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Citations to this article

How do mutations in lamins A and C cause disease?
Howard J. Worman, Jean-Claude Courvalin
Howard J. Worman, Jean-Claude Courvalin
Published February 1, 2004
Citation Information: J Clin Invest. 2004;113(3):349-351. https://doi.org/10.1172/JCI20832.
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Commentary

How do mutations in lamins A and C cause disease?

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Abstract

Mutations in lamins A and C, nuclear intermediate-filament proteins in nearly all somatic cells, cause a variety of diseases that primarily affect striated muscle, adipocytes, or peripheral nerves or cause features of premature aging. Two new studies use lamin A/C–deficient mice, which develop striated muscle disease, as a model to investigate pathogenic mechanisms. These reports provide evidence for a stepwise process in which mechanically stressed cells first develop chromatin and nuclear envelope damage and then develop secondary alterations in the transcriptional activation of genes in adaptive and protective pathways.

Authors

Howard J. Worman, Jean-Claude Courvalin

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Total citations by year

Year: 2024 2023 2022 2021 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 Total
Citations: 1 1 1 2 2 1 1 1 2 1 1 2 3 4 8 2 1 2 6 42
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article (42)

Title and authors Publication Year
The Influence of a Genetic Variant in CCDC78 on LMNA-Associated Skeletal Muscle Disease.
Mohar NP, Cox EM, Adelizzi E, Moore SA, Mathews KD, Darbro BW, Wallrath LL
International journal of molecular sciences 2024
Drosophila Models Reveal Properties of Mutant Lamins That Give Rise to Distinct Diseases
Walker SG, Langland CJ, Viles J, Hecker LA, Wallrath LL
Cells 2023
Impact of MnTBAP and Baricitinib Treatment on Hutchinson-Gilford Progeria Fibroblasts.
Vehns E, Arnold R, Djabali K
Pharmaceuticals (Basel, Switzerland) 2022
Muscle Enriched Lamin Interacting Protein (Mlip) Binds Chromatin and Is Required for Myoblast Differentiation
E Ahmady, A Blais, PG Burgon
Cells 2021
Investigating LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
Shemer Y, Mekies LN, Ben Jehuda R, Baskin P, Shulman R, Eisen B, Regev D, Arbustini E, Gerull B, Gherghiceanu M, Gottlieb E, Arad M, Binah O
International journal of molecular sciences 2021
Deciphering Nuclear Mechanobiology in Laminopathy
J Hah, DH Kim
Cells 2019
Chromatin compartment dynamics in a haploinsufficient model of cardiac laminopathy
A Bertero, PA Fields, AS Smith, A Leonard, K Beussman, NJ Sniadecki, DH Kim, HF Tse, L Pabon, J Shendure, WS Noble, CE Murry
The Journal of Cell Biology 2019
Alternative mRNA Splicing in the Pathogenesis of Obesity
CM Wong, L Xu, M Yau
International journal of molecular sciences 2018
Lamin A and microtubules collaborate to maintain nuclear morphology
Z Tariq, H Zhang, A Chia-Liu, Y Shen, Y Gete, ZM Xiong, C Tocheny, L Campanello, D Wu, W Losert, K Cao
Nucleus 2017
Skeletal myopathy in a family with lamin A/C cardiac disease.
Ghosh S, Renapurkar R, Raman SV
Cardiovascular diagnosis and therapy 2016
Myopathic Lamin Mutations Cause Reductive Stress and Activate the Nrf2/Keap-1 Pathway
G Dialynas, OK Shrestha, JM Ponce, M Zwerger, DA Thiemann, GH Young, SA Moore, L Yu, J Lammerding, LL Wallrath, KL Wilson
PLoS genetics 2015
For whom the cells pull: Hydrogel and micropost devices for measuring traction forces
AJ Ribeiro, AK Denisin, RE Wilson, BL Pruitt
Methods 2015
Nuclear localization signal deletion mutants of lamin A and progerin reveal insights into lamin A processing and emerin targeting
D Wu, AR Flannery, H Cai, E Ko, K Cao
Nucleus 2014
Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.
Brodt C, Siegfried JD, Hofmeyer M, Martel J, Rampersaud E, Li D, Morales A, Hershberger RE
Journal of Cardiac Failure 2013
Reversal of laminopathies: the curious case of SUN1.
Chi YH, Chen CY, Jeang KT
Nucleus (Austin, Tex.) 2012
Accumulation of the inner nuclear envelope protein Sun1 is pathogenic in progeric and dystrophic laminopathies.
Chen CY, Chi YH, Mutalif RA, Starost MF, Myers TG, Anderson SA, Stewart CL, Jeang KT
Cell 2012
Lamin A, farnesylation and aging
S Reddy, L Comai
Experimental Cell Research 2011
Quantitative nucleolar proteomics reveals nuclear re-organization during stress- induced senescence in mouse fibroblast.
Kar B, Liu B, Zhou Z, Lam YW
BMC cell biology 2011
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.
Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Züchner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, Hershberger RE
The American Journal of Human Genetics 2011
Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals
RE Hershberger, A Morales, JD Siegfried
Genetics in Medicine 2010
Nuclear morphology and deformation in engineered cardiac myocytes and tissues
MA Bray, WJ Adams, NA Geisse, AW Feinberg, SP Sheehy, KK Parker
Biomaterials 2010
LMNA E82K mutation activates FAS and mitochondrial pathways of apoptosis in heart tissue specific transgenic mice
D Lu, H Lian, X Zhang, H Shao, L Huang, C Qin, L Zhang
PloS one 2010
Beyond lamins other structural components of the nucleoskeleton
Z Zhong, KL Wilson, KN Dahl
Methods in cell biology 2010
A comparative study of Drosophila and human A-type lamins
SR Schulze, B Curio-Penny, S Speese, G Dialynas, DE Cryderman, CW McDonough, D Nalbant, M Petersen, V Budnik, PK Geyer, LL Wallrath
PloS one 2009
Nuclear lamins: key regulators of nuclear structure and activities
M Prokocimer, M Davidovich, M Nissim-Rafinia, N Wiesel-Motiuk, DZ Bar, R Barkan, E Meshorer, Y Gruenbaum
Journal of Cellular and Molecular Medicine 2009
Bringing KASH under the SUN: the many faces of nucleo-cytoskeletal connections
D Razafsky, D Hodzic
The Journal of Cell Biology 2009
Molecular ageing in progeroid syndromes: Hutchinson-Gilford progeria syndrome as a model
HD Coutinho, VS Falcão-Silva, GF Gonçalves, RB da Nóbrega
Immunity & Ageing 2009
Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins
C Östlund, ES Folker, JC Choi, ER Gomes, GG Gundersen, HJ Worman
Journal of cell science 2009
The nuclear envelopathies and human diseases
YH Chi, ZJ Chen, KT Jeang
Journal of Biomedical Science 2009
Reduced expression of lamin A/C correlates with poor histological differentiation and prognosis in primary gastric carcinoma
Wu Z, Wu L, Weng D, Xu D, Geng J, Zhao F
Journal of experimental & clinical cancer research : CR 2009
Requirement for Sun1 in the expression of meiotic reproductive genes and piRNA.
Chi YH, Cheng LI, Myers T, Ward JM, Williams E, Su Q, Faucette L, Wang JY, Jeang KT
Development (Cambridge, England) 2009
Microcephalia with mandibular and dental dysplasia in adult Zmpste24-deficient mice
F Carlos, I Varela, A Germanà, G Montalbano, JM Freije, JA Vega, C López-Otin, JM Cobo
Journal of Anatomy 2008
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Peterson A, Li D, Jakobs P, Litt M, Porter CB, Rahko PS, Hershberger RE
American Heart Journal 2008
Immobility, inheritance and plasticity of shape of the yeast nucleus
Hattier T, Andrulis ED, Tartakoff AM
BMC cell biology 2007
Laminopathies: Multiple disorders arising from defects in nuclear architecture
VK Parnaik, K Manju
Journal of Biosciences 2006
Emerin-Lacking Mice Show Minimal Motor and Cardiac Dysfunctions with Nuclear-Associated Vacuoles
Ozawa R, Hayashi YK, Ogawa M, Kurokawa R, Matsumoto H, Noguchi S, Nonaka I, Nishino I
The American Journal of Pathology 2006
Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy
CL Moulson, G Go, JM Gardner, AC van der Wal, JH Smitt, JM van Hagen, JH Miner
Journal of Investigative Dermatology 2005
Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress
M Paradisi, D McClintock, RL Boguslavsky, C Pedicelli, HJ Worman, K Djabali
BMC cell biology 2005
Overcoming functional redundancy to elicit pachyonychia congenita-like nail lesions in transgenic mice
P Wong, R Domergue, PA Coulombe
Molecular and cellular biology 2005
Defining the properties of the nonhelical tail domain in type II keratin 5: insight from a bullous disease-causing mutation
LH Gu, PA Coulombe
Molecular biology of the cell 2005
Functions and dysfunctions of the nuclear lamin Ig-fold domain in nuclear assembly, growth, and Emery–Dreifuss muscular dystrophy
Shumaker DK, Lopez-Soler RI, Adam SA, Herrmann H, Moir RD, Spann TP, Goldman RD
Proceedings of the National Academy of Sciences 2005
Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference.
Huang S, Chen L, Libina N, Janes J, Martin GM, Campisi J, Oshima J
Human Genetics 2005

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