Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Placental CpG methylation of infants born extremely preterm predicts cognitive impairment later in life
by
Martin, Elizabeth M.
, Joseph, Robert M.
, Heeren, Tim C.
, Tilley, Sloane K.
, O’Shea, T. Michael
, Kuban, Karl C. K.
, Smeester, Lisa
, Dammann, Olaf U.
, Fry, Rebecca C.
in
Adolescent
/ Adult
/ Biology and life sciences
/ Child
/ Cognition - physiology
/ Cognitive Dysfunction - genetics
/ Cognitive Dysfunction - metabolism
/ Cohort Studies
/ CpG Islands
/ Cytosine
/ Developmental disabilities
/ DNA Methylation
/ Female
/ Genetic aspects
/ Genome-Wide Association Study
/ Health aspects
/ Humans
/ Infant, Extremely Premature - metabolism
/ Infant, Extremely Premature - psychology
/ Male
/ Maternal Age
/ Medicine and Health Sciences
/ Methylation
/ Middle Aged
/ Neuropsychological Tests
/ People and Places
/ Physiological aspects
/ Placenta
/ Placenta - metabolism
/ Post-translational modifications
/ Pregnancy
/ Premature infants
/ Prognosis
/ Risk factors
/ Young Adult
2018
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Placental CpG methylation of infants born extremely preterm predicts cognitive impairment later in life
by
Martin, Elizabeth M.
, Joseph, Robert M.
, Heeren, Tim C.
, Tilley, Sloane K.
, O’Shea, T. Michael
, Kuban, Karl C. K.
, Smeester, Lisa
, Dammann, Olaf U.
, Fry, Rebecca C.
in
Adolescent
/ Adult
/ Biology and life sciences
/ Child
/ Cognition - physiology
/ Cognitive Dysfunction - genetics
/ Cognitive Dysfunction - metabolism
/ Cohort Studies
/ CpG Islands
/ Cytosine
/ Developmental disabilities
/ DNA Methylation
/ Female
/ Genetic aspects
/ Genome-Wide Association Study
/ Health aspects
/ Humans
/ Infant, Extremely Premature - metabolism
/ Infant, Extremely Premature - psychology
/ Male
/ Maternal Age
/ Medicine and Health Sciences
/ Methylation
/ Middle Aged
/ Neuropsychological Tests
/ People and Places
/ Physiological aspects
/ Placenta
/ Placenta - metabolism
/ Post-translational modifications
/ Pregnancy
/ Premature infants
/ Prognosis
/ Risk factors
/ Young Adult
2018
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Placental CpG methylation of infants born extremely preterm predicts cognitive impairment later in life
by
Martin, Elizabeth M.
, Joseph, Robert M.
, Heeren, Tim C.
, Tilley, Sloane K.
, O’Shea, T. Michael
, Kuban, Karl C. K.
, Smeester, Lisa
, Dammann, Olaf U.
, Fry, Rebecca C.
in
Adolescent
/ Adult
/ Biology and life sciences
/ Child
/ Cognition - physiology
/ Cognitive Dysfunction - genetics
/ Cognitive Dysfunction - metabolism
/ Cohort Studies
/ CpG Islands
/ Cytosine
/ Developmental disabilities
/ DNA Methylation
/ Female
/ Genetic aspects
/ Genome-Wide Association Study
/ Health aspects
/ Humans
/ Infant, Extremely Premature - metabolism
/ Infant, Extremely Premature - psychology
/ Male
/ Maternal Age
/ Medicine and Health Sciences
/ Methylation
/ Middle Aged
/ Neuropsychological Tests
/ People and Places
/ Physiological aspects
/ Placenta
/ Placenta - metabolism
/ Post-translational modifications
/ Pregnancy
/ Premature infants
/ Prognosis
/ Risk factors
/ Young Adult
2018
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Placental CpG methylation of infants born extremely preterm predicts cognitive impairment later in life
Journal Article
Placental CpG methylation of infants born extremely preterm predicts cognitive impairment later in life
2018
Request Book From Autostore
and Choose the Collection Method
Overview
The placenta is the central regulator of maternal and fetal interactions. Perturbations of placental structure and function have been associated with adverse neurodevelopmental outcomes later in life. Placental CpG methylation represents an epigenetic modification with the potential to impact placental function, fetal development and child health later in life.
Genome-wide placental CpG methylation levels were compared between spontaneous versus indicated deliveries from extremely preterm births (EPTBs) (n = 84). The association between the identified differentially methylated CpG sites and neurocognitive outcome at ten years of age was then evaluated.
Spontaneous EPTB was associated with differential CpG methylation levels in 250 CpG sites (217 unique genes) with the majority displaying hypermethylation. The identified genes are known to play a role in neurodevelopment and are enriched for basic helix-loop-helix transcription factor binding sites. The placental CpG methylation levels for 17 of these sites predicted cognitive function at ten years of age.
A hypermethylation signature is present in DNA from placentas in infants with spontaneous EPTB. CpG methylation levels of critical neurodevelopment genes in the placenta predicted later life cognitive function, supporting the developmental origins of health and disease hypothesis (DOHaD).
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Adult
/ Child
/ Cognitive Dysfunction - genetics
/ Cognitive Dysfunction - metabolism
/ Cytosine
/ Female
/ Genome-Wide Association Study
/ Humans
/ Infant, Extremely Premature - metabolism
/ Infant, Extremely Premature - psychology
/ Male
/ Medicine and Health Sciences
/ Placenta
This website uses cookies to ensure you get the best experience on our website.