Y Tian, W Wang, S Lautrup, H Zhao, X Li… - Nature …, 2022 - nature.com
Werner Syndrome (WS) is an autosomal recessive disorder characterized by premature aging due to mutations of the WRN gene. A classical sign in WS patients is short stature, but …
S Bardhan, N Bhargava, S Dighe, N Vats… - Current Topics in …, 2024 - europepmc.org
External bilateral symmetry is a prevalent feature in vertebrates, which emerges during early embryonic development. To begin with, vertebrate embryos are largely radially symmetric …
S Saha, C Debacq, C Audouard, T Jungas, P Dupre… - bioRxiv, 2024 - biorxiv.org
Methionine-an essential amino acid that has to be provided by nutrition-and its metabolite S- Adenosyl methionine (SAM) are indispensable for cell proliferation, stem cell maintenance …
The neocortex is unique for its evolutionary innovations such as developmental expansion and higher cognitive functions in mammals. This requires a proper coordination on the …
Werner Syndrome (WS) is an autosomal recessive disease which is characterized by accelerated aging phenotypes, such as short stature, dyslipidemia, the loss of subcutaneous …