Zobrazeno 1 - 10
of 11
pro vyhledávání: '"E M McNally"'
Autor:
Geraint Williams, Joseph R. McDermid, Joseph R. Kish, E. M. McNally, Nick Birbilis, X. Zhang, Carol Glover
A corrosion investigation of friction stir linear lap welded AM60B joints used to fabricate an Mg alloy-intensive automotive front end sub-assembly was performed. The stir zone exhibited a slightly refined grain size and significant break-up and re-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1fa13cee134a594129dd0bdf58b6214
https://cronfa.swan.ac.uk/Record/cronfa34759/Download/0034759-26072017150103.pdf
https://cronfa.swan.ac.uk/Record/cronfa34759/Download/0034759-26072017150103.pdf
Publikováno v:
The Journal of Immunology. 154:2483-2493
A longitudinal study was undertaken to characterize the autoantibodies induced during the course of procainamide treatment and to relate this information to the appearance of symptomatic drug-induced lupus. IgG, IgA, and IgM Abs to histones, native a
Publikováno v:
The Journal of biological chemistry. 276(24)
The sarcoglycan complex is found normally at the plasma membrane of muscle. Disruption of the sarcoglycan complex, through primary gene mutations in dystrophin or sarcoglycan subunits, produces membrane instability and muscular dystrophy. Restoration
Publikováno v:
Microscopy research and technique. 48(3-4)
Muscular dystrophy is a heterogeneous genetic disease that affects skeletal and cardiac muscle. The genetic defects associated with muscular dystrophy include mutations in dystrophin and its associated glycoproteins, the sarcoglycans. Furthermore, de
Publikováno v:
FEBS letters. 422(1)
The dystrophin-glycoprotein complex (DGC) is critical for muscle membrane stability. The sarcoglycans are transmembrane proteins within the DGC, and the function of the sarcoglycans is unknown. Mutations in sarcoglycan genes cause autosomal recessive
Publikováno v:
American journal of human genetics. 60(4)
Limb-girdle muscular dystrophy (LGMD) constitutes a clinically and genetically heterogeneous group of myogenic disorders with a limb-girdle distribution of weakness. One autosomal dominant family, LGMD1A, has been linked to chromosome 5q, whereas in
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 154(5)
A longitudinal study was undertaken to characterize the autoantibodies induced during the course of procainamide treatment and to relate this information to the appearance of symptomatic drug-induced lupus. IgG, IgA, and IgM Abs to histones, native a
Publikováno v:
American Heart Journal. 75:679-695
Autor:
A Benchimol, E M McNally
Publikováno v:
Heart. 29:767-769
Autor:
E M, McNally
Publikováno v:
The Western journal of medicine. 146(2)