Electromagnetic filtering effect in silicon calorimetry
- 作者E. Borchi; M. Bosetti; C. Furetta; C. Leroy; R. Paludetto; S. Pensotti; A. Penzo; P.G. Rancoita; M. Rattagi; G. Salvato; G. Terzi; L. Vismara
- 卷第32卷
- 印刷ISSN0920-5632
- 文件大小417.57KB
- 发表时间1993
- DOI10.1016/0920-5632(93)90013-v
- 页码91-96
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
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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