Results 21 to 30 of about 3,171 (209)
Modes of action of lysophospholipids as endogenous activators of the TRPV4 ion channel
The Journal of Physiology, Volume 601, Issue 9, Page 1655-1673, 1 May 2023., 2023 Abstract figure legend TRPV4 is differentially activated by distinct ligands. Lysophosphatidic acid 18:1 (LPA18:1) activates TRPV4 with a larger conductance as compared to lysophosphatidylcholine 18:1 (LPC18:1). These different modes of activation can lead to differences in cell excitability. Abstract
The Transient Receptor Potential Vanilloid 4 (TRPV4)Miguel Benítez‐Angeles, Ana E. López Romero, Itzel Llorente, Ileana Hernández‐Araiza, Ariela Vergara‐Jaque, Fernando H. Real, Óscar Eduardo Gutiérrez Castañeda, Marcelino Arciniega, Luis E. Morales‐Buenrostro, Francisco Torres‐Quiroz, Refugio García‐Villegas, Luis B. Tovar‐y‐Romo, Wolfgang B. Liedtke, León D. Islas, Tamara Rosenbaum +14 morewiley +1 more sourceProtein phosphatase 2A and complement component 4 are linked to the protective effect of APOE ɛ2 for Alzheimer's disease
Alzheimer's &Dementia, Volume 18, Issue 11, Page 2042-2054, November 2022., 2022 Abstract Introduction
The apolipoprotein E (APOE) ɛ2 allele reduces risk against Alzheimer's disease (AD) but mechanisms underlying this effect are largely unknown. Methods
We conducted a genome‐wide association study for AD among 2096 ɛ2 carriers. The potential role of the top‐ranked gene and complement 4 (C4) proteins, which were previously linked to Gyungah R. Jun, Yang You, Congcong Zhu, Gaoyuan Meng, Jaeyoon Chung, Rebecca Panitch, Junming Hu, Weiming Xia, The Alzheimer's Disease Genetics Consortium, David A. Bennett, Tatiana M. Foroud, Li‐San Wang, Jonathan L. Haines, Richard Mayeux, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Rhoda Au, Kathryn L. Lunetta, Tsuneya Ikezu, Thor D. Stein, Lindsay A. Farrer +20 morewiley +1 more sourceInformation theory approaches to improve glioma diagnostic workflows in surgical neuropathology
Brain Pathology, Volume 32, Issue 5, September 2022., 2022 Different clustering patterns with clinical, histologic, immunohistochemical, and molecular information on the brain cancer population simulation and information gain in the glioma simulation model for clinical decision‐making. Dimensionality reduction by principal component analysis is shown in A1–A4, and by t‐stochastic neighbor embedding in B1–B4 ...Lokman Cevik, Marilyn Vazquez Landrove, Mehmet Tahir Aslan, Vasilii Khammad, Francisco Jose Garagorry Guerra, Yolanda Cabello‐Izquierdo, Wesley Wang, Jing Zhao, Aline Paixao Becker, Catherine Czeisler, Anne Costa Rendeiro, Lucas Luis Sousa Véras, Maicon Fernando Zanon, Rui Manuel Reis, Marcus de Medeiros Matsushita, Koray Ozduman, M. Necmettin Pamir, Ayca Ersen Danyeli, Thomas Pearce, Michelle Felicella, Jennifer Eschbacher, Naomi Arakaki, Horacio Martinetto, Anil Parwani, Diana L. Thomas, José Javier Otero +25 morewiley +1 more sourceGenome-wide association studies of TDP-43 proteinopathy and hippocampal sclerosis reveal shared genetic associations with APOE and TMEM106B. [PDF]
Alzheimers DementAbstract INTRODUCTION
Transactive response DNA binding protein 43 kDa (TDP‐43) proteinopathy has been linked to cognitive decline and often co‐occurs with hippocampal sclerosis (HS). To identify genetic markers of TDP‐43 proteinopathy and HS, we performed genome‐wide association studies (GWASs) of HS and TDP‐43 inclusions.Godrich D, Pasteris J, Martin ER, Kunkle B, Naj AC, Hamilton K, Wang H, Lee WP, Dumitrescu L, Hohman TJ, Mayeux R, Larson EB, Crane PK, Keene CD, Latimer C, Mukherjee S, Kofler J, Kamboh MI, Bennett DA, Molina-Porcel L, Schellenberg G, Pericak-Vance MA, Cuccaro M, Scott WK, Rundek T, Kukull W, Montine T, Beecham GW, Alzheimer's Disease Genetics Consortium (ADGC). +28 moreeuropepmc +2 more sourcesConsensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA [PDF]
, 2012 The current classification of human sporadic prion diseases recognizes six major phenotypic subtypes with distinctive clinicopathological features, which largely correlate at the molecular level with the genotype at the polymorphic codon 129 (methionine, Cohen, Mark L, de Boni, Laura, Ferrer, Isidro, Gambetti, Pierluigi, Gelpi, Ellen, Giaccone, Giorgio, Giese, Armin, Hauw, Jean-Jacques, Höftberger, Romana, Ironside, James W, Jansen, Casper, Kovacs, Gabor G, Kretzschmar, Hans A, Parchi, Piero, Rozemuller, Annemieke, Saverioni, Daniela, Seilhean, Danielle, Tagliavini, Fabrizio +17 morecore +1 more sourceUnderrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions
Movement Disorders, Volume 37, Issue 8, Page 1593-1604, August 2022., 2022 Abstract Background
Human genetics research lacks diversity; over 80% of genome‐wide association studies have been conducted on individuals of European ancestry. In addition to limiting insights regarding disease mechanisms, disproportionate representation can create disparities preventing equitable implementation of personalized medicine.Artur Francisco Schumacher‐Schuh, Andrei Bieger, Olaitan Okunoye, Kin Ying Mok, Shen‐Yang Lim, Soraya Bardien, Azlina Ahmad‐Annuar, Bruno Lopes Santos‐Lobato, Matheus Zschornack Strelow, Mohamed Salama, Shilpa C. Rao, Yared Zenebe Zewde, Saiesha Dindayal, Jihan Azar, Lingappa Kukkle Prashanth, Roopa Rajan, Alastair J. Noyce, Njideka Okubadejo, Mie Rizig, Suzanne Lesage, Ignacio Fernandez Mata, On behalf of the
Global Parkinson's Genetics Program (GP2), Emilia Gatto, Marcelo Kauffman, Julie Hunter, Kishore Kumar, Miguel E. Renteria, Sulev Koks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Bruno Santos, Carlos Rieder, Vitor Tumas, Oury Monchi, Ted Fon, Marcelo David Miranda, Maria Leonor Bustamante, Patricio Olguin, Pedro Chana, Beisha Tang, Hui‐Fang Shang, Ji Feng Guo, Piu Chan, Wei Luo, Gonzalo Arboleda, Jorge Luis Orozco, Marlene Jimenez del Rio, Alvaro Hernandez, Mohamed Salama, Biniyam Ayele, Yared Zenebe, Alexis Brice, Jean‐Christophe Corvol, Anastasia Illarionova, Brit Mollenhauer, Christine Klein, Eva‐Juliane Vollstedt, Katja Lohmann, Lara Mariah Lange, Manu Sharma, Peter Heutink, Thomas Gasser, Zih‐Hua Fang, Albert Akpalu, Georgia Xiromerisiou, Leonidas Stefanis, Andrew Sobering, Alex Medina, Germaine Chan, Nancy Ip, Nelson Yuk‐Fai Cheung, Phillip Chan, XiaoPu Zhou, Asha Kishore, Pramod Pal, Roopa Rajan, Rupam Borgohain, Enza Maria Valente, Micol Avenali, Tommaso Schirinzi, Manabu Funayama, Nobu Hattori, Tomotaka Shiraishi, Tomotaka Shiraishi, Rejko Kruger, Ai Huey Tan, Azlina Ahmad‐Annuar, Nor Azian Abdul Murad, Norlinah Mohamed Ibrahim, Shahrul Azmin, Shen‐Yang Lim, Wael Mohamed, Daniel Martinez, Mayela Rodríguez Violante, Tim Anderson, Toni Pitcher, Njideka Okubadejo, Oluwadamilola Ojo, Jan Aasly, Lasse Pihlstrøm, Shoaib Urrehman, Mario Cornejo‐Olivas, Angel Vinuela, Elena Iakovenko, Jia Nee Foo, Soraya Bardien, Yun Joong Kim, Alejandro Martinez Carrasco, Janet Hoenicka, Sarah Elsadig, Chin‐Shien Lin, Ruey‐Meei Robin Wu, Serena Wu, Yih‐Ru Wu, Samia Ben Sassi, Gencer Genc, Nazli Basak, Özgür Öztop Çakmak, Sibel Ertan, Alastair Noyce, Camille Carroll, Claire Bale, Clodagh Towns, Henry Houlden, Huw Morris, John Hardy, Joseph Callanan, Kin Mok, Manuela Tan, Mie Rizig, Nick Wood, Nigel Williams, Olaitan Okunoye, Patrick Lewis, Rauan Kaiyrzanov, Rimona Weil, Simon Stott, Sumit Dey, Alyssa O'Grady, Bradford Casey, Caroline Pantazis, Claire Wegel, Dan Vitale, Deborah Hall, Ejaz Shamim, Faraz Faghri, Hampton Leonard, Hirotaka Iwaki, Ignacio Fernandez Mata, Ignacio Juan Keller Sarmiento, Jeff Kim, Joshua Shulman, Justin C. Solle, Karl Kieburtz, Ken Marek, Lana Chahine, Laurel Screven, Lisa Shulman, Maggie Kuhl, Marissa Dean, Mary Makarious, Miguel Inca, Mike Nalls, Niccolo Mencacci, Roy Alcalay, Ruqaya Murtadha, Sara Bandres‐Ciga, Schuyler Fox, Sohini Chowdhury, Steven Lubbe, Tao Xie, Tatiana Foroud, Todd Sherer, Yeajin Song, Andrew Singleton, Bernadette Siddiqi, Brian Fiske, Cornelis Blauwendraat, Ekemini Riley, Duan Nguyen, Toan Nguyen, Masharip Atadzhanov +181 morewiley +1 more source