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- [3] An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function[J]. Molecular Psychiatry, 2020, 25 : 2534 - 2555Li WangKaifang PangKihoon HanCarolyn J. AdamskiWei WangLingjie HeJason K. LaiVitaliy V BondarJoseph G. DumanRonald RichmanKimberley F. ToliasPatrick BarthTimothy PalzkillZhandong LiuJ. Lloyd HolderHuda Y. Zoghbi
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- [7] Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder[J]. PLOS ONE, 2015, 10 (02):Nemirovsky, Sergio I.Cordoba, MartaZaiat, Jonathan J.Completa, Sabrina P.Vega, Patricia A.Gonzalez-Moron, DoloresMedina, Nancy M.Fabbro, MonicaRomero, SoledadBrun, BiancaRevale, SantiagoFlorencia Ogara, MariaPecci, AdaliMarti, MarceloVazquez, MartinTurjanski, AdrianKauffman, Marcelo A.
- [8] Aberrant qNSC activity mediates decreased active neurogenesis in the Shank3 deficient Autism development[J]. Molecular Psychiatry, 2022, 27 : 2637 - 2637Hongwon KimByounggook ChoHanseul ParkJunyeop KimSiyoung KimJaein ShinChristopher J. LengnerKyoung-Jae WonJongpil Kim
- [9] Aberrant qNSC activity mediates decreased active neurogenesis in the Shank3 deficient Autism development[J]. MOLECULAR PSYCHIATRY, 2022, 27 (06) : 2637 - 2637Kim, HongwonCho, ByounggookPark, HanseulKim, JunyeopKim, SiyoungShin, JaeinLengner, Christopher J.Won, Kyoung-JaeKim, Jongpil
- [10] Single-molecule fluorescence in-situ hybridization reveals that human SHANK3 mRNA expression varies during development and in autism-associated SHANK3 heterozygosity[J]. STEM CELL RESEARCH & THERAPY, 2018, 9Taylor, Samuel E.Taylor, Ruth D.Price, JackAndreae, Laura C.