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Items: 1 to 20 of 192

1.

Pathological Fracture of Femoral Neck Leading to a Diagnosis of Wilson's Disease: A Case Report and Review of Literature.

Bhatnagar N, Lingaiah P, Lodhi JS, Karkhur Y.

J Bone Metab. 2017 May;24(2):135-139. doi: 10.11005/jbm.2017.24.2.135. Epub 2017 May 31.

2.

Phenotypes and Chronic Organ Damage May Be Different among Siblings with Wilson's Disease.

Yahata S, Yung S, Mandai M, Nagahara T, Kuzume D, Sakaeda H, Wakusawa S, Kato A, Tatsumi Y, Kato K, Hayashi H, Isaji R, Sasaki Y, Yano M, Hayashi K, Ishigami M, Goto H.

J Clin Transl Hepatol. 2017 Mar 28;5(1):27-30. doi: 10.14218/JCTH.2016.00064. Epub 2017 Feb 22.

3.

Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration.

Wilkins HM, Weidling IW, Ji Y, Swerdlow RH.

Front Immunol. 2017 Apr 26;8:508. doi: 10.3389/fimmu.2017.00508. eCollection 2017. Review.

4.

Sphingolipids and mitochondrial function, lessons learned from yeast.

Spincemaille P, Cammue BP, Thevissen K.

Microb Cell. 2014 Jun 25;1(7):210-224. doi: 10.15698/mic2014.07.156. Review.

5.

Update on the clinical management of Wilson's disease.

Hedera P.

Appl Clin Genet. 2017 Jan 13;10:9-19. doi: 10.2147/TACG.S79121. eCollection 2017. Review.

6.

Programmed Ribosomal Frameshifting Generates a Copper Transporter and a Copper Chaperone from the Same Gene.

Meydan S, Klepacki D, Karthikeyan S, Margus T, Thomas P, Jones JE, Khan Y, Briggs J, Dinman JD, Vázquez-Laslop N, Mankin AS.

Mol Cell. 2017 Jan 19;65(2):207-219. doi: 10.1016/j.molcel.2016.12.008.

PMID:
28107647
7.

On the nature of the Cu-rich aggregates in brain astrocytes.

Sullivan B, Robison G, Osborn J, Kay M, Thompson P, Davis K, Zakharova T, Antipova O, Pushkar Y.

Redox Biol. 2017 Apr;11:231-239. doi: 10.1016/j.redox.2016.12.007. Epub 2016 Dec 9.

8.

Metal Selectivity of a Cd-, Co-, and Zn-Transporting P1B-type ATPase.

Smith AT, Ross MO, Hoffman BM, Rosenzweig AC.

Biochemistry. 2017 Jan 10;56(1):85-95. doi: 10.1021/acs.biochem.6b01022. Epub 2016 Dec 21.

9.
10.

Sensitive detection of copper ions via ion-responsive fluorescence quenching of engineered porous silicon nanoparticles.

Hwang J, Hwang MP, Choi M, Seo Y, Jo Y, Son J, Hong J, Choi J.

Sci Rep. 2016 Oct 18;6:35565. doi: 10.1038/srep35565.

11.

The coming of age of the mitochondria-ER contact: a matter of thickness.

Giacomello M, Pellegrini L.

Cell Death Differ. 2016 Sep 1;23(9):1417-27. doi: 10.1038/cdd.2016.52. Epub 2016 Jun 24. Review.

PMID:
27341186
12.

Loss of divalent metal transporter 1 function promotes brain copper accumulation and increases impulsivity.

Han M, Chang J, Kim J.

J Neurochem. 2016 Sep;138(6):918-28. doi: 10.1111/jnc.13717. Epub 2016 Jul 22.

PMID:
27331785
13.

Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.

Oishi K, Arnon R, Wasserstein MP, Diaz GA.

Pediatr Transplant. 2016 Sep;20(6):756-69. doi: 10.1111/petr.12741. Epub 2016 Jun 21. Review.

PMID:
27329540
14.

Microbial peptide de-coppers mitochondria: implications for Wilson disease.

Kaler SG.

J Clin Invest. 2016 Jul 1;126(7):2412-4. doi: 10.1172/JCI88617. Epub 2016 Jun 20.

15.

Methanobactin reverses acute liver failure in a rat model of Wilson disease.

Lichtmannegger J, Leitzinger C, Wimmer R, Schmitt S, Schulz S, Kabiri Y, Eberhagen C, Rieder T, Janik D, Neff F, Straub BK, Schirmacher P, DiSpirito AA, Bandow N, Baral BS, Flatley A, Kremmer E, Denk G, Reiter FP, Hohenester S, Eckardt-Schupp F, Dencher NA, Adamski J, Sauer V, Niemietz C, Schmidt HH, Merle U, Gotthardt DN, Kroemer G, Weiss KH, Zischka H.

J Clin Invest. 2016 Jul 1;126(7):2721-35. doi: 10.1172/JCI85226. Epub 2016 Jun 20.

16.

Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines.

Chandhok G, Horvath J, Aggarwal A, Bhatt M, Zibert A, Schmidt HH.

World J Gastroenterol. 2016 Apr 28;22(16):4109-19. doi: 10.3748/wjg.v22.i16.4109.

17.

Neurological features and management of Wilson disease in children: an evaluation of 12 cases.

Bayram AK, Gümüş H, Arslan D, Özçora GK, Kumandaş S, Karacabey N, Canpolat M, Per H.

Turk Pediatri Ars. 2016 Mar 1;51(1):15-21. doi: 10.5152/TurkPediatriArs.2016.3080. eCollection 2016 Mar.

18.

Comparative study of biliary trace elements and clinical phenotypes in Wilson's disease.

Ren MS, Fan YX, Yang RM, Han YZ, Wu GJ, Xin YR, Yu L.

World J Gastroenterol. 1997 Dec 15;3(4):260-2. doi: 10.3748/wjg.v3.i4.260.

19.

Spectrum and Classification of ATP7B Variants in a Large Cohort of Chinese Patients with Wilson's Disease Guides Genetic Diagnosis.

Dong Y, Ni W, Chen WJ, Wan B, Zhao GX, Shi ZQ, Zhang Y, Wang N, Yu L, Xu JF, Wu ZY.

Theranostics. 2016 Mar 3;6(5):638-49. doi: 10.7150/thno.14596. eCollection 2016.

20.

Canine Models for Copper Homeostasis Disorders.

Wu X, Leegwater PA, Fieten H.

Int J Mol Sci. 2016 Feb 4;17(2):196. doi: 10.3390/ijms17020196. Review.

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