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There are 3215 results for: content related to: Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations

  1. Laminopathies in Russian families

    Clinical Genetics

    Volume 74, Issue 2, August 2008, Pages: 127–133, GE Rudenskaya, AV Polyakov, SM Tverskaya, EV Zaklyazminskaya, AL Chukhrova, OE Groznova and EK Ginter

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.2008.01045.x

  2. You have free access to this content
    Nuclear lamins and laminopathies

    The Journal of Pathology

    Volume 226, Issue 2, January 2012, Pages: 316–325, Howard J. Worman

    Version of Record online : 14 NOV 2011, DOI: 10.1002/path.2999

  3. Genetics of Human Laminopathies

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    eLS

    Giuseppe Novelli and Maria Rosaria D'Apice

    Published Online : 16 JAN 2017, DOI: 10.1002/9780470015902.a0024693

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    Nuclear lamins: key regulators of nuclear structure and activities

    Journal of Cellular and Molecular Medicine

    Volume 13, Issue 6, June 2009, Pages: 1059–1085, Miron Prokocimer, Maya Davidovich, Malka Nissim-Rafinia, Naama Wiesel-Motiuk, Daniel Z. Bar, Rachel Barkan, Eran Meshorer and Yosef Gruenbaum

    Version of Record online : 1 JUL 2009, DOI: 10.1111/j.1582-4934.2008.00676.x

  5. Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations

    Human Mutation

    Volume 32, Issue 2, February 2011, Pages: 152–167, Juergen Scharner, Charlotte A. Brown, Matthew Bower, Susan T. Iannaccone, Ismail A. Khatri, Diana Escolar, Erynn Gordon, Kevin Felice, Carol A. Crowe, Carla Grosmann, Matthew N. Meriggioli, Alexander Asamoah, Ora Gordon, Viola F. Gnocchi, Juliet A. Ellis, Jerry R. Mendell and Peter S. Zammit

    Version of Record online : 25 JAN 2011, DOI: 10.1002/humu.21361

  6. The laminopathies: a clinical review

    Clinical Genetics

    Volume 70, Issue 4, October 2006, Pages: 261–274, J Rankin and S Ellard

    Version of Record online : 17 AUG 2006, DOI: 10.1111/j.1399-0004.2006.00677.x

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    Corrigendum

    Vol. 71, Issue 3, 293, Version of Record online: 19 FEB 2007

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    LMNA-associated cardiocutaneous progeria: An inherited autosomal dominant premature aging syndrome with late onset

    American Journal of Medical Genetics Part A

    Volume 161, Issue 7, July 2013, Pages: 1599–1611, Megan S. Kane, Mark E. Lindsay, Daniel P. Judge, Jemima Barrowman, Colette Ap Rhys, Lisa Simonson, Harry C. Dietz and Susan Michaelis

    Version of Record online : 10 MAY 2013, DOI: 10.1002/ajmg.a.35971

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    Primary laminopathy fibroblasts display altered genome organization and apoptosis

    Aging Cell

    Volume 6, Issue 2, April 2007, Pages: 139–153, Karen J. Meaburn, Erik Cabuy, Gisele Bonne, Nicolas Levy, Glenn E. Morris, Giuseppe Novelli, Ian R. Kill and Joanna M. Bridger

    Version of Record online : 5 FEB 2007, DOI: 10.1111/j.1474-9726.2007.00270.x

  9. Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 12, 15 June 2008, Pages: 1530–1542, Julia Rankin, Michaela Auer-Grumbach, Warwick Bagg, Kevin Colclough, Nguyen Thuy Duong, Jane Fenton-May, Andrew Hattersley, Judith Hudson, Philip Jardine, Dragana Josifova, Cheryl Longman, Robert McWilliam, Katharine Owen, Mark Walker, Manfred Wehnert and Sian Ellard

    Version of Record online : 13 MAY 2008, DOI: 10.1002/ajmg.a.32331

  10. Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations

    Muscle & Nerve

    Volume 48, Issue 2, August 2013, Pages: 161–170, Nicola Carboni, Anna Mateddu, Giovanni Marrosu, Eleonora Cocco and Maria Giovanna Marrosu

    Version of Record online : 28 JUN 2013, DOI: 10.1002/mus.23827

  11. Genetics of Diseases of the Nuclear Envelope

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    eLS

    Antoine Muchir

    Published Online : 15 MAR 2013, DOI: 10.1002/9780470015902.a0023858

  12. Role of nuclear Lamin A/C in cardiomyocyte functions

    Biology of the Cell

    Volume 106, Issue 10, October 2014, Pages: 346–358, Monica Carmosino, Silvia Torretta, Giuseppe Procino, Andrea Gerbino, Cinzia Forleo, Stefano Favale and Maria Svelto

    Version of Record online : 20 AUG 2014, DOI: 10.1111/boc.201400033

  13. Laminopathies and lamin-associated signaling pathways

    Journal of Cellular Biochemistry

    Volume 112, Issue 4, April 2011, Pages: 979–992, Nadir M. Maraldi, Cristina Capanni, Vittoria Cenni, Milena Fini and Giovanna Lattanzi

    Version of Record online : 11 MAR 2011, DOI: 10.1002/jcb.22992

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    Laminopathies: Involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases

    Journal of Cellular Physiology

    Volume 203, Issue 2, May 2005, Pages: 319–327, Nadir M. Maraldi, Stefano Squarzoni, Patrizia Sabatelli, Cristina Capanni, Elisabetta Mattioli, Andrea Ognibene and Giovanna Lattanzi

    Version of Record online : 23 SEP 2004, DOI: 10.1002/jcp.20217

  15. Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 11, November 2009, Pages: 2387–2392, Agnieszka Madej-Pilarczyk, Danuta Rosińska-Borkowska, Joanna Rękawek, Michał Marchel, Ewa Szaluś, Stefania Jabłońska and Irena Hausmanowa-Petrusewicz

    Version of Record online : 19 OCT 2009, DOI: 10.1002/ajmg.a.33018

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    Atomic force microscopy and lamins: A review study towards future, combined investigations

    Microscopy Research and Technique

    Volume 80, Issue 1, January 2017, Pages: 97–108, Ilaria Pecorari, Luca Puzzi and Orfeo Sbaizero

    Version of Record online : 17 NOV 2016, DOI: 10.1002/jemt.22801

  17. Diseases of the Nucleoskeleton

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    Comprehensive Physiology

    James M. Holaska

    Published Online : 15 SEP 2016, DOI: 10.1002/cphy.c150039

  18. Association of homozygous LMNA mutation R471C with new phenotype: Mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 8, 15 April 2008, Pages: 1049–1054, Birgit Zirn, Wolfram Kress, Tiemo Grimm, Lars Daniel Berthold, Bernd Neubauer, Klaus Kuchelmeister, Ulrich Müller and Andreas Hahn

    Version of Record online : 17 MAR 2008, DOI: 10.1002/ajmg.a.32259

  19. Lamins in Inherited Disease

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    eLS

    Lucio Comai

    Published Online : 17 JUL 2017, DOI: 10.1002/9780470015902.a0027262

  20. Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations

    Clinical Genetics

    Volume 78, Issue 1, July 2010, Pages: 66–73, L Subramanyam, V Simha and A Garg

    Version of Record online : 22 DEC 2009, DOI: 10.1111/j.1399-0004.2009.01350.x