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CHOP researchers pinpoint WDR26 haploinsufficiency as cause for rare genetic syndrome

Researchers have identified a rare genetic syndrome characterized by intellectual disability, seizures, an abnormal gait and distinctive facial features.

6 Jul 2017

Study reveals link between higher BMI and increased risk of cardiometabolic diseases

Results of a new study add to the evidence of an association between higher body mass index (BMI) and increased risk of cardiometabolic diseases such as hypertension, coronary heart disease, type 2 diabetes, according to a study published by JAMA Cardiology.

5 Jul 2017

First systematic genomic analysis of patients with T-ALL may aid development of new therapies

A consortium including St. Jude Children's Research Hospital and the Children's Oncology Group has performed an unprecedented genomic sequencing analysis of hundreds of patients with T-lineage acute lymphoblastic leukemia (T-ALL).

4 Jul 2017

Research reveals biological processes that underlie comorbidity between Alzheimer's disease and cancer

Patients with Alzheimer's disease have a higher risk of developing glioblastoma and a lower risk of lung cancer.

3 Jul 2017

Cole-Parmer introduces Arcis Sample Prep Kit to extract DNA and RNA for downstream processes

Cole-Parmer, a leading supplier of laboratory equipment and reagents, is introducing the Arcis Sample Preparation System, which can extract DNA and RNA for downstream processes such as PCR/qPCR and sequencing in just three minutes.

From Cole Parmer Limited 30 Jun 2017

Psychological tools help high-risk chronic pain patients to taper opioid use

Psychological support and new coping skills are helping patients at high risk of developing chronic pain and long-term, high-dose opioid use taper their opioids and rebuild their lives with activities that are meaningful and joyful to them.

29 Jun 2017

PNNL-OHSU scientists part of NCI effort to study about role of proteins in cancer biology

The Department of Energy's Pacific Northwest National Laboratory is part of a nationwide effort to learn more about the role of proteins in cancer biology and to use that information to benefit cancer patients.

28 Jun 2017

DNA methylation can provide effective markers for major cancers, study reveals

In a new study, published online in the July 26 issue of PNAS, researchers at University of California San Diego School of Medicine, with colleagues in Xijing Hospital and Sun Yat-sen Cancer Center in China, report that DNA methylation can provide effective markers for at least four major cancers, not only correctly differentiating malignant tissues from normal, but also providing information on prognosis and survival.

28 Jun 2017

Mouse study uncovers key molecular player in heart enlargement

The heart is a dynamic muscle that grows and shrinks in response to stressors such as exercise and disease. The secret to its malleability lies in individual cells, which get bigger or smaller depending on the heart's needs.

27 Jun 2017

Cancers manipulate natural cell process to promote their survival, research suggests

Cancer tumors manipulate a natural cell process to promote their survival suggesting that controlling this mechanism could stop progress of the disease, according to new research led by the University of Oxford.

27 Jun 2017

Complete DNA sequencing should not be feared according to researchers

It is now much easier than before to do a complete DNA sequencing of patients to look at all the three billion letters that make up a person’s genetic code or genome. DNA sequencing prices have fallen and it could soon be a part of routine medical tests experts suggest. However there is public fear associated with complete sequencing. Researchers looked at the fact if this fear was actually justified.

26 Jun 2017

Combined effect of genetic change and ozone exposure could increase risk for autism

A new analysis shows that individuals with high levels of genetic variation and elevated exposure to ozone in the environment are at an even higher risk for developing autism than would be expected by adding the two risk factors together.

23 Jun 2017

Existing drugs could help subgroup of patients with osteosarcoma, suggest scientists

A subgroup of patients with osteosarcoma - a form of bone cancer - could be helped by an existing drug, suggest scientists from the Wellcome Trust Sanger Institute and their collaborators at University College London Cancer Institute and the Royal National Orthopaedic Hospital NHS Trust.

23 Jun 2017

Researchers identify first definitive risk genes for Tourette Syndrome

An international team that just conducted the largest study of Tourette Syndrome has identified genetic abnormalities that are the first definitive risk genes for the disorder.

23 Jun 2017

Scientists develop new algorithm to decipher how immune system recognizes and binds antigens

Scientists from St. Jude Children's Research Hospital and Fred Hutchinson Cancer Research Center have developed an algorithm that functions like a Rosetta Stone to help decipher how the immune system recognizes and binds antigens.

22 Jun 2017

Finnish researchers find accumulation of gene mutations in some patients with rheumatoid arthritis

Gene mutations accumulating in cells are typical of the development of cancer. Finnish researchers found that a similar accumulation of mutations occurs also in some patients with rheumatoid arthritis.

21 Jun 2017

Researchers identify new disease gene for early-onset axonal neuropathy and mild intellectual disability

Research group from the University of Helsinki, Finland, has identified a new disease gene for early-onset axonal neuropathy and mild intellectual disability through an international research network, which was brought together by "Tinder for geneticists".

20 Jun 2017

Philips introduces new web-based informatics platform to hasten drug research and biomarker discovery

Royal Philips, a global leader in health technology, today announced the launch of its Xplore web-based informatics platform for drug research and biomarker discovery.

From Philips Healthcare 20 Jun 2017

MIT biologists identify how the immune system eliminates genetically imbalanced cells

Most living cells have a defined number of chromosomes: Human cells, for example, have 23 pairs. As cells divide, they can make errors that lead to a gain or loss of chromosomes, which is usually very harmful.

20 Jun 2017

Researchers discover broad role for DNA-cutting enzyme in driving abnormal genetic rearrangements

Researchers studying a DNA-cutting enzyme with a crucial role in regulating the structure of genes have discovered a broad role for its cutting activity in driving abnormal genetic rearrangements called translocations that cause cancer, including leukemias and solid tumors.

16 Jun 2017

Genomic News and Research

CHOP researchers pinpoint WDR26 haploinsufficiency as cause for rare genetic syndrome

Study reveals link between higher BMI and increased risk of cardiometabolic diseases

First systematic genomic analysis of patients with T-ALL may aid development of new therapies

Research reveals biological processes that underlie comorbidity between Alzheimer's disease and cancer

Cole-Parmer introduces Arcis Sample Prep Kit to extract DNA and RNA for downstream processes

Psychological tools help high-risk chronic pain patients to taper opioid use

PNNL-OHSU scientists part of NCI effort to study about role of proteins in cancer biology

DNA methylation can provide effective markers for major cancers, study reveals

Mouse study uncovers key molecular player in heart enlargement

Cancers manipulate natural cell process to promote their survival, research suggests

Complete DNA sequencing should not be feared according to researchers

Combined effect of genetic change and ozone exposure could increase risk for autism

Existing drugs could help subgroup of patients with osteosarcoma, suggest scientists

Researchers identify first definitive risk genes for Tourette Syndrome

Scientists develop new algorithm to decipher how immune system recognizes and binds antigens

Finnish researchers find accumulation of gene mutations in some patients with rheumatoid arthritis

Researchers identify new disease gene for early-onset axonal neuropathy and mild intellectual disability

Philips introduces new web-based informatics platform to hasten drug research and biomarker discovery

MIT biologists identify how the immune system eliminates genetically imbalanced cells

Researchers discover broad role for DNA-cutting enzyme in driving abnormal genetic rearrangements

Genetics & Genomics - Second Edition eBook

Sensing a Healthier Future

Achieving and maintaining ISO/IEC 27001 and BS 10012 certifications

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