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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 3 |
2007 | 2 |
2008 | 1 |
2024 | 0 |
Search Results
6 results
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Page 1
Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome.
Clin Genet. 2008 Oct;74(4):374-83. doi: 10.1111/j.1399-0004.2008.01034.x. Epub 2008 Jun 28.
Clin Genet. 2008.
PMID: 18554282
Free article.
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype.
Lombardi F, Gullotta F, Columbaro M, Filareto A, D'Adamo M, Vielle A, Guglielmi V, Nardone AM, Azzolini V, Grosso E, Lattanzi G, D'Apice MR, Masala S, Maraldi NM, Sbraccia P, Novelli G.
Lombardi F, et al.
J Clin Endocrinol Metab. 2007 Nov;92(11):4467-71. doi: 10.1210/jc.2007-0116. Epub 2007 Sep 11.
J Clin Endocrinol Metab. 2007.
PMID: 17848409
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Primary laminopathy fibroblasts display altered genome organization and apoptosis.
Meaburn KJ, Cabuy E, Bonne G, Levy N, Morris GE, Novelli G, Kill IR, Bridger JM.
Meaburn KJ, et al.
Aging Cell. 2007 Apr;6(2):139-53. doi: 10.1111/j.1474-9726.2007.00270.x. Epub 2007 Feb 5.
Aging Cell. 2007.
PMID: 17274801
Free article.
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Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy.
Filesi I, Gullotta F, Lattanzi G, D'Apice MR, Capanni C, Nardone AM, Columbaro M, Scarano G, Mattioli E, Sabatelli P, Maraldi NM, Biocca S, Novelli G.
Filesi I, et al.
Physiol Genomics. 2005 Oct 17;23(2):150-8. doi: 10.1152/physiolgenomics.00060.2005. Epub 2005 Jul 26.
Physiol Genomics. 2005.
PMID: 16046620
Free article.
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Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.
Capanni C, Mattioli E, Columbaro M, Lucarelli E, Parnaik VK, Novelli G, Wehnert M, Cenni V, Maraldi NM, Squarzoni S, Lattanzi G.
Capanni C, et al.
Hum Mol Genet. 2005 Jun 1;14(11):1489-502. doi: 10.1093/hmg/ddi158. Epub 2005 Apr 20.
Hum Mol Genet. 2005.
PMID: 15843404
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Somatic and gonadal mosaicism in Hutchinson-Gilford progeria.
Wuyts W, Biervliet M, Reyniers E, D'Apice MR, Novelli G, Storm K.
Wuyts W, et al.
Am J Med Genet A. 2005 May 15;135(1):66-8. doi: 10.1002/ajmg.a.30663.
Am J Med Genet A. 2005.
PMID: 15793835
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