Format
Sort by
Items per page

Send to

Choose Destination

Best matches for van der Westhuizen FH:

The unresolved role of mitochondrial DNA in Parkinson's disease: An overview of published studies, their limitations, and future prospects. Müller-Nedebock AC et al. Neurochem Int. (2019)

Metabolomics of mitochondrial disease. Esterhuizen K et al. Mitochondrion. (2017)

The aetiology of cardiovascular disease: a role for mitochondrial DNA? Venter M et al. Cardiovasc J Afr. (2018)

Search results

Items: 1 to 20 of 65

1.

Data on the optimisation of a solid phase extraction method for fractionating estrogen metabolites from small urine volumes.

van der Berg CL, Venter G, van der Westhuizen FH, Erasmus E.

Data Brief. 2020 Feb 3;29:105222. doi: 10.1016/j.dib.2020.105222. eCollection 2020 Apr.

2.

A call for global action for rare diseases in Africa.

Baynam GS, Groft S, van der Westhuizen FH, Gassman SD, du Plessis K, Coles EP, Selebatso E, Selebatso M, Gaobinelwe B, Selebatso T, Joel D, Llera VA, Vorster BC, Wuebbels B, Djoudalbaye B, Austin CP, Kumuthini J, Forman J, Kaufmann P, Chipeta J, Gavhed D, Larsson A, Stojiljkovic M, Nordgren A, Roldan EJA, Taruscio D, Wong-Rieger D, Nowak K, Bilkey GA, Easteal S, Bowdin S, Reichardt JKV, Beltran S, Kosaki K, van Karnebeek CDM, Gong M, Shuyang Z, Mehrian-Shai R, Adams DR, Puri RD, Zhang F, Pachter N, Muenke M, Nellaker C, Gahl WA, Cederroth H, Broley S, Schoonen M, Boycott KM, Posada M.

Nat Genet. 2020 Jan;52(1):21-26. doi: 10.1038/s41588-019-0552-2. No abstract available.

PMID:
31873296
3.

Development and validation of LC-ESI-MS/MS methods for quantification of 27 free and conjugated estrogen-related metabolites.

van der Berg C, Venter G, van der Westhuizen FH, Erasmus E.

Anal Biochem. 2020 Feb 1;590:113531. doi: 10.1016/j.ab.2019.113531. Epub 2019 Dec 2.

PMID:
31805274
4.

The unresolved role of mitochondrial DNA in Parkinson's disease: An overview of published studies, their limitations, and future prospects.

Müller-Nedebock AC, Brennan RR, Venter M, Pienaar IS, van der Westhuizen FH, Elson JL, Ross OA, Bardien S.

Neurochem Int. 2019 Oct;129:104495. doi: 10.1016/j.neuint.2019.104495. Epub 2019 Jun 21. Review.

PMID:
31233840
5.

Attenuation of Endoplasmic Reticulum Stress, Impaired Calcium Homeostasis, and Altered Bioenergetic Functions in MPP+-Exposed SH-SY5Y Cells Pretreated with Rutin.

Enogieru AB, Haylett WL, Miller HC, van der Westhuizen FH, Hiss DC, Ekpo OE.

Neurotox Res. 2019 Nov;36(4):764-776. doi: 10.1007/s12640-019-00048-4. Epub 2019 May 4.

PMID:
31055769
6.

Panel-Based Nuclear and Mitochondrial Next-Generation Sequencing Outcomes of an Ethnically Diverse Pediatric Patient Cohort with Mitochondrial Disease.

Schoonen M, Smuts I, Louw R, Elson JL, van Dyk E, Jonck LM, Rodenburg RJT, van der Westhuizen FH.

J Mol Diagn. 2019 May;21(3):503-513. doi: 10.1016/j.jmoldx.2019.02.002. Epub 2019 Mar 11.

PMID:
30872186
7.

MtDNA population variation in Myalgic encephalomyelitis/Chronic fatigue syndrome in two populations: a study of mildly deleterious variants.

Venter M, Tomas C, Pienaar IS, Strassheim V, Erasmus E, Ng WF, Howell N, Newton JL, Van der Westhuizen FH, Elson JL.

Sci Rep. 2019 Feb 27;9(1):2914. doi: 10.1038/s41598-019-39060-1.

8.

Implementing a new variant load model to investigate the role of mtDNA in oxidative stress and inflammation in a bi-ethnic cohort: the SABPA study.

Venter M, Malan L, Elson JL, van der Westhuizen FH.

Mitochondrial DNA A DNA Mapp Seq Anal. 2019 Apr;30(3):440-447. doi: 10.1080/24701394.2018.1544248. Epub 2019 Jan 18.

PMID:
30657012
9.

The dilemma of diagnosing coenzyme Q10 deficiency in muscle.

Louw R, Smuts I, Wilsenach KL, Jonck LM, Schoonen M, van der Westhuizen FH.

Mol Genet Metab. 2018 Sep;125(1-2):38-43. doi: 10.1016/j.ymgme.2018.02.015. Epub 2018 Feb 23.

PMID:
29530532
10.

A urinary biosignature for mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS).

Esterhuizen K, Lindeque JZ, Mason S, van der Westhuizen FH, Suomalainen A, Hakonen AH, Carroll CJ, Rodenburg RJ, de Laat PB, Janssen MCH, Smeitink JAM, Louw R.

Mitochondrion. 2019 Mar;45:38-45. doi: 10.1016/j.mito.2018.02.003. Epub 2018 Feb 19.

PMID:
29471047
11.

A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency.

van der Westhuizen FH, Smuts I, Honey E, Louw R, Schoonen M, Jonck LM, Dercksen M.

J Neurol Sci. 2018 Jan 15;384:121-125. doi: 10.1016/j.jns.2017.11.012. Epub 2017 Nov 15.

PMID:
29249369
12.

The aetiology of cardiovascular disease: a role for mitochondrial DNA?

Venter M, van der Westhuizen FH, Elson JL.

Cardiovasc J Afr. 2018 Mar/Apr 23;29(2):122-132. doi: 10.5830/CVJA-2017-037. Epub 2017 Aug 25. Review.

13.

Metabolomics of mitochondrial disease.

Esterhuizen K, van der Westhuizen FH, Louw R.

Mitochondrion. 2017 Jul;35:97-110. doi: 10.1016/j.mito.2017.05.012. Epub 2017 May 31. Review.

PMID:
28576558
14.

A molecular analysis of the GBA gene in Caucasian South Africans with Parkinson's disease.

Barkhuizen M, Anderson DG, van der Westhuizen FH, Grobler AF.

Mol Genet Genomic Med. 2017 Feb 8;5(2):147-156. doi: 10.1002/mgg3.267. eCollection 2017 Mar.

15.

Kinetic analysis, size profiling, and bioenergetic association of DNA released by selected cell lines in vitro.

Aucamp J, Bronkhorst AJ, Peters DL, Van Dyk HC, Van der Westhuizen FH, Pretorius PJ.

Cell Mol Life Sci. 2017 Jul;74(14):2689-2707. doi: 10.1007/s00018-017-2495-z. Epub 2017 Mar 18.

PMID:
28315952
16.

Clinically proven mtDNA mutations are not common in those with chronic fatigue syndrome.

Schoeman EM, Van Der Westhuizen FH, Erasmus E, van Dyk E, Knowles CV, Al-Ali S, Ng WF, Taylor RW, Newton JL, Elson JL.

BMC Med Genet. 2017 Mar 16;18(1):29. doi: 10.1186/s12881-017-0387-6.

17.

Using MutPred derived mtDNA load scores to evaluate mtDNA variation in hypertension and diabetes in a two-population cohort: The SABPA study.

Venter M, Malan L, van Dyk E, Elson JL, van der Westhuizen FH.

J Genet Genomics. 2017 Mar 20;44(3):139-149. doi: 10.1016/j.jgg.2016.12.003. Epub 2016 Dec 26.

PMID:
28298255
18.

A 3-methylcrotonyl-CoA carboxylase deficient human skin fibroblast transcriptome reveals underlying mitochondrial dysfunction and oxidative stress.

Zandberg L, van Dyk HC, van der Westhuizen FH, van Dijk AA.

Int J Biochem Cell Biol. 2016 Sep;78:116-129. doi: 10.1016/j.biocel.2016.07.010. Epub 2016 Jul 12.

PMID:
27417235
19.

Curcumin Rescues a PINK1 Knock Down SH-SY5Y Cellular Model of Parkinson's Disease from Mitochondrial Dysfunction and Cell Death.

van der Merwe C, van Dyk HC, Engelbrecht L, van der Westhuizen FH, Kinnear C, Loos B, Bardien S.

Mol Neurobiol. 2017 May;54(4):2752-2762. doi: 10.1007/s12035-016-9843-0. Epub 2016 Mar 22.

PMID:
27003823
20.

Conservation of the coding regions of the glycine N-acyltransferase gene further suggests that glycine conjugation is an essential detoxification pathway.

van der Sluis R, Badenhorst CP, Erasmus E, van Dyk E, van der Westhuizen FH, van Dijk AA.

Gene. 2015 Oct 15;571(1):126-34. doi: 10.1016/j.gene.2015.06.081. Epub 2015 Jul 3.

PMID:
26149650

Supplemental Content

Loading ...
Support Center