Zobrazeno 1 - 10
of 195
pro vyhledávání: '"J. C. MacMillan"'
Publikováno v:
The British Medical Journal, 1959 Mar . 1(5125), 865-865.
Externí odkaz:
https://www.jstor.org/stable/25387073
Autor:
Collingwood, W. G.
Publikováno v:
Saga-Book, 1906 Jan 01. 5, 415-416.
Externí odkaz:
https://www.jstor.org/stable/48612593
Autor:
R J C MacMillan, S K Crawford
With the demand for increased availability and a higher level of safety, the defence industry is faced with reducing operational and maintenance budgets. Additional focus on acquisition programmes is being placed on through-life requirements, with de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::013cc02cf14c469cb031fd1b4f6d7a37
https://zenodo.org/record/2245043
https://zenodo.org/record/2245043
Autor:
Rodney A. Lea, Saras Menon, J C MacMillan, Hannah Cox, Sharon Anne Quinlan, Larisa M. Haupt, Melissa Kuwahata, Lyn R. Griffiths
Publikováno v:
Cephalalgia. 31:264-270
Introduction: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) shares common symptoms with migraine. Most CADASIL causative mutations occur in exons 3 and 4 of the Notch 3 gene. This study investiga
Autor:
T. P. Ses, Rybakova Mg, J. C. MacMillan, S. B. Tkachenko, Anders Kallner, N. A. Gavrisheva, J. G. Vassilyeva, Alexey V. Fedulov
Publikováno v:
Karolinska Institutet
Objectives To characterize dynamics of changes of serum levels of TGF-β1 and TNF-α in rats with cardiac fibrosis (CF) occurring during chronic renal failure (CRF), and to reveal the character pf correlations of these factors with amounts of cardiac
Autor:
Peter S. Harper, J C MacMillan
Publikováno v:
Clinical Genetics. 42:161-163
The Charcot-Marie-Tooth group of disorders cause significant morbidity in a proportion of the individuals affected. We have shown that there is a significant correlation between the objective neurological assessment of their dysfunction and the indiv
Autor:
A L Jones, Philip Thomas, S. K. Singhrao, J C MacMillan, Jonathan D. Wood, James Neal, Peter S. Harper
Publikováno v:
Experimental Neurology. 150:213-222
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease associated with a CAG trinucleotide repeat expansion in a large gene on chromosome 4. The gene encodes the protein huntingtin with a polyglutamine tract encoded by the CAG r
Publikováno v:
Human Molecular Genetics. 5:481-487
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the expansion of a CAG repeat in a gene coding for a protein of unknown function. We have raised a polyclonal antibody against a 12 amino acid peptide (residues 2110-2121
Autor:
J C MacMillan, P S Harper
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 57:7-15
Publikováno v:
Canadian family physician Medecin de famille canadien. 32
The Donwood Institute in Toronto is a public hospital dedicated to the treatment of chemical dependency. The standard program consists of three phases: detoxification and orientation to the program; active hospital treatment which includes individual