Blog Archives

Les individus de peau foncée aux cheveux blonds naturels – En génétique, tout est possible

8 août 2019 – Les cheveux blonds sont un phénotype humain plutôt rare, présent presque exclusivement en Europe et en Océanie. La pigmentation humaine varie considérablement au sein des populations et entre les populations et dépend de l’exposition aux rayons ultraviolets (UV) ainsi que du type et de la quantité de mélanine produit dans les mélanocytes et les kératinocytes.

Read more ›

Tags : , , , , , , , , , , , , , , , , , ,

thasso: conditions

thasso: tweets

thasso poste: magasin

View my Flipboard Magazine.

thasso: catégories

thasso: archives

thasso: chat simple

Vous devez être un utilisateur inscrit pour participer à ce tchat.

  • Scientists find link between genes and ability to exercise février 26, 2020
    A team of researchers have discovered a genetic mutation that reduces a patient's ability to exercise efficiently.
  • ALS mystery illuminated by blue light février 26, 2020
    A joint research group in Japan has succeeded in reproducing key ALS symptoms in a small tropical fish by remotely controlling a disease-associated protein molecule using light illumination.
  • Researchers identify novel anti-aging targets février 26, 2020
    A recent study published in Nature has reported two conserved epigenetic regulators as novel anti-aging targets. The research, by scientists from Dr. Cai Shiqing's Lab at the Center for Excellence in Brain Science and Intelligence Technology, Institute of Neuroscience of the Chinese Academy of Sciences (CAS), and Dr. Jiang Lubing's team at Institut Pasteur, Shanghai […]
  • KAT6A syndrome: advances on the genetic bases and clinical picture of a rare disease février 26, 2020
    A research team has described five new cases of a rare disease known as KAT6A syndrome, of which there are only 80 dominant cases worldwide. This neurological and developmental disorder, caused by alterations in the lysine acetyltransferase 6A gene (KAT6A), involves intellectual disability, language impairment, low muscle tone, cardiovascular malformation and eye defects, among other […]
  • Researchers outline centralized genetic testing model février 26, 2020
    The Roberts Individualized Medical Genetics Center (RIMGC) at Children's Hospital of Philadelphia (CHOP) launched in 2014 as a first-of-its-kind system to help families navigate the complex process of genetic and genomic testing and standardize how genetic testing is performed across different clinical disciplines.
Top