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A magnifying glass, decorated with DNA, showing the face of a girl with a droopy mouth due to facial weakness.

Facial weakness: A dark matter detective story

Basic/Translational, Research
Elizabeth Engle, MD, has devoted her career to finding genetic and developmental causes for disorders of eye, eyelid, and facial movement. From common conditions like strabismus to very rare disorders, these conditions can impact a person’s appearance and impair social communication, making it hard to shift one’s eyes up, down, or sideways or adjust facial expressions. Each ... Read More about Facial weakness: A dark matter detective story
Tagged: genetics and genomics, neurology, neuroscience, ophthalmology
A cartoon brain being bathed in fluid, with researchers pointing out the Alzheimer's diagnostic markers in the fluid.

Another angle on Alzheimer’s: CSF, proteomics, and metabolic enzymes

Basic/Translational, Research
Currently there are no objective, easily assessed diagnostic markers for Alzheimer’s disease, and no good therapeutic options. Taking an agnostic approach, proteomics expert Hanno Steen, PhD, and neurobiologist Judith Steen, PhD, who share a lab at Boston Children’s Hospital, teamed up to analyze proteomics data from the cerebrospinal fluid (CSF) that bathes the brain, combining ... Read More about Another angle on Alzheimer’s: CSF, proteomics, and metabolic enzymes
Tagged: alzheimers disease, metabolism, neurology, neuroscience, proteomics
A body surrounded by blood cells

Could we make blood anywhere in the body?

Basic/Translational, Research
Our bodies make blood in a specialized niche — a “nursery” within our bone marrow that nurtures blood stem cells so they can replicate and make different kinds of blood cells. The lab of Leonard Zon, MD, has even shown how blood stem cells, once they settle in the niche, are “cuddled” by nearby cells. ... Read More about Could we make blood anywhere in the body?
Tagged: blood, blood disorder, hematology, stem cell transplant, stem cells
A vacuum cleaner trying to vacuum up RNA molecules.

A new cancer mechanism: Failed cellular housekeeping

Basic/Translational, Research
Cancer can stem from mutations in many different genes. New research from Boston Children’s Hospital and Dana-Farber Cancer Institute pinpoints a gene that, when mutated, causes cancer through a mechanism not before seen: Inability of cells to dispose of their trash, namely defective strands of RNA. This mechanism appears to cut across many different malignancies, ... Read More about A new cancer mechanism: Failed cellular housekeeping
Tagged: cancer, cellular and molecular medicine, genetics and genomics, oncology
Natural killer cells attacking a tumor.

An unexpected journey reveals a potent way to attack tumors

Basic/Translational, Research
Research on the effects of prenatal exposure to the Zika virus has yielded an unexpected dividend: a potentially promising way to trigger natural killer (NK) cells to fight cancer. NK cells are first-responder immune cells. When enough of their activating receptors are triggered, they mobilize to kill infected, stressed, or cancerous cells at an early ... Read More about An unexpected journey reveals a potent way to attack tumors
Tagged: cancer, cellular and molecular medicine, immunology, immunotherapy, zika virus
Sam and his family pose at a formal event about SSADH deficiency.

Conquering a rare metabolic condition: A family, a pediatrician, and two labs join forces

Basic/Translational, Research
As a newborn, Sam Hoffman never cried or made a sound. His mother, Carolyn, often had to wake him up to feed him. He missed many of his infant milestones. At one visit, his pediatrician tapped his leg and couldn’t get a reflex. A urine test found extremely high levels of 4-hydrobutyric acid or GHB ... Read More about Conquering a rare metabolic condition: A family, a pediatrician, and two labs join forces
Tagged: epilepsy, gene therapy, metabolism, neurology, neuroscience, rare disease, stem cells
An ionocyte under magnification.

Making ionocytes: A step toward cell or gene therapy for cystic fibrosis

Basic/Translational, Research
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators were a breakthrough for cystic fibrosis, improving the movement of chloride and water and moistening mucus secretions. But these drugs are expensive, don’t work in all patients with cystic fibrosis, and have side effects and interactions with other drugs. People who do respond to CFTR modulators must take ... Read More about Making ionocytes: A step toward cell or gene therapy for cystic fibrosis
Tagged: cell therapy, cystic fibrosis, gene therapy, pulmonology, stem cells
A young woman draws blood from her fingertip to test her blood sugar.

Study shows young adults don’t easily transition to self-care of diabetes

Basic/Translational, Research
Diabetes is challenging to manage at any age, but even more so for young adults who are handling the condition on their own for the first time. They need to transition from pediatric to adult care as smoothly as possible — but a recent study finds this isn’t happening. Research led by Katharine Garvey, MD, MPH, ... Read More about Study shows young adults don’t easily transition to self-care of diabetes
Tagged: diabetes, emergency medicine, endocrinology, research
Cartoon of two researchers lifting a large pancreatic tumor out of a box.

Going out of the box to tackle pancreatic cancer

Basic/Translational, Research
Pancreatic cancers are deadly and hard to treat, in part because they are so often detected at an advanced stage; overall five-year survival rates are about 11 percent. Two separate labs at Boston Children’s Hospital took out-of-the-box approaches to this difficult cancer, and both uncovered some very promising leads. Wiping out pancreatic tumors’ immune defense ... Read More about Going out of the box to tackle pancreatic cancer
Tagged: cancer, cellular and molecular medicine, drug development, endocrinology, immunotherapy, metabolism, vascular biology
A scientist at a microscope with a brain and a double helix over her shoulder.

Could gene therapy relieve post-hemorrhagic hydrocephalus?

Basic/Translational, Research
Premature infants, especially very low birthweight babies, are at risk for intraventricular hemorrhage. A frequent complication of these brain bleeds is hydrocephalus, an accumulation of cerebrospinal fluid (CSF) in the brain ventricles that can gravely disrupt brain development. If hydrocephalus develops, a child may need shunt operations throughout life to manage the fluid buildup. Could ... Read More about Could gene therapy relieve post-hemorrhagic hydrocephalus?
Tagged: blood, gene therapy, genetics and genomics, hydrocephalus, neuroscience, neurosurgery, newborn medicine, prematurity

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