Zobrazeno 1 - 10
of 707
pro vyhledávání: '"M, Brockington"'
Autor:
DE JONG, J. W.
Publikováno v:
Indo-Iranian Journal, 1996 Jan 01. 39(1), 86-90.
Externí odkaz:
https://www.jstor.org/stable/24662219
Autor:
Kölver, Bernhard
Publikováno v:
Zeitschrift der Deutschen Morgenländischen Gesellschaft, 1995 Jan 01. 145(1), 196-197.
Externí odkaz:
https://www.jstor.org/stable/43378938
Autor:
Podzeit, U.
Publikováno v:
Wiener Zeitschrift für die Kunde Südasiens / Vienna Journal of South Asian Studies, 1993 Jan 01. 37, 229-230.
Externí odkaz:
https://www.jstor.org/stable/24006846
Akademický článek
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Autor:
Aker, Amira1,2 (AUTHOR) amaker@bu.edu, Courtemanche, Yohann3 (AUTHOR), Ayotte, Pierre3,4 (AUTHOR), Robert, Philippe5 (AUTHOR), Gaudreau, Éric4 (AUTHOR), Lemire, Mélanie3,5,6 (AUTHOR)
Publikováno v:
Environmental Health: A Global Access Science Source. 10/12/2024, Vol. 23 Issue 1, p1-14. 14p.
Autor:
Giora Proskurowski, Wayne C. Shanks, K. L. Von Damm, K. M. O'Grady, Alastair G C Graham, Eric J. Olson, Marvin D. Lilley, A.M. Bray, M. Brockington
Publikováno v:
Earth and Planetary Science Letters. 206:365-378
The discovery of Brandon vent on the southern East Pacific Rise is providing new insights into the controls on mid-ocean ridge hydrothermal vent fluid chemistry. The physical conditions at the time of sampling (287 bar and 405°C) place the Brandon f
Autor:
J. VAN REEUWIJK, M. JANSSEN, C. VAN DEN ELZEN, D. BELTRAN-VALERO DE BERNABE, P. SABATELLI, L. MERLINI, M. BOON, H. SCHEFFER, M. BROCKINGTON, F. MUNTONI, M.A. HUYNEN, A. VERRIPS, C.A. WALSH, P.G. BARTH, H.G. BRUNNER, H. VAN BOKHOVEN
Publikováno v:
42 (2005): 907–912.
info:cnr-pdr/source/autori:J. VAN REEUWIJK, M. JANSSEN, C. VAN DEN ELZEN, D. BELTRAN-VALERO DE BERNABE, P. SABATELLI, L. MERLINI, M. BOON, H. SCHEFFER, M. BROCKINGTON, F. MUNTONI, M.A. HUYNEN, A. VERRIPS, C.A. WALSH, P.G. BARTH, H.G. BRUNNER, H.G. BRUNNER, H. VAN BOKHOVEN,/titolo:POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome,/doi:/rivista:/anno:2005/pagina_da:907/pagina_a:912/intervallo_pagine:907–912/volume:42
info:cnr-pdr/source/autori:J. VAN REEUWIJK, M. JANSSEN, C. VAN DEN ELZEN, D. BELTRAN-VALERO DE BERNABE, P. SABATELLI, L. MERLINI, M. BOON, H. SCHEFFER, M. BROCKINGTON, F. MUNTONI, M.A. HUYNEN, A. VERRIPS, C.A. WALSH, P.G. BARTH, H.G. BRUNNER, H.G. BRUNNER, H. VAN BOKHOVEN,/titolo:POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome,/doi:/rivista:/anno:2005/pagina_da:907/pagina_a:912/intervallo_pagine:907–912/volume:42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::b8198ebbb523e63552c4c83bddb72288
http://www.cnr.it/prodotto/i/5272
http://www.cnr.it/prodotto/i/5272
Autor:
P. SABATELLI, M. COLUMBARO, L. MERLINI, S. SQUARZONI, F. MUNTONI, M. BROCKINGTON, N.M. MERLINI
Publikováno v:
4th AIM Conference, Taormina, 2004
info:cnr-pdr/source/autori:P. SABATELLI, M. COLUMBARO, L. MERLINI, S. SQUARZONI, F. MUNTONI, M. BROCKINGTON, N.M. MERLINI,/congresso_nome:4th AIM Conference/congresso_luogo:Taormina/congresso_data:2004/anno:2004/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:P. SABATELLI, M. COLUMBARO, L. MERLINI, S. SQUARZONI, F. MUNTONI, M. BROCKINGTON, N.M. MERLINI,/congresso_nome:4th AIM Conference/congresso_luogo:Taormina/congresso_data:2004/anno:2004/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::28f92aac9653cb5dd53fa0a5e3445164
https://publications.cnr.it/doc/99139
https://publications.cnr.it/doc/99139
Publikováno v:
Journal of the Neurological Sciences. 143:41-45
A mitochondrial myopathy associated with multiple deletions of mitochondrial DNA has been identified in pedigrees showing an autosomal dominant mode of inheritance. We report the first two British kindreds with this disorder, and two sporadic cases.
Autor:
JM Cooper, Hammans, Anthony H.V. Schapira, J. A. Morgan-Hughes, John B. Clark, Mary G. Sweeney, A. E. Harding, M. Brockington
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1271(1):135-140
This study examines the relationship of genotype to phenotype in 14 unselected patients who were found to harbour the A3243G transition in the mitochondrial transfer RNALeu(UUR) gene commonly associated with the syndrome of mitochondrial encephalopat