Process Integration of High Aspect Ratio Vias with a Comparison between Co and Ru Metallizations

Autor: Philippe Leray, N. Jourdan, O. Varela Pedreira, E. Dentoni-Litta, Thomas Witters, Werner Gillijns, Nancy Heylen, L. Ramakers, E. Grieten, Zaid El-Mekki, Gayle Murdoch, V. Vega-Gonzalez, Anne-Laure Charley, Ivan Ciofi, Zsolt Tokei, H. Vats, S. V. Gompel, M. H. van der Veen, L. Halipre, J. Swerts, A. Haider, Bilal Chehab, S. Park, N. Bazzazian, Quoc Toan Le, B. De Wachter, T. Peissker, Harinarayanan Puliyalil, Naoto Horiguchi, Miroslav Cupak, J. Versluijs, G. T. Martinez, Y. Kimura, R. Kim, J. Geypen, J. Uk-Lee, N. Nagesh, D. Montero, L. Rynders, M. Ercken, D. Batuk, K. Croes, Patrick Verdonck, Manoj Jaysankar, Y. Drissi, T. Webers

Publikováno v: 2021 IEEE International Interconnect Technology Conference (IITC).

The integration of high aspect-ratio (AR) vias or supervias (SV) with a min CD bottom = 10.5 nm and a max AR = 5.8 is demonstrated, allowing a comparison between ruthenium (Ru) and cobalt (Co) chemical vapor deposition (CVD) metallizations. Ru gave a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::775097fabe7d875876eeac9844668bb1
https://doi.org/10.1109/iitc51362.2021.9537535

Thrombotic thrombocytopenic purpura in childhood

Autor: Natasja Dors, Maria C. Bouw, Heleen van Ommen, Nicole L. Ramakers-van Woerden

Publikováno v: Pediatric Blood & Cancer. 53:537-542

Thrombotic thrombocytopenic purpura (TTP) is a rare disease, especially in childhood, and has a high mortality rate in the absence of appropriate treatment. It is characterised by microangiopathic haemolytic anaemia and consumptive thrombocytopenia.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::482eeff29eccd2a17b64cb61738db27e
https://doi.org/10.1002/pbc.22094

In vitro drug-resistance profile in infant acute lymphoblastic leukemia in relation to age, MLL rearrangements and immunophenotype

Autor: M L den Boer, Jochen Harbott, E. R. Van Wering, A H Loonen, Bruce M. Camitta, G. E. Janka-Schaub, Rosalyn Slater, W.-D. Ludwig, Rob Pieters, N L Ramakers-van Woerden, Anjo J.P. Veerman, H B Beverloo, Oskar A. Haas

Publikováno v: Leukemia, 18(3), 521-9. Nature Publishing Group
Ramakers-van Woerden, NL, Beverloo, HB, Veerman, A J P, Camitta, BM, Loonen, A H, van Wering, E R, Slater, RM, Harbott, J, den Boer, M L, Ludwig, WD, Haas, OA & Janka-Schaub, GE 2004, ' In vitro drug-resistance profile in infant acute lymphoblastic leukemia in relation to age, MLL rearrangements and immunophenotype. ', Leukemia, vol. 18, no. 3, pp. 521-9 . https://doi.org/10.1038/sj.leu.2403253
Leukemia, 18, 521-529. Nature Publishing Group

Acute lymphoblastic leukemia (ALL) in infants under 1 year is strongly associated with translocations involving 11q23 (MLL gene), CD10-negative B-lineage (proB) immunophenotype, and poor outcome. The present study analyses the relationship between ag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb65991c3bb2238ae6d2e837d6e4829b
https://doi.org/10.1038/sj.leu.2403253

In vitro drug resistance and prognostic impact of p16INK4A /P15INK4B deletions in childhood T-cell acute lymphoblastic leukaemia

Autor: Marianne G. Rots, Mats Heyman, Willem Kamps, Rob Pieters, E van Drunen, A H Loonen, H B Beverloo, N. L. Ramakers-Van Woerden, TC Moreno, E. R. Van Wering, G. E. Janka-Schaub, Rosalyn Slater, A. J. P. Veerman

Publikováno v: British Journal of Haematology. 112:680-690

p16 gene deletions are present in about 70% of primary paediatric T-cell acute lymphoblastic leukaemia (T-ALL) and 20% of common/precursor B-cell ALL cases. It is not clear what the impact of the frequent p16 deletions is within the subgroup of T-lin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f1918a9bea135a73990af8ba275decb3
https://doi.org/10.1046/j.1365-2141.2001.02586.x

Thrombotic thrombocytopenic purpura in childhood

Autor: Maria C, Bouw, Natasja, Dors, Heleen, van Ommen, Nicole L, Ramakers-van Woerden

Publikováno v: Pediatric bloodcancer. 53(4)

Thrombotic thrombocytopenic purpura (TTP) is a rare disease, especially in childhood, and has a high mortality rate in the absence of appropriate treatment. It is characterised by microangiopathic haemolytic anaemia and consumptive thrombocytopenia.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::33ae2e05ec76f78a934232dcae656234
https://pubmed.ncbi.nlm.nih.gov/19544391