Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease
by
Volta, Manuela
, Harries, Lorna W
, Powell, John
, Burrage, Joe
, Condliffe, Daniel
, Lunnon, Katie
, Katsel, Pavel
, Smith, Rebecca
, Hannon, Eilis
, Mill, Jonathan
, Kaminsky, Zachary
, Al-Sarraj, Safa
, Bennett, David A
, Schalkwyk, Leonard C
, Srivastava, Gyan
, Macdonald, Ruby
, Haroutunian, Vahram
, Lovestone, Simon
, Troakes, Claire
, De Jager, Philip L
, Joachim, Catharine
in
45
/ 45/22
/ 45/61
/ 45/77
/ 631/1647/2210/2213
/ 631/208/177
/ 631/378/1689/1283
/ Aged
/ Aged, 80 and over
/ Alzheimer Disease - epidemiology
/ Alzheimer Disease - genetics
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Animal Genetics and Genomics
/ Ankyrins - genetics
/ Behavioral Sciences
/ Biological Techniques
/ Biomedicine
/ Brain
/ Cerebellum
/ Cerebral Cortex - pathology
/ Cerebral Cortex - physiology
/ Development and progression
/ DNA methylation
/ DNA Methylation - genetics
/ Entorhinal cortex
/ Entorhinal Cortex - pathology
/ Entorhinal Cortex - physiology
/ Epigenesis, Genetic - genetics
/ Epigenetics
/ Female
/ Genetic aspects
/ Genome-Wide Association Study
/ Hospitals
/ Humans
/ Male
/ Methylation
/ Middle Aged
/ Neurobiology
/ Neurodegeneration
/ Neuropathology
/ Neurosciences
/ Patient outcomes
/ Prefrontal Cortex - pathology
/ Prefrontal Cortex - physiology
/ Psychiatry
/ Risk factors
/ Temporal Lobe - pathology
/ Temporal Lobe - physiology
/ Transcriptome
2014
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?
Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease
by
Volta, Manuela
, Harries, Lorna W
, Powell, John
, Burrage, Joe
, Condliffe, Daniel
, Lunnon, Katie
, Katsel, Pavel
, Smith, Rebecca
, Hannon, Eilis
, Mill, Jonathan
, Kaminsky, Zachary
, Al-Sarraj, Safa
, Bennett, David A
, Schalkwyk, Leonard C
, Srivastava, Gyan
, Macdonald, Ruby
, Haroutunian, Vahram
, Lovestone, Simon
, Troakes, Claire
, De Jager, Philip L
, Joachim, Catharine
in
45
/ 45/22
/ 45/61
/ 45/77
/ 631/1647/2210/2213
/ 631/208/177
/ 631/378/1689/1283
/ Aged
/ Aged, 80 and over
/ Alzheimer Disease - epidemiology
/ Alzheimer Disease - genetics
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Animal Genetics and Genomics
/ Ankyrins - genetics
/ Behavioral Sciences
/ Biological Techniques
/ Biomedicine
/ Brain
/ Cerebellum
/ Cerebral Cortex - pathology
/ Cerebral Cortex - physiology
/ Development and progression
/ DNA methylation
/ DNA Methylation - genetics
/ Entorhinal cortex
/ Entorhinal Cortex - pathology
/ Entorhinal Cortex - physiology
/ Epigenesis, Genetic - genetics
/ Epigenetics
/ Female
/ Genetic aspects
/ Genome-Wide Association Study
/ Hospitals
/ Humans
/ Male
/ Methylation
/ Middle Aged
/ Neurobiology
/ Neurodegeneration
/ Neuropathology
/ Neurosciences
/ Patient outcomes
/ Prefrontal Cortex - pathology
/ Prefrontal Cortex - physiology
/ Psychiatry
/ Risk factors
/ Temporal Lobe - pathology
/ Temporal Lobe - physiology
/ Transcriptome
2014
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?
Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease
by
Volta, Manuela
, Harries, Lorna W
, Powell, John
, Burrage, Joe
, Condliffe, Daniel
, Lunnon, Katie
, Katsel, Pavel
, Smith, Rebecca
, Hannon, Eilis
, Mill, Jonathan
, Kaminsky, Zachary
, Al-Sarraj, Safa
, Bennett, David A
, Schalkwyk, Leonard C
, Srivastava, Gyan
, Macdonald, Ruby
, Haroutunian, Vahram
, Lovestone, Simon
, Troakes, Claire
, De Jager, Philip L
, Joachim, Catharine
in
45
/ 45/22
/ 45/61
/ 45/77
/ 631/1647/2210/2213
/ 631/208/177
/ 631/378/1689/1283
/ Aged
/ Aged, 80 and over
/ Alzheimer Disease - epidemiology
/ Alzheimer Disease - genetics
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Animal Genetics and Genomics
/ Ankyrins - genetics
/ Behavioral Sciences
/ Biological Techniques
/ Biomedicine
/ Brain
/ Cerebellum
/ Cerebral Cortex - pathology
/ Cerebral Cortex - physiology
/ Development and progression
/ DNA methylation
/ DNA Methylation - genetics
/ Entorhinal cortex
/ Entorhinal Cortex - pathology
/ Entorhinal Cortex - physiology
/ Epigenesis, Genetic - genetics
/ Epigenetics
/ Female
/ Genetic aspects
/ Genome-Wide Association Study
/ Hospitals
/ Humans
/ Male
/ Methylation
/ Middle Aged
/ Neurobiology
/ Neurodegeneration
/ Neuropathology
/ Neurosciences
/ Patient outcomes
/ Prefrontal Cortex - pathology
/ Prefrontal Cortex - physiology
/ Psychiatry
/ Risk factors
/ Temporal Lobe - pathology
/ Temporal Lobe - physiology
/ Transcriptome
2014
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.
Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease
Journal Article
Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease
2014
Request Book From Autostore
and Choose the Collection Method
Overview
Alzheimer's disease (AD) is a chronic neurodegenerative disorder characterized by progressive neuropathology and cognitive decline. Here the authors describe an epigenome-wide association study (EWAS) of human post-mortem brain samples across multiple independent AD cohorts. They find consistent hypermethylation of the
ANK1
gene associated with neuropathology.
Alzheimer's disease (AD) is a chronic neurodegenerative disorder that is characterized by progressive neuropathology and cognitive decline. We performed a cross-tissue analysis of methylomic variation in AD using samples from four independent human post-mortem brain cohorts. We identified a differentially methylated region in the ankyrin 1 (
ANK1
) gene that was associated with neuropathology in the entorhinal cortex, a primary site of AD manifestation. This region was confirmed as being substantially hypermethylated in two other cortical regions (superior temporal gyrus and prefrontal cortex), but not in the cerebellum, a region largely protected from neurodegeneration in AD, or whole blood obtained pre-mortem from the same individuals. Neuropathology-associated
ANK1
hypermethylation was subsequently confirmed in cortical samples from three independent brain cohorts. This study represents, to the best of our knowledge, the first epigenome-wide association study of AD employing a sequential replication design across multiple tissues and highlights the power of this approach for identifying methylomic variation associated with complex disease.
Publisher
Nature Publishing Group US,Nature Publishing Group
Subject
/ 45/22
/ 45/61
/ 45/77
/ Aged
/ Alzheimer Disease - epidemiology
/ Alzheimer Disease - genetics
/ Alzheimer Disease - pathology
/ Animal Genetics and Genomics
/ Brain
/ Cerebral Cortex - physiology
/ Entorhinal Cortex - pathology
/ Entorhinal Cortex - physiology
/ Epigenesis, Genetic - genetics
/ Female
/ Genome-Wide Association Study
/ Humans
/ Male
/ Prefrontal Cortex - pathology
This website uses cookies to ensure you get the best experience on our website.