X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
pfic (47) 47
humans (36) 36
progressive familial intrahepatic cholestasis (26) 26
index medicus (23) 23
gastroenterology & hepatology (21) 21
cholestasis (20) 20
familial intrahepatic cholestasis (18) 18
bric (16) 16
male (15) 15
salt export pump (14) 14
female (13) 13
abcb11 (12) 12
atp-binding cassette transporters - genetics (12) 12
pediatrics (12) 12
gastroenterology and hepatology (11) 11
hereditary cholestasis (11) 11
liver (11) 11
animals (10) 10
atp binding cassette subfamily b member 11 (10) 10
bsep (10) 10
children (10) 10
infant (10) 10
liver transplantation (10) 10
liver-transplantation (10) 10
mutation (10) 10
benign recurrent intrahepatic cholestasis (9) 9
child (9) 9
child, preschool (9) 9
cholestasis, intrahepatic - genetics (9) 9
genetic aspects (9) 9
liver - metabolism (9) 9
pruritus (9) 9
bile (8) 8
cholestasis, intrahepatic - surgery (8) 8
abcb4 (7) 7
adenosine triphosphatases - genetics (7) 7
adolescent (7) 7
atp8b1 (7) 7
bile acids (7) 7
jaundice, obstructive (7) 7
mutations (7) 7
surgery (7) 7
bile acids and salts - metabolism (6) 6
biliary atresia (6) 6
biliary diversion (6) 6
byler disease (6) 6
cholestasis, intrahepatic - diagnosis (6) 6
cholestasis, intrahepatic - metabolism (6) 6
disease (6) 6
pfic, progressive familial intrahepatic cholestasis (6) 6
alagille syndrome (5) 5
article (5) 5
atp binding cassette transporter, sub-family b - genetics (5) 5
atp-binding cassette transporters - metabolism (5) 5
bile salt export pump (5) 5
bsep, bile salt export pump (5) 5
cholestasis, intrahepatic - complications (5) 5
deficiency (5) 5
diagnosis (5) 5
disease progression (5) 5
fic1 (5) 5
icp, intrahepatic cholestasis of pregnancy (5) 5
mdr3 (5) 5
mdr3 gene (5) 5
pathology (5) 5
transplantation of organs, tissues, etc (5) 5
transporter (5) 5
treatment outcome (5) 5
udca, ursodeoxycholic acid (5) 5
2 forms (4) 4
alagille-syndrome (4) 4
cholestasis - genetics (4) 4
cholestasis, intrahepatic - physiopathology (4) 4
endocrinology & metabolism (4) 4
estate tax (4) 4
farnesoid-x-receptor (4) 4
gallbladder - surgery (4) 4
hepatocytes - metabolism (4) 4
infant, newborn (4) 4
p-glycoprotein (4) 4
pregnancy (4) 4
recurrence (4) 4
retrospective studies (4) 4
taxation (4) 4
abc transporter (3) 3
adult (3) 3
analysis (3) 3
associated builders and contractors (3) 3
associated general contractors (3) 3
atp binding cassette transporter, sub-family b - deficiency (3) 3
biliary tract surgical procedures - methods (3) 3
biochemistry & molecular biology (3) 3
biopsy (3) 3
bylers-disease (3) 3
canalicular membrane (3) 3
care and treatment (3) 3
cell biology (3) 3
chamber of commerce of the u.s (3) 3
cholestasis, intrahepatic - etiology (3) 3
cholestasis, intrahepatic - therapy (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal of Hepatology, ISSN 0168-8278, 2012, Volume 58, Issue 1, pp. 155 - 168
Summary Bile acid (BA) transporters are critical for maintenance of the enterohepatic BA circulation where BAs exert their multiple physiological functions... 
Gastroenterology and Hepatology | Gallstones | Liver cancer | Bile acids | Fatty liver disease | Cholestasis | Liver regeneration | RAT-LIVER | SALT EXPORT PUMP | GROWTH-FACTOR 19 | ORGANIC ANION TRANSPORTERS | 90-PERCENT PARTIAL-HEPATECTOMY | URSODEOXYCHOLIC ACID | PRIMARY BILIARY-CIRRHOSIS | FARNESOID-X-RECEPTOR | GASTROENTEROLOGY & HEPATOLOGY | PHOSPHOLIPID-ASSOCIATED CHOLELITHIASIS | FAMILIAL INTRAHEPATIC CHOLESTASIS | Animals | Carrier Proteins - metabolism | Cholestasis - metabolism | Membrane Glycoproteins - metabolism | Humans | Liver - metabolism | Bile Acids and Salts - metabolism | Liver Diseases - metabolism | Liver Regeneration - physiology | Receptors, Cytoplasmic and Nuclear - metabolism | Drug resistance in microorganisms | Corticosteroids | Glucagon | Calcifediol | Ursodiol | Deoxycholic acid | Epidermal growth factor | Vitamin D | Physiological aspects | Fibroblast growth factors | Alfacalcidol | IBABP (FABP6, ILBP), intestinal bile acid-binding protein, fatty acid-binding protein 6 | PFIC, progressive familial intrahepatic cholestasis | TNFα, tumor necrosis factor α | 3 (human) | SRC2, p160 steroid receptor coactivator | NAFLD, non-alcoholic fatty liver disease | BA, bile acid | bile acid receptor | 8, cholesterol efflux pump, ATP-binding cassette, subfamily G, member 5 | UDCA, ursodeoxycholic acid | LRH-1 (NR5A2), liver receptor homolog-1 | LCA, lithocholic acid | LXRα (NR1H3), liver X receptor alpha | PPARγ (NR1C3), peroxisome proliferator-activated receptor gamma | OSTαβ, organic solute transporter alpha | ABCG5 | AMPK, AMP activated protein kinase | NASH, non-alcoholic steatohepatitis | SHP (NR0B2), short heterodimer partner | OATP1A2 (SLCO1A2, OATP1, OATP-A, SLC21A3), solute carrier organic anion transporter family, member 1A2 | EGFR, epidermal growth factor receptor | IL6, interleukin 6 | TGR5, G protein-coupled bile acid receptor | PH, partial hepatectomy | AE2, anion exchanger 2 | PSC, primary sclerosing cholangitis | OATP1B1 (SLCO1B1, OATP2, OATP-C, SLC21A6), solute carrier organic anion transporter family, member 1B1 | RARα (NR1B1), retinoic acid receptor alpha | GLP-1, glucagon like peptide 1 | VDR (NR1I1), vitamin D receptor. Please note that for the convenience of better readability and clarity, abbreviations for transporters and nuclear receptors were capitalized throughout this article when symbols were identical for human and rodents | MRP2 (ABCC2), multidrug resistance-associated protein 2, ATP-binding cassette, subfamily C, member 2 | NTCP (SLC10A1), sodium | CAR (NR1I3), constitutive androstane receptor | taurocholate cotransporting polypeptide, solute carrier family 10, member 1 | PPARα (NR1C1), peroxisome proliferator-activated receptor alpha | Review | GR (NR3C1), glucocorticoid receptor | Bile acids, Cholestasis, Fatty liver disease, Gallstones, Liver regeneration, Liver cancer | 19, fibroblast growth factor 15 | Mdr2 | ICP, intrahepatic cholestasis of pregnancy | BRIC, benign recurrent intrahepatic cholestasis | OATP1B3 (SLCO1B3, OATP8, SLC21A8), solute carrier organic anion transporter family, member 1B3 | MRP3 (ABCC3), multidrug resistance-associated protein 3, ATP-binding cassette, subfamily C, member 3 | beta | MDR1 (ABCB1), p-glycoprotein, ATP-binding cassette, subfamily B, member 1 | norUDCA, norursodeoxycholic acid | 6-ECDCA, 6-ethylchenodeoxycholic acid | FXR (NR1H4), farnesoid X receptor | BCRP (ABCG2), breast cancer resistance protein, ATP-binding cassette, subfamily G, member 2 | HNF4α (NR2A1), hepatocyte nuclear factor 4 alpha | PBC, primary biliary cirrhosis | MDR3 (ABCB4), multidrug resistance protein 2 (rodents) | HNF1α, hepatocyte nuclear factor 1 alpha | NR, nuclear receptor | FGF15 | RXRα (NR2B1), retinoid X receptor alpha | PXR (NR1I2), pregnane X receptor | BSEP (ABCB11), bile salt export pump | HCC, hepatocellular carcinoma | MRP4 (ABCC4), multidrug resistance-associated protein 4, ATP-binding cassette, subfamily C, member 4 | TPN, total parenteral nutrition
Journal Article
Journal of Hepatology, ISSN 0168-8278, 07/2019, Volume 71, Issue 1, pp. 153 - 162
Progressive familial intrahepatic cholestasis type 3 (PFIC3), for which there are limited therapeutic options, often leads to end-stage liver disease before... 
Adeno-associated virus | Progressive familial intrahepatic cholestasis | MDR2 | ABCB4 | AAV | PFIC type 3 | PFIC3 | Correction cholestatic phenotype | MDR3 | AAV8 | Gene therapy | HOMOZYGOUS DISRUPTION | IMMUNE-RESPONSE | HEPATOCYTES | ADENOASSOCIATED VIRUS | MDR2 P-GLYCOPROTEIN | BILIARY DIVERSION | IN-VIVO | MOUSE MODEL | DISEASE | GASTROENTEROLOGY & HEPATOLOGY | BILE
Journal Article
Journal Article
European Journal of Pediatrics, ISSN 0340-6199, 8/2018, Volume 177, Issue 8, pp. 1261 - 1269