Altered pre-lamin A processing is a common mechanism leading to lipodystrophy-Reference-Cited by-同舟云学术

Altered pre-lamin A processing is a common mechanism leading to lipodystrophy

Published:2005-04-20 Issue:11 Volume:14 Page:1489-1502
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Capanni Cristina,Mattioli Elisabetta,Columbaro Marta,Lucarelli Enrico,Parnaik Veena K.,Novelli Giuseppe,Wehnert Manfred,Cenni Vittoria,Maraldi Nadir M.,Squarzoni Stefano,Lattanzi Giovanna

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/11/1489/1659964/ddi158.pdf

Reference59 articles.

1. Hegele, R.A. (2003) Monogenic forms of insulin resistance: apertures that expose the common metabolic syndrome. Trends Endocrinol. Metab., 14, 371–377.

2. Shacketon, S., Lloyd, D.J., Jackson, SN., Evans, R., Niermeijer, M.F., Singh, B.M., Schmidt, H., Brabant, G., Kumar, S. et al. (2000) LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. Nat. Genet., 24, 153–156.

3. Novelli, G., Muchir, A., Sangiuolo, F., Helbling-Leclerc, A., D'Apice, M.R., Massart, C., Capon, F., Sbraccia, P., Federici, M., Lauro, R. et al. (2002) Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C. Am. J. Hum. Genet., 71, 426–431.

4. Bhayana, S., Siu, V.M., Joubert, G.I., Clarson, C.L., Cao, H. and Hegele, R.A. (2002) Cardiomyopathy in congenital complete lipodystrophy. Clin. Genet., 61, 283–287.

5. Magre, J.J., Delepine, M., Khallouf, E., Gedde-Dahl, T., Jr, Van Maldergem, L., Sobel, E., Papp, J., Meier, M., Megarbane, A., Bachy, A. et al. (2001) Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nat. Genet., 28, 365–370.

Cited by 192 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Evaluation of lamin A/C mechanotransduction under different surface topography in LMNA related muscular dystrophy;Cytoskeleton;2024-08

2. The Compromised Fanconi Anemia Pathway in Prelamin A‐Expressing Cells Contributes to Replication Stress‐Induced Genomic Instability;Advanced Science;2024-06-18

3. Effect of β-Estradiol on Adipogenesis in a 3T3-L1 Cell Model of Prelamin A Accumulation;International Journal of Molecular Sciences;2024-01-20

4. Mineralocorticoid Receptor Antagonism Prevents Type 2 Familial Partial Lipodystrophy Brown Adipocyte Dysfunction;Cells;2023-11-07

5. Ghrelin delays premature aging in Hutchinson‐Gilford progeria syndrome;Aging Cell;2023-10-19