DongWangMD

PubMed

• Emerging many-to-one weighted mapping in hippocampus-amygdala network underlies memory formation.
  Jun Liu, Arron F Hall, Dong V Wang> ;Biorxiv. 2023 Sep 6
• 4 citations
  The two tales of hippocampal sharp-wave ripple content: The rigid and the plastic.
  Arron F Hall, Dong V Wang> ;Progress in Neurobiology. 2023 Feb 1
• 1 citations
  Locomotor Exercise Enhances Supraspinal Control of Lower-Urinary-Tract Activity to Improve Micturition Function after Contusive Spinal-Cord Injury.
  Lingxiao Deng, Tao Sui, Dong V Wang, Shaoping Hou, Xiaojian Cao, Kaiwen Peng, Zaocheng Xu, Xiaoming Xu> ;Cells. 2022 Apr 20
• 3 citations
  Median Raphe Nonserotonergic Neurons Modulate Hippocampal Theta Oscillations.
  Wenqiang Huang, Satoshi Ikemoto, Dong V Wang> ;The Journal of Neuroscience. 2022 Mar 9
• 34 citations
  Putting Together Pieces of the Lateral Septum: Multifaceted Functions and Its Neural Pathways.
  Candace A. Rizzi-Wise, Dong V. Wang> ;Eneuro. 2021 Nov 10
• 42 citations
  A Subpopulation of Prefrontal Cortical Neurons Is Required for Social Memory.
  Bo Xing, Nancy R. Mack, Kai-Ming Guo, Yu-Xiang Zhang, Billy Ramirez, Sha-Sha Yang, Li Lin, Dong V. Wang, Yan-Chun Li, Wen-Jun Gao> ;Biological Psychiatry. 2021 Mar 1
• 8 citations
  Representation of Fear of Heights by Basolateral Amygdala Neurons.
  Jun Liu, Longnian Lin, Dong V. Wang> ;The Journal of Neuroscience. 2021 Feb 3
• 22 citations
  Hippocampal Efferents to Retrosplenial Cortex and Lateral Septum Are Required for Memory Acquisition.
  Ashley N. Opalka, Dong V. Wang> ;Learning & Memory. 2020 Aug 1
• 30 citations
  Hippocampal Ripple Coordinates Retrosplenial Inhibitory Neurons during Slow-Wave Sleep
  Ashley N. Opalka, Wen-qiang Huang, Jun Liu, Hualou Liang, Dong V. Wang> ;Cell Reports. 2020 Jan 14
• 23 citations
  Topography of brain glucose hypometabolism and epileptic network in glucose transporter 1 deficiency.
  Cigdem I. Akman, Frank A. Provenzano, Dong Wang, Kristin Engelstad, Veronica J. Hinton, Julia Yu, Ronald S. Tikofsky, Masonari Ichese, Darryl C. De Vivo> ;Epilepsy Research. 2015 Feb 1
• 8 citations
  Allelic Variations of Glut-1 Deficiency Syndrome: The Chinese Experience
  Yan-yan Liu, Xinhua Bao, Dong Wang, Na Fu, Xiaoying Zhang, Guang-na Cao, Fu-ying Song, Shuang Wang, Yuehua Zhang, Jiong Qin, Hong Yang, Kristin Engelstad, Darryl C. De...> ;Pediatric Neurology. 2012 Jul 1
• 71 citations
  Glut1 deficiency syndrome and erythrocyte glucose uptake assay.
  Hong Yang, Dong Wang, Kristin Engelstad, Leslie Bagay, Ying Wei, Michael Rotstein, Vimla Aggarwal, Brynn Levy, Lijiang Ma, Wendy K. Chung, Darryl C. De Vivo> ;Annals of Neurology. 2011 Dec 1
• 12 citations
  T295M-associated Glut1 deficiency syndrome with normal erythrocyte 3-OMG uptake
  Tatsuya Fujii, Masafumi Morimoto, Hiroshi Yoshioka, Yuan-Yuan Ho, Peggy P.Y. Law, Dong Wang, Darryl C. De Vivo> ;Brain & Development. 2011 Apr 1
• 62 citations
  Glut1 deficiency: Inheritance pattern determined by haploinsufficiency
  Michael Rotstein, Kristin Engelstad, Hong Yang, Dong Wang, Brynn Levy, Wendy K. Chung, Darryl C. De Vivo> ;Annals of Neurology. 2010 Dec 1
• 17 citations
  Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis
  Brynn Levy, Dong Wang, Paivi M. Ullner, Kristin Engelstad, Hong Yang, Odelia Nahum, Wendy K. Chung, Darryl C. De Vivo> ;Molecular Genetics and Metabolism. 2010 Jun 1
• Pyruvate Carboxylase Deficiency
  Wang D De Vivo D> ;1993
• Glucose Transporter Type 1 Deficiency Syndrome
  Wang D Pascual JM De Vivo D> ;1993
• 26 citations
  Acute hyperglycemia produces transient improvement in glucose transporter type 1 deficiency
  Cigdem I. Akman, Kristin Engelstad, Veronica J. Hinton, Paivi M. Ullner, Dorcas Koenigsberger, Linda D. Leary, Dong Wang, Darryl C. De Vivo> ;Annals of Neurology. 2010 Jan 1
• 21 citations
  Murine Glut-1 transporter haploinsufficiency: postnatal deceleration of brain weight and reactive astrocytosis
  Paivi M. Ullner, Alessia Di Nardo, James E. Goldman, Scott A. Schobel, Hong Yang, Kristin Engelstad, Dong Wang, Darryl C. De Vivo> ;Neurobiology of Disease. 2009 Oct 1
• 28 citations
  ERCC5 promoter polymorphisms at -763 and +25 predict the response to oxaliplatin-based chemotherapy in patients with advanced colorectal cancer
  Jianfang Chen, Fangwei Xie, Keli Chen, Dong Wang, Heng Jiang, Jianjun Li, Feng Pan, Shixu Chen, Yanling Zhang, Zhihua Ruan, Haihui Huang, Lan Zou, Houjie Liang> ;Cancer Biology & Therapy. 2009 Jul 15
• 6 citations
  Activity of ciprofloxacin and azithromycin on biofilms produced in vitro by Haemophilus influenzae.
  Dong Wang, Ying Wang, You-ning Liu> ;Chinese Medical Journal. 2009 Jun 5
• 2 citations
  Characterization of magnetic fluorescence Fe3O4/CdSe nanocomposites.
  Guihuan Du, Zuli Liu, Dong Wang, Xing Xia, Lihui Jia, Kailun Yao, Qian Chu, Suming Zhang> ;Journal of Nanoscience and Nanotechnology. 2009 Feb 1
• 19 citations
  Glut1 deficiency: CSF glucose. How low is too low?
  Darryl C. De Vivo, Dong Wang> ;Revue Neurologique. 2008 Nov 1
• 20 citations
  Functional studies of the T295M mutation causing Glut1 deficiency: glucose efflux preferentially affected by T295M.
  Dong Wang, Hong Yang, Lei Shi, Li Ma, Tatsuya Fujii, Kristin Engelstad, Juan M. Pascual, Darryl C. De Vivo> ;Pediatric Research. 2008 Nov 1
• 30 citations
  The molecular basis of pyruvate carboxylase deficiency: mosaicism correlates with prolonged survival.
  Dong Wang, Hong Yang, Kevin C. De Braganca, Jiesheng Lu, Ling Yu Shih, Paz Briones, Tim Lang, Darryl C. De Vivo> ;Molecular Genetics and Metabolism. 2008 Sep 1
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Journal Articles

• Allelic Variations of Glut1 Deficiency Syndrome: The Chinese Experience  
  Liu Y, Bao XH, Wang D, Fu N, Zhang XY, Cao GN, Song FY, Wang S, Zhang YH, QinJ, Yang H, Engelstad K, De Vivo DC, Wu XR, Pediatr Neurol, 1/1/2012
• T295M associated glut-1 deficiency syndrome with normal erythrocyte 3-OMG uptake  
  Fuji T, Morimoto M, Yoshioka H, Ho YY, Law PY, Wang D, De Vivo DC, Brain Dev, 1/1/2011
• Uncovering Microdeletions in Patients with Severe Glut-1 Deficiency Syndrome Using SNP Oligonucleotide Microarray Analysis  
  Levy B, Wang D, Ullner PM, Engelstad K, Yang H, Nahum O, Chung WK, De Vivo DC, Molecular Genetics and Metabolism, 1/1/2010
• Acute hyperglycemia produces transient improvement in glucose transporter type 1 deficiency  
  Akman CI, Engelstad K, Hinton VJ, Ullner P, Koenigsberger D, Leary L, Wang D, De Vivo DC, Annals of Neurology, 1/1/2009
• Methylprednisolone for Status Migrainous Vertigo and Cephalic Status Migrainosus  
  Robbins MS, Wang D,DeOrchis VS, Headache, 1/1/2009
• Murine Glut-1 transporter haploinsufficiency: postnatal deceleration of brain weight and reactive astrocytosis  
  Ullner PM, Di Nardo A, Goldman JE,Schobel S, Yang H, Engelstad K, Wang D,Sahin M, De Vivo DC, Neurobiology of Disease, 1/1/2009
• Glut 1 deficiency without epilepsy- yet another case  
  Joshi C, Greenberg CR, De Vivo DC, Wang D, Chan-Lui W and Booth F, J Child Neurol, 1/1/2008
• Membrane helix 4 and other crucial structural signatures of Glut-1: Inferences from blood brain glucose transport mutants  
  Pascual JM, Wang D, Yang R, Shi L, Yang H, and Darryl DC, JBC, 1/1/2008
• A Novel tRNAVal Mitochondrial DNA Mutation Causing MELAS  
  Tanji K, Kaufmann K, Naini AB, Parsons TC, Wang D, Wiley J, Lu JS, Shanske S, Hirano M, Khandji AJ, DiMauro S and Rowland LP, J NeurolSci, 1/1/2008
• Functional studies of the T295M mutation Causing Glut1 Deficiency: Glucose efflux preferentially affected by T295M  
  Wang D, Yang H, Shi L, Ma L, Fujii T, Engelstad K, Pascual JM, and De Vivo DC, Ped Res, 1/1/2008
• Glut1 Deficiency: CSF Glucose How low is too low?  
  De Vivo,Wang D, Revue Neurologique, 1/1/2008
• Three Japanese patients with glucose transporter type 1 deficiency syndrome  
  Fujii T, Ho YY, Wang D, De Vivo DC, Miyajima T, Wong HY, Tsang PT, Shirasaka Y, Kudo T and Ito M, Brain & Dev, 1/1/2007
• Brain glucose supply and the syndrome of infantile neuroglycopenia  
  Pascual JM, Wang D, Hinton V, Engelstad K, Saxena CM, Van Heertum RL, De Vivo DC, Archives of Neurology, 1/1/2007
• Atypical GLUT1 Deficiency: Movement Disorder and Sleep Disturbance Responsive to Ketogenic Diet  
  Friedman JR, Thiele EA, Wang D, Levine KB, Cloherty EK, Pfeifer H, De Vivo DC, Carruthers A,Natowicz M, MovDisord, 1/1/2006
• Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiencysyndrome  
  Coman DJ, Sinclair KG, Burke CJ, Appleton DB, Pelekanos JT, O'Neil CM, Wallace GB, Bowling FG, Wang D, De Vivo DC, McGill JJ, J Paediatr Child Health, 1/1/2006
• Glucose transporter protein syndromes (In Chinese)  
  Wang D,Sun RP, Wang X, Yang R, Yang H, Pascual JM, De Vivo DC, J. Chinese Pediatrics, 1/1/2005
• Type 1 glucose transporter (Glut1) deficiency: manifestations of a hereditary neurological syndrome (In Spanish)  
  Pascual JM, Lecumberri B,Wang D, Yang R, Engelstad K, De Vivo DC, Rev Neurol, 1/1/2004
• Seizure characterization and electrographic features in Glut-1 deficiency syndrome  
  Leary LD, Wang D, Nordli DR, Engelstad K, De vivo DC, Epilepsia, 1/1/2003
• Functional studies of Thr310 mutations in Glut-1: T310I is a pathogenic mutation of Glut-1 deficiency  
  Wang D, Pascual JM, Iserovich P, Yang H, Ma L, Kuang K, Kranz-Eble P, Fischbarg J, De Vivo DC, J Biol Chem, 1/1/2003
• GLUT1 deficiency without epilepsy -an exceptional case  
  Overweg-Plandsoen WCG, Groener JEM, Wang D, Onkenhout P, Brouwer OF, Bakker HD, De Vivo DC, J. Inherit. Metab. Dis., 1/1/2003
• EEG Features of Glut-1 Deficiency Syndrome  
  von Moers A, Brockmann K, Wang D, Korenke CG, Huppke P, De Vivo DC, and Hanefeld F, Epilepsia, 1/1/2002
• Imaging the metabolic footprint of Glut1 deficiency on the brain  
  Pascual JM, van Heertum RL, Wang D, Engelstad K, De Vivo DC, Ann Neurol, 1/1/2002
• Glucose transporter proteindeficiency syndromes  
  De Vivo DC, Wang D, Pascual JM, Ho Y-Y, Int Rev Neurobiol, 1/1/2002
• Glut-1 Deficiency Syndrome and Other Glycolytic Defects  
  De VivoDC, Leary L, Wang D, J Child Neurol, 1/1/2002
• Changes in glucose transport and water permeability resulting from the T310I pathogenic mutation in Glut1 are consistent with two transport channels per monomer  
  Wang D, Iserovich P, Ma L, Yang H, Zuniga FA, Shi G, Haller JF, Wen Q, Pascual JM, Kuang K, De Vivo DC, Fischbarg J, J. Biol. Chem., 1/1/2002
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Abstracts/Posters

• Functional Studies Confirm Relative Pathogenicity of Serine 66 Mutations in Glut1 Deficiency.
  Wang D, Yang H, De Vivo DC, Neurology, (poster presentation to be presented at 65th AAN Annual Meeting), 1/1/2013
• Glut1 Deficiency Syndrome -An Emerging Realization of Protean Phenotypes.
  Wang D, Yang H, Bagay L, Engelstad K, Bao XH, De Vivo DC, Neurology, (poster presentation at 63rd AAN Annual Meeting), 1/1/2012
• Glut1 Deficiency Syndrome: The Diagnostic Value of the Erythrocyte 3-O-Methyl-D-Glucose Uptake Assay.
  Wang D, Yang H, Bagay L, Engelstad K, Wei Y, Rotstein M, Chung W, De Vivo DC, Neurology, 63rd AAN Annual Meeting, 1/1/2011
• A novel mutation in pyruvate carboxylase deficiency Type C.
  Lang TF, Wang D, De Vivo DC and Loughrey CL, J Inherited Metab Dis, 1/1/2008
• GLUT1 Deficiency without Epilepsy: Yet another case.
  Joshi C, Greenberg CR, De Vivo D, Wang D, Chan-Lui W, Booth FA, J Child Neurol, 1/1/2008
• Voxel based brain mapping of glucose metabolism in children with glucose transporter Type 1 Deficiency.
  Akman CI, Provazano F, Wang D, Engelstad K, Rikofsky R, Van Heertum RL, De Vivo DC, Neurology, 1/1/2008
• Molecular genetics of Glut1 Deficiency Syndrome.
  Wang D, Yang H, Engelstad K, Min-Wei C, De Vivo DC, Neurology, 1/1/2007
• Pyruvate carboxylase deficiency: Mosaicism correlates with prolonged survival.
  Wang D, Yang H, Lu JS, De Vivo DC, Am Acad Neurol, 1/1/2007
• Aminoglycoside enhancement of glucose transport in GLUT1 Deficiency Syndrome.
  Pascual JM, Zhang XM, Wang D, and De Vivo DC, Neuropediatrics, 1/1/2006
• Glucose transporter Type 1 deficiency syndrome (Glut 1 DS): the relationship with glucose transport to brain function during development.
  De Vivo DC, Engelstad K, Pascual JM, Wang D, Neurometabolic Disease Symposium Section, 10th International Child Neurology Congress, Montreal, Canada, 1/1/2006
• Glucose Transporter Type 1 Deficiency Syndrome (GLUT 1 DS).
  De Vivo DC, Wang D, Pascual J, Neuropediatrics, 1/1/2006
• Glucose transporter type 1 deficiency syndrome (Glut1 DS). (Platform presentation)
  Wang D, Pascual JM and De Vivo DC, 10th International Child Neurology Congress, Montreal, Canada, 1/1/2006
• GLUT-1 Deficiency Syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins.
  Henneke M, Wang D, Korinthenberg R, Pascual J, Yang H, Engelstad K, Brockmann K, De Vivo DC, Gartner J, Neuropediatrics, 1/1/2005
• Functional studies of disease-associated R126 mutations in GLUT1.
  Yang R, Wang D, Yang H, Pascaul JM, De Vivo DC, Soc Neurosci, 1/1/2004
• KmtA, A putative novel potassium transporter gene.
  Yang R, Wang D, Yang H, De Vivo DC, Pascaul JM, Soc Neurosci, 1/1/2004
• Pyruvate carboxylase deficiency: genotype-phenotype correlations.
  Wang D,Pascaul JM, Yang H, Steiner D, Di Mauro S, De Vivo DC, Soc Neurosci, 1/1/2004
• Effects of valproic acid on GLUT-1 gene expression.
  Mao X, Wang D, Pascaul JM, Yang H, Stiener D, De Vivo DC, Soc Neurosci, 1/1/2004
• Water permeability of pathogenic mutants of human facilitative glucose transporter Glut-1.
  Ma L, Wang D, Zuniga F, Wang D, Kuang K, Yang H, Iserovich P, De Vivo DC, Fischbarg J, ARVO (The Association for Research in Vision and Ophthalmology) meeting, 1/1/2002
• Genotype-phenotype correlation of Glut-1 deficiency syndrome.
  Wang D, Pascual JM, Kranz-Eble P, Yang H, Alvarez MG, Sun RP, De Vivo DC, The Joint Congress of ICNA and AOCNA, 1/1/2002
• Early onset dystonia /choreoathetosls/ataxia secondary to GLUT-1 deficiency, responsible to Ketogenic diet.
  FriedmanJR, Thiele E A, Wang D, De Vivo DC, Penny P, Heidi, P, Movement disorders, 1/1/2002
• Pyruvate dehydrogenase deficiency: clinical and molecular analysis.
  GarciaAlvarez M, Wang D, Kranz-Eble P, De Vivo DC, The Joint Congress of ICNA and AOCNA, 1/1/2002
• Water passage across a water-filled pore in the Glut1 glucose transporter pathogenic mutant T310I.
  Ma L, Wang D, Kuang K, Yang H, Iserovich P, Wen Q, Pauscal JM, De Vivo DC and Fischbarg J, IOVS, 1/1/2001
• Glut-1 deficiency syndrome (Glut-1DS): Autosomal dominant transmission of the R126H missense mutation.
  Wang D, Brockmann K, Korenke CG, Moers AV, Ho YY, Pascual JM, Kuang K, Yang H, Ma L, Kranz-Eble P, Fischbarg J, Hanefeld F and De Vivo DC, Ann Neurol, 1/1/2001
• Glut-1 deficiency syndrome (Glut-1DS): A severe phenotype associated with compound heterozygosity in trans.
  Wang D, Pascual JM, Yang H, Ho YY, Hinton V, Yang H, Engelstad K, Jhung S, Miller C, Kranz-Eble P, De Vivo DC, Ann Neurol, 1/1/2001
• Glut-1 deficiency syndrome (Glut-1DS): R333W genotype and paternal mosaicism.
  Wang D, Ho Y-Y, Pascual JM, Hinton V, Yang H, Anolik M, Kranz-Eble P, Jhung S, Engelstad K, De Vivo DC, Ann Neurol, 1/1/2001
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Other

• Glucose Transporter Type 1 Deficiency Syndrome. 
  Wang D, Pascual JM, De Vivo D; Pagon RA, Bird TD, Dolan CR, et al., eds., GeneReviews™ [Internet]
  University of Washington, Seattle, Seattle, WA - 8/9/2012
• Pyruvate Carboxylase Deficiency. 
  Wang D, De Vivo D; Pagon RA, Bird TD, Dolan CR, et al., eds., GeneReviews™ [Internet]
  University of Washington, Seattle, Seattle, WA - 7/21/2011