B. Antalffy

发表

Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3

Juan I. Young, H. Zoghbi, R. Paylor, 2002, Neuron.

Learning and Memory and Synaptic Plasticity Are Impaired in a Mouse Model of Rett Syndrome

H. Zoghbi, J. Sweatt, O. Arancio, 2006, The Journal of Neuroscience.

Predominant Localization of the LIS Family of Gene Products to Cajal‐Retzius Cells and Ventricular Neuroepithelium in the Developing Human Cortex

M. Mizuguchi, B. Antalffy, G. Clark, 1997, Journal of neuropathology and experimental neurology.

The neurological mutant quakingviable is Parkin deficient

M. Justice, H. Vogel, J. Noveroske, 2004, Mammalian Genome.

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1

Michael A. Mancini, Huda Y. Zoghbi, Harry T. Orr, 1998, Nature Genetics.

Interaction of reelin signaling and Lis1 in brain development

Amir H Assadi, Joachim Herz, Michael Sheldon, 2003, Nature Genetics.

Reelin and Disabled‐1 Expression in Developing and Mature Human Cortical Neurons

K. Mikoshiba, C. Quattrocchi, G. D’Arcangelo, 2003, Journal of neuropathology and experimental neurology.

Decreased Dendritic Branching in Frontal, Motor and Limbic Cortex in Rett Syndrome Compared with Trisomy 21

B. Antalffy, D D Armstrong, D. Armstrong, 1998, Journal of neuropathology and experimental neurology.

Selective Dendritic Alterations in the Cortex of Rett Syndrome

B. Antalffy, D. Armstrong, J. Dunn, 1995, Journal of neuropathology and experimental neurology.

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.

J. Lupski, A. Goldman, R. Paylor, 2007, Human molecular genetics.

The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology.

A. Beaudet, M. Bhattacharjee, B. Antalffy, 2007, Human molecular genetics.

Intestine-specific ablation of mouse atonal homolog 1 (Math1) reveals a role in cellular homeostasis.

H. Zoghbi, M. Helmrath, S. Henning, 2007, Gastroenterology.

Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice.

H. Zoghbi, H. Orr, R. Mestril, 2001, Human molecular genetics.

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation.

H. Zoghbi, M. Shahbazian, D. Armstrong, 2002, Human molecular genetics.

Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice

Harry T Orr, Aaron Ciechanover, A. Ciechanover, 1999, Neuron.

A Long CAG Repeat in the Mouse Sca1 Locus Replicates SCA1 Features and Reveals the Impact of Protein Solubility on Selective Neurodegeneration

H. Zoghbi, M. Kano, J. Sweatt, 2002, Neuron.

Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1

Huda Y. Zoghbi, Harry T. Orr, H. Zoghbi, 2000, Nature Neuroscience.

Impaired Conditioned Fear and Enhanced Long-Term Potentiation inFmr2 Knock-Out Mice

H. Zoghbi, J. Sweatt, E. Weeber, 2002, The Journal of Neuroscience.

Expression analysis of the ataxin–1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

H. Zoghbi, H. Orr, D. Armstrong, 1995, Nature Genetics.

Association of impaired neuronal migration with cognitive deficits in extremely preterm infants.

Kenji F. Tanaka, M. Kakeyama, Toshihiro Endo, 2017, JCI insight.

Substance P immunoreactivity in the enteric nervous system in Rett syndrome

D. Glaze, D. Armstrong, B. Antalffy, 2001, Brain and Development.

Differential expression of survivin splice isoforms in medulloblastomas

K. Wong, A. Adesina, B. Antalffy, 2007, Neuropathology and applied neurobiology.

Neurobiology of Disease Learning and Memory and Synaptic Plasticity Are Impaired in a Mouse Model of Rett Syndrome

H. Zoghbi, J. Sweatt, O. Arancio, 2005 .