| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Mariana L Pais, João Martins, Miguel Castelo-Branco, Joana Gonçalve. Increased susceptibility to kainate-induced seizures in a mouse model of tuberous sclerosis complex: Importance of sex and circadian cycle. Epilepsia open. 2024-07-16. PMID:39010669. |
comorbidity of epilepsy and autism in tuberous sclerosis complex 2 (tsc2) is very frequent, but the link between these conditions is still poorly understood. |
2024-07-16 |
2024-07-18 |
mouse |
| Shiming Li, Jianfeng Li, Guoliang Chen, Tao Lin, Penghui Zhang, Kuileung Tong, Ningning Chen, Shaoyu Li. Exosomes originating from neural stem cells undergoing necroptosis participate in cellular communication by inducing TSC2 upregulation of recipient cells following spinal cord injury. Neural regeneration research. 2024-07-12. PMID:38993124. |
construction of a competing endogenous rna network identified the following hub genes: tuberous sclerosis 2 (tsc2), solute carrier family 16 member 3 (slc16a3), and forkhead box protein p1 (foxpl). |
2024-07-12 |
2024-07-14 |
mouse |
| Yi-Han Chang, Kwang-Yu Chang, Chao-Hsuan Li, Pei-Lung Chen, John A McGrath, Chao-Kai Hs. Delayed diagnosis of tuberous sclerosis complex: unveiling low-level TSC2 mosaicism using targeted next-generation sequencing. Clinical and experimental dermatology. 2024-07-06. PMID:38970490. |
delayed diagnosis of tuberous sclerosis complex: unveiling low-level tsc2 mosaicism using targeted next-generation sequencing. |
2024-07-06 |
2024-07-12 |
Not clear |
| Nuo Chen, Xiaoyu Wang, Yaxin Guo, Ming Zhao, Baihui Cao, Bing Zhan, Yubin Li, Tian Zhou, Faliang Zhu, Chun Guo, Yongyu Shi, Qun Wang, Lining Zhang, Yan L. IL-37d suppresses Rheb-mTORC1 axis independently of TCS2 to alleviate alcoholic liver disease. Communications biology. vol 7. issue 1. 2024-06-21. PMID:38907105. |
tuberous sclerosis complex 2 (tsc2) crucially suppresses rheb activity to prevent mtorc1 activation. |
2024-06-21 |
2024-06-24 |
human |
| b' Patricia Marqu\xe9s, Jes\xfas Burillo, Carlos Gonz\xe1lez-Blanco, Beatriz Jim\xe9nez, Gema Garc\xeda, Ana Garc\xeda-Aguilar, Sarai Iglesias-Fortes, \xc1ngela Lockwood, Carlos Guill\xe9. Regulation of TSC2 lysosome translocation and mitochondrial turnover by TSC2 acetylation status. Scientific reports. vol 14. issue 1. 2024-05-31. PMID:38822085.' |
sirtuin1 (sirt1) activity decreases the tuberous sclerosis complex 2 (tsc2) lysine acetylation status, inhibiting the mechanistic target of rapamycin complex 1 (mtorc1) signalling and concomitantly, activating autophagy. |
2024-05-31 |
2024-06-02 |
mouse |
| Vincent Milon, Marie-Claire Malinge, Maud Blanluet, Marine Tessarech, Clarisse Battault, Sarah Prestwich, Béatrice Vary, Pierre Gueracher, Louis Legoff, Magalie Barth, Clara Houdayer, Agnès Guichet, Audrey Rousseau, Dominique Bonneau, Vincent Procaccio, Céline Bris, Estelle Coli. Diagnosis of tuberous sclerosis in the prenatal period: a retrospective study of 240 cases and review of the literature. European journal of human genetics : EJHG. 2024-05-28. PMID:38806662. |
tuberous sclerosis complex (tsc) is a rare multisystemic disorder caused by a pathogenic variant in the tsc1 or tsc2 gene. |
2024-05-28 |
2024-06-03 |
Not clear |
| Cassie Liu, Subodh M Lele, Martin H Goodenberger, Gwendolyn M Reiser, Andrew J Christiansen, James C Padussi. Malignant tumors in tuberous sclerosis complex: a case report and review of the literature. BMC medical genomics. vol 17. issue 1. 2024-05-28. PMID:38802873. |
tuberous sclerosis complex (tsc) is a rare, autosomal dominant genetic disease that arises from tsc1 or tsc2 genetic mutations. |
2024-05-28 |
2024-05-31 |
Not clear |
| Jiahui Fu, Peili Liang, Yingchun Zheng, Cailing Xu, Fu Xiong, Fang Yan. Corrigendum to "A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K_AKT_mTOR signaling pathway" [GENE909 (2024) 148312/D-23-04187]. Gene. vol 919. 2024-04-30. PMID:38685184. |
corrigendum to "a large deletion in tsc2 causes tuberous sclerosis complex by dysregulating pi3k_akt_mtor signaling pathway" [gene909 (2024) 148312/d-23-04187]. |
2024-04-30 |
2024-05-03 |
Not clear |
| Siyao Zhang, Jiaqi Fan, Hairui Sun, Xiaoyan Hao, Yihua H. Generation of a TSC2 knockout embryonic stem cell line by CRISPR/Cas9 editing. Stem cell research. vol 77. 2024-04-04. PMID:38574666. |
tuberous sclerosis complex (tsc) is a severe developmental disorder with various clinical effects, primarily caused by tsc2 gene mutations, often involving loss of function(henske,et al., 2016).to explore role of tsc2 in human heart development, we successfully developed a tsc2 knockout (tsc2-/-) human embryonic stem cells (hescs) line using crispr/cas9 gene editing. |
2024-04-04 |
2024-04-07 |
human |
| Ananya Sharma, Bhawana Aggarwal, Aanchal Kakkar, Niraj Nirmal Pandey, Neha Tanej. Dermoscopy of hypopigmented macules unveiling genetic diagnosis of tuberous sclerosis complex type 2 in an infant presenting with sacral chordoma. Pediatric dermatology. 2024-03-19. PMID:38500310. |
the combination of these findings led to a diagnosis of tuberous sclerosis, confirmed with the finding of a heterozygous tsc2 gene deletion; treatment with sirolimus resulted in regression of cardiac rhabdomyomas and hypopigmented macules. |
2024-03-19 |
2024-03-21 |
Not clear |
| Xiao-Tong Wang, Ru Fang, Hui-Ying He, Wei Zhang, Qing Li, Su-An Sun, Xuan Wang, Ru-Song Zhang, Xiao-Dong Teng, Xiao-Jun Zhou, Qiu-Yuan Xia, Ming Zhao, Qiu Ra. Recurrent Tuberous Sclerosis Complex/Mammalian Target of Rapamycin Mutations Define Primary Renal Hemangioblastoma as a Unique Entity Distinct From Its Central Nervous System Counterpart. The American journal of surgical pathology. 2024-03-19. PMID:38501656. |
mutational analysis demonstrated that all 10 renal hbs harbored somatic mutations in tuberous sclerosis complex 1 (tsc1, 5 cases), tsc2 (3 cases), and mammalian target of rapamycin (2 cases), with the majority classified as pathogenic or likely pathogenic. |
2024-03-19 |
2024-03-21 |
Not clear |
| HaEun Kim, Benjamin Lebeau, David Papadopoli, Predrag Jovanovic, Mariana Russo, Daina Avizonis, Masahiro Morita, Farzaneh Afzali, Josie Ursini-Siegel, Lynne-Marie Postovit, Michael Witcher, Ivan Topisirovi. MTOR modulation induces selective perturbations in histone methylation which influence the anti-proliferative effects of mTOR inhibitors. iScience. vol 27. issue 3. 2024-03-04. PMID:38433910. |
our results show that mtorc1 activation caused by the abrogation of its negative regulator tuberous sclerosis complex 2 (tsc2) coincides with increased levels of the histone modification h3k27me3 but not h3k4me3 or h3k9me3. |
2024-03-04 |
2024-03-06 |
Not clear |
| Jiahui Fu, Peili Liang, Yingchun Zheng, Cailing Xu, Fu Xiong, Fang Yan. A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K/AKT/mTOR signaling pathway. Gene. 2024-02-27. PMID:38412945. |
a large deletion in tsc2 causes tuberous sclerosis complex by dysregulating pi3k/akt/mtor signaling pathway. |
2024-02-27 |
2024-03-01 |
Not clear |
| Jiahui Fu, Peili Liang, Yingchun Zheng, Cailing Xu, Fu Xiong, Fang Yan. A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K/AKT/mTOR signaling pathway. Gene. 2024-02-27. PMID:38412945. |
tuberous sclerosis complex (tsc) is a multi-system syndrome caused by loss-of-function mutation in tsc1 or tsc2. |
2024-02-27 |
2024-03-01 |
Not clear |
| Marta Banchi, Tiziana Lanzolla, Arianna Di Napoli, Arianna Bandini, Guido Bocci, Maria Christina Co. Complete Remission of a Diffuse Large B-Cell Lymphoma in a Young Patient, with Severe Tuberous Sclerosis, Treated with Metronomic Chemotherapy and Ibrutinib: A Case Report. Chemotherapy. vol 69. issue 1. 2024-02-26. PMID:37549660. |
tuberous sclerosis (ts) is a rare autosomal dominant genetic multisystem disease caused by mutations in either the tsc1 or tsc2 gene and results in the growth of non-cancerous masses in several organs. |
2024-02-26 |
2024-02-29 |
human |
| Arthur Bandeira de Mello Garcia, Guilherme Danielski Viola, Bruno da Silveira Corrêa, Taís da Silveira Fischer, Maria Clara de Freitas Pinho, Grazielle Motta Rodrigues, Patricia Ashton-Prolla, Clévia Rosse. An overview of actionable and potentially actionable TSC1 and TSC2 germline variants in an online Database. Genetics and molecular biology. vol 46. issue 3 Suppl 1. 2024-02-19. PMID:38373162. |
tuberous sclerosis complex (tsc) is caused by loss of function germline variants in the tsc1 or tsc2 tumor suppressor genes. |
2024-02-19 |
2024-02-22 |
Not clear |
| Paula Basso Dias, Anna Carolina Badotti Linhares, Ana Barbara Dias Lopes Urzedo, Rony Carlos Preti, Leandro Cabral Zacharias, Leonardo Provetti Cunha, Mário Luiz Ribeiro Monteiro, Kenzo Hokazon. Optical coherence tomography detection of retinal neural loss in patients with tuberous sclerosis. International journal of retina and vitreous. vol 10. issue 1. 2024-02-04. PMID:38311784. |
tuberous sclerosis (ts) is a rare, multisystem genetic disease caused by mutations in the tsc1 and tsc2 genes, leading to abnormalities in cell differentiation and proliferation. |
2024-02-04 |
2024-02-07 |
Not clear |
| Lijuan Wang, Huan Xin. Segmental hypopigmentation and unilateral fibrous patches: an unusual presentation of tuberous sclerosis complex with a novel TSC2 mutation. International journal of dermatology. 2024-01-25. PMID:38273422. |
segmental hypopigmentation and unilateral fibrous patches: an unusual presentation of tuberous sclerosis complex with a novel tsc2 mutation. |
2024-01-25 |
2024-01-28 |
Not clear |
| Seung Woo Ryu, Ji-Hee Yoon, Dong-Wook Kim, Beomman Han, Heonjong Han, Joohyun Han, Hane Lee, Go Hun Seo, Beom Hee Le. Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular genetics & genomic medicine. 2024-01-24. PMID:38265426. |
tuberous sclerosis complex (tsc) is an autosomal dominant multisystem disorder, caused by a loss-of-function of either tsc1 or tsc2 gene. |
2024-01-24 |
2024-01-26 |
Not clear |
| Yaewon Yang, Jisun Lee, Chang Gok Woo, Ok-Jun Lee, Seung-Myoung So. Epithelioid angiomyolipoma of the liver in a patient with Li-Fraumeni syndrome: a case report. Diagnostic pathology. vol 19. issue 1. 2024-01-19. PMID:38243242. |
most pecomas arise sporadically, but may be associated with tuberous sclerosis complex (tsc), an autosomal dominant genetic disorder characterized by germline mutations in the tsc1 or tsc2 genes. |
2024-01-19 |
2024-01-22 |
Not clear |