Zobrazeno 1 - 10
of 35
pro vyhledávání: '"J C MacMillan"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cccb1e96f72be06bdfdca5fc3f1ba2c3
https://doi.org/10.1177/0333102410381143
https://doi.org/10.1177/0333102410381143
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93db2d71ea12d7f8c119497e0e1bd66a
https://doi.org/10.1081/imm-55807
https://doi.org/10.1081/imm-55807
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c927ddb6c64f9195f37daa8fad751e07
https://doi.org/10.1111/j.1399-0004.1992.tb03231.x
https://doi.org/10.1111/j.1399-0004.1992.tb03231.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eddac7d062fa192032b2f3a64f10572
https://doi.org/10.1006/exnr.1998.6778
https://doi.org/10.1006/exnr.1998.6778
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a3ee95006e733ffb8de6f5f6a321711
https://doi.org/10.1093/hmg/5.4.481
https://doi.org/10.1093/hmg/5.4.481
Autor:
J C MacMillan, P S Harper
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 57:7-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2eae227dd59087399a089755e191b41
https://doi.org/10.1136/jnnp.57.1.7
https://doi.org/10.1136/jnnp.57.1.7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::727a6cbcb06aeff1acd4f6bf3aa3f740
https://pubmed.ncbi.nlm.nih.gov/21267260
https://pubmed.ncbi.nlm.nih.gov/21267260
Autor:
Russell G. Snell, J C MacMillan, I. Fenton, Jeremy Peter Cheadle, Peter S. Harper, Albert Tyler, L. P. Lazarou, G. D. Houlihan, J. D. Shaw
Publikováno v:
The Lancet. 342:954-958
The genetic mutation underlying Huntington's disease (HD) has been identified as an expansion and instability of a specific CAG repeat sequence in a gene (IT15) on chromosome 4. We have investigated the relation of the phenotype of HD to this molecul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d86c155f6ae974c184881ce6f80bf3d
https://doi.org/10.1016/0140-6736(93)92002-b
https://doi.org/10.1016/0140-6736(93)92002-b
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
Autor:
L. P. Lazarou, Jeremy Peter Cheadle, Marcy E. MacDonald, James F. Gusella, Peter Davies, I. Fenton, J C MacMillan, Peter S. Harper, Russell G. Snell, D.J. Shaw
Publikováno v:
Nature Genetics. 4:393-397
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 repeats in affected individuals and 9-34 in normals. We find significant n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48736441d78e414fb652114761164fc5
https://doi.org/10.1038/ng0893-393
https://doi.org/10.1038/ng0893-393