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收藏分享 收藏 分享 收藏 Memory Reconsolidation Updating in Substance Addiction: Applications, Mechanisms, and Future Prospects for Clinical Therapeutics
Huang, Shihao; Liu, Xiaoxing; Li, Zhonghao; Si, Yue; Yang, Liping; Deng, Jiahui; Luo, Yixiao; Xue, Yan-Xue; Lu, Lin 分享 收藏 Intelligent classification of major depressive disorder using rs-fMRI of the posterior cingulate cortexHuang, Shihao; Hao, Shisheng; Si, Yue; Shen, Dan; Cui, Lan; Zhang, Yuandong; Lin, Hang; Wang, Sanwang; Gao, Yujun; Guo, Xin 分享 收藏 Disparate macrophage responses are linked to infection outcome of Hantan virus in humans or rodentsMa, Hongwei; Yang, Yongheng; Nie, Tiejian; Yan, Rong; Si, Yue; Wei, Jing; Li, Mengyun; Liu, He; Ye, Wei; Zhang, Hui; Cheng, Linfeng; Zhang, Liang; Lv, Xin; Luo, Limin; Xu, Zhikai; Zhang, Xijing; Lei, Yingfeng; Zhang, Fanglin 分享 收藏 Significance of NotchScore and JAG1 in predicting prognosis and immune response of low-grade gliomaShi, Bo; Ge, Fei; Cai, Liangliang; Yang, Yi; Guo, Xiaohui; Wu, Rui; Fan, Zhehao; Cao, Binjie; Wang, Ning; Si, Yue; Lin, Xinyue; Dong, Weibing; Sun, Haibo 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signalingHoltz, Alexander M.; VanCoillie, Rachel; Vansickle, Elizabeth A.; Carere, Deanna Alexis; Withrow, Kara; Torti, Erin; Juusola, Jane; Millan, Francisca; Person, Richard; Sacoto, Maria J. Guillen; Si, Yue; Wentzensen, Ingrid M.; Pugh, Jada; Vasileiou, Georgia; Rieger, Melissa; Reis, Andr Prime E.; Argilli, Emanuela; Sherr, Elliott H.; Aldinger, Kimberly A.; Dobyns, William B.; Brunet, Theresa; Hoefele, Julia; Wagner, Matias; Haber, Benjamin; Kotzaeridou, Urania; Keren, Boris; Heron, Delphine; Mignot, Cyril; Heide, Solveig; Courtin, Thomas; Buratti, Julien; Murugasen, Serini; Donald, Kirsten A.; O'Heir, Emily; Moody, Shade; Kim, Katherine H.; Burton, Barbara K.; Yoon, Grace; Del Campo, Miguel; Masser-Frye, Diane; Kozenko, Mariya; Parkinson, Christina; Sell, Susan L.; Gordon, Patricia L.; Prokop, Jeremy W.; Karaa, Amel; Bupp, Caleb; Raby, Benjamin A. 分享 收藏 分享 收藏 分享 收藏 Expanding the phenotypic spectrum of ARCN1-related syndrome扩大ARCN1-related综合征的表型谱Ritter, Alyssa L.; Gold, Jessica; Hayashi, Hiroshi; Ackermann, Amanda M.; Hanke, Stephanie; Skraban, Cara; Cuddapah, Sanmati; Bhoj, Elizabeth; Li, Dong; Kuroda, Yukiko; Wen, Jessica; Takeda, Ryojun; Bibb, Audrey; El Chehadeh, Salima; Piton, Amelie; Ohl, Jeanine; Kukolich, Mary K.; Nagasaki, Keisuke; Kato, Kohji; Ogi, Tomoo; Bhatti, Tricia; Russo, Pierre; Krock, Bryan; Murrell, Jill R.; Sullivan, Jennifer A.; Shashi, Vandana; Stong, Nicholas; Hakonarson, Hakon; Sawano, Kentaro; Torti, Erin; Willaert, Rebecca; Si, Yue; Wilcox, William Ross; Wirgenes, Katrine Verena; Thomassen, Kristian; Carlotti, Katherine; Erwin, Angelika; Lazier, Joanna; Marquardt, Thorsten; He, Miao; Edmondson, Andrew C.; Izumi, Kosuke 分享 收藏 LncRNA NEAT1 Potentiates SREBP2 Activity to Promote Inflammatory Macrophage Activation and Limit Hantaan Virus PropagationYang, Yongheng; Li, Mengyun; Ma, Yongtao; Ye, Wei; Si, Yue; Zheng, Xuyang; Liu, He; Cheng, Linfeng; Zhang, Liang; Zhang, Hui; Zhang, Xijing; Lei, Yingfeng; Shen, Lixin; Zhang, Fanglin; Ma, Hongwei 分享 收藏 TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in DrosophilaGoodman, Lindsey D.; Cope, Heidi; Nil, Zelha; Ravenscroft, Thomas A.; Charng, Wu-Lin; Lu, Shenzhao; Tien, An-Chi; Pfundt, Rolph; Koolen, David A.; Haaxma, Charlotte A.; Veenstra-Knol, Hermine E.; Wassink-Ruiter, Jolien S. Klein; Wevers, Marijke R.; Jones, Melissa; Walsh, Laurence E.; Klee, Victoria H.; Theunis, Miel; Legius, Eric; Steel, Dora; Barwick, Katy E. S.; Kurian, Manju A.; Mohammad, Shekeeb S.; Dale, Russell C.; Terhal, Paulien A.; van Binsbergen, Ellen; Kirmse, Brian; Robinette, Bethany; Cogne, Benjamin; Isidor, Bertrand; Grebe, Theresa A.; Kulch, Peggy; Hainline, Bryan E.; Sapp, Katherine; Morava, Eva; Klee, Eric W.; Macke, Erica L.; Trapane, Pamela; Spencer, Christopher; Si, Yue; Begtrup, Amber; Moulton, Matthew J.; Dutta, Debdeep; Kanca, Oguz; Wangler, Michael F.; Yamamoto, Shinya; Bellen, Hugo J.; Tan, Queenie K-G 分享 收藏 Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological diseaseDerksen, Alexa; Shih, Hung-Yu; Forget, Diane; Darbelli, Lama; Tran, Luan T.; Poitras, Christian; Guerrero, Kether; Tharun, Sundaresan; Alkuraya, Fowzan S.; Kurdi, Wesam, I; Nguyen, Cam-Tu Emilie; Laberge, Anne-Marie; Si, Yue; Gauthier, Marie-Soleil; Bonkowsky, Joshua L.; Coulombe, Benoit; Bernard, Genevieve 分享 收藏 Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome致病性SPTBN1变异引起常染色体显性神经发育综合征Cousin, Margot A.; Creighton, Blake A.; Breau, Keith A.; Spillmann, Rebecca C.; Torti, Erin; Dontu, Sruthi; Tripathi, Swarnendu; Ajit, Deepa; Edwards, Reginald J.; Afriyie, Simone; Bay, Julia C.; Harper, Kathryn M.; Beltran, Alvaro A.; Munoz, Lorena J.; Falcon Rodriguez, Liset; Stankewich, Michael C.; Person, Richard E.; Si, Yue; Normand, Elizabeth A.; Blevins, Amy; May, Alison S.; Bier, Louise; Aggarwal, Vimla; Mancini, Grazia M. S.; van Slegtenhorst, Marjon A.; Cremer, Kirsten; Becker, Jessica; Engels, Hartmut; Aretz, Stefan; MacKenzie, Jennifer J.; Brilstra, Eva; van Gassen, Koen L. I.; van Jaarsveld, Richard H.; Oegema, Renske; Parsons, Gretchen M.; Mark, Paul; Helbig, Ingo; McKeown, Sarah E.; Stratton, Robert; Cogne, Benjamin; Isidor, Bertrand; Cacheiro, Pilar; Smedley, Damian; Firth, Helen V.; Bierhals, Tatjana; Kloth, Katja; Weiss, Deike; Fairley, Cecilia; Shieh, Joseph T.; Kritzer, Amy; Jayakar, Parul; Kurtz-Nelson, Evangeline; Bernier, Raphael A.; Wang, Tianyun; Eichler, Evan E.; van de Laar, Ingrid M. B. H.; McConkie-Rosell, Allyn; McDonald, Marie T.; Kemppainen, Jennifer; Lanpher, Brendan C.; Schultz-Rogers, Laura E.; Gunderson, Lauren B.; Pichurin, Pavel N.; Yoon, Grace; Zech, Michael; Jech, Robert; Winkelmann, Juliane; Beltran, Adriana S.; Zimmermann, Michael T.; Temple, Brenda; Moy, Sheryl S.; Klee, Eric W.; Tan, Queenie K. -G.; Lorenzo, Damaris N. 分享 收藏 Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremorWebb, Bryn D.; Evans, Anthony; Naidich, Thomas P.; Bird, Lynne M.; Parikh, Sumit; Garcia, Meilin Fernandez; Henderson, Lindsay B.; Millan, Francisca; Si, Yue; Brennand, Kristen J.; Hung, Peter; Rucker, Janet C.; Wheeler, Patricia G.; Schadt, Eric E. 分享 收藏 Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities干扰FOXP4转录阻遏物活性的杂合变异导致发育障碍，伴有言语/语言延迟和多种先天性异常Blok, Lot Snijders; Vino, Arianna; den Hoed, Joery; Underhill, Hunter R.; Monteil, Danielle; Li, Hong; Santos, Francis Jeshira Reynoso; Chung, Wendy K.; Amaral, Michelle D.; Schnur, Rhonda E.; Santiago-Sim, Teresa; Si, Yue; Brunner, Han G.; Kleefstra, Tjitske; Fisher, Simon E. 分享 收藏 
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