Cargando…

Novel lncRNA‐prader willi/angelman region RNA, SNRPN neighbour (PWARSN) aggravates tubular epithelial cell pyroptosis by regulating TXNIP via dual way in diabetic kidney disease

OBJECTIVES: Elevated thioredoxin‐interacting protein (TXNIP)‐induced pyroptosis contributes to the pathology of diabetic kidney disease (DKD). However, the molecular mechanisms in dysregulated TXNIP in DKD remain largely unclear. MATERIALS AND METHODS: Transcriptomic analysis identified a novel long...

Descripción completa

Detalles Bibliográficos
Autores principales:	Song, Yi, Guo, Feng, Zhao, Yan‐yan, Ma, Xiao‐jun, Wu, Li‐na, Yu, Ji‐feng, Ji, Hong‐fei, Shao, Ming‐wei, Huang, Feng‐juan, Zhao, Lin, Fan, Xun‐jie, Xu, Ya‐nan, Wang, Qing‐zhu, Qin, Gui‐jun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890532/ https://www.ncbi.nlm.nih.gov/pubmed/36316968 http://dx.doi.org/10.1111/cpr.13349

Ejemplares similares

Accommodative insufficiency in a patient with Prader–Willi syndrome and SNRPN gene mutation
por: Kanclerz, Piotr
Publicado: (2020)

Prader–Willi Syndrome with Angelman Syndrome in the Offspring
por: Greco, Donatella, et al.
Publicado: (2021)

Prader-Willi and Angelman Syndromes: Mechanisms and Management
por: Ma, Van K, et al.
Publicado: (2023)

Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes
por: Ramsden, Simon C, et al.
Publicado: (2010)

A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics
por: Strom, Samuel P., et al.
Publicado: (2021)

Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China
por: Liu, Chang, et al.
Publicado: (2019)

Evolution of Genomic Imprinting with Biparental Care: Implications for Prader-Willi and Angelman Syndromes
por: Úbeda, Francisco
Publicado: (2008)

Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes
por: Baker, Emma K., et al.
Publicado: (2018)

Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome
por: Zhang, Kaihui, et al.
Publicado: (2016)

Transcription Is Required to Establish Maternal Imprinting at the Prader-Willi Syndrome and Angelman Syndrome Locus
por: Smith, Emily Y., et al.
Publicado: (2011)

Clinical characteristics and epilepsy in genomic imprinting disorders: Angelman syndrome and Prader–Willi syndrome
por: Wang, Tzong-Shi, et al.
Publicado: (2019)

Loss of hierarchical imprinting regulation at the Prader–Willi/Angelman syndrome locus in human iPSCs
por: Pólvora-Brandão, Duarte, et al.
Publicado: (2018)

Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes
por: Beygo, Jasmin, et al.
Publicado: (2019)

Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader–Willi Syndrome and Angelman Syndrome
por: Kim, Boram, et al.
Publicado: (2022)

Regulatory Elements Associated with Paternally-Expressed Genes in the Imprinted Murine Angelman/Prader-Willi Syndrome Domain
por: Rodriguez-Jato, Sara, et al.
Publicado: (2013)

The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature
por: Pellikaan, Karlijn, et al.
Publicado: (2021)

Ovarian cyst torsion in Prader-Willi Syndrome
por: Zhao, Ji-cun, et al.
Publicado: (2023)

De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s
por: Rossi, Elena, et al.
Publicado: (2012)

Molecular and cytogenetic analyses of a patient with Prader-Willi syndrome who also had the phenotype of Angelman syndrome
por: Miyako, Kenichi, et al.
Publicado: (2013)

Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes
por: Salminen, Iiro Ilmari, et al.
Publicado: (2019)

A rapid and accurate methylation‐sensitive high‐resolution melting analysis assay for the diagnosis of Prader Willi and Angelman patients
por: Ribeiro Ferreira, Igor, et al.
Publicado: (2019)

Identification of novel variations of oculocutaneous albinism type 2 with Prader–Willi syndrome/Angelman syndrome in two Chinese families
por: Chen, XiaoFei, et al.
Publicado: (2023)

Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome
por: Bingeliene, Arina, et al.
Publicado: (2015)

Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS features
por: Aypar, Umut, et al.
Publicado: (2016)

Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader–Willi/Angelman syndromes?
por: Ortega, Veronica, et al.
Publicado: (2021)

Generation of isogenic models of Angelman syndrome and Prader-Willi syndrome in CRISPR/Cas9-engineered human embryonic stem cells
por: Gilmore, Rachel B., et al.
Publicado: (2023)

Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
por: Cheon, Chong Kun
Publicado: (2016)

Epigenetics in Prader-Willi Syndrome
por: Mendiola, Aron Judd P., et al.
Publicado: (2021)

The Long Non-Coding RNA Prader Willi/Angelman Region RNA5 (PAR5) Is Downregulated in Anaplastic Thyroid Carcinomas Where It Acts as a Tumor Suppressor by Reducing EZH2 Activity
por: Pellecchia, Simona, et al.
Publicado: (2020)

Prader-Willi Syndrome: Clinical Aspects
por: Elena, Grechi, et al.
Publicado: (2012)

Hyperprolactinemia in Adults with Prader-Willi Syndrome
por: Sjöström, Anna, et al.
Publicado: (2021)

Approach to the Patient With Prader–Willi Syndrome
por: Höybye, Charlotte, et al.
Publicado: (2022)

Sleep Consequences of Prader-Willi Syndrome
por: Itani, Reem, et al.
Publicado: (2023)

Prader-Willi syndrome: a single center's experience in Korea
por: Kim, Yea Ji, et al.
Publicado: (2014)

Causes of Death in Prader-Willi Syndrome: Prader-Willi Syndrome Association (USA) 40-Year Mortality Survey
por: Butler, Merlin G., et al.
Publicado: (2016)

A newborn screening pilot study using methylation-sensitive high resolution melting on dried blood spots to detect Prader-Willi and Angelman syndromes
por: Ferreira, Igor Ribeiro, et al.
Publicado: (2020)

Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
por: Heseding, Hannah M., et al.
Publicado: (2022)

Differences in circulating microRNA signature in Prader–Willi syndrome and non-syndromic obesity
por: Pascut, Devis, et al.
Publicado: (2018)

Prader-Willi syndrome: A primer for clinicians
por: Cataletto, Mary, et al.
Publicado: (2011)

Prader-Willi Syndrome and Growth Hormone Deficiency
por: Aycan, Zehra, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_208p2p0dmaculfngrfcmfe6alm