|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | A reassessment of the low molecular weight phosphoUpase A2 geue family in mammals显示文摘 | Tischfield JA | 1997 | J Biol Chem1997，272，17： | 1 |
| 2 | Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus显示文摘 | Rym Benayed Neda Gharani Ian Rossman Vincent Mancuso Gloria Lazar Silky Kamdar Shannon E. Bruse Samuel Tischfield Brett J. Smith Raymond A. Zimmerman Emanuel DiCicco-Bloom Linda M. Brzustowicz James H. Millonig | 2005 | The American Journal of Human Genetics2005，，5： | 1 |
| 3 | A reassessment of the low molecular weight phospholkipase A2 gene family in mammals显示文摘 | | 1997 | JBiolChem1997，272，17： | 1 |
| 4 | Aninherited TUBB2B mutation alters a kinesin-binding site andcauses polymicrogyria, CFEOM and axon dysinnervation 显示文摘 | Cederquist GY Luchniak A Tischfield MA | 2012 | Hum Mol Genet2012，21，26： | 1 |
| 5 | Canonical WNT signaling components in vascular development and barrier formation显示文摘 | Zhou Y Wang Y Tischfield M | 2014 | J Clin Invest2014，124，： | 1 |
| 6 | Canonical WNT signaling components in vascular development and barrier formation 显示文摘 | Zhou Y Wang Y Tischfield M | 2014 | J Clin Invest2014，124，： | 1 |
| 7 | Human TUBB3 mutations perturb microtubule dynamics,kinesin interactions,and axon guidance显示文摘 | Tischfield M A Baris H N Wu C | 2010 | Cell2010，140，1： | 1 |
| 8 | Homozygous HOXA1 mutations disrupt humanbrainstem,inner ear, cardiovascular and cognitive de-velopment显示文摘 | TISCHFIELD M A BOSLEY T M SALIH M A etal | 2005 | Nat Genet2005，37，： | 1 |
| 9 | Analysis of the secretory phospholipases A2 that mediates prostglandin production in mast cell显示文摘 | Reddy ST Winstead MV Tischfield JA Herschman HR | 1997 | J Biol Chem1997，272，： | 1 |
| 10 | Single-nucleotide polymorphism in the human mu opioid receptor gene alters beta-endorphin binding and activity: possible implications for opiate addiction 显示文摘 | Bond C LaForge KS Tian M Melia D Zhang S Borg L Gong J Schluger J Strong JA Leal SM Tischfield JA Kreek M J Yu L | 1998 | Proc Natl Acad Sci USA1998，95，16： | 1 |
| 11 | Homozygous HOXAl mutations disrupt human brainstem,inner ear, cardiovascular and cognitive development显示文摘 | Tischfield MA Bosley TM Salih MA | 2005 | Nat Genet2005，37，10： | 1 |
| 12 | Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A显示文摘 | Isabelle Richard Odile Broux Valéerie Allamand Fran?oise Fougerousse Nuchanard Chiannilkulchai Nathalie Bourg Lydie Brenguier Catherine Devaud Patricia Pasturaud Carinne Roudaut Dominique Hillaire Maria-Rita Passos-Bueno Mayana Zatz Jay A Tischfield Miche | 1995 | Cell1995，，1： | 1 |
| 13 | Human TUBB3 mutations perturb microtubule dynamics, kinesin interac- tions, and axon guidance显示文摘 | Tischfield MA Baris HN Wu C | 2010 | Cell2010，140，1： | 1 |
| 14 | Mutations in WDR62, encoding a protein, cause mi- crocephaly with simplified gyri and abnormal cortical architec- ture显示文摘 | YU TW MOCHIDA GH TISCHFIELD DJ | 2010 | Nat Genet2010，42，11： | 1 |
| 15 | Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture 显示文摘 | Yu TW Mochida GH Tischfield DJ | 2010 | Nat Genet2010，42，： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员