About: Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice

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About: Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice Goto Sponge NotDistinct Permalink

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description	artículu científicu espublizáu en 2004 (ast) vědecký článek publikovaný v roce 2004 (cs) 2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в грудні 2004 (uk) 2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած (hyw) 2004年學術文章 (zh) vedecký článok (publikovaný 2004/12/28) (sk) مقالة علمية (نشرت في 28-12-2004) (ar) im Dezember 2004 veröffentlichter wissenschaftlicher Artikel (de) wetenschappelijk artikel (gepubliceerd op 2004/12/28) (nl) article publié dans les Proceedings of the National Academy of Sciences of the United States of America (fr) scientific journal article (en)
publication date	wds:Q28505849-46AD117D-BC0B-4056-B93B-CB73BBBCEF8C
publication date	2004-12-17 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28505849-3535B438-3949-4052-8FFC-5427CFDCA676
language of work or name	English
cites work	wds:Q28505849-08AEB859-002B-4C23-A003-2FC786A2B6EE wds:Q28505849-093579A5-AC62-47E5-A198-B3195B810B53 wds:Q28505849-0E384709-7BE0-4C01-B2ED-9E7F79D5AEF7 wds:Q28505849-0F75790F-DDD0-4DA5-80E3-63A124986117 wds:Q28505849-1A91F465-681B-4AFE-94F7-2A6F497B4843 wds:Q28505849-47D163D4-6C36-4762-999D-AFCDEAC33622 wds:Q28505849-49950BAC-34E9-4AD8-A940-AC84461BEF6E wds:Q28505849-4C68387E-A780-4C48-9BEE-6FC0D6859564 wds:Q28505849-512B226B-B0AD-4E85-B80D-4E921E29B1DA wds:Q28505849-5BA6DFB8-BB43-490F-98CB-CC4433092F7C wds:Q28505849-5DFBB857-9FAA-4D3A-9EF2-1D583B2C2866 wds:Q28505849-82B2AE70-FAE8-49B2-8384-522FFD046AA5 wds:Q28505849-83166DF3-1391-4B6D-A3AC-F4F5C2CB1C17 wds:Q28505849-8B54A395-8A14-49C2-93C0-D08BD52160BA wds:Q28505849-9EF6150A-3643-4A66-AF7D-F3511A218E67 wds:Q28505849-BB574FF8-0948-4908-8CD8-0B1A00802CB4 wds:Q28505849-C894DA5E-F793-41C4-92D0-C59A5D64F917 wds:Q28505849-C9445A9E-A7BA-497A-ACF1-D45B5B496987 wds:Q28505849-E291D860-F1E3-408F-A420-0AD94A54D15D wds:Q28505849-E672E136-EC42-4166-9FE6-95E9A249B902 wds:Q28505849-EB3473EF-3D4D-40F2-8E5E-7897F11105D3 wds:Q28505849-EBEAFC6B-9AF1-4D90-98A1-0DD65563C747 wds:Q28505849-F824C98F-0563-45E9-99C1-BCF71A0849A2 wds:Q28505849-FEB18D47-B590-4957-B1E7-3C18E2424C81
cites work	Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy Prenylated prelamin A interacts with Narf, a novel nuclear protein Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect. Edible vaccines: not quite ready for prime time Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice. Dual roles for Ste24p in yeast a-factor maturation: NH2-terminal proteolysis and COOH-terminal CAAX processing Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome Quantitative studies of the growth of mouse embryo cells in culture and their development into established lines Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction. Protein-protein interactions between human nuclear lamins expressed in yeast Chapter 24 Isolation and Characterization of Intermediate Filaments Biochemical studies of Zmpste24-deficient mice Roles of prenyl protein proteases in maturation of Saccharomyces cerevisiae a-factor Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy In vitro assay and characterization of the farnesylation-dependent prelamin A endoprotease Lamin B1 is required for mouse development and nuclear integrity A progeroid syndrome in mice is caused by defects in A-type lamins The role of isoprenylation in membrane attachment of nuclear lamins. A single point mutation prevents proteolytic cleavage of the lamin A precursor and confers membrane binding properties Nucleoplasmic localization of prelamin A: implications for prenylation-dependent lamin A assembly into the nuclear lamina An antibody which specifically recognizes prelamin A but not mature lamin A: application to detection of blocks in farnesylation-dependent protein processing
author name string	wds:Q28505849-0A6A7B25-D7B1-41C2-8805-4D5AEF75A3F6 wds:Q28505849-34088054-B991-4534-AB1A-B211F29B1497 wds:Q28505849-3A60C32D-12C5-48BB-B3E6-C70DFD1957BA wds:Q28505849-3B4071D3-E545-4ABC-B677-4986EFDE3B29 wds:Q28505849-3F913F0C-77D6-4375-AE62-2D510057F6A1 wds:Q28505849-54CE1463-2AEC-4E59-8897-94094C1ACFDC wds:Q28505849-A45077FB-8331-41AA-BA99-FAA2AC12EE79 wds:Q28505849-C5CC1805-5B6D-4CE6-86A3-7D10A3592D72
OpenCitations bibliographic resource ID	wds:Q28505849-B69D599A-36D7-4BA3-92D3-D802C3028F92
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/4592395
author name string	Sharmila Majumdar Colin L Stewart Martin O Bergo Shao H Yang Andrew Burghardt Terry Sullivan Jennifer K Ng Nathan Coté
OpenCitations bibliographic resource ID	4592395
rdfs:label	Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (en) Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (nl) Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (ast)
skos:prefLabel	Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (en) Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (nl) Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (ast)
name	Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (en) Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (nl) Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice (ast)
author	wds:Q28505849-0D07D4BA-EE72-4934-AA37-A92D55AF7A5B wds:Q28505849-1B9A4C5D-2DF5-44BD-B5C8-E8862919168E wds:Q28505849-8BE2DE00-711C-4E68-812E-DFC156F60505 wds:Q28505849-A1A15702-F50B-46F4-9FE6-D1E33814EB7A
author	Stephen G. Young Karen Reue Loren G Fong

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