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Illustration of mouse with chip implant

Columbia neuroelectronic system could improve epilepsy treatment and reduce side effects

May 13, 2021
By Annette Boyle
In the last decade, responsive neurostimulation (RNS) has become a mainstay of treatment for refractory focal epilepsy, but challenges with the technology remain. Researchers at Columbia University in New York appear to have overcome some of the major limitations through development of a compact, flexible, high performance implantable device that permits reading and manipulation of brain circuits.
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Coronavirus, question marks
Origin stories

SARS-CoV-2 origin is hotly debated known unknown

May 13, 2021
By Anette Breindl
Roughly a year and a half after the start of the COVID-19 pandemic, many unknowns remain about the future of the virus. How it will mutate, how long protection from either illness or vaccination will last, when it will cease to be a pandemic and instead be endemic, even whether the worst is still ahead. And there is also an increasing acknowledgment that there remain unknowns about SARS-CoV-2’s past.
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Brain and blood cells

ASGCT 2021: Engineering blood cells can treat brain diseases

May 13, 2021
By Anette Breindl
Collectively, lysosomal storage disorders (LSDs) are caused by malfunctions in metabolic enzymes in the lysosome system. Depending on which enzyme is missing, toxic metabolites accumulate. While the LSDs are highly heterogenous – even within one disease, presentation can vary widely – neurodegeneration is a common feature in these disorders.
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N. brasiliensis

AAI 2021: In immunity, IL-33 signals stop as well as go

May 12, 2021
By Anette Breindl
Parasitic worms, or helminths, are a major global health issue. At the same time, "parasites have been a prolific area of biomedical research to emerge," De'Broski Herbert told his audience at the 2021 annual meeting of the American Association of Immunologists.
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DNA illustration

Findings bolster RAD51 as biomarker for DNA repair deficiency

May 11, 2021
By Anette Breindl
The discovery of synthetic lethality between BRCA mutations and PARP inhibitors ranks has led to major advances in the treatment of BRCA-mutated cancers. Mutations in BRCA1 and BRCA2 can leave cells with a deficiency in homologous repair (HR). And that deficiency can make them vulnerable to PARP inhibitors, which block alternate DNA repair pathways, as well as platinum-based treatment, which induces DNA mutations that BRCA-deficient cells are unable to cope with.
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Teen receiving vaccine

SARS-CoV-2 vaccines make progress in the young, the old, the in-between

May 11, 2021
By Anette Breindl
With Monday's announcement that the U.S. FDA has expanded emergency use authorization for Pfizer and BioNtech's COVID-19 vaccine, Comirnaty (tozinameran), to include adolescents 12 through 15 years of age, and the EMA expected to follow suit in short order, the COVID vaccination campaign is expanding its age range.
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DNA illustration

Findings bolster RAD51 as biomarker for DNA repair deficiency

May 10, 2021
By Anette Breindl
The discovery of synthetic lethality between BRCA mutations and PARP inhibitors ranks has led to major advances in the treatment of BRCA-mutated cancers.
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Microbiome illustration

Gut microbiome affects protein folding in brain, muscles

May 7, 2021
By Anette Breindl
Using the roundworm C. elegans as a "living test tube," researchers at the University of Florida have identified specific gut bacteria that promoted protein misfolding throughout the body, as well as others that were protective.
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Tau protein in Alzheimer's disease

Study identifies four Alzheimer’s subtypes

May 5, 2021
By John Fox
An international collaborative study led by scientists at Sweden’s Lund University has classified Alzheimer’s disease into four distinct subtypes, which has important implications for the management of the progressive neurodegenerative disease, the authors reported in the April 29, 2021, edition of Nature Medicine.
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Gene editing illustration

Prime, base editing are "finer scalpels" in dystrophy

May 5, 2021
By Nuala Moran
New genome editing techniques have opened up the number of potential mutations that could be addressed in the inherited muscle wasting disorder Duchenne muscular dystrophy, while also reducing the probability of inducing off target effects.
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