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Scientists discover new molecular drivers of Parkinson's disease

Scientists at the Icahn School of Medicine at Mount Sinai have uncovered new molecular drivers of Parkinson's disease using a sophisticated statistical technique called multiscale gene network analysis.

20 Nov 2019

Study shows gender differences in prognosis predictive utility of breast cancer recurrence score

The TAILORx study published last year offered good news for women with early-stage ER-positive breast cancer who scored at intermediate risk for recurrence according to a genetic assay test.

20 Nov 2019

Rheumatoid arthritis linked to other diseases before and after diagnosis, shows study

A Mayo Clinic-led study involving 3,276 patients has found that people with inflammatory bowel disease, Type 1 diabetes or blood clots may be at increased risk of developing rheumatoid arthritis.

20 Nov 2019

Shared reading between parents and young children associated with stronger vocabulary skills

Shared reading between parents and very young children, including infants, is associated with stronger vocabulary skills for nearly all children by age 3, say physicians at Rutgers Robert Wood Johnson Medical School and Princeton University.

19 Nov 2019

Scientists develop new therapy for acute myeloid leukemia

Cold Spring Harbor Laboratory scientists, with chemists and cancer biologists from Dana-Farber Cancer Institute, have developed a new therapy that extended the survival of mice with acute myeloid leukemia.

19 Nov 2019

CTF, DELopen jointly offer unique opportunities to neurofibromatosis research community

The Children's Tumor Foundation, an innovative and global neurofibromatosis (NF) research foundation announced today a collaboration with DELopen, a DNA-encoded library technology platform sponsored by WuXi AppTec, a leading global provider of R&D and manufacturing services enabling companies in the pharmaceutical, biotechnology and medical device industries.

19 Nov 2019

MU researchers describe Down syndrome-associated catatonia

Down syndrome, due to an extra chromosome 21, occurs in 250,000 children and adults in the United States, making it the country's most common chromosomal disorder. Inherited heart defects, thyroid cancer, celiac disease and developmental disabilities are common Down syndrome complications.

19 Nov 2019

Study of 'face blindness' provides clues to what goes wrong in the brain

People with prosopagnosia, or "face blindness," have trouble recognizing faces -- even those of close friends and family members.

19 Nov 2019

Rutgers Cancer Institute researchers awarded $2.3 million in American Cancer Society grants

More than $2.3 million in Research Scholar Grants from the American Cancer Society have been awarded to three Rutgers Cancer Institute of New Jersey researchers to examine cell metabolism and tumor formation in forms of breast cancer, lung cancer and leukemia.

19 Nov 2019

Proteomics & DIA Mass Spectrometry in Neurodegenerative Disease Research

News-Medical Life Sciences spoke to Nicholas Dupuis from Biognosys about proteomics & DIA mass spectrometry in neurodegenerative disease research.

From Biognosys 19 Nov 2019

Potential new therapy for progeria

Aging is a complex and natural process that affects all living organisms. As people age, normal biological processes are affecting, resulting in a decline in various organs and age-related conditions. Though aging is normal, some children affected by a disease called Progeria may age way faster than others.

18 Nov 2019

Study examines sexual harassment among physicians and other faculty at academic medical center

A new study has shown that the majority of women (82.5%) and men (65.1%) working at an academic medical center reported at least one incident of sexual harassment by staff, students, and faculty during the previous year.

18 Nov 2019

Tailored T-cells safe, may be effective in preventing and treating multiple viral infections

Tailored T-cells specially designed to combat a half dozen viruses are safe and may be effective in preventing and treating multiple viral infections, according to research led by Children's National Hospital faculty.

18 Nov 2019

'Dysbiosis' promotes the onset of colorectal cancer

The gastroenterology team at Henri-Mondor AP-HP Hospital and University Paris-Est Créteil, led by Professor Iradj Sobhani, together with teams from Inserm and the Institut Pasteur Molecular Microbial Pathogenesis Unit (U1202), led by Professor Philippe Sansonetti - holder of the Microbiology and Infectious Diseases Chair at the Collège de France -, have demonstrated that an imbalance in the gut microbiota, also known as "dysbiosis", promotes the onset of colorectal cancer.

18 Nov 2019

BGU researchers discover gene that causes nighttime atrial fibrillation

Genetic studies spanning three generations of a Persian Jewish family by researchers at Ben-Gurion University of the Negev. have identified a gene that causes nighttime atrial fibrillation (AFib).

18 Nov 2019

Researchers identify “mutational footprint” caused by chemotherapy that leads to side effects

Researchers have characterized the "mutational footprint" that results from chemotherapy and leads to long-term side effects.

18 Nov 2019

Study: Almost 10% of diverse Latino populations meet the criteria for mild cognitive impairment

A study of over 6,300 Latinos of Dominican, Central American, Cuban, Mexican Puerto Rican and South American heritage estimates that nearly 10% of middle-age and older Latinos in the U.S. meet the criteria for mild cognitive impairment.

18 Nov 2019

Sudden death due to heart disease – it could be in the genes

More than 220,000 American adults die suddenly of cardiac causes – a phenomenon called sudden cardiac death. Some sources put it as closer to 400,000. Both inexplicable and distressing, this has been the subject of a new study published in the Journal of the American College of Cardiology and presented at the American Heart Association’s scientific session.

17 Nov 2019

Cardiac catheterization patients practicing intermittent fasting live longer

While Intermittent fasting may sound like another dieting craze, the practice of routinely not eating and drinking for short periods of time has shown again to lead to potentially better health outcomes.

17 Nov 2019

Rare DNA variants linked to sudden cardiac death

Sudden cardiac death affects 220,000 U.S. adults annually, most of whom have no prior symptoms of a heart issue.

17 Nov 2019

Genetic News and Research

Scientists discover new molecular drivers of Parkinson's disease

Study shows gender differences in prognosis predictive utility of breast cancer recurrence score

Rheumatoid arthritis linked to other diseases before and after diagnosis, shows study

Shared reading between parents and young children associated with stronger vocabulary skills

Scientists develop new therapy for acute myeloid leukemia

CTF, DELopen jointly offer unique opportunities to neurofibromatosis research community

MU researchers describe Down syndrome-associated catatonia

Study of 'face blindness' provides clues to what goes wrong in the brain

Rutgers Cancer Institute researchers awarded $2.3 million in American Cancer Society grants

Proteomics & DIA Mass Spectrometry in Neurodegenerative Disease Research

Potential new therapy for progeria

Study examines sexual harassment among physicians and other faculty at academic medical center

Tailored T-cells safe, may be effective in preventing and treating multiple viral infections

'Dysbiosis' promotes the onset of colorectal cancer

BGU researchers discover gene that causes nighttime atrial fibrillation

Researchers identify “mutational footprint” caused by chemotherapy that leads to side effects

Study: Almost 10% of diverse Latino populations meet the criteria for mild cognitive impairment

Sudden death due to heart disease – it could be in the genes

Cardiac catheterization patients practicing intermittent fasting live longer

Rare DNA variants linked to sudden cardiac death

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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