Jun Shen, Ph.D.
Affiliations: | Harvard University, Cambridge, MA, United States |
Area:
Genes involved in the development and function of the cerebral cortexGoogle:
"Jun Shen"Mean distance: 14.84 (cluster 46) | S | N | B | C | P |
Parents
Sign in to add mentor| Chris A. Walsh | grad student | 2005 | Harvard | |
| (Using forward and reverse genetics to study genes that control the size of the brain.) | ||||
| David P. Corey | post-doc | 2003-2012 | Harvard Medical School | |
BETA: Related publications
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Publications
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| Evrony GD, Cordero DR, Shen J, et al. (2017) Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Genome Research |
| Lin SY, Vollrath MA, Mangosing S, et al. (2015) The zebrafish pinball wizard gene encodes WRB, a tail-anchored-protein receptor essential for inner-ear hair cells and retinal photoreceptors. The Journal of Physiology |
| Shen J, Scheffer DI, Kwan KY, et al. (2015) SHIELD: an integrative gene expression database for inner ear research. Database : the Journal of Biological Databases and Curation. 2015: bav071 |
| Scheffer DI, Shen J, Corey DP, et al. (2015) Gene Expression by Mouse Inner Ear Hair Cells during Development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 6366-80 |
| Scheffer DI, Zhang DS, Shen J, et al. (2015) XIRP2, an actin-binding protein essential for inner ear hair-cell stereocilia. Cell Reports. 10: 1811-8 |
| Kwan KY, Shen J, Corey DP. (2015) C-MYC transcriptionally amplifies SOX2 target genes to regulate self-renewal in multipotent otic progenitor cells. Stem Cell Reports. 4: 47-60 |
| Shen J, Gilmore EC, Marshall CA, et al. (2010) Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nature Genetics. 42: 245-9 |
| Powers SE, Taniguchi K, Yen W, et al. (2010) Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation. Development (Cambridge, England). 137: 249-59 |
| Shen J, Eyaid W, Mochida GH, et al. (2005) ASPM mutations identified in patients with primary microcephaly and seizures. Journal of Medical Genetics. 42: 725-9 |
| Shen J, Walsh CA. (2005) Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice. Molecular and Cellular Biology. 25: 3639-47 |