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13篇 您的检索式:作者名="Bellacchio"
    题名 作者 年代 出处 被引量
1Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia显示文摘Sinibaldi L De Luca A Bellacchio E 2004Hum Mutat2004,24,:1
2Spectroscopic characterization of porphyrin supramolecular aggregates on poly-lysine and their application to quantitative DNA determination显示文摘Gurrieri S Alifi A Bellacchio E 1999Inorganica Chlmica Acta1999,286,2:1
3Chiral H-and J-type aggregates of meso-tetrakis (4-sulfonatophenyl) porphine on a-helical polyglutamic acid induced by cationic porphyrins显示文摘PURRELLO R MONSU S L BELLACCHIO E 1998Inorg Chem1998,37,:1
4Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia显示文摘Sinibaldi L De Luca A Bellacchio E 2004Hum Mutat2004,24,6:1
5Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia显示文摘Sinibaldi L De Luca A Bellacchio E 2004Hum Mutat2004,24,6:1
6Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism 显示文摘Silvestri L Caputo V Bellacchio E 2005Hum Mol Genet2005,14,:1
7Interaction between the Cdk2/cyelin A complex and a small molecule derived from the pRb2/p 130 spacer domain: a theoretical model显示文摘Giordano A Bellacchio E Bagella L 2007Cell Cycle2007,6,21:1
8Spectroscopic characterization of porphyrin supramolecular aggregates on poly-lysine and their application to quantitative DNA determination显示文摘GURRIERI S ALIFFI A BELLACCHIO E 1999Inorganica Chimica Acta1999,286,:1
9Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia显示文摘Sinibaldi L De Luca A Bellacchio E 0,,06:1
10The SH2B1 obesity locus is associated with myocardial infarction in diabetic patients and with NO synthase activity in endothelial cells显示文摘Sabrina Prudente Eleonora Morini Jay Larmon Francesco Andreozzi Natalia Di Pietro Angela Nigro Ernest V. Gervino Gaia Chiara Mannino Simonetta Bacci Thomas H. Hauser Emanuele Bellacchio Gloria Formoso Fabio Pellegrini Vittoria Proto Claudia Menzaghi Lucia 2011Atherosclerosis2011,,2:1
11Interaction between the Cdk2/cyclin A complex and a small molecule derived from the pRb2/p130 spacer domain: a theoretical model显示文摘Giordano A Bellacchio E Bagella L 2007Cell Cycle2007,6,21:1
12Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism显示文摘Silvestri L Caputo V Bellacchio E 2005Human Molecular Genetics2005,14,:1
13Bile salt export pump deficiency: A de novo mutation in a child compound heterozygous for ABCB11 . Laboratory investigation to study pathogenic role and transmission of two novel ABCB11 mutations显示文摘Paola Francalanci Isabella Giovannoni Manila Candusso Emanuele Bellacchio Francesco Callea 2013Hepatology Research2013,,3:1
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