Similar articles for PMID: 30277246

Year	Number of Results
1993	1
1996	1
1997	1
1998	2
1999	3
2000	3
2001	2
2002	1
2003	1
2004	2
2005	1
2006	1
2007	2
2008	1
2009	2
2010	5
2011	7
2012	7
2014	7
2015	5
2016	8
2017	6
2018	11
2019	12
2020	8
2021	8
2022	4
2023	4
2024	1

1

Altered zinc balance in the Atp7b^-/- mouse reveals a mechanism of copper toxicity in Wilson disease.

Meacham KA, Cortés MP, Wiggins EM, Maass A, Latorre M, Ralle M, Burkhead JL. Meacham KA, et al. Metallomics. 2018 Nov 14;10(11):1595-1606. doi: 10.1039/c8mt00199e. Metallomics. 2018. PMID: 30277246 Free PMC article.

2

Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis.

Polishchuk EV, Merolla A, Lichtmannegger J, Romano A, Indrieri A, Ilyechova EY, Concilli M, De Cegli R, Crispino R, Mariniello M, Petruzzelli R, Ranucci G, Iorio R, Pietrocola F, Einer C, Borchard S, Zibert A, Schmidt HH, Di Schiavi E, Puchkova LV, Franco B, Kroemer G, Zischka H, Polishchuk RS. Polishchuk EV, et al. Gastroenterology. 2019 Mar;156(4):1173-1189.e5. doi: 10.1053/j.gastro.2018.11.032. Epub 2018 Nov 17. Gastroenterology. 2019. PMID: 30452922

3

Metallothionein is elevated in liver and duodenum of Atp7b^(-/-) mice.

Zhang CC, Volkmann M, Tuma S, Stremmel W, Merle U. Zhang CC, et al. Biometals. 2018 Aug;31(4):617-625. doi: 10.1007/s10534-018-0110-x. Epub 2018 May 7. Biometals. 2018. PMID: 29732486

4

Systemic deletion of Atp7b modifies the hepatocytes' response to copper overload in the mouse models of Wilson disease.

Muchenditsi A, Talbot CC Jr, Gottlieb A, Yang H, Kang B, Boronina T, Cole R, Wang L, Dev S, Hamilton JP, Lutsenko S. Muchenditsi A, et al. Sci Rep. 2021 Mar 11;11(1):5659. doi: 10.1038/s41598-021-84894-3. Sci Rep. 2021. PMID: 33707579 Free PMC article.

5

Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson disease.

Mordaunt CE, Shibata NM, Kieffer DA, Czlonkowska A, Litwin T, Weiss KH, Gotthardt DN, Olson K, Wei D, Cooper S, Wan YY, Ali MR, LaSalle JM, Medici V. Mordaunt CE, et al. Hum Mol Genet. 2018 Nov 15;27(22):3854-3869. doi: 10.1093/hmg/ddy262. Hum Mol Genet. 2018. PMID: 30010856 Free PMC article.

6

A systems approach implicates nuclear receptor targeting in the Atp7b(-/-) mouse model of Wilson's disease.

Wilmarth PA, Short KK, Fiehn O, Lutsenko S, David LL, Burkhead JL. Wilmarth PA, et al. Metallomics. 2012 Jul;4(7):660-8. doi: 10.1039/c2mt20017a. Epub 2012 May 8. Metallomics. 2012. PMID: 22565294 Free PMC article.

7

Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B.

Braiterman LT, Murthy A, Jayakanthan S, Nyasae L, Tzeng E, Gromadzka G, Woolf TB, Lutsenko S, Hubbard AL. Braiterman LT, et al. Proc Natl Acad Sci U S A. 2014 Apr 8;111(14):E1364-73. doi: 10.1073/pnas.1314161111. Epub 2014 Mar 24. Proc Natl Acad Sci U S A. 2014. PMID: 24706876 Free PMC article.

8

Activation of liver X receptor/retinoid X receptor pathway ameliorates liver disease in Atp7B(-/-) (Wilson disease) mice.

Hamilton JP, Koganti L, Muchenditsi A, Pendyala VS, Huso D, Hankin J, Murphy RC, Huster D, Merle U, Mangels C, Yang N, Potter JJ, Mezey E, Lutsenko S. Hamilton JP, et al. Hepatology. 2016 Jun;63(6):1828-41. doi: 10.1002/hep.28406. Epub 2016 Feb 22. Hepatology. 2016. PMID: 26679751 Free PMC article.

9

Animal models of Wilson disease.

Medici V, Huster D. Medici V, et al. Handb Clin Neurol. 2017;142:57-70. doi: 10.1016/B978-0-444-63625-6.00006-9. Handb Clin Neurol. 2017. PMID: 28433110 Review.

10

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.

Buiakova OI, Xu J, Lutsenko S, Zeitlin S, Das K, Das S, Ross BM, Mekios C, Scheinberg IH, Gilliam TC. Buiakova OI, et al. Hum Mol Genet. 1999 Sep;8(9):1665-71. doi: 10.1093/hmg/8.9.1665. Hum Mol Genet. 1999. PMID: 10441329

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