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34篇 您的检索式:作者名="MUGLIA M"
    题名 作者 年代 出处 被引量
1Mutations in the mitochondrial GTPase mitofusirr 2 cause Charcot-Marie-Tooth neuropathy type 2A显示文摘Zuchner S Mersiyanova IV Muglia M 2004J Nat Genet2004,36,44:1
2Juvenile Huntington's disease presenting as progressive myoclonic epilepsy 显示文摘Gambardella A Muglia M Labate A 2001Neurology2001,57,4:1
3Charcot-Morie-Tooth type 4B is caused by mutations in the gene encoding myombulain-lelated protein-2显示文摘Bolino A Muglia M Conforti FL 2000Nat Genet2000,25,:1
4Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia显示文摘Muglia M Magariello A Nicoletti G 2002Ann Neurol2002,51,6:1
5Association between the BDNF gene and schizophrenia显示文摘Muglia P Vicente AM Verga M 2003Mol Psychiatry2003,8,:1
6The enigma of spontaneous preterm birth 显示文摘Muglia L J Katz M 2010N Engl J Med2010,362,6:1
7Structure and function of lamellar bone 显示文摘MAROTTI G MUGLIA M A PALUMBO C 1994Clin Rheumatol1994,13,1:1
8Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22显示文摘Bilino A Levy ER Muglia M 2000G enomics2000,63,2:1
9Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2显示文摘Bilino A Muglia M Conforti FL 2000Nat Genet2000,25,1:1
10A quantitative evaluation of osteoblast-osteocyte relationships on growing endosteal surface of rabbit tibiae 显示文摘Marotti G Ferretti M Muglia MA 1992Bone1992,13,5:1
11Nonisotopic method for accurate detection of (CAG) n repeats causing Huntington disease 显示文摘Muglia M Leone O Annesi G 1996Clin Chem1996,42,10:1
12The brain-derived neuro- trophic factor gene confers susceptibility to bipolar disorder: evidence from a family-based association study显示文摘Neves-Pereira M Mundo E Muglia P 2002Am J Hum Genet2002,71,3:1
13查看详情显示文摘Züchner S Mersiyanova (IV) Muglia M 0,,:1
14Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22显示文摘Bolino A Levy ER Muglia M 2000Genomics2000,63,2:1
15Association between the BDNF gene and schizophrenia显示文摘Muglia P Vicente AM Verga M 2003Molecular Psychiatry2003,8,:1
16An Fgf8 mouse mutant phenocopies human 22qll deletion syndrome显示文摘Frank D U Fotheringham L K Brewer J A Muglia L J Tristani-Firouzi M Capecchi M R Moon A 0,,19:1
17A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies显示文摘Muglia M Patitucci A Rizzi R 2007J Neurol Sci2007,263,12:1
18The 5'-flanking region of the mouse adenylyl cyclase type gene imparts tis- sue-specific expression in transgenic mice 显示文摘Muglia L M Schaefer M L Vogt S K 1999J Neurosci1999,19,6:1
19Glutathione is involved in environmental stress responses in Rhizobium tropici, including acid tolerance显示文摘Riccillo P M Muglia C D E Bruijn F G 2000Journal of Bacteriology2000,182,:1
20A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies显示文摘Muglia M Patitucci A Rizzi R 2007J Neurol Sci2007,263,:1
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