Andere Kunden interessierten sich auch für
![Genetics Meets Metabolomics]( "Genetics Meets Metabolomics")
Genetics Meets Metabolomics115,99 €![The Male Role in Pregnancy Loss and Embryo Implantation Failure]( "The Male Role in Pregnancy Loss and Embryo Implantation Failure")
The Male Role in Pregnancy Loss and Embryo Implantation Failure74,99 €![Developmental Origins of Health and Disease (DOHaD)]( "Developmental Origins of Health and Disease (DOHaD)")
Developmental Origins of Health and Disease (DOHaD)117,99 €![Fluorescence In Situ Hybridization (FISH)]( "Fluorescence In Situ Hybridization (FISH)")
Fluorescence In Situ Hybridization (FISH)119,99 €![Periconception in Physiology and Medicine]( "Periconception in Physiology and Medicine")
Periconception in Physiology and Medicine110,99 €![Bone Quantitative Ultrasound]( "Bone Quantitative Ultrasound")
Bone Quantitative Ultrasound159,99 €![Mathematical Models and Immune Cell Biology]( "Mathematical Models and Immune Cell Biology")
Mathematical Models and Immune Cell Biology147,99 €
In Gene Regulatory Sequences and Human Disease, the Editor will introduce the different technological advances that led to this breakthrough. In addition, several examples will be provided of nucleotide variants in noncoding sequences that have been shown to be associated with various human diseases.
Genes make up less than 2% of our DNA and within the remaining 98% lie other extremely important sequences that function as gene regulatory elements, instructing genes when, where and at what levels to turn on or off. In this book, we introduce the different types of gene regulatory elements and how to identify and functionally characterize them. In addition, we describe several pioneering examples of how mutations in these elements have been found to cause human disease.With advances in DNA sequencing, the ability to identify disease-associated mutations in these regulatory elements is rapidly increasing. This book provides a great starting point for clinicians, geneticists, genomicists, developmental biologists and computational biologists to understand how to identify gene regulatory elements and associate nucleotide variation within them to human disease.
Genes make up less than 2% of our DNA and within the remaining 98% lie other extremely important sequences that function as gene regulatory elements, instructing genes when, where and at what levels to turn on or off. In this book, we introduce the different types of gene regulatory elements and how to identify and functionally characterize them. In addition, we describe several pioneering examples of how mutations in these elements have been found to cause human disease.With advances in DNA sequencing, the ability to identify disease-associated mutations in these regulatory elements is rapidly increasing. This book provides a great starting point for clinicians, geneticists, genomicists, developmental biologists and computational biologists to understand how to identify gene regulatory elements and associate nucleotide variation within them to human disease.