User profiles for J. Macmillan

John MacMillan

- Verified email at ucsc.edu - Cited by 5743

John MacMillan

- Verified email at brunel.ac.uk - Cited by 1176

[HTML][HTML] The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research

…, SN Chen, A Kutateladze, JB MacMillan… - Natural product …, 2019 - pubs.rsc.org
Covering: up to 2018 With contributions from the global natural product (NP) research
community, and continuing the Raw Data Initiative, this review collects a comprehensive …

[HTML][HTML] RNA polymerase III detects cytosolic DNA and induces type I interferons through the RIG-I pathway

YH Chiu, JB MacMillan, ZJ Chen - Cell, 2009 - cell.com
Type I interferons (IFNs) are important for antiviral and autoimmune responses. Retinoic acid-induced
gene I (RIG-I) and mitochondrial antiviral signaling (MAVS) proteins mediate IFN …

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

RG Snell, JC MacMillan, JP Cheadle, I Fenton… - Nature …, 1993 - nature.com
The molecular analysis of a specific CAG repeat sequence in the Huntington's disease
gene in 440 Huntington's disease patients and 360 normal controls reveals a range of 30–70 …

[HTML][HTML] Survival in medically treated patients with homozygous β-thalassemia

NF Olivieri, DG Nathan, JH MacMillan… - … England Journal of …, 1994 - Mass Medical Soc
Background The prognosis of patients with homozygous β-thalassemia (thalassemia major)
has been improved by transfusion and iron-chelation therapy. We analyzed outcome and …

II. A randomised controlled trial of prophylactic neuroleptic treatment

TJ Crow, JF MacMillan, AL Johnson… - The British Journal of …, 1986 - cambridge.org
Out of 253 patients fulfilling criteria for a first episode of schizophrenic illness, 120 entered a
randomised placebo-controlled trial of maintenance neuroleptic medication on discharge; …

Phenotypic characterization of individuals with 30–40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal …

…, JC Kaplan, M Losekoot, JC MacMillan… - American journal of …, 1996 - ncbi.nlm.nih.gov
Abnormal CAG expansions in the IT-15 gene are associated with Huntington disease (HD).
In the diagnostic setting it is necessary to define the limits of the CAG size ranges on normal …

Beyond the separate democratic peace

J MacMillan - Journal of Peace Research, 2003 - journals.sagepub.com
This article argues that the balance of evidence and argument supports a shift from the
conventional `separate democratic peace' position that liberal states are peace prone only in …

Biosynthesis of the gibberellin plant hormones

J MacMillan - Natural Product Reports, 1997 - pubs.rsc.org
5.1 Metabolic steps 5.1. 1 Higher plants: in vitro 5.1. 2 Higher plants: in vivo 5.1. 3 Higher
plants: other pathways 5.1. 3.1 Early 2P-hydroxylation 5.1. 3.2 12a-and 12P-Hydroxylation 5.1. …

PAK3 mutation in nonsyndromic X-linked mental retardation

…, S Bagrodia, MW Partington, JC MacMillan… - Nature …, 1998 - nature.com
… & Coyle, J. Immature cortical neurons are uniquely sensitive to glutamate toxicity by … Watson
for help with COS cell transfection and western blots, J. Fox for help with SSCP, T. Young-…

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.

…, SA Rundle, JC MacMillan, J Myring… - American journal of …, 1993 - ncbi.nlm.nih.gov
A clinical and molecular analysis of 439 individuals affected with myotonic dystrophy, from
101 kindreds, has shown that the size of the unstable CTG repeat detected in nearly all cases …