WVU and citizen scientists go fishing for answers on blotchy bass syndrome
West Virginia University researchers will have a chance to better understand a condition affecting bass to an unknown extent with data ...
West Virginia University researchers will have a chance to better understand a condition affecting bass to an unknown extent with data ...
In Rett syndrome, a genetic condition affecting girls almost exclusively, mutations in the MECP2 gene cause a regression of language ...
Using an innovative microscopy method, scientists at The Picower Institute for Learning and Memory at MIT observed how newborn neurons ...
MINNEAPOLIS – Stiff person syndrome spectrum disorders are rare autoimmune and neurological disorders that most often cause muscle stiffness and ...
4 July 2022: The world’s first IVF baby, Louise Brown born in England in 1978, was conceived from a naturally ...
Myotonic dystrophy type 1 (DM1) is the most common form of muscular dystrophy, characterized by progressive muscle wasting and weakness ...
DURHAM, NC – A single gene that was previously found to be the driving force in a rare syndrome linked ...
Lamivudine, a commonly-used antiretroviral drug for treating HIV, improves cognition in a mouse model of Down syndrome, according to the ...
June 27th, 2022. Researchers from the Cancer Epigenetics group led by Dr. Manel Esteller at the Josep Carreras Leukaemia Research ...
FOR IMMEDIATE RELEASE A common hormone disorder among women of reproductive age has been linked to an increased risk of ...
Dr. Jacqueline Harris, a pediatric neurologist and director of Kennedy Krieger’s Epigenetics Clinic, received a $125,000 grant from the Kabuki ...
European Society of Endocrinology Starling House, 1600 Bristol Parkway North, Bristol, BS34 8YU, UK Tel +44 1454 642247 [email protected] www.ese-hormones.org ...
Researchers at Eötvös Loránd University (ELTE) have created a new disease model that has contributed to a better understanding of Bloom ...
CHAPEL HILL, NC – UNC School of Medicine Scientists have shown for the first time that postnatal gene therapy may ...
An important link has been found between the intellectual disability experienced by children with the rare disease Joubert Syndrome (JS) ...
Bethesda, Maryland (April 26, 2022) – Gastrointestinal hamartomatous polyposis syndromes are rare, hereditary disorders associated with an increased risk of ...
About The Study: This study of surveillance data from the Vaccine Safety Datalink that included 15.1 million doses of COVID-19 ...
A new study found that females with Long COVID-19 syndrome were more symptomatic than males. Females were statistically significantly more ...
A new study found that older children and those with high blood markers for inflammation (ferritin) were at highest risk ...
EMBARGOED FOR RELEASE UNTIL 4 P.M. ET, WEDNESDAY, MARCH 30, 2022 MINNEAPOLIS – According to a new preliminary study, children ...
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