Deciphering Nuclear Mechanobiology in Laminopathy by Jungwon Hah, Dong-Hwee Kim

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Consequences of <i>Lmna</i> Exon 4 Mutations in Myoblast Function by Déborah Gómez-Domínguez, Carolina Epifano, Fernando de Miguel, Albert García Castaño, Borja Vilaplana-Martí, Alberto Martín, Sandra Amarilla-Quintana, Anne T Bertrand, Gisèle Bonne, Javier Ramón-Azcón, Miguel A Rodríguez-Milla, Ignacio Pérez de Castro

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Case Report: An Atypical Form of Familial Partial Lipodystrophy Type 2 Due to Mutation in the Rod Domain of Lamin A/C by Carolina Cecchetti, M. Rosaria D’Apice, Elena Morini, Giuseppe Novelli, Giuseppe Novelli, Carmine Pizzi, Uberto Pagotto, Alessandra Gambineri

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LMNA-Cardiomyopathy in Emery-Dreifuss Muscular Dystrophy by E. V. Resnik, A. A. Kovaleva, M. Kh. Shurdumova, D. E. Emelyanovich, A. P. Smirnov, V. Y. Voinova

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IFN-Aging: Coupling Aging With Interferon Response by Wei Cao

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The Interplay between Oxidative Stress and the Nuclear Lamina Contributes to Laminopathies and Age-Related Diseases by Lidya Kristiani, Youngjo Kim

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Creatine and l-carnitine attenuate muscular laminopathy in the LMNA mutation transgenic zebrafish by Shao-Wei Pan, Horng-Dar Wang, He-Yun Hsiao, Po-Jui Hsu, Yung-Che Tseng, Wen-Chen Liang, Yuh-Jyh Jong, Chiou-Hwa Yuh

Subjects: “…Striated muscle laminopathy…”
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Post-Translational Modification of Lamins: Mechanisms and Functions by Mingyue Zheng, Guoxiang Jin, Zhongjun Zhou

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Structural and Mechanical Aberrations of the Nuclear Lamina in Disease by Merel Stiekema, Marc A. M. J. van Zandvoort, Frans C. S. Ramaekers, Jos L. V. Broers

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Restrictive dermopathy: A baby with taut skin, facial dysmorphism, joint contractures, and pulmonary hypoplasia by Wei Di Ng, MBBS, MMED (Paed), Ai Ling Koh, MB, ChB, MRCPCH, MMED (Paed), Mark Jean Aan Koh, MBBS, DIP, MRCPCH, Dip Pract Derm (UK), DipDermatopathology (ICDP-UEMS, Austria), Juin Yee Kong, MD (Jefferson, FAAP, Diplomate of American Board of Pediatrics) (Peds) (Neonatology)

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PRIMARY (GENETICALLY DETERMINED) DILATION CARDIOMYOPATHY IN A PATIENT WITH NOVEL MUTATION OF LAMIN GENE: CLINICAL AND MORPHOLOGICAL MANAGEMENT by O. V. Blagova, I. N. Alieva, A. V. Nedostup, V. A. Sulimov, E. A. Kogan, A. G. Shestak, D. A. Zateyshchikov, E. V. Zaklyazminskaya

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Dilated cardiomyopathy: reconceptualization of the problem by T. G. Vaykhanskaya, L. N. Sivitskaya, T. V. Kurushko, O. D. Levdansky, N. G. Danilenko

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A new laminopathy caused by an Arg133/Leu mutation in lamin A/C and the effects thereof on adipocyte differentiation and the transcriptome by Zhe Wang, Yueting Dong, Jing Yang, Yingzi He, Xihua Lin, Fang Wu, Hong Li, Fenping Zheng

Subjects: “…laminopathy…”
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A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy by Saeed Farajzadeh Valilou, Javad Karimzad Hagh, Mohammad Salimi Asl, Isa Abdi Rad, Masoud Edizadeh, Arash Pooladi

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Rare BANF1 Alleles and Relatively Frequent EMD Alleles Including ‘Healthy Lipid’ Emerin p.D149H in the ExAC Cohort by Tejas Dharmaraj, Youchen Guan, Julie Liu, Catherine Badens, Benedicte Gaborit, Katherine L. Wilson

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Laminopathies: what can humans learn from fruit flies by Marta Pałka, Aleksandra Tomczak, Katarzyna Grabowska, Magdalena Machowska, Katarzyna Piekarowicz, Dorota Rzepecka, Ryszard Rzepecki

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A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy by Damien Galant, Bénédicte Gaborit, Camille Desgrouas, Ines Abdesselam, Monique Bernard, Nicolas Levy, Françoise Merono, Catherine Coirault, Patrice Roll, Arnaud Lagarde, Nathalie Bonello-Palot, Patrice Bourgeois, Anne Dutour, Catherine Badens

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Molecular mechanism on autophagy associated cardiovascular dysfunction in Drosophila melanogaster by Wei Zhang, Rong Zhou, Xinjuan Lei, Mofei Wang, Qinchun Duan, Yuanlin Miao, Tingting Zhang, Xinjie Li, Zhang Zutong, Liyang Wang, Odell D. Jones, Mengmeng Xu, Joseph Bryant, Jianjie Ma, Yingli Liu, Xuehong Xu

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Nuclear lamins and diabetes mellitus by Wei Xie, Brian Burke

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Thematic Review Series: Lipid Posttranslational Modifications. Prelamin A, Zmpste24, misshapen cell nuclei, and progeria—new evidence suggesting that protein farnesylation could be... by Stephen G. Young, Loren G. Fong, Susan Michaelis

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