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Feb 26, 2019 (publication date) through Jan 11, 2025
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Li JQ, Gong JY, Knisely AS, Zhang MH, Wang JS. Recurrent acute liver failure associated with novel SCYL1 mutation: A case report. World J Clin Cases 2019; 7(4): 494-499 [PMID: 30842961 DOI: 10.12998/wjcc.v7.i4.494] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v7/i4/494.htm |
| Number | Citing Articles |
| 1 |
Engin Demir, Ümmühan Öncül, Merve Havan, Ceyda Tuna Kirsaçlioğlu, Fatma Tuba Eminoğlu, Tanil Kendirli, Zarife Kuloğlu, Aydan Kansu. Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient. Clinical Dysmorphology 2023; 32(1): 25 doi: 10.1097/MCD.0000000000000435
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| 2 |
Genki Amano, Shinsuke Matsuzaki, Yasutake Mori, Ko Miyoshi, Sarina Han, Sho Shikada, Hironori Takamura, Takeshi Yoshimura, Taiichi Katayama, Kozo Kaibuchi. SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. Molecular Biology of the Cell 2020; 31(18): 1963 doi: 10.1091/mbc.E20-02-0100
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| 3 |
Bianca Peters, Tal Dattner, Lea D. Schlieben, Tian Sun, Christian Staufner, Dominic Lenz. Disorders of vesicular trafficking presenting with recurrent acute liver failure: NBAS, RINT1, and SCYL1 deficiency. Journal of Inherited Metabolic Disease 2024; doi: 10.1002/jimd.12707
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| 4 |
Sanghoon Lee, Jung Nyeo Chun, Hae-Jeung Lee, Hyun Ho Park, Insuk So, Ju-Hong Jeon, Eun-Jung Park. Transcriptome Analysis of the Anti-TGFβ Effect of Schisandra chinensis Fruit Extract and Schisandrin B in A7r5 Vascular Smooth Muscle Cells. Life 2021; 11(2): 163 doi: 10.3390/life11020163
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| 5 |
Stanley Kwong, Cherise Meyerson, Wei Zheng, Ari Kassardjian, Nicholas Stanzione, Kuixing Zhang, Hanlin L. Wang. Acute hepatitis and acute liver failure: Pathologic diagnosis and differential diagnosis. Seminars in Diagnostic Pathology 2019; 36(6): 404 doi: 10.1053/j.semdp.2019.07.005
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| 6 |
Vanda McNiven, Daniela Gattini, Iram Siddiqui, Stephane Pelletier, Herbert Brill, Yaron Avitzur, Saadet Mercimek‐Andrews. SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1. American Journal of Medical Genetics Part A 2021; 185(4): 1091 doi: 10.1002/ajmg.a.62079
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| 7 |
Long-Gang Niu, Ping Liu, Zhao-Wen Wang, Bojun Chen. Slo2 potassium channel function depends on RNA editing-regulated expression of a SCYL1 protein. eLife 2020; 9 doi: 10.7554/eLife.53986
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| 8 |
J. Chavany, A. Cano, B. Roquelaure, P. Bourgeois, J. Boubnova, P. Gaignard, C. Hoebeke, R. Reynaud, B. Rhomer, A. Slama, C. Badens, B. Chabrol, A. Fabre. Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review. Archives de Pédiatrie 2020; 27(3): 155 doi: 10.1016/j.arcped.2020.01.003
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| 9 |
Mariam Youssef, Katherine L. Mascia, Brendan McGuire, Chirag R. Patel, Sameer Al Diffalha, Deepti Dhall, Goo Lee, Mauro Vigano. CALFAN (Low γ-Glutamyl Transpeptidase (GGT) Cholestasis, Acute Liver Failure, and Neurodegeneration) Syndrome: A Case Report with 3-Year Follow-Up after Liver Transplantation in Early Adulthood. Case Reports in Hepatology 2023; 2023: 1 doi: 10.1155/2023/3010131
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| 10 |
Stéphanie Kaeser-Pebernard, Christine Vionnet, Muriel Mari, Devanarayanan Siva Sankar, Zehan Hu, Carole Roubaty, Esther Martínez-Martínez, Huiyuan Zhao, Miguel Spuch-Calvar, Alke Petri-Fink, Gregor Rainer, Florian Steinberg, Fulvio Reggiori, Jörn Dengjel. mTORC1 controls Golgi architecture and vesicle secretion by phosphorylation of SCYL1. Nature Communications 2022; 13(1) doi: 10.1038/s41467-022-32487-7
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| 11 |
Hasan M Isa, Jawaher F Alkaabi, Wasan H Alhammadi, Khadija A Marjan. Recurrent Acute Liver Failure in a Bahraini Child With a Novel Mutation of Spinocerebellar Ataxia-21. Cureus 2023; doi: 10.7759/cureus.36249
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| 12 |
Barath Jagadisan, Anil Dhawan. Emergencies in paediatric hepatology. Journal of Hepatology 2022; 76(5): 1199 doi: 10.1016/j.jhep.2021.12.027
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| 13 |
Bingxin Jiang, Fangfei Xiao, Xiaolu Li, Yongmei Xiao, Yizhong Wang, Ting Zhang. Case Report: Pediatric Recurrent Acute Liver Failure Caused by Neuroblastoma Amplified Sequence (NBAS) Gene Mutations. Frontiers in Pediatrics 2021; 8 doi: 10.3389/fped.2020.607005
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| 14 |
Narges Zare, Hosein Saneian, Majid Khademian. A Rare Case of Spinocerebellar Ataxia Autosomal Recessive 21 Presented with Liver Disease. Advanced Biomedical Research 2023; 12(1) doi: 10.4103/abr.abr_139_22
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