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Items: 1 to 20 of 54

1.

Association between polymorphisms in CTR1, CTR2, ATP7A, and ATP7B and platinum resistance in epithelial ovarian cancer.

Li T, Peng J, Zeng F, Zhang K, Liu J, Li X, Ouyang Q, Wang G, Wang L, Liu Z, Liu Y.

Int J Clin Pharmacol Ther. 2017 Oct;55(10):774-780. doi: 10.5414/CP202907.

PMID:
28737129
2.

Dynamics of the metal binding domains and regulation of the human copper transporters ATP7B and ATP7A.

Yu CH, Dolgova NV, Dmitriev OY.

IUBMB Life. 2017 Apr;69(4):226-235. doi: 10.1002/iub.1611. Epub 2017 Mar 8. Review.

PMID:
28271598
3.

Multiple di-leucines in the ATP7A copper transporter are required for retrograde trafficking to the trans-Golgi network.

Zhu S, Shanbhag V, Hodgkinson VL, Petris MJ.

Metallomics. 2016 Sep 1;8(9):993-1001. doi: 10.1039/c6mt00093b. Epub 2016 Jun 23.

4.

Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX).

Perez-Siles G, Grant A, Ellis M, Ly C, Kidambi A, Khalil M, Llanos RM, Fontaine SL, Strickland AV, Züchner S, Bermeo S, Neist E, Brennan-Speranza TC, Takata RI, Speck-Martins CE, Mercer JF, Nicholson GA, Kennerson ML.

Metallomics. 2016 Sep 1;8(9):981-92. doi: 10.1039/c6mt00082g. Epub 2016 Jun 13.

5.

pH-regulated metal-ligand switching in the HM loop of ATP7A: a new paradigm for metal transfer chemistry.

Kline CD, Gambill BF, Mayfield M, Lutsenko S, Blackburn NJ.

Metallomics. 2016 Aug 1;8(8):729-33. doi: 10.1039/c6mt00062b.

6.

miR-133a enhances the sensitivity of Hep-2 cells and vincristine-resistant Hep-2v cells to cisplatin by downregulating ATP7B expression.

Wang X, Zhu W, Zhao X, Wang P.

Int J Mol Med. 2016 Jun;37(6):1636-42. doi: 10.3892/ijmm.2016.2569. Epub 2016 Apr 20.

PMID:
27121102
7.

Dual role of LRRC8A-containing transporters on cisplatin resistance in human ovarian cancer cells.

Sørensen BH, Dam CS, Stürup S, Lambert IH.

J Inorg Biochem. 2016 Jul;160:287-95. doi: 10.1016/j.jinorgbio.2016.04.004. Epub 2016 Apr 13.

PMID:
27112899
8.

Human Pigmentation, Cutaneous Vitamin D Synthesis and Evolution: Variants of Genes (SNPs) Involved in Skin Pigmentation Are Associated with 25(OH)D Serum Concentration.

Rossberg W, Saternus R, Wagenpfeil S, Kleber M, März W, Reichrath S, Vogt T, Reichrath J.

Anticancer Res. 2016 Mar;36(3):1429-37.

PMID:
26977047
9.

Gene expression of membrane transporters: Importance for prognosis and progression of ovarian carcinoma.

Elsnerova K, Mohelnikova-Duchonova B, Cerovska E, Ehrlichova M, Gut I, Rob L, Skapa P, Hruda M, Bartakova A, Bouda J, Vodicka P, Soucek P, Vaclavikova R.

Oncol Rep. 2016 Apr;35(4):2159-70. doi: 10.3892/or.2016.4599. Epub 2016 Jan 28.

PMID:
26820484
10.

The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders.

Fieten H, Gill Y, Martin AJ, Concilli M, Dirksen K, van Steenbeek FG, Spee B, van den Ingh TS, Martens EC, Festa P, Chesi G, van de Sluis B, Houwen RH, Watson AL, Aulchenko YS, Hodgkinson VL, Zhu S, Petris MJ, Polishchuk RS, Leegwater PA, Rothuizen J.

Dis Model Mech. 2016 Jan;9(1):25-38. doi: 10.1242/dmm.020263.

11.

Unresolved questions in human copper pump mechanisms.

Wittung-Stafshede P.

Q Rev Biophys. 2015 Nov;48(4):471-8. doi: 10.1017/S0033583515000128. Review.

PMID:
26537407
12.

Copper Transport Protein Antioxidant-1 Promotes Inflammatory Neovascularization via Chaperone and Transcription Factor Function.

Chen GF, Sudhahar V, Youn SW, Das A, Cho J, Kamiya T, Urao N, McKinney RD, Surenkhuu B, Hamakubo T, Iwanari H, Li S, Christman JW, Shantikumar S, Angelini GD, Emanueli C, Ushio-Fukai M, Fukai T.

Sci Rep. 2015 Oct 6;5:14780. doi: 10.1038/srep14780.

13.

Impaired osteogenesis in Menkes disease-derived induced pluripotent stem cells.

Kim D, Choi J, Han KM, Lee BH, Choi JH, Yoo HW, Han YM.

Stem Cell Res Ther. 2015 Sep 7;6:160. doi: 10.1186/s13287-015-0147-5.

14.

Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry.

Protasova MS, Grigorenko AP, Tyazhelova TV, Andreeva TV, Reshetov DA, Gusev FE, Laptenko AE, Kuznetsova IL, Goltsov AY, Klyushnikov SA, Illarioshkin SN, Rogaev EI.

Eur J Hum Genet. 2016 Apr;24(4):550-5. doi: 10.1038/ejhg.2015.139. Epub 2015 Aug 5.

15.

Menkes disease with discordant phenotype in female monozygotic twins.

Burgemeister AL, Zirn B, Oeffner F, Kaler SG, Lemm G, Rossier E, Büttel HM.

Am J Med Genet A. 2015 Nov;167A(11):2826-9. doi: 10.1002/ajmg.a.37276. Epub 2015 Aug 4.

PMID:
26239182
16.

A Truncating De Novo Point Mutation in a Young Infant with Severe Menkes Disease.

Lin YJ, Ho CS, Hsu CH, Lin JL, Chuang CK, Tsai JD, Chiu NC, Lin HY, Lin SP.

Pediatr Neonatol. 2017 Feb;58(1):89-92. doi: 10.1016/j.pedneo.2014.05.008. Epub 2014 Nov 14.

17.

Molecular basis of neurodegeneration and neurodevelopmental defects in Menkes disease.

Zlatic S, Comstra HS, Gokhale A, Petris MJ, Faundez V.

Neurobiol Dis. 2015 Sep;81:154-61. doi: 10.1016/j.nbd.2014.12.024. Epub 2015 Jan 10. Review.

18.
19.

Carboplatin and taxol resistance develops more rapidly in functional BRCA1 compared to dysfunctional BRCA1 ovarian cancer cells.

Busschots S, O'Toole S, O'Leary JJ, Stordal B.

Exp Cell Res. 2015 Aug 1;336(1):1-14. doi: 10.1016/j.yexcr.2014.12.001. Epub 2014 Dec 12.

PMID:
25499884
20.

Molecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse model.

Haddad MR, Patel KD, Sullivan PH, Goldstein DS, Murphy KM, Centeno JA, Kaler SG.

Mol Genet Metab. 2014 Dec;113(4):294-300. doi: 10.1016/j.ymgme.2014.10.001. Epub 2014 Oct 13.

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