Role of Lamin A/C as Candidate Biomarker of Aggressiveness and Tumorigenicity in Glioblastoma Multiforme by Giuliana Gatti, Laura Vilardo, Carla Musa, Chiara Di Pietro, Fabrizio Bonaventura, Ferdinando Scavizzi, Alessio Torcinaro, Barbara Bucci, Raffaele Saporito, Ivan Arisi, Francesca De Santa, Marcello Raspa, Loredana Guglielmi, Igea D’Agnano

Subjects: “…Lamin A/C…”
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Anti-lamin A/C antibodies in patients with Behçet’s disease by Peng Chen, Hai Yan, Wen Zhang, Chunhe Yang, Hongwu Du

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Phenotypic spectrum of mutations in cardiolaminopathies by Ali J. Marian

Subjects: “…Cardiolaminopathies, Lamin A/C, dilated cardiomyopathy.…”
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TPX2 promotes ovarian tumorigenesis by interacting with Lamin A/C and affecting its stability by Xin Meng, Jiazhen Cao, Hui Zheng, Xiaolu Ma, Yanchun Wang, Ying Tong, Suhong Xie, Renquan Lu, Lin Guo

Subjects: “…Lamin A/C…”
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FAK Executes Anti-Senescence via Regulating EZH2 Signaling in Non-Small Cell Lung Cancer Cells by Hsiang-Hao Chuang, Ming-Shyan Huang, Yen-Yi Zhen, Cheng-Hao Chuang, Ying-Ray Lee, Michael Hsiao, Chih-Jen Yang

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Construction of HEK293 and C2C12 cell models transfected by LMNA mutant and related intracellular sublocalization of lamin A/C by TAN Dan-dan, CHAI Jing-yan, LIU Jian-yun, NIE Hong-bing, XIONG Hui, WU Xiang-bin

Subjects: “…lmna gene|lamin a/c|lentivirus|mutation…”
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A novel role of lamins from genetic disease to cancer biomarkers by Kunnathur Murugesan Sakthivel, Poonam Sehgal

Subjects: “…Lamin A/C…”
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Role of Nuclear Lamin A/C in the Regulation of Nav1.5 Channel and Microtubules: Lesson From the Pathogenic Lamin A/C Variant Q517X by Roberta De Zio, Giusy Pietrafesa, Serena Milano, Giuseppe Procino, Manuela Bramerio, Martino Pepe, Cinzia Forleo, Stefano Favale, Maria Svelto, Andrea Gerbino, Monica Carmosino

Subjects: “…lamin A/C…”
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Pregnancy and Progression of Cardiomyopathy in Women With LMNA Genotype‐Positive by Anna I. Castrini, Eystein Skjølsvik, Mette E. Estensen, Vibeke M. Almaas, Helge Skulstad, Erik Lyseggen, Thor Edvardsen, Øyvind H. Lie, Kermshlise C. I. Picard, Neal K. Lakdawala, Kristina H. Haugaa

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ZMPSTE24 Is Associated with Elevated Inflammation and Progerin mRNA by Moritz Messner, Santhosh Kumar Ghadge, Thomas Maurer, Michael Graber, Simon Staggl, Sarah Christine Maier, Gerhard Pölzl, Marc-Michael Zaruba

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Biological Aging Modulates Cell Migration via Lamin A/C-Dependent Nuclear Motion by Jung-Won Park, Seong-Beom Han, Jungwon Hah, Geonhui Lee, Jeong-Ki Kim, Soo Hyun Kim, Dong-Hwee Kim

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Exercise is Associated With Impaired Left Ventricular Systolic Function in Patients With Lamin A/C Genotype by Eystein T. Skjølsvik, Nina E. Hasselberg, Lars A. Dejgaard, Øyvind H. Lie, Kjell Andersen, Torbjørn Holm, Thor Edvardsen, Kristina H. Haugaa

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Lamin-A/C variants found in patients with cardiac conduction disease reduce sodium currents by Michael A. Olaopa, Katherine G. Spoonamore, Deepak Bhakta, Zhenhui Chen, Patricia B.S. Celestino-Soper, Peng-Sheng Chen, Tomohiko Ai, Matteo Vatta

Subjects: “…Lamin A/C…”
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Perinuclear organelle trauma at the nexus of cardiomyopathy pathogenesis arising from loss of function LMNA mutation by Jason C. Choi

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Clinical and diagnostic difficulties in management of patients with laminopathies by O. V. Melnik, A. B. Malashicheva, Yu. V. Fomicheva, A. A. Khudyakov, A. Ya. Gudkova, D. I. Rudenko, M. A. Simonenko, Е. N. Mikhailov, D. S. Lebedev, E. S. Vasichkina, T. M. Pervunina, A. A. Kostareva

Subjects: “…lamin a/c…”
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Targeting unfolded protein response reverts ER stress and ER Ca2+ homeostasis in cardiomyocytes expressing the pathogenic variant of Lamin A/C R321X by Giusy Pietrafesa, Roberta De Zio, Simona Ida Scorza, Maria Francesca Armentano, Martino Pepe, Cinzia Forleo, Giuseppe Procino, Andrea Gerbino, Maria Svelto, Monica Carmosino

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Sensing the squeeze: nuclear mechanotransduction in health and disease by Luv Kishore Srivastava, Allen J. Ehrlicher

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DNA Damage Accumulation and TRF2 Degradation in Atypical Werner Syndrome Fibroblasts with LMNA mutations by Bidisha eSaha, Galynn eZitnik, Simon C Johnson, Quyen eNguyen, Rosa Ana eRisques, George M Martin, Junko eOshima

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An Intronic Heterozygous <i>SYNE2</i> Splice Site Mutation: A Rare Cause for Myalgia and hyperCKemia? by Theresa Paulus, Natalie Young, Emily Jessop, Carolin Berwanger, Christoph Stephan Clemen, Rolf Schröder, Rafal Ploski, Christian Hagel, Yorck Hellenbroich, Andreas Moser, Iakowos Karakesisoglou

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The Pathogenic Mechanisms of and Novel Therapies for Lamin A/C-Related Dilated Cardiomyopathy Based on Patient-Specific Pluripotent Stem Cell Platforms and Animal Models by Xin-Yi Wu, Yee-Ki Lee, Yee-Man Lau, Ka-Wing Au, Yiu-Lam Tse, Kwong-Man Ng, Chun-Ka Wong, Hung-Fat Tse

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