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New approach identifies genes that help microbes to survive in the human gut

Trillions of tiny microbes and bacteria live in your gut, each with their own set of genes. These gut microbes can have both beneficial and harmful effects on your health, from protecting you against inflammation to causing life-threatening infections.

10 Aug 2018

Scientists are one step closer to understanding autistic disorders

Autism spectrum disorders are a heterogeneous group of neurodevelopmental disorders, one of the main characteristics of which is impaired social communication.

10 Aug 2018

Researchers discover genetic mutation underlying debilitating childhood brain disorder

Ashleigh Schaffer, PhD, assistant professor of genetics at Case Western Reserve University School of Medicine, and a team of global genetics experts have discovered a genetic mutation and the faulty development process it triggers, causing a debilitating brain-based disorder in children.

9 Aug 2018

Scientists find genetic marker that indicates a person's risk for tachycardia-induced cardiomyopathy

Scientists in Japan have found a potential marker to identify which people with abnormally fast heartbeats are at high risk of developing heart failure.

9 Aug 2018

Study identifies key role of TLK1 and TLK2 enzymes in DNA replication

During cell growth, cells copy their DNA through a process called DNA replication. For this process to be accurate, the genetic and epigenetic information must be copied flawlessly.

9 Aug 2018

ETH scientists discover new cancer-specific molecular changes in tumor tissues

A research team led by Gunnar Raetsch, Professor of Biomedical Informatics at ETH Zurich, has evaluated the largest set of genetic data in cancer medicine: The Cancer Genome Atlas in the United States.

9 Aug 2018

Scientists uncover reason for similarity between cells in malignant cancers and embryonic cells

Using just a microscope, Italian surgeon Francesco Durante was struck by the similarities between cells in the most malignant cancers and the embryonic cells of the organ in which the cancer originated.

9 Aug 2018

Atlas of the nervous system provides new clues about origin of neurological diseases

Researchers at Karolinska Institutet have created a systematic and detailed map of the cell types of the mouse nervous system.

9 Aug 2018

Scientists turn to C. elegans for new model of peripheral neuropathy

Studying transthyretin amyloidoses - a group of progressive nerve and cardiac degenerative diseases caused by the buildup of misfolded transthyretin proteins in the body - has long been hampered by the lack of animal models of the disease.

9 Aug 2018

New method evaluates effectiveness of interventions in mitigating spread of HIV

Using genetic sequencing to understand the evolutionary relationships among pathogens, an international team of researchers - including several from the Center for Drug Use and HIV/HCV Research at New York University - has developed a new method to determine how effective interventions are against the spread of infectious diseases like HIV.

9 Aug 2018

Defects in RNA modification can cause altered smooth muscle contraction

Genetic information is stored in DNA and is passed on in a very stable manner from one cell to the next or from one generation to the next.

9 Aug 2018

Cleveland Clinic awarded $4.7 million grant to study prevention of cancer-associated blood clots

The National Heart, Lung and Blood Institute (NHLBI), part of the National Institutes of Health, awarded a $4.7 million grant to Cleveland Clinic to study the prevention of life-threatening, cancer-associated blood clots.

9 Aug 2018

Study identifies distinct genetic mutations in appendix cancer that may impact treatment

The rarity of appendix cancer, accounting for less than 1 percent of tumors that originate in the gastrointestinal tract, and the lack of scientific data for this disease means that current treatment guidelines recommend applying therapies to people with appendix cancer that are intended for those with colon cancer.

9 Aug 2018

Researchers develop new method for capturing dynamic processes in individual cells

Researchers at Karolinska Institutet and Harvard Medical School report in the journal Nature that they have developed a technique for capturing dynamic processes in individual cells. Apart from studying disease processes, the method can be used to observe in detail how specialised cells are formed during embryonic development.

9 Aug 2018

Researchers provide new insight on origins and global spread of HBV

Researchers have provided new insight on the geographical origins and global spread of two classes of the hepatitis B virus (HBV), according to a study in eLife.

7 Aug 2018

New study identifies genes linked to higher risk for triple-negative breast cancer

A new study published in the Journal of the National Cancer Institute has identified specific genes associated with increased risk for triple-negative breast cancer, providing the basis for better risk management.

7 Aug 2018

Scientists create new tool to precisely control 3D architecture of linkages in drugs

When it comes to certain molecules, shape makes all the difference. The shape of limonene, for instance, a compound produced by citrus fruits, determines whether it tastes like orange juice or turpentine.

7 Aug 2018

Study could help explain why Asians often develop diabetes at a lower body weight

A new UC San Francisco study has discovered a key biological difference in how people of European and Chinese descent put on weight -- a finding that could help explain why Asians often develop type 2 diabetes at a much lower body weight than Caucasians.

7 Aug 2018

Researchers identify specific genes linked to increased risk for triple-negative breast cancer

A research team led by Fergus Couch, Ph.D., a geneticist at Mayo Clinic, has identified specific genes associated with an increased risk for developing triple-negative breast cancer. Their research was published in the Journal of the National Cancer Institute.

7 Aug 2018

Inhibition of NOVA1 gene helps prevent growth of lung cancer tumors

Researchers have identified a gene that when inhibited or reduced, in turn, reduced or prevented human non-small cell lung cancer tumors from growing.

7 Aug 2018

Genetic News and Research

New approach identifies genes that help microbes to survive in the human gut

Scientists are one step closer to understanding autistic disorders

Researchers discover genetic mutation underlying debilitating childhood brain disorder

Scientists find genetic marker that indicates a person's risk for tachycardia-induced cardiomyopathy

Study identifies key role of TLK1 and TLK2 enzymes in DNA replication

ETH scientists discover new cancer-specific molecular changes in tumor tissues

Scientists uncover reason for similarity between cells in malignant cancers and embryonic cells

Atlas of the nervous system provides new clues about origin of neurological diseases

Scientists turn to C. elegans for new model of peripheral neuropathy

New method evaluates effectiveness of interventions in mitigating spread of HIV

Defects in RNA modification can cause altered smooth muscle contraction

Cleveland Clinic awarded $4.7 million grant to study prevention of cancer-associated blood clots

Study identifies distinct genetic mutations in appendix cancer that may impact treatment

Researchers develop new method for capturing dynamic processes in individual cells

Researchers provide new insight on origins and global spread of HBV

New study identifies genes linked to higher risk for triple-negative breast cancer

Scientists create new tool to precisely control 3D architecture of linkages in drugs

Study could help explain why Asians often develop diabetes at a lower body weight

Researchers identify specific genes linked to increased risk for triple-negative breast cancer

Inhibition of NOVA1 gene helps prevent growth of lung cancer tumors

Sequencing & Genomics: Elevating Science and Healthcare eBook

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

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