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Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder.

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Activating and inactivating mutations in the human GNAS1 gene.

Human mutation·2000

A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted region.

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Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.

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The niche-metabolism axis: reprogramming tumor-associated macrophages for precision immunotherapy.

Trends in molecular medicine·2026

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Formicitoxins: membrane-targeting antifungal peptides from carpenter ant venoms.

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Trends in molecular medicine·2026

Statins suppress colon tumors by inhibiting KRAS condensates.

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RNA translational control in skeletal development, homeostasis, and disease.

Trends in molecular medicine·2026

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Current medical research and opinion·2026

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Physics in medicine and biology·2026

Brain alterations detected by multiplex magnetic resonance imaging in nasopharyngeal carcinoma patients after induction chemotherapy: a longitudinal study.

PeerJ·2026

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Cureus·2026

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Three decades of occupational individual monitoring at the University of São Paulo.

Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder.

Activating and inactivating mutations in the human GNAS1 gene.

A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted region.

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