Add BrightSurf on Google Email

Johns Hopkins Medicine


Marfan, a 'look-alike' disorder, or neither?

Researchers developed lists of physical features to aid in early detection of Marfan and Loeys-Dietz syndromes, which can be life-threatening if left untreated. These lists are reliable without imaging tests and can help doctors spot the disorders during a physical exam.

SourceJohns Hopkins Medicine·JournalJournal of Bone and Joint Surgery·DateAug 4, 2010

Double-teaming a whole-genome hunt

Scientists combined new and classic approaches to identify a single genetic mutation causing metachondromatosis, a disorder characterized by bony growths. The study demonstrates the power of whole-genome sequencing technology in efficiently identifying genes responsible for Mendelian diseases.

SourceJohns Hopkins Medicine·JournalPLOS Genetics·DateJul 12, 2010

Genetic septet in control of blood platelet clotting

Researchers found a group of seven genes that significantly impact platelet clumping, offering new targets for developing diagnostic tests and treatments for arterial disease. The study used data from two large studies to identify the genetic factors behind blood clotting, providing insights into promoting healing and stalling disease ...

SourceJohns Hopkins Medicine·JournalNature Genetics·DateJun 22, 2010

Fly cells flock together, follow the light

Researchers at Johns Hopkins Medicine used a laser beam to activate a protein that makes a cluster of fruit fly cells behave like a school of fish, following the lead of one stimulated with light. This study holds potential importance for understanding embryonic development and tumor metastasis.

SourceJohns Hopkins Medicine·JournalNature Cell Biology·DateJun 18, 2010

Improving recovery from spinal cord injury

A team of researchers at Johns Hopkins University School of Medicine has shown that treating injured rat spinal cords with the enzyme sialidase improves nerve regrowth, motor recovery, and nervous system function. The treatment also showed improvements in blood pressure control and increased number of sprouted nerve ends.

SourceJohns Hopkins Medicine·JournalProceedings of the National Academy of Sciences·DateJun 9, 2010

Children who lose a parent to suicide more likely to die the same way

A study led by Johns Hopkins Children's Center found that children who lose a parent to suicide are three times more likely to commit suicide than those with living parents. The researchers also found that these children are nearly twice as likely to be hospitalized for depression and have an increased risk of committing violent crimes.

SourceJohns Hopkins Medicine·JournalJournal of the American Academy of Child & Adolescent Psychiatry·DateApr 21, 2010

STI, HIV counseling inadequate in male teens

A recent study by Johns Hopkins Medicine found that most sexually active male teens receive inadequate HIV and STI counseling during doctor visits, even among those with high-risk behaviors. The study highlights the need for better counseling to minimize risky behaviors.

SourceJohns Hopkins Medicine·JournalJournal of Adolescent Health·DateApr 13, 2010

Donor kidneys from hepatitis C patients needlessly denied to patients with that infection

A Johns Hopkins study found that more than half of donor kidneys infected with hepatitis C are discarded, despite the need among hepatitis C patients who may die waiting for an infection-free organ. The study suggests that using hepatitis C-positive kidneys could help those with hepatitis C and expand the organ supply.

SourceJohns Hopkins Medicine·JournalAmerican Journal of Transplantation·DateApr 1, 2010

Understanding night blindness and calcium

Johns Hopkins researchers discovered that a tail module in a calcium channel protein controls its sensitivity to calcium, potentially leading to neurodegenerative diseases. This finding has implications for conditions like schizophrenia, Alzheimer's, Parkinson's, and Huntington's.

SourceJohns Hopkins Medicine·JournalNature·DateApr 1, 2010

Causes found for stiff skin conditions

A study by Johns Hopkins Medicine reveals that a rare inherited disorder called stiff skin syndrome shares genetic similarities with the debilitating condition scleroderma, affecting about one in 5,000 people. The findings suggest a potential treatment strategy involving the protein fibrillin-1 and its role in regulating TGFbeta activity.

SourceJohns Hopkins Medicine·JournalScience Translational Medicine·DateMar 19, 2010