Cellular interplay via cytokine hierarchy causes pathological cardiac hypertrophy in RAF1-mutant Noonan syndrome
出版年份 2017 全文链接
标题
Cellular interplay via cytokine hierarchy causes pathological cardiac hypertrophy in RAF1-mutant Noonan syndrome
作者
关键词
-
出版物
Nature Communications
Volume 8, Issue -, Pages 15518
出版商
Springer Nature
发表日期
2017-05-26
DOI
10.1038/ncomms15518
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- A novel rasopathy caused by recurrent de novo missense mutations inPPP1CBclosely resembles Noonan syndrome with loose anagen hair
- (2016) Karen W. Gripp et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Developmental SHP2 dysfunction underlies cardiac hypertrophy in Noonan syndrome with multiple lentigines
- (2016) Jessica Lauriol et al. JOURNAL OF CLINICAL INVESTIGATION
- Autonomous and Non-autonomous Defects Underlie Hypertrophic Cardiomyopathy in BRAF-Mutant hiPSC-Derived Cardiomyocytes
- (2016) Rebecca Josowitz et al. Stem Cell Reports
- Left Ventricular Hypertrophy in Valvular Aortic Stenosis: Mechanisms and Clinical Implications
- (2015) Florian Rader et al. AMERICAN JOURNAL OF MEDICINE
- Elevated Ca2+ transients and increased myofibrillar power generation cause cardiac hypercontractility in a model of Noonan syndrome with multiple lentigines
- (2015) Sarah A. Clay et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Rare variants inSOS2andLZTR1are associated with Noonan syndrome
- (2015) Guilherme Lopes Yamamoto et al. JOURNAL OF MEDICAL GENETICS
- Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis
- (2014) E. Flex et al. HUMAN MOLECULAR GENETICS
- Resident fibroblast lineages mediate pressure overload–induced cardiac fibrosis
- (2014) Thomas Moore-Morris et al. JOURNAL OF CLINICAL INVESTIGATION
- Next-generation sequencing identifies rare variants associated with Noonan syndrome
- (2014) P.-C. Chen et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Lack of specificity of fibroblast-specific protein 1 in cardiac remodeling and fibrosis
- (2013) Ping Kong et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- The RASopathies
- (2013) Katherine A. Rauen Annual Review of Genomics and Human Genetics
- Priming with synthetic oligonucleotides attenuates pressure overload-induced inflammation and cardiac hypertrophy in mice
- (2012) Markus Velten et al. CARDIOVASCULAR RESEARCH
- Endocardial Cells Form the Coronary Arteries by Angiogenesis through Myocardial-Endocardial VEGF Signaling
- (2012) Bingruo Wu et al. CELL
- Importance of Myocyte-Nonmyocyte Interactions in Cardiac Development and Disease
- (2012) Ying Tian et al. CIRCULATION RESEARCH
- Hypertrophic cardiomyopathy
- (2012) Barry J Maron et al. LANCET
- Unknown
- (2012) Valentina Sala et al. MOLECULAR MEDICINE
- The Progression of Hypertensive Heart Disease
- (2011) Mark H. Drazner CIRCULATION
- RAS signaling pathway mutations and hypertrophic cardiomyopathy: getting into and out of the thick of it
- (2011) Bruce D. Gelb et al. JOURNAL OF CLINICAL INVESTIGATION
- MEK-ERK pathway modulation ameliorates disease phenotypes in a mouse model of Noonan syndrome associated with the Raf1L613V mutation
- (2011) Xue Wu et al. JOURNAL OF CLINICAL INVESTIGATION
- Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome–associated PTPN11 mutation
- (2011) Talita M. Marin et al. JOURNAL OF CLINICAL INVESTIGATION
- Mechanisms of disease: hypertrophic cardiomyopathy
- (2011) Norbert Frey et al. Nature Reviews Cardiology
- Reversible Heart Failure in a Patient Receiving Etanercept for Ankylosing Spondylitis
- (2010) Francisco Airton Castro Rocha et al. JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
- Mouse intact cardiac myocyte mechanics: cross-bridge and titin-based stress in unactivated cells
- (2010) Nicholas M.P. King et al. JOURNAL OF GENERAL PHYSIOLOGY
- The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation
- (2009) William E Tidyman et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Severe cardiomyopathy following treatment with the tumour necrosis factor-α inhibitor adalimumab for Crohn's disease
- (2009) Maximilian Y. Emmert et al. EUROPEAN JOURNAL OF HEART FAILURE
- Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
- (2009) Viviana Cordeddu et al. NATURE GENETICS
- A restricted spectrum of NRAS mutations causes Noonan syndrome
- (2009) Ion C Cirstea et al. NATURE GENETICS
- Molecular targets and regulators of cardiac hypertrophy
- (2009) Agrawal Rohini et al. PHARMACOLOGICAL RESEARCH
- Noonan syndrome cardiac defects are caused by PTPN11 acting in endocardium to enhance endocardial-mesenchymal transformation
- (2009) T. Araki et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Myofilament proteins: From cardiac disorders to proteomic changes
- (2008) Chao Yuan et al. Proteomics Clinical Applications
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now