Tsc1 is a Critical Regulator of Macrophage Survival and Function by Chunmin Fang, Juan Yu, Yuechen Luo, Song Chen, Weiqiang Wang, Chunxiao Zhao, Zhina Sun, Wantong Wu, Wei Guo, Zhongchao Han, Xiao Hu, Fang Liao, Xiaoming Feng

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Hamartin: An Endogenous Neuroprotective Molecule Induced by Hypoxic Preconditioning by Sijie Li, Sijie Li, Changhong Ren, Changhong Ren, Christopher Stone, Ankush Chandra, Jiali Xu, Ning Li, Cong Han, Yuchuan Ding, Xunming Ji, Guo Shao, Guo Shao, Guo Shao, Guo Shao

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Mutations in ALK and TSC1 in a gastrointestinal stromal tumor: a case report by Qingzhi Song, Guan Li, Zhuofei Li, Sheng Ao, Jianing Hou, Guoqing Lv

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The effect of high-intensity interval swimming training on ULK and TSC1/2 proteins of hippocampus tissue in elderly rats by Mostafa Salmanizadeh Qomi, Saeedeh Shadmehri

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mTORC1 signalling mediates PI3K-dependent large lipid droplet accumulation in Drosophila ovarian nurse cells by Lawrence B. Mensah, Deborah C. I. Goberdhan, Clive Wilson

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A Human TSC1 Variant Screening Platform in Gabaergic Cortical Interneurons for Genotype to Phenotype Assessments by Dean Wundrach, Luis E. Martinetti, Luis E. Martinetti, April M. Stafford, Stephanie M. Bilinovich, Kartik Angara, Jeremy W. Prokop, Jeremy W. Prokop, Jeremy W. Prokop, Shane R. Crandall, Shane R. Crandall, Daniel Vogt, Daniel Vogt, Daniel Vogt

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DYRK1A reinforces epithelial-mesenchymal transition and metastasis of hepatocellular carcinoma via cooperatively activating STAT3 and SMAD by Yang-ling Li, Man-man Zhang, Lin-wen Wu, Ye-han Liu, Zuo-yan Zhang, Ling-hui Zeng, Neng-ming Lin, Chong Zhang

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Co-occurrence of leukemia, Crohn’s disease, and tuberous sclerosis in one patient by Yoon Ji Ahn, Dasom Park, Mi Jin Kim, Yon Ho Choe, Youngse Kwon, Yiyoung Kwon

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Tuberous sclerosis complex: Clinical spectrum and epilepsy: A retrospective chart review study by Almobarak Sulaiman, Almuhaizea Mohammad, Abukhaled Musaad, Alyamani Suad, Dabbagh Omar, Chedrawi Aziza, Khan Sameena, Aldhalaan Hesham

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Clinical and Molecular Spectrum of Tuberous Sclerosis Complex Patients: Identification of Three Novel Mutations by Esra Işık, Hüseyin Onay, Tahir Atık, Aslı Ece Solmaz, Demet Terek, Sarenur Gökben, Hasan Tekgül, Ertürk Levent, Mehmet Kantar, Nilgün Kültürsay, Özgür Çoğulu, Ferda Özkınay

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Osteocyte TSC1 promotes sclerostin secretion to restrain osteogenesis in mice by Wen Liu, Zhenyu Wang, Jun Yang, Yongkui Wang, Kai Li, Bin Huang, Bo Yan, Ting Wang, Mangmang Li, Zhipeng Zou, Jian Yang, Guozhi Xiao, Zhong-Kai Cui, Anling Liu, Xiaochun Bai

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Identification of genetic variants in two families with Keratoconus by Qinghong Lin, Xuejun Wang, Tian Han, Xingtao Zhou

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Identification of a novel TSC1 gene variant in a patient with atypical vitiligo‐like skin lesions: Unveiling the hidden tuberous sclerosis complex by Linli Liu, Yanbo Wang, Zhengzhong Zhang, Chunshui Yu, Jin Chen

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FoxO suppresses endoplasmic reticulum stress to inhibit growth of Tsc1-deficient tissues under nutrient restriction by Avantika Gupta, Hugo Stocker

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Electro-clinical and neurodevelopmental outcome in six children with early diagnosis of tuberous sclerosis complex and role of the genetic background by M. N. Savini, A. Mingarelli, A. Peron, F. La Briola, F. Cervi, R. M. Alfano, M. P. Canevini, A. Vignoli

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Tsc1 deletion in Purkinje neurons disrupts the axon initial segment, impairing excitability and cerebellar function by Samuel P. Brown, Achintya K. Jena, Joanna J. Osko, Joseph L. Ransdell

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Renal phenotypes correlate with genotypes in unrelated individuals with tuberous sclerosis complex in China by Cong Luo, Ye Zhang, Yu-shi Zhang, Ming-Xin Zhang, Jun Ning, Min-Feng Chen, Yuan Li, Lin Qi, Xiong-Bing Zu, Yang-Le Li, Yi Cai

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miR-301a Suppression within Fibroblasts Limits the Progression of Fibrosis through the TSC1/mTOR Pathway by Jiexuan Wang, Xun Li, Mingtian Zhong, Yansheng Wang, Liming Zou, Miaomiao Wang, Xiaoli Gong, Xinjie Wang, Chengzhi Zhou, Xiaodong Ma, Ming Liu

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<i>Tsc1</i> Loss in VIP-Lineage Cortical Interneurons Results in More VIP+ Interneurons and Enhanced Excitability by Jia Sheng Hu, Ruchi Malik, Vikaas S. Sohal, John L. Rubenstein, Daniel Vogt

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The association of neurodevelopmental abnormalities, congenital heart and renal defects in a tuberous sclerosis complex patient cohort by Jessica Robinson, Orhan Uzun, Ne Ron Loh, Isabelle Rose Harris, Thomas E. Woolley, Adrian J. Harwood, Jennifer Frances Gardner, Yasir Ahmed Syed

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