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Hepatology International, ISSN 1936-0533, 9/2017, Volume 11, Issue 5, pp. 409 - 411
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s12072-017-9823-0 
Medicine & Public Health | Colorectal Surgery | Hepatology | Surgery | PATHOGENESIS | SCLEROSIS | LIVER-DISEASE | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | VENOPATHY | Hypertension
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Journal of Gastroenterology, ISSN 0944-1174, 4/2013, Volume 48, Issue 4, pp. 526 - 534
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Journal of Human Genetics, ISSN 1434-5161, 05/2018, Volume 63, Issue 5, pp. 569 - 577
The bile salt export pump (BSEP) plays an important role in biliary secretion. Mutations in ABCB11, the gene encoding BSEP, induce progressive familial... 
GENE-MUTATIONS | LIVER-TRANSPLANTATION | SALT EXPORT PUMP | GENETICS & HEREDITY | PFIC2 | PATIENT | 4-PHENYLBUTYRATE THERAPY | TYPE-2 | DEFICIENCY | FAMILIAL INTRAHEPATIC CHOLESTASIS | CHILDREN
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Hepatology research : the official journal of the Japan Society of Hepatology, ISSN 1386-6346, 10/2009, Volume 39, Issue 10, p. 1015
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Hepatology Research, ISSN 1386-6346, 10/2009, Volume 39, Issue 10, pp. 1015 - 1015
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International Journal of Clinical Oncology, ISSN 1341-9625, 4/2013, Volume 18, Issue 2, pp. 293 - 304
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Cancer Science, ISSN 1347-9032, 05/2016, Volume 107, Issue 5, pp. 590 - 600
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Hepatology Research, ISSN 1386-6346, 2009, Volume 39, Issue 10, pp. 1015 - 1015
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Journal of Pediatrics, The, ISSN 0022-3476, 2014, Volume 164, Issue 5, pp. 1219 - 1227.e3
To examine the effects of 4-phenylbutyrate (4PB) therapy in a patient with progressive familial intrahepatic cholestasis type 2. A homozygous c.3692G>A... 
Pediatrics | TfR | Gamma-glutamyl transferase | Direct bilirubin | Aspartate aminotransaminase | Hemagglutinin | ALT | mRNA | UDCA | Alanine aminotransaminase | D-Bil | Ursodeoxycholic acid | Messenger RNA | T-Bil | cDNA | qPCR | WT | Adenosine triphosphate | G protein-coupled receptor | AST | Empty vector | BSEP | OTCD | P-gp | Quantitative polymerase chain reaction | 4PB | PFIC2 | 4-Phenylbutyrate | Wild type | Progressive familial intrahepatic cholestasis type 2 | Transferrin receptor | P-glycoprotein | Polymerase chain reaction | EV | Complementary DNA | GGT | Ornithine transcarbamylase deficiency | Glyceraldehyde-3-phosphate dehydrogenase | GPCR | HA | ATP | GAPDH | Bile salt export pump | PCR | Total bilirubin | TRANSPORT | SALT EXPORT PUMP | PEDIATRICS | MUTATIONS | EXPRESSION | DEFICIENCY | BILE | Liver Function Tests | Phenylbutyrates - therapeutic use | Cholestasis, Intrahepatic - genetics | Humans | Infant | Cholestasis, Intrahepatic - drug therapy | Genetic Markers | Homozygote | Point Mutation | ATP-Binding Cassette Transporters - genetics | ATP Binding Cassette Subfamily B Member 11 | Pruritus - drug therapy | Gastrointestinal Agents - therapeutic use | Female | Pruritus - etiology | Cholestasis, Intrahepatic - complications | Medical colleges | Care and treatment | Jaundice, Obstructive | Liver | Genetic aspects | Pruritus | Cholestasis
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