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Study identifies a genetic mutation linked to high risk of lethal childhood leukemia

A genetic variant changing just one base pair of nucleotides greatly increases risk of a high-risk subtype of childhood acute lymphoblastic leukemia (ALL), according to a Northwestern Medicine study published in Nature Genetics. ....

Feng Yue , Emily Henderson , Jude Children Research Hospital , Roberth Lurie Comprehensive Cancer Center , Institute For Augmented Intelligence In Medicine , Northwestern University , Northwestern Medicine , Susan Burnham Professor , Molecular Medicine , Molecular Genetics , Cancer Genomics , Comprehensive Cancer Center , Jude Children , Research Hospital , Advanced Molecular Analysis , Augmented Intelligence , Acute Lymphoblastic Leukemia ,

Study finds minimal genetic difference between healthy sea stars and those with wasting syndrome

Healthy-looking ochre sea stars have minimal genetic difference from those displaying symptoms of sea star wasting syndrome, say Oregon State University researchers who examined whether genetic variation was the reason some animals went unaffected during an epidemic of the deadly disease. ....

United States , Oregon State University , Andrea Burton , Pacific Ocean , Sarah Gravem , Felipe Barreto , Emily Henderson , Baja California , Oregon State , Genetic Variation Study ,

Researchers identify genetic cause of rare interstitial lung disease in a young child

New research from Washington University School of Medicine in St. Louis has solved the medical mystery of why a 2-year-old child seemingly healthy at birth succumbed to an undiagnosed, rare illness. ....

Hubertc Moog , Stephenc Pak , Huiyan Winnie Huang , Stevenl Brody , Jennifera Wambach , Emily Henderson , Diseases Network , Washington University , Proceedings Of The National Academy Sciences , National Institutes Of Health , Washington University School Of Medicine , Baylor College Of Medicine , Washington University School , National Institutes , Undiagnosed Diseases Network , National Academy , Baylor College , Interstitial Lung Disease , Ung Disease ,

Oligodendrocytes may have a different role in the development of multiple sclerosis, study finds

An international team of researchers led by Karolinska Institutet in Sweden have discovered that a cell type in the central nervous system known as oligodendrocytes might have a different role in the development of multiple sclerosis (MS) than previously thought. ....

Mandy Meijer , Karolinska Institutet , Eneritz Agirre , Emily Henderson , Department Of Medical Biochemistry , Medical Biochemistry , Multiple Sclerosis , Central Nervous System , Nervous System ,

Low-cost test could open new avenues for earlier diagnosis, treatment of rare genetic disorders

A newly developed test to screen for three rare genetic disorders simultaneously in newborns was feasible, reliable and scalable, according to a new study. ....

United States , David Amor , David Godler , Chrissy Cimino , Prader Willi , Doris Hamilton Brown , Jaala Pulford , Emily Henderson , Journal Of The American Medical Association Network , Victorian Medical Research Acceleration Fund , Murdoch Children Research Institute , Murdoch Children , Research Institute , American Medical Association Network Open , Methylation Specific Quantitative Melt Analysis , Victorian State Government , Medical Research Acceleration Fund , Research Minister Jaala Pulford , Professor David Godler , Professor Godler , Angelman Syndrome , Hromosome 15 , Growth Hormone , Medical Research , Newborn Screening ,