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anti-Human ABCG8 Antikörper:
anti-Mouse (Murine) ABCG8 Antikörper:
anti-Rat (Rattus) ABCG8 Antikörper:
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Human Polyclonal ABCG8 Primary Antibody für ICC, IF - ABIN152894
Mathur, Watt, Field: Regulation of intestinal NPC1L1 expression by dietary fish oil and docosahexaenoic acid. in Journal of lipid research 2007
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Human Monoclonal ABCG8 Primary Antibody für ICC, IF - ABIN4277252
Graf, Yu, Li, Gerard, Tuma, Cohen, Hobbs: ABCG5 and ABCG8 are obligate heterodimers for protein trafficking and biliary cholesterol excretion. in The Journal of biological chemistry 2003
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Polyclonal ABCG8 Primary Antibody für WB - ABIN540800
Garcia, Wilund, Arca, Zuliani, Fellin, Maioli, Calandra, Bertolini, Cossu, Grishin, Barnes, Cohen, Hobbs: Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein. in Science (New York, N.Y.) 2001
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Human Polyclonal ABCG8 Primary Antibody für WB - ABIN152887
Lu, Lee, Hazard, Brooks-Wilson, Hidaka, Kojima, Ose, Stalenhoef, Mietinnen, Bjorkhem, Bruckert, Pandya, Brewer, Salen, Dean, Srivastava, Patel: Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively. in American journal of human genetics 2001
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Human Polyclonal ABCG8 Primary Antibody für WB - ABIN438154
Maqdasy, El Hajjaji, Baptissart, Viennois, Oumeddour, Brugnon, Trousson, Tauveron, Volle, Lobaccaro, Baron: Identification of the Functions of Liver X Receptor-β in Sertoli Cells Using a Targeted Expression-Rescue Model. in Endocrinology 2015
Human Polyclonal ABCG8 Primary Antibody für ICC, IF - ABIN4277253
Ahn, Jang, Jun, Lee, Shin: Expression of liver X receptor correlates with intrahepatic inflammation and fibrosis in patients with nonalcoholic fatty liver disease. in Digestive diseases and sciences 2014
we identified a novel mutation in the ABCG8 gene, which in the homozygous form was associated with generalized xanthomatosis, and in the heterozygous form was associated with isolated xanthelasmas
Case Reports: compound heterozygous for nonsense mutations in ABCG8 responsible for sitosterolemia.
ABCG8 genetic variants may have role in the development of cholelithiasis in patients with Gaucher disease type 1.
Genetic polymorphism within the ABCG8 gene is a risk factor for diabetes.
crystallization in lipid bilayers to determine the X-ray structure of human G5G8 in a nucleotide-free state at 3.9 A resolution, generating the first atomic model of an ABC (zeige ABCB6 Antikörper) sterol transporter
A polymorphism of the sterol transporter ABCG8 has been associated with the prevalence of end-stage renal disease
Mutation in ABCG8 is associated with sitosterolaemia.
ATP-binding cassette (ABC (zeige ABCB6 Antikörper)) transporters G5 (ABCG5 (zeige ABCG5 Antikörper)) and G8 (ABCG8) form an obligate heterodimer that limits intestinal absorption and facilitates biliary secretion of cholesterol and phytosterols.
ABCG5 (zeige ABCG5 Antikörper)/8 variants are associated with susceptibility to coronary heart disease.
Sitosterolemia is caused by a genetic defect of sterolins (ABCG5 (zeige ABCG5 Antikörper)/ABCG8) mapped to the STSL (zeige ABCG5 Antikörper) locus. Polymorphic variations in STSL (zeige ABCG5 Antikörper) have been linked to lipid levels and gallstone disease
ABCG5 (zeige ABCG5 Antikörper) and ABCG8 mRNA levels were significantly increased in cholesterol group and less increased in myriocin group, relative to that in normal group.
The ABCG5 (zeige ABCG5 Antikörper)/G8-independent pathway plays an important role in regulating biliary cholesterol secretion, and gallstone formation, which works independently of the ABCG5 (zeige ABCG5 Antikörper)/G8 pathway.
ABCG5 (zeige ABCG5 Antikörper)/G8 mediate mass biliary cholesterol secretion but not from a reverse cholesterol transport-relevant pool.
AdGRP78 reduced expression of lipogenic genes and plasma triglycerides in the db/db (zeige LEPR Antikörper) strain. Both G5 and G8 protein levels increased as did total biliary cholesterol
The data demonstrate that Abcg5 (zeige ABCG5 Antikörper)/Abcg8 deficiency reduces the uptake and secretion of both dietary triacylglycerols and cholesterol by the intestine, suggesting a novel role for the sterol transporter in the formation and secretion of chylomicrons.
Sitosterolemia is caused by a genetic defect of sterolins (ABCG5 (zeige ABCG5 Antikörper)/ABCG8) mapped to the STSL locus. Polymorphic variations in STSL have been linked to lipid levels and gallstone disease
The absence of an ABCG5 (zeige ABCG5 Antikörper)/ABCG8 expression.
biliary cholesterol mass secretion under maximal bile salt-stimulated conditions is fully dependent on ABCG5 (zeige ABCG5 Antikörper)/G8
This study is the first to report such toxic effects of phytosterol accumulation in ABCG5 (zeige ABCG5 Antikörper)/G8 knockout mice.
handling of sterols by the intestine involves both G5G8 and ACAT2 but that an additional factor (possibly Niemann-Pick C1-like 1) may be key in determining absorption efficiency
high expression levels of both ATP-binding cassette sub-family G member 5 (zeige ABCG5 Antikörper) and 8 (ABCG5 (zeige ABCG5 Antikörper) and ABCG8) were present in bovine liver and digestive tract samples, and in the mammary gland
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. The protein encoded by this gene functions to exclude non-cholesterol sterol entry at the intestinal level, promote excretion of cholesterol and sterols into bile, and to facilitate transport of sterols back into the intestinal lumen. It is expressed in a tissue-specific manner in the liver, intestine, and gallbladder. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG5. Mutations in this gene may contribute to sterol accumulation and atherosclerosis, and have been observed in patients with sitosterolemia.
ATP-binding cassette, sub-family G (WHITE), member 8 (sterolin 2)
, sterolin 2
, ATP-binding cassette sub-family G member 8
, ATP-binding cassette, sub-family G (WHITE), member 8
, ATP-binding cassette sub-family G member 8-like
, ATP-binding cassette, subfamily G, member 8