Genetic News and Research

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New research describes genetic switches that ignite axon formation

While the neural architecture responsible for the transmission of electrical impulses has been known for more than a century, the basic biology behind how a neuron acquires its one and only axon -- a fundamental component of how neurons communicate -- remains a mystery.

5 Feb 2019

Scientists shed light on biological process that helps production of healthy cells

Scientists have shed light on a biological process that helps the production of healthy cells, which may aid understanding of neurological diseases and other conditions.

5 Feb 2019

Study uncovers new clues to lung transplant rejection

A lung transplant often remains the only option for many patients with end-stage lung disease, a condition that can be brought on by emphysema, pulmonary fibrosis, cystic fibrosis and other lung disorders.

4 Feb 2019

Researchers identify treatable mechanism in patients with schizophrenia

For reasons that are unclear, schizophrenia patients have fewer connections between the neurons in the brain. Researchers at Karolinska Institutet, Sweden, and Massachusetts General Hospital, USA, have now succeeded in creating human cell models that show that there is an excessive degradation of connections in the brain of these patients, and they have been able to link this to a genetic risk variant for the disease.

4 Feb 2019

Study sheds new light on genetics of diabetes in Japanese population

The genetic and genomic revolutions have led to an abundance of data about the genetic factors that confer a predisposition to type 2 diabetes, alongside environmental and lifestyle-related causes.

4 Feb 2019

Developing a Cervical Cancer Test That’s 100% Predictive

An interview with Professor Attila Lorincz, discussing the development of a new cervical cancer test that is able to predict cervical cancer and pre-cancer in 100% cases.

4 Feb 2019

Newly launched CINECA enables researchers to access clinical research data

Registered researchers will have rapid access to an "unprecedented scale" of clinical research data through the new Common Infrastructure for National Cohorts in Europe, Canada and Africa, launched today.

4 Feb 2019

Cancer among Israeli men on the decline says report

According to a report from the Israel Cancer Association yesterday (3rd February 2019), there has been a significant fall in the number of Israeli men getting cancers over that last decade.

3 Feb 2019

Researchers reveal risks of eating disorders from childhood

Eating disorders — anorexia nervosa, bulimia nervosa or hyperphagia — usually appear in adolescence and often leave young patients and their families helpless. These disorders, whose prevalence is increasing, raise the question of early detection.

1 Feb 2019

Genetic testing improves diagnoses of abnormalities in developing babies

Genetic testing improves the diagnoses of abnormalities in developing babies that are picked up during ultrasound scans, scientists report today (31 January) in The Lancet.

1 Feb 2019

New genetic technique could allow scientists to study how smell affects behavior

Take a whiff when it rains after a dry spell, and breathe in the earthy scent that pervades the air. That smell comes from decomposing bacteria, and scientists call the compound geosmin.

1 Feb 2019

Oxford Genetics signs licensing agreement with Aldevron to market lentiviral packaging plasmids

Oxford Genetics, a leading innovator of biopharmaceutical technologies, has signed a licensing agreement with world-class service organization, Aldevron to bring to market a standardized range of its plasmids for lentiviral manufacture.

1 Feb 2019

Johns Hopkins Greenberg Bladder Cancer Institute awards research grants to study how bladder cancer affects women

The Johns Hopkins Greenberg Bladder Cancer Institute awarded research grants to four projects that focus on understanding how treatment of bladder cancer affects women, why the disease has a less favorable outcome for women than men, and how biology could play a role in offering new targets for cancer therapy.

1 Feb 2019

Research could potentially lead to new treatments for neurodegenerative diseases

Scientists from the University of Sheffield have identified new messenger molecules shuttled between cells which could help to protect the survival of neurones - potentially leading to new treatments for MND .

1 Feb 2019

Discovery of proteins that control mucin secretion reveals clues to treating colon, airway diseases

Cells produce mucins at a constant rate, and when exposed to an allergen or pathogen, they produce more mucin in a rapid burst. Both the constant and rapid mucin secretion is controlled by calcium.

1 Feb 2019

Persistent low BMI in children may be a risk factor for developing anorexia nervosa

A new study has found that a persistent low body mass index in children, starting as young as age 2 for boys and 4 for girls, may be a risk factor for the development of anorexia nervosa in adolescence.

1 Feb 2019

Study reveals mechanisms responsible for embryonic development in fruit flies

The first moments of life unfold with incredible precision. Now, using mathematical tools and the help of fruit flies, researchers at Princeton have uncovered new findings about the mechanisms behind this precision.

1 Feb 2019

Researchers identify regulatory mechanism underlying obesity

Obesity − as research in the past decade has shown − is first and foremost a brain disease. Researchers at Helmholtz Zentrum München, partners in the German Center for Diabetes Research, have now discovered a molecular switch that controls the function of satiety neurons and therefore body weight. The findings were published in the journal 'Nature Metabolism'.

31 Jan 2019

New understanding could help improve prediction and prevention of depression

In a new study, researchers from the Danish iPSYCH project demonstrate that people with the highest genetic propensity are over two and a half times as likely to be treated in a psychiatric hospital for depression compared to people with the lowest propensity.

31 Jan 2019

New link found between psychiatric disorders and events during the prenatal stage

Particular genetic variants in the human genome that are important for the development of the brain early in the life of the fetus are frequently found in psychiatric disorders. This is shown by a study carried out by iPSYCH.

31 Jan 2019

Genetic News and Research

New research describes genetic switches that ignite axon formation

Scientists shed light on biological process that helps production of healthy cells

Study uncovers new clues to lung transplant rejection

Researchers identify treatable mechanism in patients with schizophrenia

Study sheds new light on genetics of diabetes in Japanese population

Developing a Cervical Cancer Test That’s 100% Predictive

Newly launched CINECA enables researchers to access clinical research data

Cancer among Israeli men on the decline says report

Researchers reveal risks of eating disorders from childhood

Genetic testing improves diagnoses of abnormalities in developing babies

New genetic technique could allow scientists to study how smell affects behavior

Oxford Genetics signs licensing agreement with Aldevron to market lentiviral packaging plasmids

Johns Hopkins Greenberg Bladder Cancer Institute awards research grants to study how bladder cancer affects women

Research could potentially lead to new treatments for neurodegenerative diseases

Discovery of proteins that control mucin secretion reveals clues to treating colon, airway diseases

Persistent low BMI in children may be a risk factor for developing anorexia nervosa

Study reveals mechanisms responsible for embryonic development in fruit flies

Researchers identify regulatory mechanism underlying obesity

New understanding could help improve prediction and prevention of depression

New link found between psychiatric disorders and events during the prenatal stage

Genetics & Genomics - Second Edition 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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