ATPase phospholipid transporting 8B1 ; Homo sapiens






102 Article(s)
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1 1326803 Characterization of the large tegument protein (ICP1/2) of herpes simplex virus type 1. Virology 1992 Sep 1
2 1702290 The membrane domain of the human erythrocyte anion transport protein. Epitope mapping of a monoclonal antibody defines the location of a cytoplasmic loop near the C-terminus of the protein. Biochem J 1990 Nov 15 1
3 1847560 Immunochemical studies on the differential binding properties of two monoclonal antibodies reacting with Tn red cells. Transfusion 1991 Feb 9
4 2001409 Role of ABH blood group antigens in the stimulation of a DIDS-sensitive Ca2+ influx pathway in human erythrocytes by Ulex europaeus agglutinin I and a monoclonal anti A1 antibody. Biochim Biophys Acta 1991 Feb 19 2
5 2744357 Benign recurrent intrahepatic cholestasis: altered bile acid metabolism. Gastroenterology 1989 Aug 10
6 3135800 Monoclonal antibodies that recognize different membrane proteins that are deficient in Rhnull human erythrocytes. One group of antibodies reacts with a variety of cells and tissues whereas the other group is erythroid-specific. Biochem J 1988 Apr 15 1
7 3678736 Benign recurrent intrahepatic cholestasis. Evidence for an intrinsic abnormality in hepatocyte secretion. Gastroenterology 1987 Dec 5
8 6413884 Effect of mannitol on increased intracranial pressure. Neurosurgery 1983 Sep 1
9 7250892 A distinctive pattern of serum bile acid and bilirubin concentrations in benign recurrent intrahepatic cholestasis. Hepatogastroenterology 1981 Jun 1
10 7259083 Serum bile acid concentrations in the course of benign recurrent intrahepatic cholestasis. Ann Clin Res 1980 Aug 1
11 7655458 Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region. Hum Mol Genet 1995 Jun 2
12 7912266 Clinical and biochemical findings in progressive familial intrahepatic cholestasis. J Pediatr Gastroenterol Nutr 1994 Feb 1
13 10223112 [Progressive familial intrahepatic cholestasis and hereditary anomalies lf hepatocellular metabolism of bile acids]. Arch Pediatr 1998 Jan 1
14 10385071 Progressive familial intrahepatic cholestasis. J Gastroenterol Hepatol 1999 Jun 1
15 10679031 Progressive familial intrahepatic cholestasis: a personal perspective. Pediatr Dev Pathol 2000 Mar-Apr 1
16 10975791 Advances in familial and congenital cholestatic diseases. Clinical and diagnostic implications. Dig Liver Dis 2000 Mar 3
17 11151888 Progressive familial intrahepatic cholestasis: partial biliary diversion normalizes serum lipids and improves growth in noncirrhotic patients. Am J Gastroenterol 2000 Dec 2
18 11682038 FIC1: another bile salt carrier within the enterohepatic circulation? J Hepatol 2001 Oct 1
19 12076045 The FIC1 gene: structure and polymorphisms in baboon. J Med Primatol 2002 Feb 1
20 12220310 Extracorporal albumin dialysis (MARS) improves cholestasis and normalizes low apo A-I levels in a patient with benign recurrent intrahepatic cholestasis (BRIC). Liver 2002 3
21 12481430 A novel indolocarbazole, ICP-1, abrogates DNA damage-induced cell cycle arrest and enhances cytotoxicity: similarities and differences to the cell cycle checkpoint abrogator UCN-01. Mol Cancer Ther 2002 Oct 1
22 12596388 Progressive familial intrahepatic cholestasis. Acta Biomed 2002 1
23 12880872 FIC1, a P-type ATPase linked to cholestatic liver disease, has homologues (ATP8B2 and ATP8B3) expressed throughout the body. Biochim Biophys Acta 2003 Jul 21 3
24 12887856 [Ursodeoxycholic acid treatment shortens the course of cholestasis in two patients with benign recurrent intrahepatic cholestasis]. Gastroenterol Hepatol 2003 Aug-Sep 1
25 14976163 A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion. Hum Mol Genet 2004 Apr 15 1
26 15209631 Taurocholate transport by hepatic and intestinal bile acid transporters is independent of FIC1 overexpression in Madin-Darby canine kidney cells. J Gastroenterol Hepatol 2004 Jul 1
27 15300568 Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11. Gastroenterology 2004 Aug 3
28 15448432 Resistance to parathyroid hormone in two patients with familial intrahepatic cholestasis: possible involvement of the ATP8B1 gene in calcium regulation via parathyroid hormone. J Pediatr Gastroenterol Nutr 2004 Oct 1
29 15756213 Evaluation of risk for atherosclerosis in Alagille syndrome and progressive familial intrahepatic cholestasis: two congenital cholestatic diseases with different lipoprotein metabolisms. J Pediatr 2005 Mar 2
30 16374853 Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis. Hepatology 2006 Jan 1
31 16628629 Altered hepatobiliary gene expressions in PFIC1: ATP8B1 gene defect is associated with CFTR downregulation. Hepatology 2006 May 2
32 16799980 Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transport. Hepatology 2006 Jul 3
33 16819395 Bile salt excretory pump: biology and pathobiology. J Pediatr Gastroenterol Nutr 2006 Jul 3
34 18186923 CD47 associates with alpha 5 integrin and regulates responses of human articular chondrocytes to mechanical stimulation in an in vitro model. Arthritis Res Ther 2008 2
35 18379143 Successful treatment with colestimide for a bout of cholestasis in a Japanese patient with benign recurrent intrahepatic cholestasis caused by ATP8B1 mutation. Intern Med 2008 5
36 18466903 Abcg5/8 independent biliary cholesterol excretion in Atp8b1-deficient mice. Gastroenterology 2008 Jun 2
37 18575333 [Study on relationship between expression of familial intrahepatic cholestasis 1 mRNA in placenta and Intrahepatic cholestasis of pregnancy]. Sichuan Da Xue Xue Bao Yi Xue Ban 2008 May 1
38 18668687 The membrane protein ATPase class I type 8B member 1 signals through protein kinase C zeta to activate the farnesoid X receptor. Hepatology 2008 Dec 2
39 18770956 [Benign recurrent intrahepatic cholestasis type-II--a rare cause of direct hyperbilirubinemia exacerbations with hepatic fibrosis]. Harefuah 2008 May 2
40 18937870 Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary Diversion. BMC Gastroenterol 2008 Oct 20 1
41 19001830 Phosphate binder impact on bone remodeling and coronary calcification--results from the BRiC study. Nephron Clin Pract 2008 1
42 19027009 ATP8B1 deficiency disrupts the bile canalicular membrane bilayer structure in hepatocytes, but FXR expression and activity are maintained. Gastroenterology 2009 Mar 2
43 19059530 Effects of bezafibrate on dyslipidemia with cholestasis in children with familial intrahepatic cholestasis-1 deficiency manifesting progressive familial intrahepatic cholestasis. Metabolism 2009 Jan 1
44 19228886 Knockdown of ATP8B1 expression leads to specific downregulation of the bile acid sensor FXR in HepG2 cells: effect of the FXR agonist GW4064. Am J Physiol Gastrointest Liver Physiol 2009 May 3
45 19479804 Allograft steatohepatitis in progressive familial intrahepatic cholestasis type 1 after living donor liver transplantation. Liver Transpl 2009 Jun 1
46 19882051 Bile acid transport correlative protein mRNA expression profile in human placenta with intrahepatic cholestasis of pregnancy. Saudi Med J 2009 Nov 1
47 19918981 Folding defects in P-type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4-phenylbutyrate. Hepatology 2010 Jan 3
48 20034695 Liver disease associated with canalicular transport defects: current and future therapies. J Hepatol 2010 Feb 1
49 20414253 DHPLC screening for mutations in progressive familial intrahepatic cholestasis patients. J Hum Genet 2010 May 1
50 20422494 Progressive familial intrahepatic cholestasis type 1. Semin Liver Dis 2010 May 2