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Results for
""Copper-Transporting ATPases""[mesh_terms]

144 Results

Searching titles within these results

Wilson's disease: best practice.

Paul Cook, Patrick J Twomey, Aidan Ryan

Journal of clinical pathology 2023;76(7):435-441

Wilson's disease: A new perspective review on its genetics, diagnosis and treatment.

Jasjit S Suri, Madhusudhan B K, Narendra N Khanna, Christopher Kwaku Asare, Rui Tato Marinho, Carlo Carcassi, J Miguel Sanches, Sandro Orru, Harman S Suri, Monika Turk, Amrita Chaturvedi, Elisa Godia-Cuadrado, Suneet Kumar Gupta, Mainak Biswas, Anurag Tiwari, Luca Saba

Frontiers in bioscience (Elite edition) 2020;11(1):166-185

Copper-independent lysosomal localisation of the Wilson disease protein ATP7B.

Marinella Pirozzi, Raviranjan Pandey, Tamal Ghosh, Santanu Das, Arnab Gupta, Saptarshi Maji

Traffic (Copenhagen, Denmark) 2023;24(12):587-609

The genetics of Wilson disease.

Irene J Chang, Si Houn Hahn

Handbook of clinical neurology 2018;142():19-34

Epidemiology of Wilson's Disease and Pathogenic Variants of the Gene Leading to Diversified Protein Disfunctions.

Vadim Vladimirovich Kumeiko, Anna Aleksandrovna Ovchinnikova, Mikhail Maksimovich Garbuz, Elena Vasilievna Ovchinnikova

International journal of molecular sciences 2024;25(4):

Structure and mechanism of the human copper transporting ATPases: Fitting the pieces into a moving puzzle.

Oleg Y Dmitriev, Jaala Patry

Biochimica et biophysica acta. Biomembranes 2024;1866(4):184306

Wilson disease and related copper disorders.

Matthew T Lorincz

Handbook of clinical neurology 2018;147():279-292

A Systematic Review and Meta-Analysis of the R778L Mutation in ATP7B With Wilson Disease in China.

Peifang Jiang, Lan Yu, Hongyu Chen, Ziru Xue

Pediatric neurology 2023;145():135-147

Clinical and Molecular Spectrum of Wilson Disease in the Arab World: A Systematic Review.

Majida Charif, Mohammed Bellaoui, Meryem Ouarzane, Maria Rkain, Saida Lhousni, Halima Benzine, Redouane Boulouiz

Biochemical genetics 2025;63(2):1198-1218

Stem Cells Treatment for Wilson Disease.

Sujun Zheng, Zhongping Duan, Li Bai, Shan Tang

Current stem cell research & therapy 2022;17(8):712-719

Non-ceruloplasmin bound copper and ATP7B gene variants in Alzheimer's disease.

R Squitti, M Siotto, M Arciello, L Rossi

Metallomics : integrated biometal science 2017;8(9):863-73

Psychiatric Symptoms in Wilson's Disease-Consequence of Gene Mutations or Just Coincidence?-Possible Causal Cascades and Molecular Pathways.

Tomasz Litwin, Zofia Sorysz, Grażyna Gromadzka, Agnieszka Antos

International journal of molecular sciences 2024;25(22):

Copper efflux transporters ATP7A and ATP7B: Novel biomarkers for platinum drug resistance and targets for therapy.

Yue-Qin Li, Zhao-Qian Liu, Xiang-Ping Li, Ji-Ye Yin

IUBMB life 2019;70(3):183-191

Hepatic features of Wilson disease.

Michael L Schilsky, Salih Boga, Aftab Ala

Handbook of clinical neurology 2018;142():91-99

Currently Clinical Views on Genetics of Wilson's Disease.

Chen Chen, Bo Shen, Jia-Jia Xiao, Rong Wu, Sarah Jane Duff Canning, Xiao-Ping Wang

Chinese medical journal 2016;128(13):1826-30

Results: 1 – 15 / 144

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