| Year |
Citation |
Score |
| 2020 |
Goulding DS, Vogel RC, Pandya CD, Shula C, Gensel JC, Mangano FT, Goto J, Miller BA. Neonatal hydrocephalus leads to white matter neuroinflammation and injury in the corpus callosum of Ccdc39 hydrocephalic mice. Journal of Neurosurgery. Pediatrics. 1-8. PMID 32032950 DOI: 10.3171/2019.12.Peds19625 |
0.333 |
|
| 2019 |
Emmert AS, Iwasawa E, Shula C, Schultz P, Lindquist D, Dunn RS, Fugate EM, Hu YC, Mangano FT, Goto J. Impaired neural differentiation and glymphatic CSF flow in the rat model of neonatal hydrocephalus: genetic interaction with . Disease Models & Mechanisms. 12. PMID 31771992 DOI: 10.1242/Dmm.040972 |
0.367 |
|
| 2019 |
Emmert AS, Vuong SM, Shula C, Lindquist D, Yuan W, Hu YC, Mangano FT, Goto J. Characterization of a novel rat model of X-linked hydrocephalus by CRISPR-mediated mutation in L1cam. Journal of Neurosurgery. 1-14. PMID 30738385 DOI: 10.3171/2018.10.Jns181015 |
0.301 |
|
| 2018 |
Abdelhamed Z, Vuong SM, Hill L, Shula C, Timms A, Beier D, Campbell K, Mangano FT, Stottmann RW, Goto J. A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development (Cambridge, England). 145. PMID 29317443 DOI: 10.1242/Dev.154500 |
0.35 |
|
| 2015 |
Hu Z, Wang Y, Huang F, Chen R, Li C, Wang F, Goto J, Kwiatkowski DJ, Wdzieczak-Bakala J, Tu P, Liu J, Zha X, Zhang H. Brain Expressed X-Linked 2 Is Pivotal for Hyperactive mTOR-Mediated Tumorigenesis. The Journal of Biological Chemistry. PMID 26296882 DOI: 10.1074/Jbc.M115.665208 |
0.359 |
|
| 2015 |
Prabhakar S, Zhang X, Goto J, Han S, Lai C, Bronson R, Sena-Esteves M, Ramesh V, Stemmer-Rachamimov A, Kwiatkowski DJ, Breakefield XO. Survival benefit and phenotypic improvement by hamartin gene therapy in a tuberous sclerosis mouse brain model. Neurobiology of Disease. 82: 22-31. PMID 26019056 DOI: 10.1016/J.Nbd.2015.04.018 |
0.351 |
|
| 2015 |
Prabhakar S, Zhang X, Goto J, Sena-Esteves M, Ramesh V, Bronson R, Chen JW, Stemmer-Rachamimov AO, Kwiatkowski DJ, Breakefield XO. 196. AAV-Mediated Gene Replacement Therapy in Mouse Model of Tuberous Sclerosis Molecular Therapy. 23. DOI: 10.1016/S1525-0016(16)33801-1 |
0.393 |
|
| 2013 |
Prabhakar S, Goto J, Zhang X, Zuang X, Sena-Esteves M, Bronson R, Brockmann J, Gianni D, Wojtkiewicz GR, Chen JW, Stemmer-Rachamimov A, Kwiatkowski DJ, Breakefield XO. Stochastic model of Tsc1 lesions in mouse brain. Plos One. 8: e64224. PMID 23696872 DOI: 10.1371/Journal.Pone.0064224 |
0.361 |
|
| 2011 |
Goto J, Talos DM, Klein P, Qin W, Chekaluk YI, Anderl S, Malinowska IA, Di Nardo A, Bronson RT, Chan JA, Vinters HV, Kernie SG, Jensen FE, Sahin M, Kwiatkowski DJ. Regulable neural progenitor-specific Tsc1 loss yields giant cells with organellar dysfunction in a model of tuberous sclerosis complex. Proceedings of the National Academy of Sciences of the United States of America. 108: E1070-9. PMID 22025691 DOI: 10.1073/Pnas.1106454108 |
0.334 |
|
| 2011 |
Anderl S, Freeland M, Kwiatkowski DJ, Goto J. Therapeutic value of prenatal rapamycin treatment in a mouse brain model of tuberous sclerosis complex. Human Molecular Genetics. 20: 4597-604. PMID 21890496 DOI: 10.1093/Hmg/Ddr393 |
0.36 |
|
| 2011 |
Malhowski AJ, Hira H, Bashiruddin S, Warburton R, Goto J, Robert B, Kwiatkowski DJ, Finlay GA. Smooth muscle protein-22-mediated deletion of Tsc1 results in cardiac hypertrophy that is mTORC1-mediated and reversed by rapamycin. Human Molecular Genetics. 20: 1290-305. PMID 21212099 DOI: 10.1093/Hmg/Ddq570 |
0.321 |
|
| 2009 |
Pollizzi K, Malinowska-Kolodziej I, Doughty C, Betz C, Ma J, Goto J, Kwiatkowski DJ. A hypomorphic allele of Tsc2 highlights the role of TSC1/TSC2 in signaling to AKT and models mild human TSC2 alleles. Human Molecular Genetics. 18: 2378-87. PMID 19357198 DOI: 10.1093/Hmg/Ddp176 |
0.354 |
|
| 2008 |
Goto J, Tezuka T, Nakazawa T, Sagara H, Yamamoto T. Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development. Molecular and Cellular Neurosciences. 38: 203-12. PMID 18403215 DOI: 10.1016/J.Mcn.2008.02.009 |
0.458 |
|
| 2006 |
Nakazawa T, Komai S, Watabe AM, Kiyama Y, Fukaya M, Arima-Yoshida F, Horai R, Sudo K, Ebine K, Delawary M, Goto J, Umemori H, Tezuka T, Iwakura Y, Watanabe M, et al. NR2B tyrosine phosphorylation modulates fear learning as well as amygdaloid synaptic plasticity. The Embo Journal. 25: 2867-77. PMID 16710293 DOI: 10.1038/Sj.Emboj.7601156 |
0.41 |
|
| 2004 |
Goto J, Tezuka T, Nakazawa T, Tsukamoto N, Nakamura T, Ajima R, Yokoyama K, Ohta T, Ohki M, Yamamoto T. Altered gene expression in the adult brain of fyn-deficient mice. Cellular and Molecular Neurobiology. 24: 149-59. PMID 15049519 DOI: 10.1023/B:Cemn.0000012720.71630.14 |
0.467 |
|
| Show low-probability matches. |