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Research advances offer hope for patient-tailored AML treatment

Advances in rapid screening of leukemia cells for drug susceptibility and resistance are bringing scientists closer to patient-tailored treatment for acute myeloid leukemia.

10 Dec 2018

High intensity statin treatment and adherence could save more lives

Thousands of heart attacks and deaths from cardiovascular disease could be prevented by patients taking higher doses of statins and taking the drugs as advised by doctors.

7 Dec 2018

Surgical choices may have long-term impact on quality of life for breast cancer patients

Even as more young women with breast cancer opt to have mastectomies, many experience a persistent decline in their sexual and psychosocial well-being following the procedure, as detailed in new research by Dana-Farber/Brigham and Women's Cancer Center.

7 Dec 2018

Researchers confirm link between neonatal vitamin D deficiency and schizophrenia

Newborns with vitamin D deficiency have an increased risk of schizophrenia later in life, a team of Australian and Danish researchers has reported.

7 Dec 2018

New technology for profiling genetic makeup of myeloma tumor cells developed

Cancer arises when cells lose control. Deciphering the "blueprint" of cancer cells - outlining how cancer cells hijack specific pathways for uncontrolled proliferation - will lead to more efficient ways to fight it.

7 Dec 2018

MUHC's 'Dr. House' discovers new genetic disease and the gene responsible for it

A team from the Research Institute of the McGill University Health Centre led by Dr. Donald Vinh, the RI's so-called "Dr. House" because of his research into rare diseases, has discovered a new human disease and the gene responsible for it, paving the way for the proper diagnosis of patients globally and the development of new therapies.

7 Dec 2018

New booklet could help improve conditions of young pupils with albinism

A booklet, in Swahili and English, could help teachers in Tanzania improve conditions for pupils with albinism in their schools.

7 Dec 2018

New way of controlling HIV latency to completely eradicate the virus

A new study suggests that a genetic switch that causes latent HIV inside cells to begin to replicate can be manipulated to completely eradicate the virus from the human body. Cells harboring latent HIV are "invisible" to the natural defenses of the immune system.

7 Dec 2018

Earliest strain of plague bacteria found in neolithic Swedish mass grave

Researchers have unearthed a strain of plague bacteria Yersinia pestis, in a woman who was buried in Sweden during the stone ages.

6 Dec 2018

World's first robot-assisted bilateral breast reconstruction performed by Penn surgeons

A team of surgeons from the Perelman School of Medicine at the University of Pennsylvania are the first in the world to use a surgical robot to assist with a bilateral free flap breast reconstruction - a procedure in which tissue is taken from the lower abdomen - similar to a "tummy tuck" - and used to rebuild the breast.

6 Dec 2018

New way to trace the transmission histories of rare genetic diseases

There are only 25 people in the whole of Quebec at the moment who have a rare recessive genetic disease called chronic atrial and intestinal dysrhythmia. Now, scientists have begun tracing the origins of these diseases.

6 Dec 2018

New EU-funded project provides insight into how the brain develops

The human brain is comprised of billions of different types of cells. These cells are then organized into sophisticated networks, each of which determines a specific function of the brain. But how do the neurons, or nerve cells that form these networks, find the right network? And what happens when they don’t?

6 Dec 2018

Newborns with vitamin D deficiency have increased risk of schizophrenia later in life

Newborns with Vitamin D deficiency have an increased risk of schizophrenia later in life, researchers from Aarhus University and the University of Queensland report.

6 Dec 2018

CHOP celebrates EC approval of first and only gene therapy for patients with inherited retinal disease

Children's Hospital of Philadelphia celebrates a pivotal moment in medicine: approval by the European Commission of LUXTURNA (voretigene neparvovec), the first and only gene therapy for patients with an inherited retinal disease, last month.

6 Dec 2018

Mapping brain microglia

Microglia are known to be important to brain function. The immune cells have been found to protect the brain from injury and infection and are critical during brain development, helping circuits wire properly. They also seem to play a role in disease -- showing up, for example, around brain plaques in people with Alzheimer's.

6 Dec 2018

Study reveals how the absence of Dna2 enzyme affects chromosome instability

Cells have in place a number of mechanisms to protect the integrity of the genome, including processes that repair mistakes that may occur during DNA replication.

6 Dec 2018

Study shows correlation between childhood infections and increased risk of mental disorders

A new study from iPSYCH shows that the infections children contract during their childhood increase the risk of mental disorders during childhood and adolescence. This knowledge expands our understanding of the role of the immune system in the development of mental disorders.

6 Dec 2018

CWRU researcher secures $14.6 million funding for genetic study into Alzheimer's disease

Alzheimer's disease symptoms, such as memory loss or cognitive decline, can present in different ways among people with diverse ethnic backgrounds. Researchers know that a complex mix of social, behavioral, and genetic variables can impact the onset and progression of this disease.

6 Dec 2018

Scientists identify new drug target for potential blood pressure treatment

Scientists have identified a key player in blood pressure regulation and have shown that switching it off reduces blood pressure in mice, according to new research in eLife.

6 Dec 2018

New massive sequencing platform implemented for double factor preimplantation genetic testing

A research team from the Universitat Autònoma de Barcelona, in collaboration with the Blood and Tissue Bank of Catalonia, has managed to implement a massive sequencing platform for Preimplantation Genetic Testing for the first time in history.

5 Dec 2018

Genetic News and Research

Research advances offer hope for patient-tailored AML treatment

High intensity statin treatment and adherence could save more lives

Surgical choices may have long-term impact on quality of life for breast cancer patients

Researchers confirm link between neonatal vitamin D deficiency and schizophrenia

New technology for profiling genetic makeup of myeloma tumor cells developed

MUHC's 'Dr. House' discovers new genetic disease and the gene responsible for it

New booklet could help improve conditions of young pupils with albinism

New way of controlling HIV latency to completely eradicate the virus

Earliest strain of plague bacteria found in neolithic Swedish mass grave

World's first robot-assisted bilateral breast reconstruction performed by Penn surgeons

New way to trace the transmission histories of rare genetic diseases

New EU-funded project provides insight into how the brain develops

Newborns with vitamin D deficiency have increased risk of schizophrenia later in life

CHOP celebrates EC approval of first and only gene therapy for patients with inherited retinal disease

Mapping brain microglia

Study reveals how the absence of Dna2 enzyme affects chromosome instability

Study shows correlation between childhood infections and increased risk of mental disorders

CWRU researcher secures $14.6 million funding for genetic study into Alzheimer's disease

Scientists identify new drug target for potential blood pressure treatment

New massive sequencing platform implemented for double factor preimplantation genetic testing

eBook: Using iPSCs models for human disease research and drug discovery 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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