Dissecting primary and secondary senescence to enable new senotherapeutic strategies
TD Admasu, MJ Rae, A Stolzing - Ageing Research Reviews, 2021 - Elsevier
Cellular senescence is a state of stable cell cycle arrest that is known to be elicited in
response to different stresses or forms of damage. Senescence limits the replication of old …
response to different stresses or forms of damage. Senescence limits the replication of old …
Congenital hydrocephalus: a review of recent advances in genetic etiology and molecular mechanisms
XY Liu, X Song, M Czosnyka, C Robba… - Military Medical …, 2024 - Springer
The global prevalence rate for congenital hydrocephalus (CH) is approximately one out of
every five hundred births with multifaceted predisposing factors at play. Genetic influences …
every five hundred births with multifaceted predisposing factors at play. Genetic influences …
Origin of cytoplasmic GDP-fucose determines its contribution to glycosylation reactions
Biosynthesis of macromolecules requires precursors such as sugars or amino acids,
originating from exogenous/dietary sources, reutilization/salvage of degraded molecules, or …
originating from exogenous/dietary sources, reutilization/salvage of degraded molecules, or …
Dietary diversification and specialization in neotropical bats facilitated by early molecular evolution
JHT Potter, KTJ Davies, LR Yohe… - Molecular Biology …, 2021 - academic.oup.com
Dietary adaptation is a major feature of phenotypic and ecological diversification, yet the
genetic basis of dietary shifts is poorly understood. Among mammals, Neotropical leaf …
genetic basis of dietary shifts is poorly understood. Among mammals, Neotropical leaf …
FUT10 and FUT11 are protein O-fucosyltransferases that modify protein EMI domains
O-Fucosylation plays crucial roles in various essential biological events. Alongside the well-
established O-fucosylation of epidermal growth factor-like repeats by protein O …
established O-fucosylation of epidermal growth factor-like repeats by protein O …
O-fucosylation of thrombospondin type 1 repeats is essential for ECM remodeling and signaling during bone development
S Neupane, SJ Berardinelli, DC Cameron, RC Grady… - Matrix Biology, 2022 - Elsevier
Many extracellular matrix (ECM) associated proteins that influence ECM properties have
Thrombospondin type 1 repeats (TSRs) which are modified with O-linked fucose. The O …
Thrombospondin type 1 repeats (TSRs) which are modified with O-linked fucose. The O …
O-Fucosylation of ADAMTSL2 is required for secretion and is impacted by geleophysic dysplasia-causing mutations
A Zhang, SJ Berardinelli, C Leonhard-Melief… - Journal of Biological …, 2020 - ASBMB
ADAMTSL2 mutations cause an autosomal recessive connective tissue disorder,
geleophysic dysplasia 1 (GPHYSD1), which is characterized by short stature, small hands …
geleophysic dysplasia 1 (GPHYSD1), which is characterized by short stature, small hands …
Passing the post: roles of posttranslational modifications in the form and function of extracellular matrix
JC Adams - American Journal of Physiology-Cell …, 2023 - journals.physiology.org
The extracellular matrix (ECM) is central to the physiology of animal tissues, through its
multifaceted roles in tissue structure, mechanical properties, and cell interactions, and by its …
multifaceted roles in tissue structure, mechanical properties, and cell interactions, and by its …
CEBPB regulates the migration, invasion and EMT of breast cancer cells by inhibiting THBS2 expression and O-fucosylation
L Qi, B Sun, B Yang, S Lu - Human Molecular Genetics, 2023 - academic.oup.com
Breast cancer (bc) is the second most common type of human malignancies with highest
morbidity and mortality in the female population. Therefore, it is essential to develop novel …
morbidity and mortality in the female population. Therefore, it is essential to develop novel …
Hydrocephalus in mouse B3glct mutants is likely caused by defects in multiple B3GLCT substrates in ependymal cells and subcommissural organ
Peters plus syndrome, characterized by defects in eye and skeletal development with
isolated cases of ventriculomegaly/hydrocephalus, is caused by mutations in the β3 …
isolated cases of ventriculomegaly/hydrocephalus, is caused by mutations in the β3 …