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Xiaolin Lin

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Xiaolin Lin

Researcher
Department of Clinical and Molecular Medicine

xiaolin.lin@ntnu.no
Publications

Publications

  • Chronological
  • By category
  • All publications registered in NVA

2025

  • Li, Yanjiao; Wang, Yunhao; Cengiz, Aylin; Jin, Kang-Xuan; Castroviejo, Blanca Corral; Lin, Xiaolin. (2025) The RNA m6A landscape during human oocyte-to-embryo transition. EMBO Journal
    Academic article

2023

  • Lin, Xiaolin; Wang, Wei; Yang, Mingyi; Damseh, Nadirah; Sousa, Mirta; Jacob, Fadi. (2023) A loss-of-function mutation in human Oxidation Resistance 1 disrupts the spatial–temporal regulation of histone arginine methylation in neurodevelopment. Genome Biology
    Academic article

2022

  • Kennedy, Lauritz Hagen; Glesaaen, Emilie Rylund; Palibrk, Vuk; Pannone, Marco; Wang, Wei; Al-Jabri, Ali. (2022) Lactate receptor HCAR1 regulates neurogenesis and microglia activation after neonatal hypoxia-ischemia. eLIFE
    Academic article

2020

  • Yang, Mingyi; Lin, Xiaolin; Segers, Filip; Suganthan, Rajikala; Hildrestrand, Gunn Annette; Rinholm, Johanne Egge. (2020) OXR1A, a Coactivator of PRMT5 Regulating Histone Arginine Methylation. Cell reports
    Academic article

2017

  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying. (2017) Corrigendum: Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics
    Errata
  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying. (2017) Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics
    Academic article

2015

  • Yang, Mingyi; Lin, Xiaolin; Rowe, Alexander D.; Rognes, Torbjørn; Eide, Lars; Bjørås, Magnar. (2015) Transcriptome analysis of human OXR1 depleted cells reveals its role in regulating the p53 signaling pathway. Scientific Reports
    Academic article

Journal publications

  • Li, Yanjiao; Wang, Yunhao; Cengiz, Aylin; Jin, Kang-Xuan; Castroviejo, Blanca Corral; Lin, Xiaolin. (2025) The RNA m6A landscape during human oocyte-to-embryo transition. EMBO Journal
    Academic article
  • Lin, Xiaolin; Wang, Wei; Yang, Mingyi; Damseh, Nadirah; Sousa, Mirta; Jacob, Fadi. (2023) A loss-of-function mutation in human Oxidation Resistance 1 disrupts the spatial–temporal regulation of histone arginine methylation in neurodevelopment. Genome Biology
    Academic article
  • Kennedy, Lauritz Hagen; Glesaaen, Emilie Rylund; Palibrk, Vuk; Pannone, Marco; Wang, Wei; Al-Jabri, Ali. (2022) Lactate receptor HCAR1 regulates neurogenesis and microglia activation after neonatal hypoxia-ischemia. eLIFE
    Academic article
  • Yang, Mingyi; Lin, Xiaolin; Segers, Filip; Suganthan, Rajikala; Hildrestrand, Gunn Annette; Rinholm, Johanne Egge. (2020) OXR1A, a Coactivator of PRMT5 Regulating Histone Arginine Methylation. Cell reports
    Academic article
  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying. (2017) Corrigendum: Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics
    Errata
  • Rydning, Siri Lynne; Backe, Paul Hoff; Sousa, Mirta; Iqbal, Zafar; Øye, Ane-Marte; Sheng, Ying. (2017) Novel UCHL1 mutations reveal new insights into ubiquitin processing. Human Molecular Genetics
    Academic article
  • Yang, Mingyi; Lin, Xiaolin; Rowe, Alexander D.; Rognes, Torbjørn; Eide, Lars; Bjørås, Magnar. (2015) Transcriptome analysis of human OXR1 depleted cells reveals its role in regulating the p53 signaling pathway. Scientific Reports
    Academic article

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