Cargando…

Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells

Detalles Bibliográficos
Autores principales:	Parisi, Silvia, Polishchuk, Elena V., Allocca, Simona, Ciano, Michela, Musto, Anna, Gallo, Maria, Perone, Lucia, Ranucci, Giusy, Iorio, Raffaele, Polishchuk, Roman S., Bonatti, Stefano
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2020
Materias:	Author Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308340/ https://www.ncbi.nlm.nih.gov/pubmed/32572046 http://dx.doi.org/10.1038/s41598-020-65961-7

Ejemplares similares

Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells
por: Parisi, Silvia, et al.
Publicado: (2018)

An αB-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population
por: Allocca, Simona, et al.
Publicado: (2018)

Wilson’s disease: Prospective developments towards new therapies
por: Ranucci, Giusy, et al.
Publicado: (2017)

Zinc monotherapy is effective in Wilson’s disease patients with mild liver disease diagnosed in childhood: a retrospective study
por: Ranucci, Giusy, et al.
Publicado: (2014)

Wilson Disease Protein ATP7B Utilizes Lysosomal Exocytosis to Maintain Copper Homeostasis
por: Polishchuk, Elena V., et al.
Publicado: (2014)

Identification of p38 MAPK and JNK as new targets for correction of Wilson disease‐causing ATP7B mutants
por: Chesi, Giancarlo, et al.
Publicado: (2016)

Differential phosphorylation-based regulation of αB-crystallin chaperone activity for multipass transmembrane proteins
por: Ciano, Michela, et al.
Publicado: (2016)

Infantile ATP7B-Related End-Stage Liver Disease: An Exceptional Wilson Disease Phenotype From Consecutive Generations
por: Nicastro, Emanuele, et al.
Publicado: (2021)

Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice
por: Padula, Agnese, et al.
Publicado: (2022)

Systemic deletion of Atp7b modifies the hepatocytes’ response to copper overload in the mouse models of Wilson disease
por: Muchenditsi, Abigael, et al.
Publicado: (2021)

Obese children with fatty liver: Between reality and disease mongering
por: Ranucci, Giusy, et al.
Publicado: (2017)

Autophagy delays progression of the two most frequent human monogenetic lethal diseases: cystic fibrosis and Wilson disease
por: Maiuri, Luigi, et al.
Publicado: (2018)

CRISPR-targeted genome editing of human induced pluripotent stem cell-derived hepatocytes for the treatment of Wilson’s disease
por: Wei, Rui, et al.
Publicado: (2021)

ATP7B gene therapy of autologous reprogrammed hepatocytes alleviates copper accumulation in a mouse model of Wilson’s disease
por: Cai, Hongxia, et al.
Publicado: (2022)

The Paradox of Copper Deficiency in Wilson's Disease Patients
por: Iorio, Raffaele, et al.
Publicado: (2023)

Structure of the Wilson disease copper transporter ATP7B
por: Bitter, Ryan M., et al.
Publicado: (2022)

On the Most Frequented Watering Places on the Continent
Publicado: (1837)

Where to look for the most frequent biases?
por: Jager, Kitty J., et al.
Publicado: (2020)

Prevalence of ATP7B Gene Mutations in Iranian Patients With Wilson Disease
por: Zali, Narges, et al.
Publicado: (2011)

Functional Characterization of Novel ATP7B Variants for Diagnosis of Wilson Disease
por: Guttmann, Sarah, et al.
Publicado: (2018)

Observations on One of the Most Frequent Causes of Abortion
Publicado: (1829)

The 100 Most Frequently Cited Articles on Myopia
por: Shemesh, Rachel, et al.
Publicado: (2023)

A High-Calorie Diet Aggravates Mitochondrial Dysfunction and Triggers Severe Liver Damage in Wilson Disease Rats
por: Einer, Claudia, et al.
Publicado: (2018)

Retinoids rescue ceruloplasmin secretion and alleviate oxidative stress in Wilson’s disease-specific hepatocytes
por: Song, Dan, et al.
Publicado: (2022)

Novel mutations found in the ATP7B gene in Chinese patients with Wilson's disease
por: Qian, Zhiling, et al.
Publicado: (2019)

Genetic analysis of ATP7B in 102 south Indian families with Wilson disease
por: Singh, Nivedita, et al.
Publicado: (2019)

A Novel Mutation of ATP7B Gene in a Case of Wilson Disease
por: Kahraman, Cigdem Yuce, et al.
Publicado: (2021)

A case of Wilson disease with the ATP7B mutation presenting movement disorders
por: Van Nguyen, Huong, et al.
Publicado: (2021)

Mutation spectrum of ATP7B gene in pediatric patients with Wilson disease in Vietnam
por: Huong, Nguyen Thi Mai, et al.
Publicado: (2022)

Analysis of Wilson disease mutations in copper binding domain of ATP7B gene
por: Gul, Bushra, et al.
Publicado: (2022)

New ATP7B Gene Mutation in a Brazilian Patient with Wilson Disease
por: Barros de Oliveira Sá, Marcus Villander, et al.
Publicado: (2022)

The most frequent short sequences in non-coding DNA
por: Subirana, Juan A., et al.
Publicado: (2010)

Vestibular migraine: the most frequent entity of episodic vertigo
por: Dieterich, Marianne, et al.
Publicado: (2016)

An Account of the Most Frequented Watering Places on the Continent, &c.
Publicado: (1837)

Observations on Some of the Most Frequent and Important Diseases of the Heart
Publicado: (1809)

Focus on the agents most frequently responsible for perioperative anaphylaxis
por: Di Leo, E., et al.
Publicado: (2018)

On Tubercular Degeneration as the Most Frequent Cause of Acute Hydrocephalus
Publicado: (1841)

The hundred most frequently cited studies on sleeve gastrectomy
por: Stefura, Tomasz, et al.
Publicado: (2019)

The Most Frequently Observed Oto-Laryngeal Affections and Wounds
por: Hautant, A.
Publicado: (1918)

Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease
por: Merle, Uta, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_qj6cp7u3oh996dbrnc2tb87cdj