C MacMillan
Overview
Explore the profile of C MacMillan including associated specialties, affiliations and a list of published articles.
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Articles
46
Citations
508
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Recent Articles
1.
Olivier B, Boulle N, Jacobs J, Obiora O, MacMillan C, Liebenberg J, et al.
S Afr J Sports Med
. 2024 Jan;
35(1):v35i1a15144.
PMID: 38249757
Background: Despite differences between left- and right-handed athletes in other sports, minimal evidence exists regarding biomechanical similarities and differences between left- and right-handed cricket fast bowlers performing an equivalent task....
2.
Hyles J, Vautrin S, Pettolino F, MacMillan C, Stachurski Z, Breen J, et al.
J Exp Bot
. 2017 Apr;
68(7):1519-1529.
PMID: 28369427
The tiller inhibition gene (tin) that reduces tillering in wheat (Triticum aestivum) is also associated with large spikes, increased grain weight, and thick leaves and stems. In this study, comparison...
3.
Chauhan S, Kaur J, Kumar M, Matta A, Srivastava G, Alyass A, et al.
Oncogenesis
. 2015 Apr;
4:e147.
PMID: 25893634
Loco-regional recurrence in 50% of oral squamous cell carcinoma (OSCC) patients poses major challenge for oncologists. Lack of biomarkers that can predict disease aggressiveness and recurrence risk makes the scenario...
4.
Davis L, Maltman N, Mosconi M, MacMillan C, Schmitt L, Moore K, et al.
Am J Med Genet A
. 2012 Jun;
158A(7):1654-61.
PMID: 22678932
Ataxin 2 binding protein 1 (A2BP1 aka FOX1, RBFOX1) is an RNA binding protein responsible for regulation of pre-mRNA splicing events in a number of critical developmental genes expressed in...
5.
6.
Singla M, John E, Hidalgo G, Grewal D, MacMillan C
Neuropediatrics
. 2008 Aug;
39(2):128-30.
PMID: 18671191
Moyamoya disease is a cerebral vasculopathy of unknown etiology frequently seen in the Asian population. We report a case of moyamoya vasculopathy in an African-American child who had renal failure...
7.
Bradley G, Tremblay S, Irish J, MacMillan C, Baker G, Gullane P, et al.
Br J Cancer
. 2007 Apr;
96(9):1425-32.
PMID: 17437012
The Pidd (p53-induced protein with death domain) gene was shown to be induced by the tumour suppressor p53 and to mediate p53-dependent apoptosis in mouse and human cells, through interactions...
8.
Freisinger P, Horvath R, MacMillan C, Peters J, Jaksch M
J Inherit Metab Dis
. 2004 Feb;
27(1):67-79.
PMID: 14970747
Mutations in Sco2, a protein involved in copper trafficking to the terminal enzyme of the respiratory chain, cytochrome c oxidase, results in infantile hypertrophic cardioencephalomyopathy. We have recently shown that...
9.
Braun M, Adab F, Bradley C, McAdam K, Thomas G, Wadd N, et al.
Br J Cancer
. 2003 Oct;
89(7):1155-8.
PMID: 14520437
We previously reported high activity for oxaliplatin and a modified de Gramont regimen (OxMdG) in a single centre study of patients with metastatic colorectal cancer. We now report results with...
10.
Jaksch M, Horvath R, Horn N, Auer D, MacMillan C, Peters J, et al.
Neurology
. 2001 Oct;
57(8):1440-6.
PMID: 11673586
Objective: To report three unrelated infants with a distinctive phenotype of Leigh-like syndrome, neurogenic muscular atrophy, and hypertrophic obstructive cardiomyopathy. The patients all had a homozygous missense mutation in SCO2....