Role of Genomics in the Management of Hypertension

Arterial hypertension affects about 1 billion people worldwide and it is the strongest modifiable risk factor for cardiovascular disease and related disability. Since the initial discovery of rare monogenic disorders with large effects, the role of genomics has evolved into large genome-wide associa...

Full description

Saved in:
Bibliographic Details
HerausgeberIn:
Sonstige:
Year of Publication:2020
Language:English
Physical Description:1 electronic resource (200 p.)
Tags: Add Tag
No Tags, Be the first to tag this record!
id 993545997904498
ctrlnum (CKB)5400000000045926
(oapen)https://directory.doabooks.org/handle/20.500.12854/68974
(EXLCZ)995400000000045926
collection bib_alma
record_format marc
spelling Mulatero, Paolo edt
Role of Genomics in the Management of Hypertension
Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2020
1 electronic resource (200 p.)
text txt rdacontent
computer c rdamedia
online resource cr rdacarrier
Arterial hypertension affects about 1 billion people worldwide and it is the strongest modifiable risk factor for cardiovascular disease and related disability. Since the initial discovery of rare monogenic disorders with large effects, the role of genomics has evolved into large genome-wide association studies detecting common variants with a modest effect size. Similarly, pharmacogenomics has emerged as a new tool for understanding variability in drug response, to maximize efficacy and reduce toxicity. This book presents the most recent advances in the field of genetics and genomics of arterial hypertension and their potential impact on clinical management. The book is a useful tool for clinicians but also to the research community and those who want to be updated in the field.
English
Research & information: general bicssc
Biology, life sciences bicssc
atrial natriuretic peptide
T2238C variant
endothelial dysfunction
smooth muscle cells contraction
platelet aggregation
epigenetics
cardiovascular diseases
renin
low-renin
hypertension
mineralocorticoid receptor
genetics
aldosterone
essential hypertension
blood pressure
genome-wide association studies
exome microarray
next-generation sequencing
rare variants
rare-variants association testing
burden test
sequence kernel association test
hypokalemia
low renin hypertension
monogenic hypertension
Liddle syndrome
SCNN1A
SCNN1B
SCNN1G
non-coding RNA
micro RNA
primary aldosteronism
aldosterone-producing adenoma
transcriptome profiing
DNA methylation
histone modifications
vascular smooth muscle cells
endothelial cells
Kruppel-like factor 15
left ventricular hypertrophy
cardiac hypertrophy
heart failure
genetics of left ventricular hypertrophy
fibromuscular dysplasia
non atherosclerotic vascular stenosis
PHACTR1
genetic association
cervical artery dissection
spontaneous coronary arteries dissection
CRY1
CRY2
HSD3B1
HSD3B2
cardio-tonic steroids
endogenous ouabain
adducin
renal damage
African American
ARMC5
GRK4
CACNA1D
endocrine hypertension
3-03936-627-0
3-03936-628-9
Monticone, Silvia edt
Mulatero, Paolo oth
Monticone, Silvia oth
language English
format eBook
author2 Monticone, Silvia
Mulatero, Paolo
Monticone, Silvia
author_facet Monticone, Silvia
Mulatero, Paolo
Monticone, Silvia
author2_variant p m pm
s m sm
author2_role HerausgeberIn
Sonstige
Sonstige
title Role of Genomics in the Management of Hypertension
spellingShingle Role of Genomics in the Management of Hypertension
title_full Role of Genomics in the Management of Hypertension
title_fullStr Role of Genomics in the Management of Hypertension
title_full_unstemmed Role of Genomics in the Management of Hypertension
title_auth Role of Genomics in the Management of Hypertension
title_new Role of Genomics in the Management of Hypertension
title_sort role of genomics in the management of hypertension
publisher MDPI - Multidisciplinary Digital Publishing Institute
publishDate 2020
physical 1 electronic resource (200 p.)
isbn 3-03936-627-0
3-03936-628-9
illustrated Not Illustrated
work_keys_str_mv AT mulateropaolo roleofgenomicsinthemanagementofhypertension
AT monticonesilvia roleofgenomicsinthemanagementofhypertension
status_str n
ids_txt_mv (CKB)5400000000045926
(oapen)https://directory.doabooks.org/handle/20.500.12854/68974
(EXLCZ)995400000000045926
carrierType_str_mv cr
is_hierarchy_title Role of Genomics in the Management of Hypertension
author2_original_writing_str_mv noLinkedField
noLinkedField
noLinkedField
_version_ 1796652211968671744
fullrecord <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>03977nam-a2201069z--4500</leader><controlfield tag="001">993545997904498</controlfield><controlfield tag="005">20231214133155.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr|mn|---annan</controlfield><controlfield tag="008">202105s2020 xx |||||o ||| 0|eng d</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(CKB)5400000000045926</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(oapen)https://directory.doabooks.org/handle/20.500.12854/68974</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLCZ)995400000000045926</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Mulatero, Paolo</subfield><subfield code="4">edt</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Role of Genomics in the Management of Hypertension</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Basel, Switzerland</subfield><subfield code="b">MDPI - Multidisciplinary Digital Publishing Institute</subfield><subfield code="c">2020</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 electronic resource (200 p.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Arterial hypertension affects about 1 billion people worldwide and it is the strongest modifiable risk factor for cardiovascular disease and related disability. Since the initial discovery of rare monogenic disorders with large effects, the role of genomics has evolved into large genome-wide association studies detecting common variants with a modest effect size. Similarly, pharmacogenomics has emerged as a new tool for understanding variability in drug response, to maximize efficacy and reduce toxicity. This book presents the most recent advances in the field of genetics and genomics of arterial hypertension and their potential impact on clinical management. The book is a useful tool for clinicians but also to the research community and those who want to be updated in the field.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Research &amp; information: general</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Biology, life sciences</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">atrial natriuretic peptide</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">T2238C variant</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">endothelial dysfunction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">smooth muscle cells contraction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">platelet aggregation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">epigenetics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cardiovascular diseases</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">renin</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">low-renin</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">hypertension</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">mineralocorticoid receptor</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">genetics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">aldosterone</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">essential hypertension</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">blood pressure</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">genome-wide association studies</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">exome microarray</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">next-generation sequencing</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">rare variants</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">rare-variants association testing</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">burden test</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">sequence kernel association test</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">hypokalemia</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">low renin hypertension</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">monogenic hypertension</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Liddle syndrome</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">SCNN1A</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">SCNN1B</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">SCNN1G</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">non-coding RNA</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">micro RNA</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">primary aldosteronism</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">aldosterone-producing adenoma</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">transcriptome profiing</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">DNA methylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">histone modifications</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">vascular smooth muscle cells</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">endothelial cells</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Kruppel-like factor 15</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">left ventricular hypertrophy</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cardiac hypertrophy</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">heart failure</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">genetics of left ventricular hypertrophy</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">fibromuscular dysplasia</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">non atherosclerotic vascular stenosis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">PHACTR1</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">genetic association</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cervical artery dissection</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">spontaneous coronary arteries dissection</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CRY1</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CRY2</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">HSD3B1</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">HSD3B2</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cardio-tonic steroids</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">endogenous ouabain</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">adducin</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">renal damage</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">African American</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">ARMC5</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">GRK4</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CACNA1D</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">endocrine hypertension</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-03936-627-0</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-03936-628-9</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Monticone, Silvia</subfield><subfield code="4">edt</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mulatero, Paolo</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Monticone, Silvia</subfield><subfield code="4">oth</subfield></datafield><datafield tag="906" ind1=" " ind2=" "><subfield code="a">BOOK</subfield></datafield><datafield tag="ADM" ind1=" " ind2=" "><subfield code="b">2023-12-15 05:45:33 Europe/Vienna</subfield><subfield code="f">system</subfield><subfield code="c">marc21</subfield><subfield code="a">2022-04-04 09:22:53 Europe/Vienna</subfield><subfield code="g">false</subfield></datafield><datafield tag="AVE" ind1=" " ind2=" "><subfield code="i">DOAB Directory of Open Access Books</subfield><subfield code="P">DOAB Directory of Open Access Books</subfield><subfield code="x">https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&amp;portfolio_pid=5338061890004498&amp;Force_direct=true</subfield><subfield code="Z">5338061890004498</subfield><subfield code="b">Available</subfield><subfield code="8">5338061890004498</subfield></datafield></record></collection>