| Year |
Citation |
Score |
| 2017 |
Muthusamy B, Selvan LDN, Nguyen TT, Manoj J, Stawiski EW, Jaiswal BS, Wang W, Raja R, Ramprasad VL, Gupta R, Murugan S, Kadandale JS, Prasad TSK, Reddy K, Peterson A, et al. Next-Generation Sequencing Reveals Novel Mutations in X-linked Intellectual Disability. Omics : a Journal of Integrative Biology. 21: 295-303. PMID 28481730 DOI: 10.1089/Omi.2017.0009 |
0.305 |
|
| 2017 |
Wu C, Li J, Peterson A, Tao K, Wang B. Loss of dynein-2 intermediate chain Wdr34 results in defects in retrograde ciliary protein trafficking and Hedgehog signaling in the mouse. Human Molecular Genetics. PMID 28379358 DOI: 10.1093/hmg/ddx127 |
0.441 |
|
| 2012 |
Ashique AM, May SR, Kane MA, Folias AE, Phamluong K, Choe Y, Napoli JL, Peterson AS. Morphological defects in a novel Rdh10 mutant that has reduced retinoic acid biosynthesis and signaling. Genesis (New York, N.Y. : 2000). 50: 415-23. PMID 22162152 DOI: 10.1002/Dvg.22002 |
0.465 |
|
| 2010 |
Tang T, Li L, Tang J, Li Y, Lin WY, Martin F, Grant D, Solloway M, Parker L, Ye W, Forrest W, Ghilardi N, Oravecz T, Platt KA, Rice DS, ... ... Peterson A, et al. A mouse knockout library for secreted and transmembrane proteins. Nature Biotechnology. 28: 749-55. PMID 20562862 DOI: 10.1038/Nbt.1644 |
0.375 |
|
| 2010 |
Endoh-Yamagami S, Karkar KM, May SR, Cobos I, Thwin MT, Long JE, Ashique AM, Zarbalis K, Rubenstein JL, Peterson AS. A mutation in the pericentrin gene causes abnormal interneuron migration to the olfactory bulb in mice. Developmental Biology. 340: 41-53. PMID 20096683 DOI: 10.1016/J.Ydbio.2010.01.017 |
0.691 |
|
| 2009 |
Ashique AM, Choe Y, Karlen M, May SR, Phamluong K, Solloway MJ, Ericson J, Peterson AS. The Rfx4 transcription factor modulates Shh signaling by regional control of ciliogenesis. Science Signaling. 2: ra70. PMID 19887680 DOI: 10.1126/scisignal.2000602 |
0.475 |
|
| 2009 |
Siegenthaler JA, Ashique AM, Zarbalis K, Patterson KP, Hecht JH, Kane MA, Folias AE, Choe Y, May SR, Kume T, Napoli JL, Peterson AS, Pleasure SJ. Retinoic acid from the meninges regulates cortical neuron generation. Cell. 139: 597-609. PMID 19879845 DOI: 10.1016/j.cell.2009.10.004 |
0.735 |
|
| 2009 |
Zoltewicz JS, Ashique AM, Choe Y, Lee G, Taylor S, Phamluong K, Solloway M, Peterson AS. Wnt signaling is regulated by endoplasmic reticulum retention. Plos One. 4: e6191. PMID 19593386 DOI: 10.1371/journal.pone.0006191 |
0.498 |
|
| 2009 |
Shen Y, Peterson AS. Atrophins' emerging roles in development and neurodegenerative disease. Cellular and Molecular Life Sciences : Cmls. 66: 437-46. PMID 18953689 DOI: 10.1007/S00018-008-8403-9 |
0.718 |
|
| 2007 |
Zarbalis K, Siegenthaler JA, Choe Y, May SR, Peterson AS, Pleasure SJ. Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development. Proceedings of the National Academy of Sciences of the United States of America. 104: 14002-7. PMID 17715063 DOI: 10.1073/pnas.0702618104 |
0.743 |
|
| 2007 |
Shen Y, Lee G, Choe Y, Zoltewicz JS, Peterson AS. Functional architecture of atrophins. The Journal of Biological Chemistry. 282: 5037-44. PMID 17150957 DOI: 10.1074/Jbc.M610274200 |
0.733 |
|
| 2007 |
Dow LE, Kauffman JS, Caddy J, Zarbalis K, Peterson AS, Jane SM, Russell SM, Humbert PO. The tumour-suppressor Scribble dictates cell polarity during directed epithelial migration: regulation of Rho GTPase recruitment to the leading edge. Oncogene. 26: 2272-82. PMID 17043654 DOI: 10.1038/sj.onc.1210016 |
0.673 |
|
| 2005 |
May SR, Ashique AM, Karlen M, Wang B, Shen Y, Zarbalis K, Reiter J, Ericson J, Peterson AS. Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli. Developmental Biology. 287: 378-89. PMID 16229832 DOI: 10.1016/J.Ydbio.2005.08.050 |
0.73 |
|
| 2004 |
Zarbalis K, May SR, Shen Y, Ekker M, Rubenstein JL, Peterson AS. A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development. Plos Biology. 2: E219. PMID 15314648 DOI: 10.1371/Journal.Pbio.0020219 |
0.737 |
|
| 2004 |
Zoltewicz JS, Stewart NJ, Leung R, Peterson AS. Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis Development. 131: 3-14. PMID 14645126 DOI: 10.1242/dev.00908 |
0.305 |
|
| 1998 |
Womack M, Thompson K, Fanselow E, Augustine GJ, Peterson A. Elevated intracellular calcium levels in cerebellar granule neurons of weaver mice. Neuroreport. 9: 3391-5. PMID 9855287 DOI: 10.1097/00001756-199810260-00011 |
0.326 |
|
| 1995 |
Patil N, Cox DR, Bhat D, Faham M, Myers RM, Peterson AS. A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nature Genetics. 11: 126-9. PMID 7550338 DOI: 10.1038/ng1095-126 |
0.465 |
|
| 1994 |
Patil N, Peterson A, Rothman A, De Jong PJ, Myers RM, Cox DR. A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21 Human Molecular Genetics. 3: 1811-1817. PMID 7849705 DOI: 10.1093/Hmg/3.10.1811 |
0.426 |
|
| 1994 |
Peterson A, Patil N, Robbins C, Wang L, Cox DR, Myers RM. A transcript map of the Down syndrome critical region on chromosome 21 Human Molecular Genetics. 3: 1735-1742. PMID 7849696 DOI: 10.1093/Hmg/3.10.1735 |
0.453 |
|
| 1991 |
Maricq AV, Peterson AS, Brake AJ, Myers RM, Julius D. Primary structure and functional expression of the 5HT3 receptor, a serotonin-gated ion channel. Science (New York, N.Y.). 254: 432-7. PMID 1718042 DOI: 10.1126/Science.1718042 |
0.373 |
|
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