Functions of the SNAI family in chondrocyte‐to‐osteocyte development

E Razmara, A Bitaraf, B Karimi… - Annals of the New York …, 2021 - Wiley Online Library
Different cellular mechanisms contribute to osteocyte development. And while critical roles
for members of the zinc finger protein SNAI family (SNAIs) have been discussed in cancer …

WRN promotes bone development and growth by unwinding SHOX-G-quadruplexes via its helicase activity in Werner Syndrome

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 …

Emergence of a left-right symmetric body plan in vertebrate embryos.

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 …

Acute dietary methionine restriction highlights sensitivity of neocortex development to metabolic variations

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 …

Role of one-carbon metabolism in neocortex development

S Saha - 2024 - theses.hal.science
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 …

Elucidation of the Molecular Mechanisms of Werner Syndrome with Stem Cell Models

Y Tian - 2021 - search.proquest.com
Werner Syndrome (WS) is an autosomal recessive disease which is characterized by
accelerated aging phenotypes, such as short stature, dyslipidemia, the loss of subcutaneous …