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Items: 15

1.

Disruption of mitochondrial dynamics affects behaviour and lifespan in Caenorhabditis elegans.

Byrne JJ, Soh MS, Chandhok G, Vijayaraghavan T, Teoh JS, Crawford S, Cobham AE, Yapa NMB, Mirth CK, Neumann B.

Cell Mol Life Sci. 2019 Mar 6. doi: 10.1007/s00018-019-03024-5. [Epub ahead of print]

PMID:
30840087
2.

Portal Hypertensive Polyposis in Advanced Liver Cirrhosis: The Unknown Entity?

Kara D, Hüsing-Kabar A, Schmidt H, Grünewald I, Chandhok G, Maschmeier M, Kabar I.

Can J Gastroenterol Hepatol. 2018 Aug 1;2018:2182784. doi: 10.1155/2018/2182784. eCollection 2018.

3.

Organic cation transporter 3 mediates cisplatin and copper cross-resistance in hepatoma cells.

Guttmann S, Chandhok G, Groba SR, Niemietz C, Sauer V, Gomes A, Ciarimboli G, Karst U, Zibert A, Schmidt HH.

Oncotarget. 2017 Dec 12;9(1):743-754. doi: 10.18632/oncotarget.23142. eCollection 2018 Jan 2.

4.

Structure, function, and regulation of mitofusin-2 in health and disease.

Chandhok G, Lazarou M, Neumann B.

Biol Rev Camb Philos Soc. 2018 May;93(2):933-949. doi: 10.1111/brv.12378. Epub 2017 Oct 25. Review.

PMID:
29068134
5.

FAP plasma-induced cellular toxicity.

Niemietz C, Chandhok G, Fleischhauer L, Ballmaier P, Sauer V, Guttmann S, Zibert A, Schmidt H.

Amyloid. 2017 Mar;24(sup1):87-88. doi: 10.1080/13506129.2017.1278692. No abstract available.

PMID:
28434333
6.

Evaluation of Therapeutic Oligonucleotides for Familial Amyloid Polyneuropathy in Patient-Derived Hepatocyte-Like Cells.

Niemietz CJ, Sauer V, Stella J, Fleischhauer L, Chandhok G, Guttmann S, Avsar Y, Guo S, Ackermann EJ, Gollob J, Monia BP, Zibert A, Schmidt HH.

PLoS One. 2016 Sep 1;11(9):e0161455. doi: 10.1371/journal.pone.0161455. eCollection 2016.

7.

Identification of survival-promoting OSIP108 peptide variants and their internalization in human cells.

Verbandt S, Henriques ST, Spincemaille P, Harvey PJ, Chandhok G, Sauer V, De Coninck B, Cassiman D, Craik DJ, Cammue BPA, De Cremer K, Thevissen K.

Mech Ageing Dev. 2017 Jan;161(Pt B):247-254. doi: 10.1016/j.mad.2016.07.013. Epub 2016 Aug 1.

PMID:
27491841
8.

Presynaptic Deficits at Neuromuscular Junctions: A Specific Cause and Potential Target of Axonal Neuropathy in Type 2 Charcot-Marie-Tooth Disease.

Chandhok G, Soh MS.

J Neurosci. 2016 Aug 3;36(31):8067-9. doi: 10.1523/JNEUROSCI.1515-16.2016. Review. No abstract available.

9.

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.

10.

Therapeutic Oligonucleotides Targeting Liver Disease: TTR Amyloidosis.

Niemietz C, Chandhok G, Schmidt H.

Molecules. 2015 Sep 30;20(10):17944-75. doi: 10.3390/molecules201017944. Review.

11.

Angiotensin II type 1 receptor blockers increase tolerance of cells to copper and cisplatin.

Spincemaille P, Chandhok G, Zibert A, Schmidt H, Verbeek J, Chaltin P, Cammue BP, Cassiman D, Thevissen K.

Microb Cell. 2014 Oct 24;1(11):352-364. doi: 10.15698/mic2014.11.175.

12.

The plant decapeptide OSIP108 prevents copper-induced toxicity in various models for Wilson disease.

Spincemaille P, Pham DH, Chandhok G, Verbeek J, Zibert A, Libbrecht L, Schmidt H, Esguerra CV, de Witte PA, Cammue BP, Cassiman D, Thevissen K.

Toxicol Appl Pharmacol. 2014 Oct 15;280(2):345-51. doi: 10.1016/j.taap.2014.08.005. Epub 2014 Aug 16.

PMID:
25134866
13.

The effect of zinc and D-penicillamine in a stable human hepatoma ATP7B knockout cell line.

Chandhok G, Schmitt N, Sauer V, Aggarwal A, Bhatt M, Schmidt HH.

PLoS One. 2014 Jun 3;9(6):e98809. doi: 10.1371/journal.pone.0098809. eCollection 2014.

14.

The plant decapeptide OSIP108 prevents copper-induced apoptosis in yeast and human cells.

Spincemaille P, Chandhok G, Newcomb B, Verbeek J, Vriens K, Zibert A, Schmidt H, Hannun YA, van Pelt J, Cassiman D, Cammue BPA, Thevissen K.

Biochim Biophys Acta. 2014 Jun;1843(6):1207-1215. doi: 10.1016/j.bbamcr.2014.03.004. Epub 2014 Mar 13.

15.

Wilson disease mutation pattern with genotype-phenotype correlations from Western India: confirmation of p.C271* as a common Indian mutation and identification of 14 novel mutations.

Aggarwal A, Chandhok G, Todorov T, Parekh S, Tilve S, Zibert A, Bhatt M, Schmidt HH.

Ann Hum Genet. 2013 Jul;77(4):299-307. doi: 10.1111/ahg.12024. Epub 2013 Apr 2.

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