PMC Links for Gene (Select 5621) - PMC

Jacqueline Marcia Boccacino, Rafael dos Santos Peixoto, Camila Felix de Lima Fernandes, Giovanni Cangiano, Paula Rodrigues Sola, Bárbara Paranhos Coelho, Mariana Brandão Prado, Maria Isabel Melo-Escobar, Breno Pereira de Sousa, Shamini Ayyadhury, Gary D. Bader, Sueli Mieko Oba Shinjo, Suely Kazue Nagahashi Marie, Edroaldo Lummertz da Rocha, Marilene Hohmuth Lopes

BMC Cancer. 2024; 24: 199. Published online 2024 Feb 13. doi: 10.1186/s12885-024-11914-6

PMCID:: PMC10863147

Abstract Article PDF–5.2M

Select item 107093754.

Excess PrP^C inhibits muscle cell differentiation via miRNA-enhanced liquid–liquid phase separation implicated in myopathy

Jing Tao, Yanping Zeng, Bin Dai, Yin Liu, Xiaohan Pan, Li-Qiang Wang, Jie Chen, Yu Zhou, Zuneng Lu, Liwei Xie, Yi Liang

Nat Commun. 2023; 14: 8131. Published online 2023 Dec 8. doi: 10.1038/s41467-023-43826-7

PMCID:: PMC10709375

Abstract Article PDF–6.1M

Select item 105735345.

Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt–Jakob Disease (CJD)

Sae-Young Won, Yong-Chan Kim, Byung-Hoon Jeong

Int J Mol Sci. 2023 Oct; 24(19): 14831. Published online 2023 Oct 2. doi: 10.3390/ijms241914831

PMCID:: PMC10573534

Abstract Article PDF–1.4M

Select item 103997386.

Copper homeostasis-associated gene PRNP regulates ferroptosis and immune infiltration in breast cancer

Changwei Lin, Jiaqing He, Xiaopei Tong, Liying Song

PLoS One. 2023; 18(8): e0288091. Published online 2023 Aug 3. doi: 10.1371/journal.pone.0288091

PMCID:: PMC10399738

Abstract Article PDF–3.6M

Select item 101664637.

A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques

Rabeah Bayazid, Christina Orru’, Rabail Aslam, Yvonne Cohen, Amelia Silva-Rohwer, Seong-Ki Lee, Rossana Occhipinti, Qingzhong Kong, Shashirekha Shetty, Mark L. Cohen, Byron Caughey, Lawrence B. Schonberger, Brian S. Appleby, Ignazio Cali

Acta Neuropathol. 2023; 146(1): 121–143. Published online 2023 May 8. doi: 10.1007/s00401-023-02581-1

Correction in:: Acta Neuropathol. 2023; 146(1): 167–170.

PMCID:: PMC10166463

Abstract Article PDF–4.3M

Select item 101092498.

PRNP expression predicts imaging findings in sporadic Creutzfeldt‐Jakob disease

Iris J. Broce, Eduardo Caverzasi, Simone Sacco, Ryan Michael Nillo, Matteo Paoletti, Rahul S. Desikan, Michael Geschwind, Leo P. Sugrue

Ann Clin Transl Neurol. 2023 Apr; 10(4): 536–552. Published online 2023 Feb 6. doi: 10.1002/acn3.51739

PMCID:: PMC10109249

Abstract Article PDF–3.4M

Select item 97370459.

Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt–Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene

Taiki Matsubayashi, Nobuo Sanjo

Int J Mol Sci. 2022 Dec; 23(23): 15172. Published online 2022 Dec 2. doi: 10.3390/ijms232315172

PMCID:: PMC9737045

Abstract Article PDF–1.5M

Select item 953700710.

Downregulated PRNP Facilitates Cell Proliferation and Invasion and Has Effect on the Immune Regulation in Ovarian Cancer

Kuan Hu, Xiaofang Zhang, Lei Zhou, Juanni Li

J Immunol Res. 2022; 2022: 3205040. Published online 2022 Sep 29. doi: 10.1155/2022/3205040

PMCID:: PMC9537007

Abstract Article PDF–2.7M

Select item 951327911.

Met/Val129 polymorphism of the full-length human prion protein dictates distinct pathways of amyloid formation

Thomas Pauly, Najoua Bolakhrif, Jesko Kaiser, Luitgard Nagel-Steger, Lothar Gremer, Holger Gohlke, Dieter Willbold

J Biol Chem. 2022 Oct; 298(10): 102430. Published online 2022 Aug 28. doi: 10.1016/j.jbc.2022.102430

PMCID:: PMC9513279

Abstract Article PDF–1.4M

Select item 950006712.

Hereditary E200K mutation within the prion protein gene alters human iPSC derived cardiomyocyte function

Aleksandar R. Wood, Simote T. Foliaki, Bradley R. Groveman, Ryan O. Walters, Katie Williams, Jue Yuan, Wen-Quan Zou, Cathryn L. Haigh

Sci Rep. 2022; 12: 15788. Published online 2022 Sep 22. doi: 10.1038/s41598-022-19631-5

PMCID:: PMC9500067

Abstract Article PDF–7.5M

Select item 946420613.

Characteristic distribution and molecular properties of normal cellular prion protein in human endocrine and exocrine tissues

Sachiko Koyama, Hideko Noguchi, Kaoru Yagita, Hideomi Hamasaki, Masahiro Shijo, Motoi Yoshimura, Kohei Inoshita, Naokazu Sasagasako, Hiroyuki Honda

Sci Rep. 2022; 12: 15289. Published online 2022 Sep 10. doi: 10.1038/s41598-022-19632-4

PMCID:: PMC9464206

Abstract Article PDF–2.3M

Select item 870459814.

Extracellular Prion Protein Aggregates in Nine Gerstmann–Sträussler–Scheinker Syndrome Subjects with Mutation P102L: A Micromorphological Study and Comparison with Literature Data

Nikol Jankovska, Radoslav Matej, Tomas Olejar

Int J Mol Sci. 2021 Dec; 22(24): 13303. Published online 2021 Dec 10. doi: 10.3390/ijms222413303

PMCID:: PMC8704598

Abstract Article PDF–3.9M

Select item 862749715.

Novel quaternary structures of the human prion protein globular domain

Leandro Oliveira Bortot, Victor Lopes Rangel, Francesca A. Pavlovici, Kamel El Omari, Armin Wagner, Jose Brandao-Neto, Romain Talon, Frank von Delft, Andrew G Reidenbach, Sonia M Vallabh, Eric Vallabh Minikel, Stuart Schreiber, Maria Cristina Nonato

Biochimie. Author manuscript; available in PMC 2022 Dec 1.

Published in final edited form as: Biochimie. 2021 Dec; 191: 118–125. Published online 2021 Sep 10. doi: 10.1016/j.biochi.2021.09.005

PMCID:: PMC8627497

Abstract Article PDF–1.1M

Select item 861874116.

The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene (PRNP) with Sporadic Creutzfeldt–Jakob Disease

Yong-Chan Kim, Byung-Hoon Jeong

Cells. 2021 Nov; 10(11): 3132. Published online 2021 Nov 11. doi: 10.3390/cells10113132

PMCID:: PMC8618741

Abstract Article PDF–724K

Select item 859375717.

Characteristics of Chinese patients with genetic CJD who have E196A or E196K mutation in PRNP: comparative analysis of patients identified in the Chinese National CJD Surveillance System

Qi Shi, Kang Xiao, Cao Chen, Wei Zhou, Li-Ping Gao, Yue-Zhang Wu, Yuan Wang, Chao Hu, Chen Gao, Xiao-Ping Dong

BMJ Open. 2021; 11(11): e054551. Published online 2021 Nov 15. doi: 10.1136/bmjopen-2021-054551

PMCID:: PMC8593757

Abstract Article PDF–1.1M

Select item 854076518.

The First Sporadic Creutzfeldt–Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in PRNP

Aušrinė Areškevičiūtė, Eva Løbner Lund, Sabina Capellari, Piero Parchi, Christian Tersbøl Pinkowsky

Viruses. 2021 Oct; 13(10): 2061. Published online 2021 Oct 14. doi: 10.3390/v13102061

PMCID:: PMC8540765

Abstract Article PDF–988K

Select item 852488619.

Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease

Teresa Ximelis, Alba Marín-Moreno, Juan Carlos Espinosa, Hasier Eraña, Jorge M. Charco, Isabel Hernández, Carmen Riveira, Daniel Alcolea, Eva González-Roca, Iban Aldecoa, Laura Molina-Porcel, Piero Parchi, Marcello Rossi, Joaquín Castilla, Raquel Ruiz-García, Ellen Gelpi, Juan María Torres, Raquel Sánchez-Valle

Alzheimers Res Ther. 2021; 13: 176. Published online 2021 Oct 18. doi: 10.1186/s13195-021-00912-6

PMCID:: PMC8524886

Abstract Article PDF–3.2M

Select item 844289820.

Genetic prion disease–related mutation E196K displays a novel amyloid fibril structure revealed by cryo-EM

Li-Qiang Wang, Kun Zhao, Han-Ye Yuan, Xiang-Ning Li, Hai-Bin Dang, Yeyang Ma, Qiang Wang, Chen Wang, Yunpeng Sun, Jie Chen, Dan Li, Delin Zhang, Ping Yin, Cong Liu, Yi Liang

Sci Adv. 2021 Sep; 7(37): eabg9676. Published online 2021 Sep 8. doi: 10.1126/sciadv.abg9676

PMCID:: PMC8442898

Abstract Article PDF–1.3M

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