Literature DB >> 15254580

Determination of the molecular basis of Marfan syndrome: a growth industry.

Peter H Byers1.   

Abstract

Although it has been known for more than a decade that Marfan syndrome - a dominantly inherited connective tissue disorder characterized by tall stature, arachnodactyly, lens subluxation, and a high risk of aortic aneurysm and dissection - results from mutations in the FBN1 gene, which encodes fibrillin-1, the precise mechanism by which the pleiotropic phenotype is produced has been unclear. A report in this issue now proposes that loss of fibrillin-1 protein by any of several mechanisms and the subsequent effect on the pool of TGF-beta may be more relevant in the development of Marfan syndrome than mechanisms previously proposed in a dominant-negative disease model. The model proposed in this issue demonstrates several strategies for clinical intervention.

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Year:  2004        PMID: 15254580      PMCID: PMC449756          DOI: 10.1172/JCI22399

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  24 in total

Review 1.  Nonsense-mediated mRNA decay in health and disease.

Authors:  P A Frischmeyer; H C Dietz
Journal:  Hum Mol Genet       Date:  1999       Impact factor: 6.150

2.  Segregation of a novel FBN1 gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of vertebral dysplasia in three generations.

Authors:  Lesley C Adès; Darshikka Sreetharan; Ella Onikul; Vivienne Stockton; Karen C Watson; Katherine J Holman
Journal:  Am J Med Genet       Date:  2002-05-15

Review 3.  Making sense of latent TGFbeta activation.

Authors:  Justin P Annes; John S Munger; Daniel B Rifkin
Journal:  J Cell Sci       Date:  2003-01-15       Impact factor: 5.285

4.  Structure of the mutant fibrillin-1 gene in the tight skin (TSK) mouse.

Authors:  C A Bona; C Murai; S Casares; K Kasturi; H Nishimura; T Honjo; F Matsuda
Journal:  DNA Res       Date:  1997-08-31       Impact factor: 4.458

5.  Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1.

Authors:  R E Magenis; C L Maslen; L Smith; L Allen; L Y Sakai
Journal:  Genomics       Date:  1991-10       Impact factor: 5.736

6.  Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome.

Authors:  S Sood; Z A Eldadah; W L Krause; I McIntosh; H C Dietz
Journal:  Nat Genet       Date:  1996-02       Impact factor: 38.330

7.  In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome.

Authors:  L Faivre; R J Gorlin; M K Wirtz; M Godfrey; N Dagoneau; J R Samples; M Le Merrer; G Collod-Beroud; C Boileau; A Munnich; V Cormier-Daire
Journal:  J Med Genet       Date:  2003-01       Impact factor: 6.318

8.  Missense mutations impair intracellular processing of fibrillin and microfibril assembly in Marfan syndrome.

Authors:  T Aoyama; K Tynan; H C Dietz; U Francke; H Furthmayr
Journal:  Hum Mol Genet       Date:  1993-12       Impact factor: 6.150

9.  Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.

Authors:  E A Putnam; H Zhang; F Ramirez; D M Milewicz
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330

10.  Expression of a mutant human fibrillin allele upon a normal human or murine genetic background recapitulates a Marfan cellular phenotype.

Authors:  Z A Eldadah; T Brenn; H Furthmayr; H C Dietz
Journal:  J Clin Invest       Date:  1995-02       Impact factor: 14.808

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  8 in total

1.  Novel FBN1 mutations are responsible for cardiovascular manifestations of Marfan syndrome.

Authors:  Jin'e Wang; Yupeng Yan; Jinxing Chen; Ling Gong; Yu Zhang; Mengmeng Yuan; Bing Cui; Yibo Wang
Journal:  Mol Biol Rep       Date:  2016-08-24       Impact factor: 2.316

Review 2.  Current themes in molecular pediatrics: molecular medicine and its applications.

Authors:  Andrea Superti-Furga; Livia Garavelli
Journal:  Ital J Pediatr       Date:  2010-02-19       Impact factor: 2.638

3.  Dilatation of the great arteries in an infant with marfan syndrome and ventricular septal defect.

Authors:  L Rozendaal; N A Blom; Y Hilhorst-Hofstee; A D J Ten Harkel
Journal:  Case Rep Med       Date:  2011-07-12

4.  TGFBR3 variation is not a common cause of Marfan-like syndrome and Loeys-Dietz-like syndrome.

Authors:  Krishna K Singh; Joerg Schmidtke; Britta Keyser; Mine Arslan-Kirchner
Journal:  J Negat Results Biomed       Date:  2012-02-02

5.  Fibrillin-1, induced by Aurora-A but inhibited by BRCA2, promotes ovarian cancer metastasis.

Authors:  Ziliang Wang; Yang Liu; Lili Lu; Lina Yang; Sheng Yin; Yan Wang; Zihao Qi; Jiao Meng; Rongyu Zang; Gong Yang
Journal:  Oncotarget       Date:  2015-03-30

Review 6.  The ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment.

Authors:  Stefano Stagi; Loredana Cavalli; Salvatore Seminara; Maurizio de Martino; Maria Luisa Brandi
Journal:  Ital J Pediatr       Date:  2014-06-07       Impact factor: 2.638

7.  Assessment of bone mineral status in children with Marfan syndrome.

Authors:  Monica Grover; Nicola Brunetti-Pierri; John Belmont; Kelly Phan; Alyssa Tran; Roman J Shypailo; Kenneth J Ellis; Brendan H Lee
Journal:  Am J Med Genet A       Date:  2012-08-07       Impact factor: 2.802

8.  The zinc transporter SLC39A13/ZIP13 is required for connective tissue development; its involvement in BMP/TGF-beta signaling pathways.

Authors:  Toshiyuki Fukada; Natacha Civic; Tatsuya Furuichi; Shinji Shimoda; Kenji Mishima; Hiroyuki Higashiyama; Yayoi Idaira; Yoshinobu Asada; Hiroshi Kitamura; Satoru Yamasaki; Shintaro Hojyo; Manabu Nakayama; Osamu Ohara; Haruhiko Koseki; Heloisa G Dos Santos; Luisa Bonafe; Russia Ha-Vinh; Andreas Zankl; Sheila Unger; Marius E Kraenzlin; Jacques S Beckmann; Ichiro Saito; Carlo Rivolta; Shiro Ikegawa; Andrea Superti-Furga; Toshio Hirano
Journal:  PLoS One       Date:  2008-11-05       Impact factor: 3.240

  8 in total

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