Year |
Citation |
Score |
2017 |
Driver AM, Shumrick C, Stottmann RW. Ttc21b Is Required in Bergmann Glia for Proper Granule Cell Radial Migration. Journal of Developmental Biology. 5. PMID 29615573 DOI: 10.3390/jdb5040018 |
0.578 |
|
2017 |
DiStasio A, Driver A, Sund K, Donlin M, Muraleedharan RM, Pooya S, Kline-Fath B, Kaufman KM, Prows CA, Schorry E, DasGupta B, Stottmann RW. Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly. Human Molecular Genetics. PMID 29036432 DOI: 10.1093/Hmg/Ddx362 |
0.425 |
|
2017 |
Li Z, Peng Y, Hufnagel RB, Hu YC, Zhao C, Queme LF, Khuchua Z, Driver AM, Dong F, Lu QR, Lindquist DM, Jankowski MP, Stottmann RW, Kao WWY, Huang T. Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice. Human Molecular Genetics. 26: 3776-3791. PMID 28934388 DOI: 10.1093/Hmg/Ddx262 |
0.61 |
|
2016 |
Stottmann RW, Driver A, Gutierrez A, Skelton MR, Muntifering M, Stepien C, Knudson L, Kofron M, Vorhees CV, Williams MT. A HETEROZYGOUS MUTATION IN TUBULIN, BETA 2B (TUBB2B) CAUSES COGNITIVE DEFICITS AND HIPPOCAMPAL DISORGANIZATION. Genes, Brain, and Behavior. PMID 27594048 DOI: 10.1111/Gbb.12327 |
0.66 |
|
2016 |
Driver AM, Kratz LE, Kelley RI, Stottmann RW. Altered cholesterol biosynthesis causes precocious neurogenesis in the developing mouse forebrain. Neurobiology of Disease. PMID 26921468 DOI: 10.1016/J.Nbd.2016.02.017 |
0.628 |
|
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