Identification of Rare Variants inATP8B4as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing
出版年份 2015 全文链接
标题
Identification of Rare Variants inATP8B4as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing
作者
关键词
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出版物
Arthritis & Rheumatology
Volume 68, Issue 1, Pages 191-200
出版商
Wiley
发表日期
2015-10-17
DOI
10.1002/art.39449
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility
- (2014) Elena López-Isac et al. ARTHRITIS RESEARCH & THERAPY
- Updated Clinical Classification of Pulmonary Hypertension
- (2013) Gerald Simonneau et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
- (2013) Karen A. Hunt et al. NATURE
- The promise of single-cell sequencing
- (2013) James Eberwine et al. NATURE METHODS
- A Novel Channelopathy in Pulmonary Arterial Hypertension
- (2013) Lijiang Ma et al. NEW ENGLAND JOURNAL OF MEDICINE
- Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies
- (2012) Seunggeun Lee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Detection of asymmetric distribution of phospholipids by fluorescence resonance energy transfer
- (2012) Yoko Nishimura et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Phospholipid flippases: Building asymmetric membranes and transport vesicles
- (2012) Tessy T. Sebastian et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
- Whole Exome Sequencing to Identify a Novel Gene (Caveolin-1) Associated With Human Pulmonary Arterial Hypertension
- (2012) Eric D. Austin et al. Circulation-Cardiovascular Genetics
- Epidemiology of systemic sclerosis
- (2012) Jammie Barnes et al. CURRENT OPINION IN RHEUMATOLOGY
- Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD
- (2012) Nadia N. Hansel et al. HUMAN GENETICS
- Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up
- (2012) Jose-Ezequiel Martin et al. HUMAN MOLECULAR GENETICS
- Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
- (2012) Mary J Emond et al. NATURE GENETICS
- Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness
- (2012) Saskia B Wortmann et al. NATURE GENETICS
- Erythroid-Specific Transcriptional Changes in PBMCs from Pulmonary Hypertension Patients
- (2012) Chris Cheadle et al. PLoS One
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- (2012) J. A. Tennessen et al. SCIENCE
- The dynamic relationships between the three events that release individual Na+ ions from the Na+/K+-ATPase
- (2012) David C. Gadsby et al. Nature Communications
- Persistent pulmonary hypertension results in reduced tetralinoleoyl-cardiolipin and mitochondrial complex II + III during the development of right ventricular hypertrophy in the neonatal pig heart
- (2011) Harjot K. Saini-Chohan et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- P-Type ATPases
- (2011) Michael G. Palmgren et al. Annual Review of Biophysics
- Insights into the pathogenesis of systemic sclerosis based on the gene expression profile of progenitor-derived endothelial cells
- (2011) Jérôme Avouac et al. ARTHRITIS AND RHEUMATISM
- A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations
- (2011) Lara Bossini-Castillo et al. HUMAN MOLECULAR GENETICS
- Late-age Onset Systemic Sclerosis
- (2011) R. L. MANNO et al. JOURNAL OF RHEUMATOLOGY
- Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy
- (2011) Olga Gorlova et al. PLoS Genetics
- Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis
- (2011) Yannick Allanore et al. PLoS Genetics
- Pulmonary arterial hypertension associated with systemic sclerosis
- (2011) Stephen C Mathai et al. Expert Review of Respiratory Medicine
- Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population
- (2010) P. Dieude et al. ANNALS OF THE RHEUMATIC DISEASES
- Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
- (2010) Timothy R D J Radstake et al. NATURE GENETICS
- Dynamic regulation of cardiolipin by the lipid pump Atp8b1 determines the severity of lung injury in experimental pneumonia
- (2010) Nancy B Ray et al. NATURE MEDICINE
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- The ins and outs of phospholipid asymmetry in the plasma membrane: roles in health and disease
- (2009) Bengt Fadeel et al. CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY
- Candidate Single-Nucleotide Polymorphisms From a Genomewide Association Study of Alzheimer Disease
- (2007) Hao Li et al. ARCHIVES OF NEUROLOGY
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