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An athlete recovers from a sports injury.

Not just a physical thing: The psychology of sports injuries and recovery

Research
“Nobody plays sports expecting to get injured, but unfortunately, injuries are part of sports,” says Melissa Christino, MD. As a surgeon in the Sports Medicine Division at Boston Children’s Hospital, Christino helps athletes recover from sports injuries, some of which keep her patients on the sidelines for weeks or months at a time. Key takeaways ... Read More about Not just a physical thing: The psychology of sports injuries and recovery
Tagged: female athletes, mental health, orthopedics, sports behavioral health, sports injury, sports medicine
asthma genetics precision medicine duplimab

Trial for severe asthma targets a mutation common in children of color

Clinical, Research
Children and adults of color have higher rates of asthma than white people, as well as more hospitalizations and deaths. There are many reasons for this disparity, including more exposure to allergens and pollutants and differences in asthma care. One difference, however, is genetic. A mutation that causes severe, hard-to-treat asthma, in the gene ILR4, ... Read More about Trial for severe asthma targets a mutation common in children of color
Tagged: asthma, clinical trials, genetics and genomics, precision medicine
understanding interferon's role COVID-19

Unpacking the body’s interferon response to COVID-19

Basic/Translational, Research
Interferons are potent natural antivirals, rallying other parts of the immune system to defend against viruses. Some clinical trials have tested interferons as a treatment for COVID-19, but results have been mixed. And the science has been unclear about whether interferons are helpful or harmful. Key takeawayAn early, protective interferon response in the upper respiratory ... Read More about Unpacking the body’s interferon response to COVID-19
Tagged: cellular and molecular medicine, coronavirus, immunology, infectious diseases
MIS-C genetic variants concept

Why do some children get MIS-C after COVID-19? Some early clues

Clinical, Research
Several months into the COVID-19 pandemic, a small number of children began to develop a cluster of mysterious symptoms. These included rashes, red eyes, gastrointestinal symptoms and, most worrisome, heart problems. Why does this serious illness, now known as multisystem inflammatory disorder in children (MIS-C), strike some previously healthy children? And who is most at ... Read More about Why do some children get MIS-C after COVID-19? Some early clues
Tagged: coronavirus, genetics and genomics, immune disorders, immunology, infectious diseases, mis-c
home saliva test that detects COVID-19 variants

Rapid saliva test detects COVID-19 variants, at home or point of care

Research, Therapeutics/Diagnostics/Devices
COVID-19 tests are now widely available, including FDA-approved tests like BinaxNOW that people can do at home. But none of the home tests — or any hospital test — can distinguish between specific SARS-CoV-2 variants. Detecting and tracking variants, essential for public health efforts, requires complete nucleic acid sequencing of the virus. Currently, only specialized ... Read More about Rapid saliva test detects COVID-19 variants, at home or point of care
Tagged: coronavirus, diagnostics, infectious diseases
cancerous cell transformation concept

RNA-modifying protein offers a possible lead for treating aggressive cancers

Basic/Translational, Research
A protein that modifies RNAs, called METTL1, could be a target for treating some aggressive, difficult-to-treat cancers, suggests new research in Molecular Cell. The study provides evidence that blocking METTL1 curbs cancer cells’ ability to grow, selectively killing them, and the researchers believe it could be targeted with drugs. METTL1 and related proteins had previously ... Read More about RNA-modifying protein offers a possible lead for treating aggressive cancers
Tagged: cancer, drug development, genetics and genomics
an infant with spinal muscular atrophy receiving an oral medication (risdiplam)

Risdiplam improves motor function in infants with spinal muscular atrophy

Clinical, Research
Until recently, babies and children with spinal muscular atrophy (SMA) lacked any type of treatment capable of stopping the neuromuscular disease from progressing. In SMA, damaged motor neurons in the spinal cord fail to correctly send messages to the muscle cells. As a result, infants and children with SMA may not be able to hold ... Read More about Risdiplam improves motor function in infants with spinal muscular atrophy
Tagged: clinical trials, spinal muscular atrophy
an illustration of a baby bottle to suggest thickened feeds

Thickened feeds — but not acid-suppressing medications — help treat laryngomalacia in infants

Research
In laryngomalacia, the soft tissues of the larynx fall over the airway opening and partially block it, which can result in stridor, feeding difficulties, and other symptoms. Infants with this condition are frequently treated with acid-suppressing medications, based on the belief that gastroesophageal reflux might worsen the problem. However, there’s little evidence to support the ... Read More about Thickened feeds — but not acid-suppressing medications — help treat laryngomalacia in infants
Tagged: aerodigestive, dysphagia, reflux, research
COVID-19 nasal swab with different cell types in the nasopharynx

Why do some people get severe COVID-19? The nose may know

Basic/Translational, Research
The body’s first encounter with SARS-CoV-2, the virus behind COVID-19, happens in the nose and throat, or nasopharynx. A new study in the journal Cell suggests that the first responses in this battleground help determine who will develop severe disease and who will get through with mild or no illness. Building on work published last ... Read More about Why do some people get severe COVID-19? The nose may know
Tagged: coronavirus, genetics and genomics, immunology, infectious diseases
illustration of the genetics of joint disease - hip dysplasia and knee osteoarthritis

The surprisingly specific genetics of joint disease

Basic/Translational, Research
A new study provides unexpected insights into the biology of two common, heritable orthopedic conditions: developmental dysplasia of the hip (DDH) and knee osteoarthritis (OA). The findings, published July 6 in Nature Communications, show how a gene can have different effects in different parts of the body. They also raise the possibility of preventive measures ... Read More about The surprisingly specific genetics of joint disease
Tagged: epigenetics, genetics and genomics, hip dysplasia, orthopedics, personalized medicine, sports medicine

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