201 related articles for article (PubMed ID: 20683201)
1. Analysis of gene mutations in children with cholestasis of undefined etiology.
Matte U; Mourya R; Miethke A; Liu C; Kauffmann G; Moyer K; Zhang K; Bezerra JA
J Pediatr Gastroenterol Nutr; 2010 Oct; 51(4):488-493. PubMed ID: 20683201
[TBL] [Abstract][Full Text] [Related]
2. Novel resequencing chip customized to diagnose mutations in patients with inherited syndromes of intrahepatic cholestasis.
Liu C; Aronow BJ; Jegga AG; Wang N; Miethke A; Mourya R; Bezerra JA
Gastroenterology; 2007 Jan; 132(1):119-26. PubMed ID: 17241866
[TBL] [Abstract][Full Text] [Related]
3. Sequencing of FIC1, BSEP and MDR3 in a large cohort of patients with cholestasis revealed a high number of different genetic variants.
Dröge C; Bonus M; Baumann U; Klindt C; Lainka E; Kathemann S; Brinkert F; Grabhorn E; Pfister ED; Wenning D; Fichtner A; Gotthardt DN; Weiss KH; McKiernan P; Puri RD; Verma IC; Kluge S; Gohlke H; Schmitt L; Kubitz R; Häussinger D; Keitel V
J Hepatol; 2017 Dec; 67(6):1253-1264. PubMed ID: 28733223
[TBL] [Abstract][Full Text] [Related]
4. 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
J Gastroenterol; 2018 Aug; 53(8):945-958. PubMed ID: 29238877
[TBL] [Abstract][Full Text] [Related]
5. ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes.
Al-Hussaini A; Lone K; Bashir MS; Alrashidi S; Fagih M; Alanazi A; AlYaseen S; Almayouf A; Alruwaithi M; Asery A
J Pediatr; 2021 Sep; 236():113-123.e2. PubMed ID: 33915153
[TBL] [Abstract][Full Text] [Related]
6. Advances in familial and congenital cholestatic diseases. Clinical and diagnostic implications.
Colombo C; Okolicsanyi L; Strazzabosco M
Dig Liver Dis; 2000 Mar; 32(2):152-9. PubMed ID: 10975791
[TBL] [Abstract][Full Text] [Related]
7. Molecular basis of intrahepatic cholestasis.
Carlton VE; Pawlikowska L; Bull LN
Ann Med; 2004; 36(8):606-17. PubMed ID: 15768832
[TBL] [Abstract][Full Text] [Related]
8. Review article: liver disease in adults with variants in the cholestasis-related genes ABCB11, ABCB4 and ATP8B1.
Nayagam JS; Williamson C; Joshi D; Thompson RJ
Aliment Pharmacol Ther; 2020 Dec; 52(11-12):1628-1639. PubMed ID: 33070363
[TBL] [Abstract][Full Text] [Related]
9. ABCB4 and ABCB11 mutations in intrahepatic cholestasis of pregnancy in an Italian population.
Anzivino C; Odoardi MR; Meschiari E; Baldelli E; Facchinetti F; Neri I; Ruggiero G; Zampino R; Bertolotti M; Loria P; Carulli L
Dig Liver Dis; 2013 Mar; 45(3):226-32. PubMed ID: 23022423
[TBL] [Abstract][Full Text] [Related]
10. Clinical characteristics and genetic profiles of young and adult patients with cholestatic liver disease.
Huynh MT; Nguyen TT; Grison S; Lascols O; Fernandez E; Barbu V
Rev Esp Enferm Dig; 2019 Oct; 111(10):775-788. PubMed ID: 31538484
[TBL] [Abstract][Full Text] [Related]
11. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort.
Mínguez Rodríguez B; Molera Busoms C; Martorell Sampol L; García Romero R; Colomé Rivero G; Martín de Carpi J
Gastroenterol Hepatol; 2022 Oct; 45(8):585-592. PubMed ID: 34942279
[TBL] [Abstract][Full Text] [Related]
12. [Childhood cholestasis and bile transporters].
Hierro L; Jara P
Gastroenterol Hepatol; 2005; 28(7):388-95. PubMed ID: 16137474
[TBL] [Abstract][Full Text] [Related]
13. Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1.
Nayagam JS; Foskett P; Strautnieks S; Agarwal K; Miquel R; Joshi D; Thompson RJ
Hepatol Commun; 2022 Oct; 6(10):2654-2664. PubMed ID: 35894240
[TBL] [Abstract][Full Text] [Related]
14. Mutations and polymorphisms in the bile salt export pump and the multidrug resistance protein 3 associated with drug-induced liver injury.
Lang C; Meier Y; Stieger B; Beuers U; Lang T; Kerb R; Kullak-Ublick GA; Meier PJ; Pauli-Magnus C
Pharmacogenet Genomics; 2007 Jan; 17(1):47-60. PubMed ID: 17264802
[TBL] [Abstract][Full Text] [Related]
15. NR1H4 analysis in patients with progressive familial intrahepatic cholestasis, drug-induced cholestasis or intrahepatic cholestasis of pregnancy unrelated to ATP8B1, ABCB11 and ABCB4 mutations.
Davit-Spraul A; Gonzales E; Jacquemin E
Clin Res Hepatol Gastroenterol; 2012 Dec; 36(6):569-73. PubMed ID: 23142591
[TBL] [Abstract][Full Text] [Related]
16. The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency.
Wang NL; Li LT; Wu BB; Gong JY; Abuduxikuer K; Li G; Wang JS
PLoS One; 2016; 11(4):e0153114. PubMed ID: 27050426
[TBL] [Abstract][Full Text] [Related]
17. The role of genetic mutations in intrahepatic cholestasis of pregnancy.
Aydın GA; Özgen G; Görükmez O
Taiwan J Obstet Gynecol; 2020 Sep; 59(5):706-710. PubMed ID: 32917322
[TBL] [Abstract][Full Text] [Related]
18. An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy.
Dixon PH; Sambrotta M; Chambers J; Taylor-Harris P; Syngelaki A; Nicolaides K; Knisely AS; Thompson RJ; Williamson C
Sci Rep; 2017 Sep; 7(1):11823. PubMed ID: 28924228
[TBL] [Abstract][Full Text] [Related]
19. Common ABCB4 and ABCB11 Genotypes Are Associated with Idiopathic Chronic Cholestasis in Adults.
Jüngst C; Justinger C; Fischer J; Berg T; Lammert F
Dig Dis; 2022; 40(4):489-496. PubMed ID: 34348275
[TBL] [Abstract][Full Text] [Related]
20. Molecular findings in children with inherited intrahepatic cholestasis.
Wang NL; Lu Y; Gong JY; Xie XB; Lin J; Abuduxikuer K; Zhang MH; Wang JS
Pediatr Res; 2020 Jan; 87(1):112-117. PubMed ID: 31450232
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]