X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
atp8b1 (61) 61
humans (46) 46
index medicus (46) 46
adenosine triphosphatases - genetics (30) 30
familial intrahepatic cholestasis (28) 28
gastroenterology & hepatology (28) 28
cholestasis, intrahepatic - genetics (27) 27
mutation (27) 27
hereditary cholestasis (25) 25
canalicular membrane (24) 24
cholestasis (24) 24
animals (23) 23
salt export pump (22) 22
abcb11 (21) 21
progressive familial intrahepatic cholestasis (19) 19
bile (18) 18
liver (18) 18
atp8b1 deficiency (16) 16
expression (16) 16
male (16) 16
atp-binding cassette transporters - genetics (15) 15
biochemistry & molecular biology (15) 15
female (15) 15
mice (15) 15
atp binding cassette subfamily b member 11 (14) 14
pediatrics (14) 14
cell biology (13) 13
mutations (12) 12
transport (12) 12
abcb4 (11) 11
farnesoid-x-receptor (11) 11
intrahepatic cholestasis (11) 11
child (10) 10
child, preschool (10) 10
cholestasis, intrahepatic - diagnosis (10) 10
fic1 (10) 10
adenosine triphosphatases - metabolism (9) 9
children (9) 9
jaundice, obstructive (9) 9
plasma-membrane (9) 9
analysis (8) 8
benign recurrent intrahepatic cholestasis (8) 8
genetic aspects (8) 8
infant (8) 8
liver-transplantation (8) 8
phospholipid transfer proteins (8) 8
research (8) 8
adenosine triphosphatase (7) 7
atp binding cassette transporter, sub-family b - genetics (7) 7
atp8b1 gene (7) 7
bile acids and salts - metabolism (7) 7
bric (7) 7
deficiency (7) 7
disease (7) 7
gallbladder diseases (7) 7
liver transplantation (7) 7
liver-disease (7) 7
medicine, research & experimental (7) 7
p-type atpases (7) 7
phenotype (7) 7
pregnancy (7) 7
transplantation (7) 7
adolescent (6) 6
bile salt export pump (6) 6
bsep (6) 6
cdc50 proteins (6) 6
cholestasis, intrahepatic - pathology (6) 6
cholestasis, intrahepatic - therapy (6) 6
disease progression (6) 6
genetics (6) 6
genetics & heredity (6) 6
lipids (6) 6
liver - metabolism (6) 6
liver - pathology (6) 6
pfic (6) 6
phospholipid transfer proteins - genetics (6) 6
phospholipid transfer proteins - metabolism (6) 6
pruritus (6) 6
signal transduction (6) 6
2 forms (5) 5
adult (5) 5
biopsy (5) 5
byler disease (5) 5
care and treatment (5) 5
cholestasis, intrahepatic - surgery (5) 5
external biliary diversion (5) 5
gastroenterology and hepatology (5) 5
gene (5) 5
in-vivo (5) 5
kinase-c zeta (5) 5
pathology (5) 5
pfic2 (5) 5
phospholipids (5) 5
physiological aspects (5) 5
proteins (5) 5
type-1 (5) 5
young adult (5) 5
adenosine triphosphatases (4) 4
adenosine triphosphatases - deficiency (4) 4
adenosine triphosphatases - physiology (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Pediatric Gastroenterology, Hepatology & Nutrition, ISSN 2234-8646, 2019, Volume 22, Issue 5, pp. 479 - 486
Progressive familial intrahepatic cholestasis (PFIC) is a group of severe genetic disorders, inherited in an autosomal recessive manner, causing cholestasis of... 
ATP8B1 | Intrahepatic cholestasis | Child | Case Report | 소아과학
Journal Article
EMBO Molecular Medicine, ISSN 1757-4676, 09/2012, Volume 4, Issue 9, pp. 882 - 895
Journal Article
FRONTIERS IN PHYSIOLOGY, ISSN 1664-042X, 07/2016, Volume 7
P4-ATPases comprise a family of P-type ATPases that actively transport or flip phospholipids across cell membranes. This generates and maintains membrane lipid... 
CANALICULAR MEMBRANE | MOLECULAR-MECHANISM | P-type ATPases | PHYSIOLOGY | ATP8A2 | P4-ATPases | CRYSTAL-STRUCTURE | ATP8B1 DEFICIENCY | SUBCELLULAR-LOCALIZATION | membrane asymmetry | flippases | CDC50 | PLASMA-MEMBRANE | PUTATIVE AMINOPHOSPHOLIPID TRANSLOCASE | phospholipid transport | LIPID ASYMMETRY | TRANS-GOLGI NETWORK
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2014, Volume 289, Issue 48, pp. 33543 - 33556
Type IV P-type ATPases (P4-ATPases) are believed to translocate aminophospholipids from the exoplasmic to the cytoplasmic leaflets of cellular membranes. The... 
ATP8B1 DEFICIENCY | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VIVO | SUBCELLULAR-LOCALIZATION | BILE CANALICULAR MEMBRANE | AMINOPHOSPHOLIPID TRANSLOCASE | HEREDITARY CHOLESTASIS | CDC50 PROTEINS | EXPRESSION | PHOSPHATIDYLSERINE | FAMILIAL INTRAHEPATIC CHOLESTASIS
Journal Article
Journal of Biomedical Physics and Engineering, ISSN 2251-7200, 02/2019, Volume 9, Issue 1, pp. 105 - 120
Progressive familial intrahepatic cholestases (PFIC) are a spectrum of autosomal progressive liver diseases developing to end-stage liver disease. ATP8B1... 
Bioinformatics analysis | Rare codon | Progressive familial intrahepatic cholestasis | ATP8b1 | Progressive Familial Intrahepatic Cholestasis | Bioinformatics Analysis | Rare Codon
Journal Article
FASEB JOURNAL, ISSN 0892-6638, 03/2019, Volume 33, Issue 3, pp. 3087 - 3096
Journal Article
Pediatria Polska, ISSN 0031-3939, 09/2017, Volume 92, Issue 5, pp. 575 - 578
The article constitutes an up-to-day overview on pathogenesis, clinical manifestation and treatment of benign recurrent intrahepatic cholestasis in children. 
drenaż nosowo-żółciowy | Naso-biliary drainage | Progressive familial intrahepatic cholestasis | postępująca rodzinna cholestaza wewnątrzwątrobowa | BRIC | Gene ATP8B1 | Protein FIC-1 | gen ATP8B1 | białko FIC-1
Journal Article
PEDIATRICS, ISSN 0031-4005, 05/2019, Volume 143, Issue 5, p. e20182146
A 27-month-old girl with severe cholestasis, a compound heterozygote for PFIC2-associated and BRIC2-associated ABCB11 mutations, over 5 years developed... 
RENAL DYSFUNCTION | ATP8B1 | ARTHROGRYPOSIS | MEMBRANE | PEDIATRICS | DEFICIENCY | FAMILIAL INTRAHEPATIC CHOLESTASIS | TJP2 | Jaundice | Cefprozil | g-Glutamyltransferase | Nonsense mutation | Syngeneic grafts | Liver | Gallbladder diseases | Girls | Exports | Heterozygosity | Ursodeoxycholic acid | Cirrhosis | Hyperbilirubinemia | Missense mutation | Allografts | Biopsy | Fibrosis | Mutation | Cholestasis | Cystitis | Bile | Liver transplantation
Journal Article
Siriraj Medical Journal, 11/2015, Volume 67, Issue 6, pp. 296 - 300
Benign recurrent intrahepatic cholestasis (BRIC) is an autosomal recessive cholestatic liver disease. Recurrent self-limited episodes of jaundice and severe... 
severe pruritus | ATP8B1 | gene mutation | ABCB11 | Cholestasis
Journal Article
Journal Article
Clinics and Research in Hepatology and Gastroenterology, ISSN 2210-7401, 02/2019, Volume 43, Issue 1, pp. 20 - 36
Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of rare genetic disorders associated with bile acid secretion or transport... 
Bile secretion | Pruritus | ABCB11 | Byler’s disease | ATP8B1 | ABCB4 | Byler's disease | LIVER-DISEASES | SPECTRUM | GASTROENTEROLOGY & HEPATOLOGY | EXTERNAL BILIARY DIVERSION | CHILDREN | BILE
Journal Article
BBA - Molecular and Cell Biology of Lipids, ISSN 1388-1981, 2010, Volume 1801, Issue 7, pp. 683 - 692
The nuclear receptor Farnesoid X Receptor (FXR) critically regulates nascent bile formation and bile acid enterohepatic circulation. Bile acids and FXR play a... 
Inflammation | Enterohepatic circulation | Farnesoid X Receptor | Carcinogenesis | Bile acid | CANALICULAR MEMBRANE | NEGATIVE FEEDBACK-REGULATION | SALT EXPORT PUMP | ATP8B1 DEFICIENCY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-PROTEIN | BARRETTS-ESOPHAGUS | CELL BIOLOGY | BIOPHYSICS | ALPHA-OST-BETA | FARNESOID-X-RECEPTOR | NF-KAPPA-B | FAMILIAL INTRAHEPATIC CHOLESTASIS
Journal Article
Journal Article
BBA - Molecular Cell Research, ISSN 0167-4889, 09/2016, Volume 1863, Issue 9, pp. 2280 - 2288
Progressive familial intrahepatic cholestasis type 1 (PFIC1) is caused by mutations in the gene encoding the phospholipid flippase ATP8B1. Apart from severe... 
PFIC1 | Cystic fibrosis | ATP8B1 | Trafficking | CFTR | Chloride transport | CANALICULAR MEMBRANE | CFTR FUNCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CONDUCTANCE REGULATOR | DEFICIENCY | CELL BIOLOGY | THERAPY | EPITHELIAL-CELLS | GENE | MICE | EXPRESSION | FAMILIAL INTRAHEPATIC CHOLESTASIS | Phospholipids | Liver diseases | Analysis | Liver
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2010, Volume 53, Issue 1, pp. 170 - 178
Background & Aims Progressive familial intrahepatic cholestasis (PFIC) with normal serum levels of gamma-glutamyltranspeptidase can result from mutations in... 
Gastroenterology and Hepatology | Pediatrics | FIC1 | ATP binding cassette protein | BSEP | ATP8B1 | Genetics | Transport protein | ABCB11 | P-type ATPase | Cholestasis | MANAGEMENT | DIARRHEA | SALT EXPORT PUMP | EXTERNAL BILIARY DIVERSION | CHILDREN | LIVER | SECRETION | GASTROENTEROLOGY & HEPATOLOGY | FAMILIAL INTRAHEPATIC CHOLESTASIS | ABCB11 MUTATIONS | BILE | gamma-Glutamyltransferase - blood | Humans | Child, Preschool | Infant | Male | Young Adult | ATP-Binding Cassette Transporters - genetics | ATP-Binding Cassette Transporters - metabolism | Adult | Female | Retrospective Studies | Child | Infant, Newborn | Adenosine Triphosphatases - deficiency | Diagnosis, Differential | Cholestasis, Intrahepatic - genetics | Kaplan-Meier Estimate | Bile Acids and Salts - metabolism | Disease Progression | Pregnancy | Cholestasis, Intrahepatic - metabolism | Phenotype | Cholestasis, Intrahepatic - diagnosis | ATP Binding Cassette Subfamily B Member 11 | Adolescent | Age of Onset | Adenosine Triphosphatases - genetics | Mutation | Evaluation | Medical colleges | Bile acids | Phosphatases | Children's hospitals | Oncology, Experimental | Aspartate | Research | Food and nutrition | Armed Forces | Medical genetics | Transplantation of organs, tissues, etc | Anesthesia | Children | Arctic peoples | Health aspects | Adenosine triphosphatase | Cancer | Protein binding | transport protein | genetics | cholestasis | pediatrics
Journal Article