Electrical characterization of amorphous Al2O3 dielectric films on n-type 4H-SiC

Autor: R. Y. Khosa, E. B. Thorsteinsson, M. Winters, N. Rorsman, R. Karhu, J. Hassan, E. Ö. Sveinbjörnsson

Publikováno v: AIP Advances, Vol 8, Iss 2, Pp 025304-025304-8 (2018)

We report on the electrical properties of Al2O3 films grown on 4H-SiC by successive thermal oxidation of thin Al layers at low temperatures (200°C - 300°C). MOS capacitors made using these films contain lower density of interface traps, are more im

Externí odkaz: https://doaj.org/article/b4b65a01a17a48f38be1820a2829f70f

Genotypic Stability, Segregation and Selection in Heteroplasmic Human Cell Lines Containing np 3243 Mutant mtDNA

Autor: Howard T. Jacobs, Johannes N. Spelbrink, Sara Lehtinen, Ian J. Holt, Martti Juhola, N. Hance, R Karhu, A. El Meziane, K M Juhola

Publikováno v: Europe PubMed Central

The mitochondrial genotype of heteroplasmic human cell lines containing the pathological np 3243 mtDNA mutation, plus or minus its suppressor at np 12300, has been followed over long periods in culture. Cell lines containing various different proport

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa18fdc361c5fd03d3171fa8499061be
https://doi.org/10.1093/genetics/154.1.363

Contents Vol. 88, 2000

Autor: P.A. Voûte, D. Baudry, C.L. Keck-Waggoner, K. White, P.I. Patel, J.C. McHale, M. Busson-Leconiat, M. Pagano, C. Wiesmeijer, G.W. Conrad, M. Pettenati, P. Staeheli, E.R. Zabarovsky, C. Tiziana Storlazzi, Y. Xie, Z.E. Zehner, E. Gabrielson, C.A. Griffin, C. Geffrotin, E.A. Isakova, P. Spencer, J.E. Hewitt, A. Barbon, E. Sonnhammer, R.M. Schmid, B. Kazmierczak, P. Munclinger, F. Vitelli, N.A. Serdyukova, S.W. Scherer, B.G. Beatty, S. Meloche, M. Schmid, Y. Nakajima, M. Riemann, B. Brintnell, J. Laborda, N. Zijlstra, P.M. Brickell, L.A. James, J. Pellerin, T.K. Kwon, K. Yamakawa, P. van Tuinen, B.S. Klein, H.-J. Han, H. Winton, S.H. Elsea, D. Frynta, Y. Nakamura, M. Guttenbach, L. Carim, V.G. Malikov, M. van Geel, J.C.T. van Deutekom, U. Zechner, S. Barlati, P.A. Kroner, C.N. Vlangos, R. Podowski, N.C. Popescu, M.N. Meyer, I. Kärkkäinen, Ian Dunham, L. Leikepová, S. Beck, M. Escarceller, S. Bonné, F. Favara, S. Fineschi, F. Van Roy, J. Zima, E.S. Tasheva, T.P. Lushnikova, H.C. Duba, A.L. Hawkins, R. Berger, S. Sanders, J.M. Varley, Y. Furukawa, A.V. Polyakov, A. Protopopov, E.R. Werner, R.J.L.F. Lemmers, N. Andreu, A. van Staalduinen, J. Piálek, P.J. de Jong, E. Gubina, P.L. Perelman, L. Sumoy, M. Iizaka, A. Renieri, M. Loda, S. Ferraboli, C. Wahlestedt, M.H. Hofker, K. Vehse, H.M. Cann, C.F. Inglehearn, Lidia Larizza, P. Adamson, M.D. Torres, P. Benda, J. van Hengel, I. Meloni, E. Aikawa, H. Himmelbauer, M.A. Alvarez Soria, O.V. Sablina, E.E. Tarttelin, J. Justesen, R. Gizatullin, M.N. Ahmed, R. Karhu, Andries Westerveld, R.R. Frants, Mariano Rocchi, Cécile Jeanpierre, A. Marquardt, H. Hayes, S. Behrends, M. Erdel, P. Das, D.J Haile, J. Sádlová, R. Godbout, H. Markholst, N.V. Vorobieva, V.A. Trifonov, A.S. Graphodatsky, M. Ogawa, B.H.F. Weber, D.S. Chiaur, A. Duval, Marja Steenman, I. Nanda, C. Von Kap-Her, C. Cenciarelli, Marcel M.A.M. Mannens, K. Imai, W. Parks, T. Ueda, L. Hornum, H. Scholz, H. Akashi, D.L. Kruitbosch, W. Bradford, V. Kashuba, G. Inghirami, A.B. McKie, H. Hameister, K. Gopalbhai, Y. Hey, M.J. Ruiz-Hidalgo, S.S. Thorgeirsson, L.L. Hansen, D.B. Zimonjic, G.W. Padberg, A.J. Mungall, X. Estivill, J. Bullerdiek, D. Demetrick, G. Frelat, M.B. Qumsiyeh, G. Werner-Felmayer, I. Leverkoehne, S. Ganesh, S. Halford, K.-R. Kim, J. Greenwood, N. Kanda, C. Le Chalony, M.C. Dickson, H. Stöhr, J. Trowsdale, K. Amano, R. Hamelin, S. Sugano, S. Liptay, K. Sakamaki, A.-P.J. Huovila, A. Ziegler, A.D. Gruber, G. Zhao, S. Nagata, L. Zhu, V. Baladrón, P.M. Borodin, S. Murthy, D.M. Hunt, M. Meyer

Publikováno v: Cytogenetic and Genome Research. 88:337-339

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::659295b074d9fc4bfd4382ff1dade74e
https://doi.org/10.1159/000015526

Loss at 12p detected by comparative genomic hybridization (CGH): association with TEL-AML1 fusion and favorable prognostic features in childhood acute lymphoblastic leukemia (ALL). A multi-institutional study

Autor: J, Kanerva, T, Niini, K, Vettenranta, P, Riikonen, A, Mäkipernaa, R, Karhu, S, Knuutila, U M, Saarinen-Pihkala

Publikováno v: Medical and pediatric oncology. 37(5)

Genetic aberrations provide prognostic information in childhood ALL. The proportion of patients with detectable aberrations can be increased by combining G-banding with comparative genomic hybridization (CGH).We studied 79 children with ALL by CGH an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6d2626a016fde14ba1f0b0b8a9e717d7
https://pubmed.ncbi.nlm.nih.gov/11745869

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