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SEC23A gene

Known as: SEC23, S. CEREVISIAE, HOMOLOG OF, A, SEC23A, Sec23 homolog A, coat complex II component 
National Institutes of Health

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Related topics

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SEC23B gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Amentoflavone induces cell cycle arrest, apoptosis, and autophagy in BV-2 cells.
Previous studies have shown that amentoflavone (AF) elicits anti-inflammatory and neuroprotective effects. To further investigate… 
2018
2018
Pull down assay for GTP-bound form of Sar1a reveals its activation during morphological differentiation.
2016
2016
Insulin sends SEC16A packing
Study reveals that a protein known for its role in ER–Golgi transport also controls GLUT4 trafficking in adipocytes. 
2016
2016
Pancreatic SEC 23 B deficiency is sufficient to explain the perinatal lethality of germline SEC 23 B deficiency in mice
In humans, loss of function mutations in SEC23B result in Congenital Dyserythropoietic Anemia type II (CDAII), a disease limited… 
2016
2016
The Biological Effects of Sec23a Knockdown in Human Oligometastatic Breast Cancer Cells In Vitro
2015
2015
SEC23A Functionally Compensates for SEC23B Deficiency in Mice
Congenital Dyserythropoietic Anemia type II (CDAII) is a disease of ineffective erythropoiesis characterized by moderate anemia… 
2014
2014
Endoplasmic reticulum stress reduces COPII vesicles formation and modifies Sec23a cycling at ERESsG. Amodio1, O. Moltedo1, S. Franceschelli1, P. Remondelli2 1Dipartimento di Farmacia, Univ. of…
2013
2013
Hrd1 participates in the regulation of collagen I synthesis in renal fibrosis
The production and accumulation of collagen-rich extracellular matrix are common hallmarks during the process of renal… 
2013
2013
The function of mammalian COPII components Sec23a and Sec23b
The Endoplasmic Reticulum (ER) is an important organelle for protein synthesis and is an early step in the secretory pathway of… 
2010
2010
Cranio-lenticulo-sutural dysplasia associated with defects in collagen secretion
Cranio-lenticulo-sutural dysplasia (CLSD) is a rare autosomal recessive syndrome manifesting with large and late-closing… 
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