Results 151 to 160 of about 2,570 (163)
Some of the next articles are maybe not open access.
Biochemistry, 2011
Human membrane primary amine oxidase (hAOC3; also known as vascular adhesion protein-1, VAP-1) is expressed upon inflammation in most tissues, where its enzymatic activity plays a crucial role in leukocyte trafficking. We have determined two new structures of a soluble, proteolytically cleaved form of hAOC3 (sAOC3), which was extracted from human ...
Elovaara, Heli +10 more
openaire +3 more sources
Human membrane primary amine oxidase (hAOC3; also known as vascular adhesion protein-1, VAP-1) is expressed upon inflammation in most tissues, where its enzymatic activity plays a crucial role in leukocyte trafficking. We have determined two new structures of a soluble, proteolytically cleaved form of hAOC3 (sAOC3), which was extracted from human ...
Elovaara, Heli +10 more
openaire +3 more sources
Histamine oxidation in mouse adipose tissue is controlled by the AOC3 gene-encoded amine oxidase
Inflammation Research, 2009Histaminergic status can modify adipose tissue (AT) development: histamine-free mice exhibit visceral obesity, and treatments with H3-antagonists reduce body weight gain. However, direct histamine effects on AT remain poorly documented: it has been observed that histamine stimulates lipolysis in rodent adipocytes when its oxidation by amine oxidases ...
Iffiú-Soltész, Zsuzsa +4 more
exaly +4 more sources
Molecular Carcinogenesis
ABSTRACT Gastrointestinal stromal tumor (GIST) frequently develops resistance to imatinib (IM). This study identifies AOC3 downregulation as a critical contributor to IM resistance. Analyzing clinical samples and IM‐sensitive/resistant GIST cell lines, we found AOC3 significantly decreased in resistant states.
Zhiyuan Guo +4 more
exaly +3 more sources
ABSTRACT Gastrointestinal stromal tumor (GIST) frequently develops resistance to imatinib (IM). This study identifies AOC3 downregulation as a critical contributor to IM resistance. Analyzing clinical samples and IM‐sensitive/resistant GIST cell lines, we found AOC3 significantly decreased in resistant states.
Zhiyuan Guo +4 more
exaly +3 more sources
Journal of Neural Transmission, 2007
Substrates of semicarbazide-sensitive amine oxidases (SSAO) stimulate glucose transport in adipocytes. To definitively demonstrate the involvement of SSAO in this insulin-like effect, glucose transport has been studied in fat cells from mice with a targeted deletion of AOC3, a gene encoding a SSAO called vascular adhesion protein-1.
S, Bour +6 more
openaire +2 more sources
Substrates of semicarbazide-sensitive amine oxidases (SSAO) stimulate glucose transport in adipocytes. To definitively demonstrate the involvement of SSAO in this insulin-like effect, glucose transport has been studied in fat cells from mice with a targeted deletion of AOC3, a gene encoding a SSAO called vascular adhesion protein-1.
S, Bour +6 more
openaire +2 more sources
Journal of Physiology and Biochemistry, 2012
Semicarbazide-sensitive amine oxidase (SSAO) is a transmembrane enzyme that metabolizes primary amines from endogenous or dietary origin. SSAO is highly expressed in adipose, smooth muscle and endothelial cells. In each of these cell types, SSAO is implicated in different biological functions, such as glucose transport activation, extracellular matrix ...
Grès, Sandra +3 more
openaire +2 more sources
Semicarbazide-sensitive amine oxidase (SSAO) is a transmembrane enzyme that metabolizes primary amines from endogenous or dietary origin. SSAO is highly expressed in adipose, smooth muscle and endothelial cells. In each of these cell types, SSAO is implicated in different biological functions, such as glucose transport activation, extracellular matrix ...
Grès, Sandra +3 more
openaire +2 more sources
The above is a plain language summary of a publication developed with the authors of the original content which is published in a peer-reviewed scientific journal.
Dong Nguyen, Quan +5 more
openaire +1 more source
Dong Nguyen, Quan +5 more
openaire +1 more source
The function of proto-adipokine AOC3 during adipose tissue dysfunction in metabolic diseases
2022Topel Batarlar, Hande +5 more
openaire +1 more source
Inhibition of AOC3 protects against islet cell death caused by glucolipotoxicity
Diabetologie und StoffwechselLisa Naundorf +3 more
openaire +1 more source

