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Genetics and Genomics of Pulmonary Arterial Hypertension

Genetics and Genomics of Pulmonary Arterial Hypertension

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Pulmonary arterial hypertension is a severe and progressive disorder affecting the blood vessels in the lungs. Typically, symptoms first appear at around 30–40 years of age and, without treatment, can lead to fatal heart disease within a few years. Genetic studies over the past decade have identified numerous genes that contribute to disease progression but, for many sufferers, the underlying genetic cause remains elusive. The collection of reviews and original research articles contained within this book provide an overview of recent advancements in understanding the genetic risk factors for pulmonary arterial hypertension. We further examine the emerging interplay between genetic variants and clinical outcomes, providing a framework for new treatments and improved patient care.

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Keywords

  • and genetics
  • Biology, Life Sciences
  • Blood
  • BMPR2
  • BMPR2 promoter
  • bone morphogenetic protein receptor 2
  • bone morphogenetic protein receptor type 2
  • clinical trials
  • digenic inheritance
  • DNA Damage
  • DNA Repair
  • EIF2AK4
  • endothelial cells
  • epigenetic inheritance
  • eQTL
  • estradiol
  • estrogen
  • exome sequencing
  • expression quantitative trait locus
  • familial
  • forward genetics
  • forward phenotyping
  • GDF2
  • gender
  • genetic analysis
  • Genetic Heterogeneity
  • Genetics
  • Genetics (non-medical)
  • Genomics
  • heritable
  • heritable pulmonary arterial hypertension
  • intermediate phenotypes
  • Life sciences: general issues
  • lung disease
  • massive parallel sequencing
  • Mathematics & science
  • miRNA
  • Molecular genetics
  • n/a
  • NGS
  • NGS gene panel
  • paediatrics
  • PAH
  • pathogenic variant
  • Pediatrics
  • penetrance
  • pharmaceuticals
  • phenotypic heterogeneity
  • pulmonary arterial hypertension
  • pulmonary hypertension
  • Reference, information & interdisciplinary subjects
  • repurposed drugs
  • Research & information: general
  • Reverse genetics
  • reverse phenotyping
  • signaling
  • smooth muscle cells
  • TBX4
  • whole-genome sequencing

Links

DOI: 10.3390/books978-3-0365-4830-2

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