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Molecular and Cellular Biology
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  • Defect of FANCJ in FANCG Patient (hFANCGR22P) Cell.
    Defect of FANCJ in FANCG Patient (hFANCGR22P) Cell.
  • Geldanamycin-Derived HSP90 Inhibitors Are Synthetic Lethal with NRF2.
    Geldanamycin-Derived HSP90 Inhibitors Are Synthetic Lethal with NRF2.
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Research Articles

  • The Endoplasmic Reticulum Cargo Receptor SURF4 Facilitates Efficient Erythropoietin Secretion
    Research Article | Spotlight
    The Endoplasmic Reticulum Cargo Receptor SURF4 Facilitates Efficient Erythropoietin Secretion

    Erythropoietin (EPO) stimulates erythroid differentiation and maturation. Though the transcriptional regulation of EPO has been well studied, the molecular determinants of EPO secretion remain unknown. Here, we generated a HEK293T reporter cell line that provides a quantifiable and selectable readout of intracellular EPO levels and performed a genome-scale CRISPR screen that identified SURF4 as an important mediator of EPO secretion....

    Zesen Lin, Richard King, Vi Tang, Greggory Myers, Ginette Balbin-Cuesta, Ann Friedman, Beth McGee, Karl Desch, Ayse Bilge Ozel, David Siemieniak, Pavan Reddy, Brian Emmer, Rami Khoriaty
  • Loss of Mitochondrial Localization of Human FANCG Causes Defective FANCJ Helicase
    Research Article
    Loss of Mitochondrial Localization of Human FANCG Causes Defective FANCJ Helicase

    Fanconi anemia (FA) is a unique DNA damage repair pathway. To date, 22 genes have been identified that are associated with the FA pathway. A defect in any of those genes causes genomic instability, and the patients bearing the mutation become susceptible to cancer. In our earlier work, we identified that Fanconi anemia protein G (FANCG) protects the mitochondria from oxidative stress. In this report, we have identified eight patients...

    Jagadeesh Chandra Bose K, Bishwajit Singh Kapoor, Kamal Mandal, Shubhrima Ghosh, Raveendra B. Mokhamatam, Sunil K. Manna, Sudit S. Mukhopadhyay

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    Correction for Adon et al., “Cdk2 and Cdk4 Regulate the Centrosome Cycle and Are Critical Mediators of Centrosome Amplification in p53-Null Cells”
    Author Correction
    Correction for Adon et al., “Cdk2 and Cdk4 Regulate the Centrosome Cycle and Are Critical Mediators of Centrosome Amplification in p53-Null Cells”
    Arsene M. Adon, Xiangbin Zeng, Mary K. Harrison, Stacy Sannem, Hiroaki Kiyokawa, Philipp Kaldis, Harold I. Saavedra

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NEW:COVID-19 Research and News from ASM Journals

Molecular and Cellular Biology: 40 (23)

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volume 40, issue 23
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  • When Long Noncoding Becomes Protein Coding
  • Age-Dependent Ribosomal DNA Variations in Mice
  • Mutations Outside the Ure2 Amyloid-Forming Region Disrupt [URE3] Prion Propagation and Alter Interactions with Protein Quality Control Factors
  • Transcriptional and Epigenomic Regulation of Adipogenesis
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