Silicon tracker for LHC
- 作者G. Bencze; M. Bosteels; R. Brenner; S. Czellar; K. Ekman; A. Hentinen; I. Hietanen; M. Huhtinen; S. Inkinen; V. Karimäki; T. Karttaavi; R. Kinnunen; J. Lindgren; J.P. Merlo; T. Oksakivi; A. Onnela; R. orava; E. Pietarinen; M. Pimiä; W. Roth; C. Rönnqvist; J-P. Saarikko; T. Schulman; T. Tuuva; M. Voutilainen; J. Vuoskoski; K. Österberg
- 卷第32卷
- 印刷ISSN0920-5632
- 文件大小667.13KB
- 发表时间1993
- DOI10.1016/0920-5632(93)90022-x
- 页码172-180
The Two Different Receptors for Tumor Necrosis Factor Mediate Distinct Cellular ResponsesLouis A. Tartaglia, Richard F. Weber, Irene S. Figari, Carmen Reynolds, Michael A. Palladino, Jr. and David V. Goeddel · Proceedings of the National Academy of Sciences of the United States of America · 1991
Detection of early locomotor abnormalities in a Drosophila model of Alzheimer's diseaseThomas R. Jahn; Kai J. Kohlhoff; Michael Scott; Gian Gaetano Tartaglia; David A. Lomas; Christopher M. Dobson; Michele Vendruscolo; Damian C. Crowther · 2011
Genotypic and phenotypic characterization of Noonan syndrome: New data and review of the literatureMarjolijn Jongmans; Erik A. Sistermans; Alwin Rikken; Willy M. Nillesen; Rienk Tamminga; Michael Patton; Esther M. Maier; Marco Tartaglia; Kees Noordam; Ineke van der Burgt · 2005
Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutationsKristin Becker; Helen Hughes; Karol Howard; Maggie Armstrong; Devender Roberts; Edgar J. Lazda; John P. Short; Adam Shaw; Michael A. Patton; Marco Tartaglia · 2007
FGFR3 regulates brain size by controlling progenitor cell proliferation and apoptosis during embryonic developmentSuzanne L. Inglis-Broadgate; Rachel E. Thomson; Francesca Pellicano; Michael A. Tartaglia; Charlie C. Pontikis; Jonathan D. Cooper; Tomoko Iwata · 2005
Paternal Germline Origin and Sex-Ratio Distortion in Transmission of PTPN11 Mutations in Noonan SyndromeMarco Tartaglia; Viviana Cordeddu; Hong Chang; Adam Shaw; Kamini Kalidas; Andrew Crosby; Michael A. Patton; Mariella Sorcini; Ineke van der Burgt; Steve Jeffery; Bruce D. Gelb · 2004
PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic HeterogeneityMarco Tartaglia; Kamini Kalidas; Adam Shaw; Xiaoling Song; Dan L. Musat; Ineke van der Burgt; Han G. Brunner; Débora R. Bertola; Andrew Crosby; Andra Ion; Raju S. Kucherlapati; Steve Jeffery; Michael A. Patton; Bruce D. Gelb · 2002