These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

48 related articles for article (PubMed ID: 29935878)

  • 21. ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): phenotypic differences between PFIC1 and PFIC2 and natural history.
    Davit-Spraul A; Fabre M; Branchereau S; Baussan C; Gonzales E; Stieger B; Bernard O; Jacquemin E
    Hepatology; 2010 May; 51(5):1645-55. PubMed ID: 20232290
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Morphologic findings in progressive familial intrahepatic cholestasis 2 (PFIC2): correlation with genetic and immunohistochemical studies.
    Evason K; Bove KE; Finegold MJ; Knisely AS; Rhee S; Rosenthal P; Miethke AG; Karpen SJ; Ferrell LD; Kim GE
    Am J Surg Pathol; 2011 May; 35(5):687-96. PubMed ID: 21490445
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hepatotoxicity from anabolic androgenic steroids marketed as dietary supplements: contribution from ATP8B1/ABCB11 mutations?
    El Sherrif Y; Potts JR; Howard MR; Barnardo A; Cairns S; Knisely AS; Verma S
    Liver Int; 2013 Sep; 33(8):1266-70. PubMed ID: 23750872
    [TBL] [Abstract][Full Text] [Related]  

  • 24. ABCB11 gene mutations in Chinese children with progressive intrahepatic cholestasis and low gamma glutamyltransferase.
    Liu LY; Wang ZL; Wang XH; Zhu QR; Wang JS
    Liver Int; 2010 Jul; 30(6):809-15. PubMed ID: 19845854
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis.
    Qiu YL; Gong JY; Feng JY; Wang RX; Han J; Liu T; Lu Y; Li LT; Zhang MH; Sheps JA; Wang NL; Yan YY; Li JQ; Chen L; Borchers CH; Sipos B; Knisely AS; Ling V; Xing QH; Wang JS
    Hepatology; 2017 May; 65(5):1655-1669. PubMed ID: 28027573
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital Hypopituitarism.
    Grammatikopoulos T; Deheragoda M; Strautnieks S; Neves Souza L; Hinds R; Thompson RJ; Hadzic N
    J Pediatr; 2018 Sep; 200():181-187. PubMed ID: 29935878
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Relationship between phenotype and genotype of ABCB11 deficiency in siblings and literature review].
    Peng XR; Lu Y; Zhang MH; Li LT; Xie XB; Gong JY; Wang JS
    Zhonghua Er Ke Za Zhi; 2018 Jun; 56(6):440-444. PubMed ID: 29886607
    [No Abstract]   [Full Text] [Related]  

  • 28. Progressive familial intrahepatic cholestasis.
    Jacquemin E
    Clin Res Hepatol Gastroenterol; 2012 Sep; 36 Suppl 1():S26-35. PubMed ID: 23141890
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Progressive familial intrahepatic cholestasis type 1.
    Paulusma CC; Elferink RP; Jansen PL
    Semin Liver Dis; 2010 May; 30(2):117-24. PubMed ID: 20422494
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Clinical features of a Chinese infant with inborn error of bile acid metabolism-3β-hydroxy-Δ(5)-C27-steroid dehydrogenase deficiency and review of the literature].
    Yang TJ; Xie XB; Yao WL; Wang HJ; Yu H; Wang XH
    Zhonghua Er Ke Za Zhi; 2013 Aug; 51(8):625-9. PubMed ID: 24225297
    [TBL] [Abstract][Full Text] [Related]  

  • 31. BSEP: function and role in progressive familial intrahepatic cholestasis.
    Thompson R; Strautnieks S
    Semin Liver Dis; 2001 Nov; 21(4):545-50. PubMed ID: 11745042
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Trafficking and transporter disorders in pediatric cholestasis.
    Knisely AS; Gissen P
    Clin Liver Dis; 2010 Nov; 14(4):619-33. PubMed ID: 21055686
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic defects in hepatocanalicular transport.
    Thompson R; Jansen PL
    Semin Liver Dis; 2000; 20(3):365-72. PubMed ID: 11076402
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasis.
    Imagawa K; Hayashi H; Sabu Y; Tanikawa K; Fujishiro J; Kajikawa D; Wada H; Kudo T; Kage M; Kusuhara H; Sumazaki R
    J Hum Genet; 2018 May; 63(5):569-577. PubMed ID: 29507376
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The role of the sodium-taurocholate cotransporting polypeptide (NTCP) and of the bile salt export pump (BSEP) in physiology and pathophysiology of bile formation.
    Stieger B
    Handb Exp Pharmacol; 2011; (201):205-59. PubMed ID: 21103971
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Pathologic Features of Hereditary Cholestatic Diseases.
    Clouston AD
    Surg Pathol Clin; 2018 Jun; 11(2):313-327. PubMed ID: 29751877
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Function and regulation of ATP-binding cassette transport proteins involved in hepatobiliary transport.
    Hooiveld GJ; van Montfoort JE; Meijer DK; Müller M
    Eur J Pharm Sci; 2001 Feb; 12(4):525-43. PubMed ID: 11231121
    [TBL] [Abstract][Full Text] [Related]  

  • 38.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 39.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.