M P Marx
Overview
Explore the profile of M P Marx including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
59
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0
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Recent Articles
1.
Goldberg P, Madden M, Harocopos C, Grobbelaar J, Kotze M, Marx M, et al.
S Afr Med J
. 2000 Sep;
90(7):703-4.
PMID: 10985131
No abstract available.
2.
Hayes V, Bleeker W, Verlind E, Timmer T, Karrenbeld A, Plukker J, et al.
Diagn Mol Pathol
. 1999 Jul;
8(1):2-10.
PMID: 10408787
A comprehensive mutation detection assay is described for the entire coding region and all splice site junctions of TP53. The assay is based on denaturing gradient gel electrophoresis, which follows...
3.
DE VILLIERS J, Hillerman R, de Jong G, Langenhoven E, Rossouw H, Marx M, et al.
S Afr Med J
. 1999 May;
89(3):279-82.
PMID: 10226674
Objective: The aim of the study was to investigate the molecular basis of hereditary haemochromatosis (HH) in South Africa in order to establish a reliable, cost-effective molecular diagnostic service for...
4.
du Plessis L, Dietzsch E, Van Gele M, van Roy N, van Helden P, Parker M, et al.
Cancer Res
. 1999 Apr;
59(8):1877-83.
PMID: 10213495
Esophageal cancer (EC) is the leading cause of cancer death in the Black male population in South Africa. Although several oncogenes and tumor suppressor genes have previously been found altered...
5.
Thiart R, Loubser O, DE VILLIERS J, Marx M, Zaire R, Raal F, et al.
Hum Mutat
. 1998 Feb;
Suppl 1:S232-3.
PMID: 9452095
No abstract available.
6.
Hayes V, Oosthuizen C, Kotze M, Marx M, Buys C
Mol Cell Probes
. 1996 Oct;
10(5):393-5.
PMID: 8910896
In a search for mutations of the TP53 tumour suppressor gene in lung cancer samples from gold miners in the Witwatersrand, South Africa, using heteroduplex and single strand conformation polymorphism...
7.
Kotze M, Langenhoven E, Theart L, Marx M, Oosthuizen C
Genet Couns
. 1994 Jan;
5(1):15-21.
PMID: 8031531
The development of DNA-based methods for the direct detection of specific low density lipoprotein receptor (LDLR) gene mutations enabled us to establish a molecular diagnostic service for familial hypercholesterolemia (FH)....
8.
Apfelberg D, Lane B, Marx M
Plast Reconstr Surg
. 1991 Jul;
88(1):71-82.
PMID: 2052663
Thirteen patients have been treated over a 2-year period utilizing a team approach between the radiology and surgical services. Initial diagnostic evaluation is directed at determining the size and anatomic...
9.
Kotze M, Langenhoven E, Warnich L, du Plessis L, Marx M, Oosthuizen C, et al.
S Afr Med J
. 1989 Oct;
76(8):399-401.
PMID: 2799589
Two point mutations were discovered in the low-density lipoprotein genes of patients with familial hypercholesterolaemia (FH). Defective genes were cloned and/or amplified by the polymerase chain reaction (PCR) method and...
10.
Kotze M, Langenhoven E, Warnich L, Marx M, Retief A
S Afr Med J
. 1989 Oct;
76(8):402-5.
PMID: 2572061
The prevalence of familial hypercholesterolaemia (FH), an autosomal dominant disease characterised by raised low-density lipoprotein (LDL) cholesterol levels, is at least five times higher in the white Afrikaner population than...