Literature DB >> 22705998

Marfan syndrome: from gene to therapy.

Nikhita Bolar1, Lut Van Laer, Bart L Loeys.   

Abstract

PURPOSE OF REVIEW: Although historically Marfan syndrome (MFS) has always been considered as a condition caused by the deficiency of a structural extracellular matrix protein, fibrillin-1, the study of Marfan mouse models and Marfan-related conditions has shifted our current understanding to a pathogenic model that involves dysregulation of the cytokine-transforming growth factor beta (TGF-β) signaling. RECENT
FINDINGS: In this review, we focus on the impact of the revised MFS clinical diagnostic criteria. We discuss lessons that have been learned from molecular findings in relevant Marfan-related conditions, such as sporadic thoracic aortic aneurysm/dissection, stiff skin syndrome, acromelic dysplasias and Loeys-Dietz syndrome. We explore the latest insights into the role of the alternative TGF-β signaling pathways in MFS pathogenesis. Finally, we give an update on the current and future treatment strategies.
SUMMARY: The recent insights into the pathogenesis of MFS and related disorders have offered a prime example of translational medicine with immediate bridge between molecular findings and therapeutic options.

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Year:  2012        PMID: 22705998     DOI: 10.1097/MOP.0b013e3283557d4c

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  13 in total

Review 1.  Aetiology and management of hereditary aortopathy.

Authors:  Aline Verstraeten; Ilse Luyckx; Bart Loeys
Journal:  Nat Rev Cardiol       Date:  2017-01-19       Impact factor: 32.419

Review 2.  Height matters-from monogenic disorders to normal variation.

Authors:  Claudia Durand; Gudrun A Rappold
Journal:  Nat Rev Endocrinol       Date:  2013-01-22       Impact factor: 43.330

3.  Panlobular Emphysema: Enhancing Visibility with Quantitative Computed Tomography.

Authors:  Surya P Bhatt
Journal:  Chronic Obstr Pulm Dis       Date:  2016-05-23

4.  Correlation between Fibrillin-1 Degradation and mRNA Downregulation and Myofibroblast Differentiation in Cultured Human Dental Pulp Tissue.

Authors:  Nagako Yoshiba; Kunihiko Yoshiba; Naoto Ohkura; Erika Takei; Naoki Edanami; Youhei Oda; Akihiro Hosoya; Hiroaki Nakamura; Takashi Okiji
Journal:  J Histochem Cytochem       Date:  2015-03-24       Impact factor: 2.479

5.  Exome Sequencing Identifies Genetic Variants Associated with Extreme Manifestations of the Cardiovascular Phenotype in Marfan Syndrome.

Authors:  Yanireth Jimenez; Cesar Paulsen; Eduardo Turner; Sebastian Iturra; Oscar Cuevas; Guillermo Lay-Son; Gabriela M Repetto; Marcelo Rojas; Juan F Calderon
Journal:  Genes (Basel)       Date:  2022-06-08       Impact factor: 4.141

6.  Neonatal Marfan Syndrome: Report of a Case with an Inherited Splicing Mutation outside the Neonatal Domain.

Authors:  Laurianne Le Gloan; Quentin Hauet; Albert David; Nadine Hanna; Chloé Arfeuille; Pauline Arnaud; Catherine Boileau; Bénédicte Romefort; Nadir Benbrik; Véronique Gournay; Nicolas Joram; Olivier Baron; Bertrand Isidor
Journal:  Mol Syndromol       Date:  2016-02-02

7.  Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis.

Authors:  Carl Friedrich Classen; Vera Riehmer; Christina Landwehr; Anne Kosfeld; Stefanie Heilmann; Caroline Scholz; Sarah Kabisch; Hartmut Engels; Sascha Tierling; Miroslav Zivicnjak; Frank Schacherer; Dieter Haffner; Ruthild G Weber
Journal:  Hum Genet       Date:  2013-04-04       Impact factor: 4.132

8.  The genetics and genomics of thoracic aortic disease.

Authors:  Pawel Pomianowski; John A Elefteriades
Journal:  Ann Cardiothorac Surg       Date:  2013-05

9.  The economic impact of Marfan syndrome: a non-experimental, retrospective, population-based matched cohort study.

Authors:  Dmitrij Achelrod; Carl Rudolf Blankart; Roland Linder; Yskert von Kodolitsch; Tom Stargardt
Journal:  Orphanet J Rare Dis       Date:  2014-06-23       Impact factor: 4.123

10.  Integration of multiple signaling pathways determines differences in the osteogenic potential and tissue regeneration of neural crest-derived and mesoderm-derived calvarial bones.

Authors:  Kshemendra Senarath-Yapa; Shuli Li; Nathaniel P Meyer; Michael T Longaker; Natalina Quarto
Journal:  Int J Mol Sci       Date:  2013-03-15       Impact factor: 5.923

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