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| p369 |
A W148R mutation in the human FOXD4 gene segregating with dilated cardiomyopathy, obsessive-compulsive disorder, and suicidality |
Piercarlo Minoretti, Mariarosa Arra, Enzo Emanuele, Valentina Olivieri, Alessia Aldeghi, Pierluigi Politi, Valentina Martinelli, Sara Pesenti, Colomba Falcone
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| p429 |
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies |
Emanuele Panza, Giorgio Gimelli, Mario Passalacqua, Amnon Cohen, Stefania Gimelli, Sabrina Giglio, Cristina Ghezzi, Bianca Sparatore, Babett Heye, Orsetta Zuffardi, Elena Rugarli, Thomas Meitinger, Giovanni Romeo, Roberto Ravazzolo, Marco Seri
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| p461 |
Analysis of differentially expressed genes in early- and late-stage APPsw-transgenic and normal mice using cDNA microarray |
Seung W. Jee, Jung S. Cho, Chuel K. Kim, Dae Y. Hwang, Sun B. Shim, Su H. Lee, Ji S. Sin, Yang S. Kim, Jin H. Park, Se H. Lee, Soo Y. Choi, Yong K. Kim
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| p535 |
Inhibitory effect of Artemisia capillaris extract on cytokine-induced nitric oxide formation and cytotoxicity of RINm5F cells |
Eun-Kyung Kim, Kang-Beom Kwon, Mi-Jeong Han, Mi-Young Song, Ji-Hyun Lee, Na Lv, Ki-Bang Choi, Do-Gon Ryu, Kang-San Kim, Jin-Woo Park, Byung-Hyun Park
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