CC Applegate, MA Lane - World journal of gastrointestinal …, 2015 - ncbi.nlm.nih.gov
Vitamin A and its derivatives, retinoids, have been widely studied for their use as cancer chemotherapeutic agents. With respect to colorectal cancer (CRC), several critical mutations …
P Nighot, T Ma - Tissue Barriers, 2016 - Taylor & Francis
Autophagy is a cell survival mechanism by which bulk cytoplasmic material, including soluble macromolecules and organelles, is targeted for lysosomal degradation. The role of …
LV Albrecht, MH Bui… - Proceedings of the …, 2019 - National Acad Sciences
The nutrient-sensing metabolite S-adenosylmethionine (SAM) controls one-carbon metabolism by donating methyl groups to biochemical building blocks, DNA, RNA, and …
Z Li, Y Wang, M Zhang, P Xu, H Huang, D Wu… - Journal of Biological …, 2012 - ASBMB
The Motin family proteins can regulate cell polarity, cell mobility, and proliferation during embryonic development by controlling distinct signaling pathways. In this study, we …
D Kravtsov, A Mashukova, R Forteza… - American Journal …, 2014 - journals.physiology.org
Microvillus inclusion disease (MVID) is an autosomal recessive condition resulting in intractable secretory diarrhea in newborns due to loss-of-function mutations in myosin Vb …
R Yu, Z Cui, M Li, Y Yang, J Zhong - PloS one, 2014 - journals.plos.org
The high expression of PACAP (pituitary adenylate cyclase-activating polypeptide)- preferring receptor PAC1 is associated with nerve injury and tumors. Our previous report (Yu …
J Blackburn, A Ohazama, K Kawasaki… - Developmental …, 2012 - Elsevier
Thickening and the subsequent invagination of the epithelium are an important initial step in ectodermal organ development. Ikkα has been shown to play a critical role in controlling …
Biological information processing in living systems like cells, tissues and organs critically depends on the physical interactions of molecular signaling components in time and space …
A Ameen, PJ Salas - 2014 - journals.physiology.org
Microvillus Inclusion Disease (MVID) is an autosomal recessive condition resulting in intractable 27 secretory diarrhea in newborns due to loss-of-function mutations in myosin Vb …