Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1994 2
1996 6
1997 7
1998 10
1999 12
2000 20
2001 26
2002 31
2003 35
2004 33
2005 27
2006 46
2007 44
2008 43
2009 44
2010 50
2011 39
2012 54
2013 57
2014 75
2015 70
2016 58
2017 58
2018 50
2019 52
2020 8
Text availability
Article attribute
Article type
Publication date

Search Results

833 results
Results by year
Filters applied: . Clear all
Page 1
ABC Family Transporters.
Liu X. Liu X. Adv Exp Med Biol. 2019;1141:13-100. doi: 10.1007/978-981-13-7647-4_2. Adv Exp Med Biol. 2019. PMID: 31571164 Review.
The processes are usually mediated by specific transporters. One of the largest transporter families is the ATP-binding cassette (ABC) family. ...Several human diseases such as cystic fibrosis, sitosterolemia, Tangier disease, intrahepati …
The processes are usually mediated by specific transporters. One of the largest transporter families is the ATP-bind
Biliary transporter gene mutations in severe intrahepatic cholestasis of pregnancy: Diagnostic and management implications.
Yeap SP, Harley H, Thompson R, Williamson KD, Bate J, Sethna F, Farrell G, Hague WB. Yeap SP, et al. J Gastroenterol Hepatol. 2019 Feb;34(2):425-435. doi: 10.1111/jgh.14376. Epub 2018 Aug 6. J Gastroenterol Hepatol. 2019. PMID: 29992621
In five women with identified genetic mutations of such transporters, with eight observed pregnancies complicated by ICP, we examined relationships between transporter mutations, clinical phenotypes, and treatment outcomes. ...CONCLUSIONS: Early-onset or recurrent I …
In five women with identified genetic mutations of such transporters, with eight observed pregnancies complicated by ICP, we examined …
Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing.
Vitale G, Gitto S, Raimondi F, Mattiaccio A, Mantovani V, Vukotic R, D'Errico A, Seri M, Russell RB, Andreone P. Vitale G, et al. J Gastroenterol. 2018 Aug;53(8):945-958. doi: 10.1007/s00535-017-1423-1. Epub 2017 Dec 13. J Gastroenterol. 2018. PMID: 29238877
BACKGROUND: Mutations in ATP-transporters ATPB81, ABCB11, and ABCB4 are responsible for progressive familial intrahepatic cholestasis (PFIC) 1, 2 and 3, and recently the gene for tight junction protein-2 (TJP2) has been linked to PFIC4. ...CONCLUSIONS: Mutati …
BACKGROUND: Mutations in ATP-transporters ATPB81, ABCB11, and ABCB4 are responsible for progressive familial intrahepatic c
ABCB4 Gene Aberrations in Human Liver Disease: An Evolving Spectrum.
Reichert MC, Lammert F. Reichert MC, et al. Semin Liver Dis. 2018 Nov;38(4):299-307. doi: 10.1055/s-0038-1667299. Epub 2018 Oct 24. Semin Liver Dis. 2018. PMID: 30357767 Review.
ATP-binding cassette subfamily B member 4 (ABCB4) is a phospholipid translocator at the canalicular membrane of the hepatocyte, which "flops" phosphatidylcholine into bile. Dysfunction of this transporter due to ABCB4 gene variants can cause liver dise
ATP-binding cassette subfamily B member 4 (ABCB4) is a phospholipid translocator at the canalicular membrane of the hep
Trafficking and transporter disorders in pediatric cholestasis.
Knisely AS, Gissen P. Knisely AS, et al. Clin Liver Dis. 2010 Nov;14(4):619-33. doi: 10.1016/j.cld.2010.08.001. Clin Liver Dis. 2010. PMID: 21055686 Review.
This article describes the uses of immunostaining in the diagnosis of cholestasis. To immunostain for bile salt export pump (BSEP) and multidrug resistance protein 3 in severe hepatobiliary disease manifest early in life can rapidly identify whether sequencing of ABCB11 or …
This article describes the uses of immunostaining in the diagnosis of cholestasis. To immunostain for bile salt export pump (BSEP) an …
Geniposide attenuates ANIT-induced cholestasis through regulation of transporters and enzymes involved in bile acids homeostasis in rats.
Wang L, Wu G, Wu F, Jiang N, Lin Y. Wang L, et al. J Ethnopharmacol. 2017 Jan 20;196:178-185. doi: 10.1016/j.jep.2016.12.022. Epub 2016 Dec 14. J Ethnopharmacol. 2017. PMID: 27988401
GE also markedly enhanced mRNA level of basolateral transporter OSTβ (P<0.01). Bile acids transported to the plasma were cleared into the urine, resulting in down-regulation of plasma bile acids. ...CONCLUSION: GE attenuates ANIT-induced hepatotoxicity and cholestasi
GE also markedly enhanced mRNA level of basolateral transporter OSTβ (P<0.01). Bile acids transported to the plasma were cleared i …
Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters.
Liu L, Zhang L, Zhang L, Yang F, Zhu X, Lu Z, Yang Y, Lu H, Feng L, Wang Z, Chen H, Yan S, Wang L, Ju Z, Jin H, Zhu X. Liu L, et al. Am J Pathol. 2017 Dec;187(12):2775-2787. doi: 10.1016/j.ajpath.2017.08.011. Epub 2017 Sep 15. Am J Pathol. 2017. PMID: 28919113 Free article.
The proteasome inhibitor bortezomib partially restored total protein levels of BS transporters but not the localization of BS transporters in the membrane. ...TMEM30A deficiency led to intrahepatic cholestasis in mice by impairing the expression and localizat …
The proteasome inhibitor bortezomib partially restored total protein levels of BS transporters but not the localization of BS tran
Intrahepatic cholestasis of pregnancy (ICP): case report and review of the literature.
Keitel V, Dröge C, Stepanow S, Fehm T, Mayatepek E, Köhrer K, Häussinger D. Keitel V, et al. Z Gastroenterol. 2016 Dec;54(12):1327-1333. doi: 10.1055/s-0042-118388. Epub 2016 Dec 9. Z Gastroenterol. 2016. PMID: 27936482 Review. English.
Intrahepatic cholestasis of pregnancy is associated with increased perinatal complications, such as premature delivery, meconium staining of the amniotic fluid, respiratory distress, low Apgar scores, and even stillbirth. ...An important factor for ICP development is a ris …
Intrahepatic cholestasis of pregnancy is associated with increased perinatal complications, such as premature delivery, meconium stai …
Progressive familial intrahepatic cholestasis.
Jacquemin E. Jacquemin E. Clin Res Hepatol Gastroenterol. 2012 Sep;36 Suppl 1:S26-35. doi: 10.1016/S2210-7401(12)70018-9. Clin Res Hepatol Gastroenterol. 2012. PMID: 23141890 Review.
Progressive familial intrahepatic cholestasis (PFIC) refers to a heterogeneous group of autosomal-recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. ...The main clinical manifestations include chole
Progressive familial intrahepatic cholestasis (PFIC) refers to a heterogeneous group of autosomal-recessive disorders of childhood th …
ATP-Binding Cassette Transporter A Subfamily 8 Is a Sinusoidal Efflux Transporter for Cholesterol and Taurocholate in Mouse and Human Liver.
Sasaki K, Tachikawa M, Uchida Y, Hirano S, Kadowaki F, Watanabe M, Ohtsuki S, Terasaki T. Sasaki K, et al. Mol Pharm. 2018 Feb 5;15(2):343-355. doi: 10.1021/acs.molpharmaceut.7b00679. Epub 2018 Jan 24. Mol Pharm. 2018. PMID: 29300488
The ATP-binding cassette (ABC) transporter A subfamily 8 (ABCA8) belongs to the ABCA6-like transporters subgroup, which is distinct from the ABCA1-like subgroup in the ABCA family. The expression and function of the short-size human ABCA8 …
The ATP-binding cassette (ABC) transporter A subfamily 8 (ABCA8) belongs to the ABCA6-like transporter
833 results
Jump to page
Feedback