G Steel
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Explore the profile of G Steel including associated specialties, affiliations and a list of published articles.
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41
Citations
706
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Recent Articles
1.
Mehta U, Dheda M, Steel G, Blockman M, Ntilivamunda A, Maartens G, et al.
S Afr Med J
. 2014 Jun;
104(2):104-6.
PMID: 24893535
This report outlines findings and recommendations of a national pharmacovigilance workshop held in August 2012 in South Africa (SA). A survey of current pharmacovigilance activities, conducted in preparation for the...
2.
Rustomjee R, McClain B, Brennan M, McLeod R, Chetty-Makkan C, McShane H, et al.
Tuberculosis (Edinb)
. 2012 Dec;
93(2):136-42.
PMID: 23266259
This article summarises the consensus arrived at a meeting of South African and international stakeholders on specific late phase clinical trial design issues integrating the investigation of immune correlates as...
3.
Rustomjee R, McLeod R, Hanekom W, Steel G, Mahomed H, Hawkridge A, et al.
Tuberculosis (Edinb)
. 2012 Jun;
92(5):359-64.
PMID: 22698868
Significant progress has been made in advancing the development pipeline for a new and more effective TB vaccine with some candidate vaccines now in late stage clinical evaluation. However, progress...
4.
Steel G, Lutz E
J Neuroendocrinol
. 2006 Dec;
19(1):14-25.
PMID: 17184482
The VPAC(2) receptor is a seven transmembrane spanning G protein-coupled receptor for two neuropeptides, vasoactive intestinal peptide (VIP) and pituitary adenylate cyclase-activating polypeptide (PACAP). It has a distinct tissue-specific, developmental...
5.
Baumgartner M, Hu C, Almashanu S, Steel G, Obie C, Aral B, et al.
Hum Mol Genet
. 2000 Nov;
9(19):2853-8.
PMID: 11092761
delta(1)-pyrroline-5-carboxylate synthase (P5CS), a bifunctional ATP- and NADPH-dependent mitochondrial enzyme, catalyzes the reduction of glutamate to delta(1)-pyrroline-5-carboxylate, a critical step in the biosynthesis of proline, ornithine and arginine. Recently, we...
6.
Braverman N, Steel G, Lin P, Moser A, Moser H, Valle D
Genomics
. 2000 Feb;
63(2):181-92.
PMID: 10673331
We recently reported cloning a cDNA encoding Pex7p, the peroxisomal PTS2 receptor. PEX7 mutations cause the peroxisome biogenesis disorder (PBD) rhizomelic chondrodysplasia punctata (RCDP). In a survey of 44 RCDP...
7.
Wang T, Steel G, Milam A, Valle D
Proc Natl Acad Sci U S A
. 2000 Feb;
97(3):1224-9.
PMID: 10655512
Deficiency of ornithine-delta-aminotransferase (OAT) in humans results in gyrate atrophy of the choroid and retina (GA), an autosomal recessive disorder characterized by ornithine accumulation and a progressive chorioretinal degeneration of...
8.
Camacho J, Obie C, Biery B, Goodman B, Hu C, Almashanu S, et al.
Nat Genet
. 1999 Jun;
22(2):151-8.
PMID: 10369256
Neurospora crassa ARG13 and Saccharomyces cerevisiae ARG11 encode mitochondrial carrier family (MCF) proteins that transport ornithine across the mitochondrial inner membrane. We used their sequences to identify EST candidates that...
9.
Shani N, Jimenez-Sanchez G, Steel G, Dean M, Valle D
Hum Mol Genet
. 1997 Sep;
6(11):1925-31.
PMID: 9302272
Three half ATP-binding cassette transporters (ALDP, ALDR, PMP70) are known to be present in the human peroxisome membrane. Mutations in the gene encoding ALDP cause X-linked adrenoleukodystrophy; the role of...
10.
Braverman N, Steel G, Obie C, Moser A, Moser H, Gould S, et al.
Nat Genet
. 1997 Apr;
15(4):369-76.
PMID: 9090381
Rhizomelic chondrodysplasia punctata (RCDP) is a rare autosomal recessive phenotype that comprises complementation group 11 of the peroxisome biogenesis disorders (PBD). PEX7, a candidate gene for RCDP identified in yeast,...