP and characterize the effectors of humoral and cellular autoimmunity mediating epithelial tissue damage.
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Genomic and Transcriptomic Analysis Reveals Incremental Disruption of Key Signaling Pathways during Melanoma Evolution.

TL;DR: Genomic and transcriptomic changes that accompany the evolution of melanoma from pre-malignant lesions are elucidated by sequencing DNA and RNA from primary melanomas and their adjacent precursors, as well as matched primary tumors and regional metastases.