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22 Results Found

  • Article
  • Open Access
10 Citations
4,729 Views
13 Pages

UBQLN2 Promotes the Production of Type I Interferon via the TBK1-IRF3 Pathway

  • Tianhong Chen,
  • Wenjuan Zhang,
  • Bo Huang,
  • Xuan Chen and
  • Cao Huang

13 May 2020

Mutations of Ubiquilin 2 (UBQLN2) or TANK-binding kinase 1 (TBK1) are associated with amyotrophic lateral sclerosis and frontotemporal degeneration (ALS/FTD). However, the mechanisms whereby UBQLN2 or TBK1 mutations lead to ALS and FTD remain unclear...

  • Article
  • Open Access
7 Citations
3,352 Views
11 Pages

Proteasomal dysfunction is known to be associated with amyotrophic lateral sclerosis and frontotemporal degeneration (ALS/FTD). Our previous reports have shown that a mutant form of ubiquilin-2 (UBQLN2) linked to ALS/FTD leads to neurodegeneration ac...

(This article belongs to the Section Molecular Neurobiology)
  • Article
  • Open Access
7 Citations
3,348 Views
22 Pages

Chronic Oxidative Stress and Stress Granule Formation in UBQLN2 ALS Neurons: Insights into Neuronal Degeneration and Potential Therapeutic Targets

  • Ao Gu,
  • Yiti Zhang,
  • Jianfeng He,
  • Mingri Zhao and ,
  • Lingjie Ding,
  • Wanxi Liu,
  • Jianing Xiao,
  • Jiali Huang,
  • Mujun Liu and
  • Xionghao Liu
  • + 5 authors+ 0 author

15 December 2024

The pathogenesis of neurodegenerative diseases results from the interplay between genetic and environmental factors. Aging and chronic oxidative stress are critical contributors to neurodegeneration. UBQLN2, a ubiquitin-related protein, aids in prote...

(This article belongs to the Special Issue Molecular Research on the Neurodegenerative Diseases)
  • Article
  • Open Access
1 Citations
2,308 Views
16 Pages

28 June 2023

The ubiquilin family (UBQLN) of proteins consists of five closely related members (UBQLN1, UBQLN2, UBQLN3, UBQLN4, and UBQLNL) that have a high degree of similarity at the level of both amino acid and domain structure. The role of UBQLN1 and UBQLN2 i...

(This article belongs to the Section Molecular Cancer Biology)
  • Article
  • Open Access
11 Citations
6,586 Views
19 Pages

28 July 2020

Amyotrophic lateral sclerosis is a progressive neurodegenerative disorder, characterized by cytoplasmic inclusions of RNA-binding protein TDP-43. Despite decades of research and identification of more than 50 genes associated with amyotrophic lateral...

(This article belongs to the Section Cellular Pathology)
  • Article
  • Open Access
409 Views
17 Pages

UBQLN4 Is a Prognostic Biomarker in Intrahepatic Cholangiocarcinoma That Is Associated with Cisplatin Resistance

  • Kodai Abe,
  • Kelly Chong,
  • Yuta Abe,
  • Minoru Kitago and ,
  • Motonori Edanami,
  • Yosuke Uematsu,
  • Yohei Masugi,
  • Akihisa Ueno,
  • Matias A. Bustos and
  • Dave S. B. Hoon
  • + 8 authors+ 3 authors

18 September 2026

Background: Intrahepatic cholangiocarcinoma (iCCA) is an aggressive biliary tract malignancy with limited treatment options and poor prognosis. Platinum-based drugs are one of the major therapies; however, resistance remains a major therapeutic chall...

  • Article
  • Open Access
8 Citations
2,359 Views
12 Pages

Knockdown of UBQLN1 Functions as a Strategy to Inhibit CRC Progression through the ERK-c-Myc Pathway

  • Ruoxuan Ni,
  • Jianwei Jiang,
  • Mei Zhao,
  • Shengkai Huang and
  • Changzhi Huang

7 June 2023

Purpose: Colorectal cancer (CRC) is characterized by the absence of obvious symptoms in the early stage. Due to the high rate of late diagnosis of CRC patients, the mortality rate of CRC is higher than that of other malignant tumors. Accumulating evi...

(This article belongs to the Special Issue Molecular Biology of Colorectal Cancers)
  • Article
  • Open Access
4 Citations
3,443 Views
15 Pages

Damaged DNA Is an Early Event of Neurodegeneration in Induced Pluripotent Stem Cell-Derived Motoneurons with UBQLN2P497H Mutation

  • Yiti Zhang,
  • Baitao Zeng,
  • Ao Gu,
  • Qinyu Kang and ,
  • Mingri Zhao,
  • Guangnan Peng,
  • Miaojin Zhou,
  • Wanxi Liu,
  • Min Liu and
  • Mujun Liu
  • + 8 authors+ 3 authors

26 September 2022

Ubiquilin-2 (UBQLN2) mutations lead to familial amyotrophic lateral sclerosis (FALS)/and frontotemporal dementia (FTLD) through unknown mechanisms. The combination of iPSC technology and CRISPR-mediated genome editing technology can generate an iPSC-...

(This article belongs to the Special Issue Stem Cell Activation in Adult Organism 2023)
  • Communication
  • Open Access
12 Citations
4,115 Views
13 Pages

Autophagy Markers Are Altered in Alzheimer’s Disease, Dementia with Lewy Bodies and Frontotemporal Dementia

  • Antonio Longobardi,
  • Marcella Catania,
  • Andrea Geviti,
  • Erika Salvi and ,
  • Elena Rita Vecchi,
  • Sonia Bellini,
  • Claudia Saraceno,
  • Roland Nicsanu,
  • Rosanna Squitti and
  • Roberta Ghidoni
  • + 7 authors+ 2 authors

17 January 2024

The accumulation of protein aggregates defines distinct, yet overlapping pathologies such as Alzheimer’s disease (AD), dementia with Lewy bodies (DLB), and frontotemporal dementia (FTD). In this study, we investigated ATG5, UBQLN2, ULK1, and LC...

(This article belongs to the Section Molecular Pathology, Diagnostics, and Therapeutics)
  • Article
  • Open Access
5 Citations
4,007 Views
16 Pages

Genomic Amplification of UBQLN4 Is a Prognostic and Treatment Resistance Factor

  • Yuta Kobayashi,
  • Matias A. Bustos,
  • Yoshiaki Shoji,
  • Ron D. Jachimowicz and ,
  • Yosef Shiloh and
  • Dave S. B. Hoon
  • + 1 author+ 0 author

21 October 2022

Ubiquilin-4 (UBQLN4) is a proteasomal shuttle factor that directly binds to ubiquitylated proteins and delivers its cargo to the 26S proteasome for degradation. We previously showed that upregulated UBQLN4 determines the DNA damage response (DDR) thr...

(This article belongs to the Special Issue DNA Damage Response Regulation and Cancer)
  • Article
  • Open Access
5 Citations
3,915 Views
20 Pages

GABAA Receptor-Stabilizing Protein Ubqln1 Affects Hyperexcitability and Epileptogenesis after Traumatic Brain Injury and in a Model of In Vitro Epilepsy in Mice

  • Tabea Kürten,
  • Natascha Ihbe,
  • Timo Ueberbach,
  • Ute Distler and ,
  • Malte Sielaff,
  • Stefan Tenzer and
  • Thomas Mittmann
  • + 2 authors+ 0 author

Posttraumatic epilepsy (PTE) is a major public health concern and strongly contributes to human epilepsy cases worldwide. However, an effective treatment and prevention remains a matter of intense research. The present study provides new insights int...

(This article belongs to the Section Molecular Neurobiology)
  • Review
  • Open Access
16 Citations
5,063 Views
17 Pages

Ubiquilin Networking in Cancers

  • Salinee Jantrapirom,
  • Luca Lo Piccolo,
  • Dumnoensun Pruksakorn,
  • Saranyapin Potikanond and
  • Wutigri Nimlamool

15 June 2020

Ubiquilins or UBQLNs, members of the ubiquitin-like and ubiquitin-associated domain (UBL-UBA) protein family, serve as adaptors to coordinate the degradation of specific substrates via both proteasome and autophagy pathways. The UBQLN substrates reve...

(This article belongs to the Special Issue Ubiquitin-Related Cancer)
  • Case Report
  • Open Access
1 Citations
3,701 Views
8 Pages

De Novo 1q21.3q22 Duplication Revaluation in a “Cold” Complex Neuropsychiatric Case with Syndromic Intellectual Disability

  • Roberta Milone,
  • Roberta Scalise,
  • Rosa Pasquariello,
  • Stefano Berloffa and ,
  • Ivana Ricca and
  • Roberta Battini
  • + 1 author+ 0 author

31 March 2021

Syndromic intellectual disability often obtains a genetic diagnosis due to the combination of first and next generation sequencing techniques, although their interpretation may require revaluation over the years. Here we report on a composite neurops...

(This article belongs to the Special Issue Genetics of Primary Microcephaly and Intellectual Disability)
  • Article
  • Open Access
14 Citations
5,885 Views
15 Pages

Identification and Validation of Novel Reference Genes in Acute Lymphoblastic Leukemia for Droplet Digital PCR

  • Vanessa Villegas-Ruíz,
  • Karina Olmos-Valdez,
  • Kattia Alejandra Castro-López,
  • Victoria Estefanía Saucedo-Tepanecatl and ,
  • Josselen Carina Ramírez-Chiquito,
  • Eleazar Israel Pérez-López,
  • Isabel Medina-Vera and
  • Sergio Juárez-Méndez
  • + 3 authors+ 0 author

17 May 2019

Droplet digital PCR is the most robust method for absolute nucleic acid quantification. However, RNA is a very versatile molecule and its abundance is tissue-dependent. RNA quantification is dependent on a reference control to estimate the abundance....

(This article belongs to the Section Human Genomics and Genetic Diseases)
  • Article
  • Open Access
2 Citations
3,274 Views
12 Pages

10 July 2021

Ubiquitin (Ub) specifically interacts with the Ub-associating domain (UBA) in a proteasomal shuttle factor, while the latter is involved in either proteasomal targeting or self-assembly coacervation. PINK1 phosphorylates Ub at S65 and makes Ub altern...

(This article belongs to the Section Chemical Biology)
  • Feature Paper
  • Article
  • Open Access
33 Citations
8,262 Views
37 Pages

Unstructured Biology of Proteins from Ubiquitin-Proteasome System: Roles in Cancer and Neurodegenerative Diseases

  • Kundlik Gadhave,
  • Prateek Kumar,
  • Shivani K. Kapuganti,
  • Vladimir N. Uversky and
  • Rajanish Giri

The 26S proteasome is a large (~2.5 MDa) protein complex consisting of at least 33 different subunits and many other components, which form the ubiquitin proteasomal system (UPS), an ATP-dependent protein degradation system in the cell. UPS serves as...

(This article belongs to the Special Issue The Amazing World of IDPs in Human Diseases)
  • Case Report
  • Open Access
7 Citations
3,227 Views
5 Pages

Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous Mutations

  • Julian Theuriet,
  • Antoine Pegat,
  • Pascal Leblanc,
  • Sandra Vukusic and ,
  • Cécile Cazeneuve,
  • Stéphanie Millecamps,
  • Guillaume Banneau,
  • Marine Guillaud-Bataille and
  • Emilien Bernard
  • + 4 authors+ 0 author

25 November 2021

Biallelic mutations in the CYP7B1 gene lead to spastic paraplegia-5 (SPG5). We report herein the case of a patient whose clinical symptoms began with progressive lower limb spasticity during childhood, and who secondly developed amyotrophic lateral s...

(This article belongs to the Special Issue Genetics of Motor Neuron Diseases)
  • Article
  • Open Access
4 Citations
3,214 Views
13 Pages

Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

  • Shanez Haouari,
  • Christian Robert Andres,
  • Debora Lanznaster,
  • Sylviane Marouillat and ,
  • Céline Brulard,
  • Audrey Dangoumau,
  • Devina Ung,
  • Charlotte Veyrat-Durebex,
  • Frédéric Laumonnier and
  • Patrick Vourc’h
  • + 8 authors+ 3 authors

The ubiquitin pathway, one of the main actors regulating cell signaling processes and cellular protein homeostasis, is directly involved in the pathophysiology of amyotrophic lateral sclerosis (ALS). We first analyzed, by a next-generation sequencing...

(This article belongs to the Section Molecular Neurobiology)
  • Review
  • Open Access
1 Citations
1,215 Views
21 Pages

25 June 2026

Ring finger protein 126 (RNF126) is a RING-type E3 ubiquitin ligase that has recently emerged as a multifaceted regulator of cellular homeostasis, stress adaptation, and disease progression. Through its structurally distinct zinc-finger and catalytic...

  • Article
  • Open Access
57 Citations
6,056 Views
12 Pages

Cancer Metastasis Prediction and Genomic Biomarker Identification through Machine Learning and eXplainable Artificial Intelligence in Breast Cancer Research

  • Burak Yagin,
  • Fatma Hilal Yagin,
  • Cemil Colak,
  • Feyza Inceoglu and ,
  • Seifedine Kadry and
  • Jungeun Kim
  • + 1 author+ 0 author

26 October 2023

Aim: Method: This research presents a model combining machine learning (ML) techniques and eXplainable artificial intelligence (XAI) to predict breast cancer (BC) metastasis and reveal important genomic biomarkers in metastasis patients. Method: A to...

(This article belongs to the Section Machine Learning and Artificial Intelligence in Diagnostics)
  • Article
  • Open Access
775 Views
29 Pages

Serum Peptidomic Analysis in a Comparative Study of the Efficacy of Benjakul Remedy Versus Loratadine in Allergic Rhinitis Patients

  • Vilailak Tiyao,
  • Sittiruk Roytrakul,
  • Janthima Jaresitthikunchai,
  • Sawanya Charoenlappanit and ,
  • Narumon Phaonakrop,
  • Katanchalee Houngiam,
  • Nichamon Mukkasombut,
  • Pranporn Kuropakornpong,
  • Sunita Makchuchit and
  • Arunporn Itharat
  • + 7 authors+ 2 authors

18 August 2026

Benjakul (BJK) remedy, traditionally used to balance the four elements, has demonstrated clinical efficacy in relieving inflammation and allergic rhinitis (AR) symptoms. This study investigated differential serum peptide expression in AR patients tre...

(This article belongs to the Special Issue Plant Extracts and Natural Products: Molecular Insights into the Biofunctional Properties)
  • Review
  • Open Access
40 Citations
9,128 Views
21 Pages

Omics and Male Infertility: Highlighting the Application of Transcriptomic Data

  • Temidayo S. Omolaoye,
  • Victor A. Omolaoye,
  • Richard K. Kandasamy,
  • Mahmood Yaseen Hachim and
  • Stefan S. Du Plessis

14 February 2022

Male infertility is a multifaceted disorder affecting approximately 50% of male partners in infertile couples. Over the years, male infertility has been diagnosed mainly through semen analysis, hormone evaluations, medical records and physical examin...

(This article belongs to the Collection Male Infertility: Current Knowledge and Future Perspectives)