W J de Wet
Overview
Explore the profile of W J de Wet including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
22
Citations
227
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
van der Westhuizen F, Pretorius P, de Wet W
Biochem Biophys Res Commun
. 1996 Oct;
227(2):576-80.
PMID: 8878555
The effect of the presence of the regions 5' and 3' of the hIL-5 gene on the expression of recombinant hIL-5 in CHO-cells was investigated. The 3.2 kb hIL-5 gene-fragment...
2.
3.
van Rooyen J, Mienie L, Erasmus E, de Wet W, Duran M, WADMAN S
Clin Chim Acta
. 1994 Oct;
230(1):91-9.
PMID: 7850997
The identity of two formerly novel citric acid analogues, homocitric acid and methylhomocitric acid, in urine samples from patients with propionic acidaemia was confirmed by gas chromatography and mass spectrometry....
4.
Jooste S, Erasmus E, Mienie L, de Wet W, Gibson K
Clin Chim Acta
. 1994 Oct;
230(1):1-8.
PMID: 7850987
Two patients, diagnosed with 3-methylglutaconic aciduria, who presented with diverse clinical and metabolic manifestations, were studied. Glycine conjugation as a possible detoxification mechanism in these two patients yielded negative results....
5.
van Rooyen J, Mienie L, Erasmus E, de Wet W, Ketting D, Duran M, et al.
J Inherit Metab Dis
. 1994 Jan;
17(6):738-47.
PMID: 7707698
The absolute separation of the four stereoisomeric configurations of methylcitric acid can be achieved on a nonchiral stationary phase SE30 capillary column using the corresponding O-acetylated (tri-(-)-2-butyl ester derivatives. Identification...
6.
Wirtz M, Rao V, Glanville R, Labhard M, Pretorius P, de Vries W, et al.
Connect Tissue Res
. 1993 Jan;
29(1):1-11.
PMID: 8339541
The molecular basis for Osteogenesis Imperfecta in a large kindred with a highly variable phenotype was identified by sequencing the mutant pro alpha 1 (I) protein, cDNA and genomic DNA...
7.
Erasmus E, Mienie L, de Vries W, de Wet W, Carlsson B, Larsson A
J Inherit Metab Dis
. 1993 Jan;
16(5):837-43.
PMID: 8295398
Prenatal diagnosis was performed in a family affected by generalized glutathione synthetase deficiency. The disorder is transmitted by autosomal recessive inheritance. The first child born in this family died of...
8.
Pihlajaniemi T, McKeon J, Gay S, Gay R, de Wet W, Myers J, et al.
Biochem J
. 1989 Jan;
257(2):439-45.
PMID: 2649075
Fibroblasts from two lethal variants of osteogenesis imperfecta were shown to synthesize increased amounts of type IV procollagen. Previous studies established that one of these variants had a non-functional allele...
9.
Rossouw C, Vergeer W, du Plooy S, Bernard M, Ramirez F, de Wet W
J Biol Chem
. 1987 Nov;
262(31):15151-7.
PMID: 2822714
A chimeric gene was constructed in which sequences between 253 base pairs (bp) upstream of the start of transcription of the human pro-alpha 1(I) collagen gene and 117 bp downstream...
10.