Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.

Albert Friedrich Stättermayer; Stefan Traussnigg; Hans-Peter Dienes; Elmar Aigner; Rudolf Stauber; Karoline Lackner; Harald Hofer; Judith Stift; Friedrich Wrba; Andreas Stadlmayr; Christian Datz; Michael Strasser; Andreas Maieron; Michael Trauner; Peter Ferenci

doi:10.1016/j.jhep.2015.01.034

Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.

Albert Friedrich Stättermayer
, Stefan Traussnigg
, Hans-Peter Dienes
, Elmar Aigner (Co-author)
, Rudolf Stauber
, Karoline Lackner
, Harald Hofer
, Judith Stift
, Friedrich Wrba
, Andreas Stadlmayr
, Christian Datz (Co-author)
, Michael Strasser (Co-author)
, Andreas Maieron
, Michael Trauner
, Peter Ferenci

Research output: Contribution to journal › Original Article › peer-review

83 Citations (Web of Science)

Original language	English
Pages (from-to)	156-163
Journal	JOURNAL OF HEPATOLOGY
Volume	63
Issue number	1
DOIs	https://doi.org/10.1016/j.jhep.2015.01.034
Publication status	Published - 2015

Keywords

FATTY LIVER-DISEASE
SYNTHASE GENE-TRANSCRIPTION
TX-J MOUSE
I148M POLYMORPHISM
LIPID DROPLETS
RATS
DEFICIENCY
METABOLISM
MODEL
EXPRESSION

Access to Document

10.1016/j.jhep.2015.01.034

Cite this

Stättermayer, A. F., Traussnigg, S., Dienes, H.-P., Aigner, E., Stauber, R., Lackner, K., Hofer, H., Stift, J., Wrba, F., Stadlmayr, A., Datz, C., Strasser, M., Maieron, A., Trauner, M., & Ferenci, P. (2015). Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations. JOURNAL OF HEPATOLOGY , 63(1), 156-163. https://doi.org/10.1016/j.jhep.2015.01.034

Stättermayer, Albert Friedrich ; Traussnigg, Stefan ; Dienes, Hans-Peter et al. / Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations. In: JOURNAL OF HEPATOLOGY 2015 ; Vol. 63, No. 1. pp. 156-163.

@article{6dc5f3fd1346485f97eda9fe0fd2858d,

title = "Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.",

keywords = "FATTY LIVER-DISEASE, SYNTHASE GENE-TRANSCRIPTION, TX-J MOUSE, I148M POLYMORPHISM, LIPID DROPLETS, RATS, DEFICIENCY, METABOLISM, MODEL, EXPRESSION",

author = "St{\"a}ttermayer, \{Albert Friedrich\} and Stefan Traussnigg and Hans-Peter Dienes and Elmar Aigner and Rudolf Stauber and Karoline Lackner and Harald Hofer and Judith Stift and Friedrich Wrba and Andreas Stadlmayr and Christian Datz and Michael Strasser and Andreas Maieron and Michael Trauner and Peter Ferenci",

note = "Aigner, Strasser: Department of Internal Medicine I, Paracelsus Private Medical University, Salzburg, Austria; Stadlmayr, Datz: Department of Internal Medicine, KH Oberndorf, Oberndorf, Austria",

year = "2015",

doi = "10.1016/j.jhep.2015.01.034",

language = "English",

volume = "63",

pages = "156--163",

journal = "JOURNAL OF HEPATOLOGY ",

issn = "0168-8278",

publisher = "Elsevier ",

number = "1",

}

Stättermayer, AF, Traussnigg, S, Dienes, H-P, Aigner, E, Stauber, R, Lackner, K, Hofer, H, Stift, J, Wrba, F, Stadlmayr, A, Datz, C , Strasser, M, Maieron, A, Trauner, M & Ferenci, P 2015, 'Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.', JOURNAL OF HEPATOLOGY , vol. 63, no. 1, pp. 156-163. https://doi.org/10.1016/j.jhep.2015.01.034

Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations. / Stättermayer, Albert Friedrich; Traussnigg, Stefan; Dienes, Hans-Peter et al.
In: JOURNAL OF HEPATOLOGY , Vol. 63, No. 1, 2015, p. 156-163.

Research output: Contribution to journal › Original Article › peer-review

TY - JOUR

T1 - Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.

AU - Stättermayer, Albert Friedrich

AU - Traussnigg, Stefan

AU - Dienes, Hans-Peter

AU - Aigner, Elmar

AU - Stauber, Rudolf

AU - Lackner, Karoline

AU - Hofer, Harald

AU - Stift, Judith

AU - Wrba, Friedrich

AU - Stadlmayr, Andreas

AU - Datz, Christian

AU - Strasser, Michael

AU - Maieron, Andreas

AU - Trauner, Michael

AU - Ferenci, Peter

N1 - Aigner, Strasser: Department of Internal Medicine I, Paracelsus Private Medical University, Salzburg, Austria; Stadlmayr, Datz: Department of Internal Medicine, KH Oberndorf, Oberndorf, Austria

PY - 2015

Y1 - 2015

KW - FATTY LIVER-DISEASE

KW - SYNTHASE GENE-TRANSCRIPTION

KW - TX-J MOUSE

KW - I148M POLYMORPHISM

KW - LIPID DROPLETS

KW - RATS

KW - DEFICIENCY

KW - METABOLISM

KW - MODEL

KW - EXPRESSION

U2 - 10.1016/j.jhep.2015.01.034

DO - 10.1016/j.jhep.2015.01.034

M3 - Original Article

C2 - 25678388

SN - 0168-8278

VL - 63

SP - 156

EP - 163

JO - JOURNAL OF HEPATOLOGY

JF - JOURNAL OF HEPATOLOGY

IS - 1

ER -

Stättermayer AF, Traussnigg S, Dienes HP, Aigner E, Stauber R, Lackner K et al. Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations. JOURNAL OF HEPATOLOGY . 2015;63(1):156-163. doi: 10.1016/j.jhep.2015.01.034