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Brain epigenome changes from birth to adolescence

Researchers discovered significant brain epigenome changes from birth to adolescence, transforming the frontal cortex and shaping communication spaces between neurons. The study's findings have profound implications for understanding brain biology and potentially treating neurodevelopmental disorders like autism and schizophrenia.

SourceIDIBELL-Bellvitge Biomedical Research Institute·JournalScience·DateJul 4, 2013

Unique epigenomic code identified during human brain development

A new study by Salk scientists reveals that the landscape of DNA methylation in brain cells is highly dynamic during brain circuitry formation, helping to understand how information in the genome is controlled from fetal development to adulthood. The discovery opens a deeper understanding of how intricate patterns of connectivity in th...

SourceSalk Institute·JournalScience·DateJul 4, 2013
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Mapping the embryonic epigenome

A large research team elucidated how precise chemical modifications across the genome turn genes on and off during early human development. The study found that master genes governing development are silenced by histone methylation, while genes orchestrating cellular differentiation are primarily silenced by DNA methylation.

SourceLudwig Institute for Cancer Research·JournalCell·DateMay 9, 2013

New insights into how genes turn on and off

Researchers have discovered that 37% of the placental genome has regions of lower methylation, called partially methylated domains (PMDs), where gene expression is turned off. This could enhance our understanding of epigenetics and its impact on human development, cancer research and autism.

SourceUniversity of California - Davis Health·JournalProceedings of the National Academy of Sciences·DateMar 27, 2013

Scientists identify gene that is consistently altered in obese individuals

Researchers have identified the LY86 gene as a key contributor to obesity, finding high methylation levels associated with increased inflammation and insulin resistance. This association held up across various populations, suggesting a potential link between environmental factors and genetic expression.

SourceMedical College of Georgia at Augusta University·DateMar 21, 2013

New clues in hunt for heredity in type 2 diabetes

A new study by Lund University researchers has found that epigenetic changes, such as DNA methylation, can influence the function of insulin-producing cells and alter genetic risk variants for type 2 diabetes. The findings suggest that these modifications may play a key role in the development of the disease.

SourceLund University·JournalDiabetologia·DateMar 19, 2013
GoPro HERO13 Black

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Paternal obesity impacts child's chances of cancer

A study published in BMC Medicine found that newborns of obese fathers have lower DNA methylation levels of the IGF2 gene, which codes for a growth factor important during fetal development. This can lead to increased cancer risk later in life.

SourceBMC (BioMed Central)·JournalBMC Medicine·DateFeb 5, 2013

Obesity in dads may be associated with offspring's increased risk of disease

A new study from Duke University Medical Center suggests that a father's obesity may alter a genetic mechanism in the next generation, potentially raising the risk for diseases like cancer. Researchers found that paternal obesity was associated with lower DNA methylation at the IGF2 gene in offspring.

SourceDuke University Medical Center·JournalBMC Medicine·DateFeb 5, 2013
Apple iPhone 17 Pro

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Genes and immune system shaped by childhood poverty, stress

A University of British Columbia study reveals that childhood poverty and stress as an adult leave imprints on genes and predict future immune responses. The research found correlations between DNA methylation patterns and early life experiences.

SourceUniversity of British Columbia·JournalProceedings of the National Academy of Sciences·DateOct 18, 2012

Tying our fate to molecular markings

A Simon Fraser University physicist has discovered a link between variable methylation in DNA and various attributes such as age, gender, stress, and socioeconomic status. The study found that childhood poverty left a detectable molecular mark on an individual's DNA, which correlated with gene expression.

SourceSimon Fraser University·JournalProceedings of the National Academy of Sciences·DateOct 11, 2012
SAMSUNG T9 Portable SSD 2TB

SAMSUNG T9 Portable SSD 2TB transfers large imagery and model outputs quickly between field laptops, lab workstations, and secure archives.

Scientists find missing link between players in the epigenetic code

Researchers from the University of North Carolina School have established a connection between histone H3 lysine 9 methylation and DNA methylation, implicating protein UHRF1 in their maintenance. This finding may provide clues to the underlying causes of disease and cancer.

SourceUniversity of North Carolina Health Care·JournalNature Structural & Molecular Biology·DateSep 30, 2012

Columbia awarded 1 of first 'Provocative Questions' grants from NCI

Dr. Timothy Bestor's research could overturn a 20-year-old theory of carcinogenesis, instead proposing that methylation changes kill incipient cancer cells. The study aims to develop new methods to differentiate between 'driver' and 'passenger' epigenetic events in tumor development.

SourceColumbia University Irving Medical Center·DateSep 19, 2012

Epigenetics emerges powerfully as a clinical tool

Recent research in epigenetics has identified two key tests that can predict brain tumor sensitivity to temozolomide and distinguish prostate cancer from benign growth. New epigenetic biomarkers are being rapidly developed to predict treatment performance and weaknesses of tumors.

SourceIDIBELL-Bellvitge Biomedical Research Institute·JournalNature Reviews Genetics·DateSep 12, 2012

Epigenetic causes of prostate cancer

Researchers found that fusion-negative prostate cancers have different DNA methylation patterns than healthy cells, with increased EZH2 enzyme activity. This discovery may lead to more specific treatments and improved diagnosis for prostate cancer patients.

SourceMax-Planck-Gesellschaft·JournalCancer Discovery·DateSep 5, 2012

More clues about why chimps and humans are genetically different

Researchers found that DNA methylation modifications may contribute to phenotypic changes in humans and chimps. The study suggests that methylation differences between the species might be linked to human disease vulnerability.

SourceGeorgia Institute of Technology·JournalAmerican Journal of Human Genetics·DateAug 23, 2012
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Acute stress alters control of gene activity

Researchers at Ruhr-University Bochum found that acute stress increases DNA methylation of the oxytocin receptor gene, leading to excessive receptor production. This change may contribute to the development of chronic diseases such as cancer or depression.

SourceRuhr-University Bochum·JournalTranslational Psychiatry·DateAug 15, 2012
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Planting the seeds of defense

Scientists discovered that exposure to pathogens causes significant changes in a plant's epigenetic code, which helps the plant develop resistance. These epigenetic changes are linked to genes responsible for coordinating stress responses, suggesting the epigenome plays a role in disease resistance.

SourceSalk Institute·JournalProceedings of the National Academy of Sciences·DateAug 7, 2012

Epigenetics alters genes in rheumatoid arthritis

Research found epigenetic changes, specifically DNA methylation, alter genes contributing to rheumatoid arthritis (RA) inflammation and joint damage. RA fibroblast-like synoviocytes display a unique DNA methylome signature compared to normal FLS.

SourceUniversity of California - San Diego·JournalAnnals of the Rheumatic Diseases·DateJul 3, 2012
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Epigenetic changes in blood samples may point to schizophrenia

A new study by Karolinska Institutet researchers found that DNA methylation levels in white blood cells are lower in patients with schizophrenia and related to age of disease onset and treatment response. The discovery may lead to the development of a simple test to diagnose schizophrenia.

SourceKarolinska Institutet·JournalThe FASEB Journal·DateMar 27, 2012

R-loops break down gene silencing

Researchers at UC Davis found that R-loops prevent methylation at CG island promoters, which are essential for 60% of human genes. This breakthrough could lead to treatments for autoimmune diseases by reversing cytosine methylation.

SourceUniversity of California - Davis·JournalMolecular Cell·DateMar 2, 2012
Sony Alpha a7 IV (Body Only)

Sony Alpha a7 IV (Body Only) delivers reliable low-light performance and rugged build for astrophotography, lab documentation, and field expeditions.

Express yourself: How zygotes sort out imprinted genes

A team of scientists led by Bing Ren has discovered how differential DNA methylation in the parental genomes sets the stage for selective expression of imprinted genes. The study found parent-of-origin specific DNA methylation imprints at 1,952 dinucleotide sequences, including previously unknown regions.

SourceUniversity of California - San Diego·JournalCell·DateFeb 16, 2012

Gene regulator in brain's executive hub tracked across lifespan -- NIH study

A new NIH study reveals that certain genes implicated in schizophrenia and autism show increased regulatory activity during a critical period of development, influenced by environmental factors. This discovery highlights the importance of epigenetic mechanisms like DNA methylation in shaping brain function and behavior.

SourceNIH/National Institute of Mental Health·JournalAmerican Journal of Human Genetics·DateFeb 2, 2012

How protein networks stabilize muscle fibers: Same mechanism as for DNA

A research team led by Prof. Dr. Wolfgang Linke has discovered that protein networks play a crucial role in stabilizing muscle fibers using the same mechanism as DNA methylation. The study found that disrupting this network leads to significant changes in muscle structure and function.

SourceRuhr-University Bochum·JournalGenes & Development·DateJan 23, 2012

Environment and diet leave their prints on the heart

Researchers at University of Cambridge have mapped DNA methylation in human heart, revealing its connection to environmental factors such as diet and lifestyle. The study provides new insights into the genetic changes that can lead to heart disease and potential ways to identify and treat it.

SourceUniversity of Cambridge·JournalCirculation·DateNov 29, 2011

Johns Hopkins scientists discover 'fickle' DNA changes in brain

Researchers found evidence of large-scale dynamic DNA demethylation in non-dividing brain cells, challenging scientific dogma. This discovery has major implications for understanding learning, memory, and mood regulation, as well as potential new treatments for depression and neurodegenerative disorders.

SourceJohns Hopkins Medicine·JournalNature Neuroscience·DateSep 30, 2011
Sky & Telescope Pocket Sky Atlas, 2nd Edition

Sky & Telescope Pocket Sky Atlas, 2nd Edition is a durable star atlas for planning sessions, identifying targets, and teaching celestial navigation.

Research reveals how dynamic changes in methylation can determine cell fate

A study by CSHL and USC researchers reveals that methylation patterns are dynamic and can influence cell fate. The team observed that subtle changes in methylation within specific regions can lead to the activation of genes associated with particular cell types, challenging traditional views on epigenetics.

SourceCold Spring Harbor Laboratory·JournalMolecular Cell·DateSep 26, 2011

Epigenetic changes don't last

Scientists discovered that epigenetic modifications in plants, such as DNA methylation, are unstable and often disappear after a few generations. These changes can occur frequently but usually do not contribute significantly to long-term evolution.

SourceMax-Planck-Gesellschaft·JournalNature·DateSep 20, 2011

Are genes our destiny?

Researchers at Salk Institute discover a "hidden" code linked to DNA that allows plants to develop and pass down new biological traits rapidly. The epigenetic code is found to evolve more quickly than the genetic code and strongly influence biological traits.

SourceSalk Institute·JournalScience·DateSep 16, 2011
GQ GMC-500Plus Geiger Counter

GQ GMC-500Plus Geiger Counter logs beta, gamma, and X-ray levels for environmental monitoring, training labs, and safety demonstrations.

Parents' stress leaves lasting marks on children’s genes: UBC-CFRI research

A UBC study found that parents' stress during their child's early years can leave lasting marks on their genes, affecting behavior and health in adolescence. Higher stress levels reported by mothers and fathers correlated with specific DNA methylation sites, including those involved in insulin production and brain development.

SourceUniversity of British Columbia·JournalChild Development·DateAug 30, 2011

Maternal smoking causes changes in fetal DNA

Research suggests maternal smoking during pregnancy may alter DNA methylation levels in the AXL gene, associated with increased asthma risk in children. The study found a stronger association between maternal smoking and DNA methylation in girls than boys.

SourceAmerican Thoracic Society·DateMay 18, 2011

Study gives clue as to how notes are played on the genetic piano

Researchers found that a small RNA pathway is required to establish DNA methylation, a process that silences genes. This discovery may lead to new therapies for cancer and other diseases by reactivating silenced tumor-suppressor genes.

SourceUniversity of Texas Health Science Center at San Antonio·JournalScience·DateMay 12, 2011
Kestrel 3000 Pocket Weather Meter

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Epigenetic study reveals new insights into breast cancer

Researchers have identified two major sub-types of breast cancer based on DNA methylation profiles, which could help refine cancer classification and predict treatment response. The study also revealed new information about sub-types of breast cancer and the potential for epigenetic therapy.

SourceEuropean Society for Medical Oncology·JournalAnnals of Oncology·DateMay 5, 2011

Hopkins team discovers how DNA changes

Researchers identified a step-by-step process involving TET1 and Apobec1 that converts methylated cytosine into hydroxymethylated cytosine, indicating a potential unified mechanism for DNA methylation status change. The discovery has implications for understanding diseases associated with epigenetic abnormality.

SourceJohns Hopkins Medicine·JournalCell·DateApr 14, 2011

Gag order: how DNA silencing can promote cancer

Research suggests that specific genes are silenced by DNA methylating enzyme Dnmt3b, similar to those found in human tumors. This targeted silencing may be an initiating event in cancer development.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateApr 1, 2011

Cell reprogramming leaves a 'footprint' behind

Scientists found reprogramming errors in iPS cells, including a common defect near telomeres and centromeres. These hotspots resist non-CG methylation, but CG islands are affected, potentially limiting the fate of iPS cells.

SourceSalk Institute·JournalNature·DateFeb 2, 2011
Anker Laptop Power Bank 25,000mAh (Triple 100W USB-C)

Anker Laptop Power Bank 25,000mAh (Triple 100W USB-C) keeps Macs, tablets, and meters powered during extended observing runs and remote surveys.

Biomarker test shows promise for melanoma diagnosis

A new study reveals that a biomarker test for DNA methylation is technically feasible and could aid in earlier and more precise diagnosis of melanoma. The test distinguishes malignant melanomas from non-malignant moles, with high predictive value.

SourceUniversity of North Carolina Health Care·JournalPigment Cell & Melanoma Research·DateJan 24, 2011

Insight offers new angle of attack on variety of brain tumors

A new research paper published in the Journal of the National Cancer Institute reveals a genetic mutation that leads to abnormal metabolic processes in gliomas, potentially leading to targeted therapies. The study shows that almost all tumors with IDH mutations have the same methylation pattern.

SourceBrown University·JournalJNCI Journal of the National Cancer Institute·DateDec 15, 2010
Aranet4 Home CO2 Monitor

Aranet4 Home CO2 Monitor tracks ventilation quality in labs, classrooms, and conference rooms with long battery life and clear e-ink readouts.

New labeling method expands ability to read DNA modification

Researchers developed a method to label and map the sixth nucleotide, 5-hydroxymethylcytosine (5-hmC), which is enriched on active genes. The method reveals its genome-wide distribution and functional significance in gene regulation and neurodegeneration.

SourceEmory Health Sciences·JournalNature Biotechnology·DateDec 12, 2010

DNA repair protein caught in act of molecular theft

Researchers trap and observe intermediate stage of DNA repair protein Al McBiotically theft, a process that regulates health conditions such as obesity, cancer, and diabetes. The study provides new insights into how proteins chemically alter biological molecules via oxidative demethylation.

SourceUniversity of Chicago·JournalNature·DateNov 10, 2010

BGI researchers sequenced the human methylome at single base-pair resolution

The study sequenced the human methylome from peripheral blood mononuclear cells, identifying allele-specific methylation differences associated with gene expression. The findings suggest that parental gene imprinting may be more common than previously thought, with implications for understanding human health and disease.

SourcePLOS·JournalPLOS Biology·DateNov 9, 2010
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Study reveals cancer-linked epigenetic effects of smoking

UK scientists have reported direct evidence that taking up smoking results in epigenetic changes associated with cancer. A study funded by Cancer Research UK found women who started smoking had a higher risk of acquiring p16 methylation, a type of epigenetic change linked to tumor suppressor genes.

SourceEuropean Society for Medical Oncology·JournalAnnals of Oncology·DateOct 9, 2010

TGen-Mayo Clinic study discovers role of DNA methylation in multiple myeloma blood cancer

A study by Mayo Clinic and TGen reveals that DNA methylation is altered with increasing severity in multiple myeloma, leading to the overexpression of oncogenes. The researchers found hypomethylation at specific points of DNA, associated with myeloma development, and suggest it may have prognostic value.

SourceThe Translational Genomics Research Institute·JournalCancer Prevention Research·DateSep 30, 2010

Johns Hopkins scientists find genes related to body mass

Researchers at Johns Hopkins University have identified 13 genes associated with human body mass index, shedding light on the complex relationship between epigenetics and obesity. The study, published in Science Translational Medicine, used genome-wide profiling to uncover epigenetic fingerprints that correlate with body weight.

SourceJohns Hopkins Medicine·JournalScience Translational Medicine·DateSep 15, 2010
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