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Select item 60387071.

Lamins and Lamin-associated Proteins in Gastrointestinal Health and Disease

Graham F. Brady, Raymond Kwan, Juliana Bragazzi Cunha, Jared S. Elenbaas, M. Bishr Omary

Gastroenterology. Author manuscript; available in PMC 2019 May 1.

Published in final edited form as: Gastroenterology. 2018 May; 154(6): 1602–1619.e1. Published online 2018 Mar 13. doi: 10.1053/j.gastro.2018.03.026

PMCID:: PMC6038707

Abstract Article PDF–592K

Select item 59225322.

Upregulation of the aging related LMNA splice variant progerin in dilated cardiomyopathy

Moritz Messner, Santhosh Kumar Ghadge, Valentina Goetsch, Andreas Wimmer, Jakob Dörler, Gerhard Pölzl, Marc-Michael Zaruba

PLoS One. 2018; 13(4): e0196739. Published online 2018 Apr 27. doi: 10.1371/journal.pone.0196739

PMCID:: PMC5922532

Abstract Article PDF–6.4M

Select item 59333953.

Association of Lonafarnib Treatment vs No Treatment With Mortality Rate in Patients With Hutchinson-Gilford Progeria Syndrome

Leslie B. Gordon, Heather Shappell, Joe Massaro, Ralph B. D’Agostino, Sr, Joan Brazier, Susan E. Campbell, Monica E. Kleinman, Mark W. Kieran

JAMA. 2018 Apr 24; 319(16): 1687–1695. Published online 2018 Apr 24. doi: 10.1001/jama.2018.3264

PMCID:: PMC5933395

Abstract Article

Select item 59396244.

Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

Nina Eide Hasselberg, Trine Fink Haland, Jørg Saberniak, Pål Haugar Brekke, Knut Erik Berge, Trond Paul Leren, Thor Edvardsen, Kristina Hermann Haugaa

Eur Heart J. 2018 Mar 7; 39(10): 853–860. Published online 2017 Oct 31. doi: 10.1093/eurheartj/ehx596

PMCID:: PMC5939624

Abstract Article PDF–451K

Select item 59465155.

The renal manifestations of type 4 familial partial lipodystrophy: a case report and review of literature

Ru-Xuan Chen, Lei Zhang, Wei Ye, Yu-Bing Wen, Nuo Si, Hang Li, Ming-Xi Li, Xue-Mei Li, Ke Zheng

BMC Nephrol. 2018; 19: 111. Published online 2018 May 10. doi: 10.1186/s12882-018-0913-6

PMCID:: PMC5946515

Abstract Article PDF–3.4M

Select item 59532346.

Three new cases of dilated cardiomyopathy caused by mutations in LMNA gene

LARYSA N. SIVITSKAYA, NINA G. DANILENKO, TATIYANA G. VAIKHANSKAYA, TATSIYANA V. KURUSHKA, OLEG G. DAVYDENKO

Acta Myol. 2017 Dec; 36(4): 207–212. Published online 2017 Dec 1.

PMCID:: PMC5953234

Abstract Article PDF–170K

Select item 59676057.

A pharmacogenetic approach to the treatment of patients with PPARG mutations

Maura Agostini, Erik Schoenmakers, Junaid Beig, Louise Fairall, Istvan Szatmari, Odelia Rajanayagam, Fred Muskett, Claire Adams, A. David Marais, Stephen O’Rahilly, Robert K. Semple, Laszlo Nagy, Amit R. Majithia, John Schwabe, Dirk J. Blom, Rinki Murphy, Krishna Chatterjee, David B. Savage

Diabetes. Author manuscript; available in PMC 2018 Jul 1.

Published in final edited form as: Diabetes. 2018 Jun; 67(6): 1086–1092. Published online 2018 Apr 5. doi: 10.2337/db17-1236

PMCID:: PMC5967605

Abstract Article PDF–1.3M

Select item 59731678.

Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes

Pia Bernasconi, Nicola Carboni, Giulia Ricci, Gabriele Siciliano, Luisa Politano, Lorenzo Maggi, Tiziana Mongini, Liliana Vercelli, Carmelo Rodolico, Elena Biagini, Giuseppe Boriani, Lucia Ruggiero, Lucio Santoro, Elisa Schena, Sabino Prencipe, Camilla Evangelisti, Elena Pegoraro, Lucia Morandi, Marta Columbaro, Chiara Lanzuolo, Patrizia Sabatelli, Paola Cavalcante, Cristina Cappelletti, Gisèle Bonne, Antoine Muchir, Giovanna Lattanzi

Nucleus. 2018; 9(1): 292–304. Published online 2018 May 18. doi: 10.1080/19491034.2018.1467722

PMCID:: PMC5973167

Abstract Article PDF–1.3M

Select item 59732429.

Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives

Corinne Vigouroux, Anne-Claire Guénantin, Camille Vatier, Emilie Capel, Caroline Le Dour, Pauline Afonso, Guillaume Bidault, Véronique Béréziat, Olivier Lascols, Jacqueline Capeau, Nolwenn Briand, Isabelle Jéru

Nucleus. 2018; 9(1): 235–248. Published online 2018 Apr 16. doi: 10.1080/19491034.2018.1456217

PMCID:: PMC5973242

Abstract Article PDF–1018K

Select item 597325510.

Clinical aspects of Emery-Dreifuss muscular dystrophy

Agnieszka Madej-Pilarczyk

Nucleus. 2018; 9(1): 268–274. Published online 2018 Apr 10. doi: 10.1080/19491034.2018.1462635

PMCID:: PMC5973255

Abstract Article PDF–383K

Select item 597325711.

Laminopathy-causing lamin A mutations reconfigure lamina-associated domains and local spatial chromatin conformation

Nolwenn Briand, Philippe Collas

Nucleus. 2018; 9(1): 216–226. Published online 2018 Mar 8. doi: 10.1080/19491034.2018.1449498

PMCID:: PMC5973257

Abstract Article PDF–889K

Select item 597326512.

Causes and consequences of genomic instability in laminopathies: Replication stress and interferon response

Simona Graziano, Ray Kreienkamp, Nuria Coll-Bonfill,, Susana Gonzalo

Nucleus. 2018; 9(1): 258–275. Published online 2018 May 7. doi: 10.1080/19491034.2018.1454168

PMCID:: PMC5973265

Abstract Article PDF–1.1M

Select item 597664013.

The ¹³C hyperpolarized pyruvate generated by ParaHydrogen detects the response of the heart to altered metabolism in real time

Eleonora Cavallari, Carla Carrera, Matteo Sorge, Gisèle Bonne, Antoine Muchir, Silvio Aime, Francesca Reineri

Sci Rep. 2018; 8: 8366. Published online 2018 May 30. doi: 10.1038/s41598-018-26583-2

PMCID:: PMC5976640

Abstract Article PDF–1.2M

Select item 598822914.

Activation of Yap1/Taz signaling in ischemic heart disease and dilated cardiomyopathy

Ning Hou, Ying Wen, Xun Yuan, Haodong Xu, Xuejun Wang, Faqian Li, Bo Ye

Exp Mol Pathol. Author manuscript; available in PMC 2018 Jun 5.

Published in final edited form as: Exp Mol Pathol. 2017 Dec; 103(3): 267–275. Published online 2017 Nov 15. doi: 10.1016/j.yexmp.2017.11.006

PMCID:: PMC5988229

Abstract Article PDF–1.0M

Select item 600910315.

Gene Expression Profiling of Fibroblasts From a Human Progeroid Disease (Mandibuloacral Dysplasia, MAD #248370) Through cDNA Microarrays

Francesca Amati, Michela Biancolella, Maria Rosaria D’Apice, Stefano Gambardella, Ruggiero Mango, Paolo Sbraccia, Monica D’Adamo, Katia Margiotti, Annamaria Nardone, Marc Lewis, Giuseppe Novelli

Gene Expr. 2004; 12(1): 39–47. Published online 2018 Jun 20. doi: 10.3727/000000004783992189

PMCID:: PMC6009103

Abstract Article PDF–187K

Select item 603431016.

Laminopathies: what can humans learn from fruit flies

Marta Pałka, Aleksandra Tomczak, Katarzyna Grabowska, Magdalena Machowska, Katarzyna Piekarowicz, Dorota Rzepecka, Ryszard Rzepecki

Cell Mol Biol Lett. 2018; 23: 32. Published online 2018 Jul 6. doi: 10.1186/s11658-018-0093-1

PMCID:: PMC6034310

Abstract Article PDF–3.0M

Select item 591087317.

Everolimus rescues multiple cellular defects in laminopathy-patient fibroblasts

Amanda J. DuBose, Stephen T. Lichtenstein, Noreen M. Petrash, Michael R. Erdos, Leslie B. Gordon, Francis S. Collins

Proc Natl Acad Sci U S A. 2018 Apr 17; 115(16): 4206–4211. Published online 2018 Mar 26. doi: 10.1073/pnas.1802811115

Correction in:: Proc Natl Acad Sci U S A. 2018 Apr 24; 115(17): E4140.

PMCID:: PMC5910873

Abstract Article PDF–1.0M

Select item 605247418.

Mice with reduced expression of the telomere‐associated protein Ft1 develop p53‐sensitive progeroid traits

Mattia La Torre, Chiara Merigliano, Romina Burla, Carla Mottini, Giorgia Zanetti, Simona Del Giudice, Mariateresa Carcuro, Ilaria Virdia, Elisabetta Bucciarelli, Isabella Manni, Gianluca Rampioni Vinciguerra, Giulia Piaggio, Mara Riminucci, Ana Cumano, Armando Bartolazzi, Fiammetta Vernì, Silvia Soddu, Maurizio Gatti, Isabella Saggio

Aging Cell. 2018 Aug; 17(4): e12730. Published online 2018 Apr 10. doi: 10.1111/acel.12730