T. Tamura

发表

Aging Specifically Impairs amnesiac-Dependent Memory in Drosophila

A. Chiang, T. Tully, Hsin-Ping Liu, 2003, Neuron.

Developmental YAPdeltaC determines adult pathology in a model of spinocerebellar ataxia type 1

M. Sudol, K. Tagawa, H. Okazawa, 2017, Nature Communications.

Sox2 Transcriptionally Regulates Pqbp1, an Intellectual Disability-Microcephaly Causative Gene, in Neural Stem Progenitor Cells

K. Tagawa, H. Okazawa, T. Tamura, 2013, PloS one.

Glial Cell Lineage Expression of Mutant Ataxin-1 and Huntingtin Induces Developmental and Late-Onset Neuronal Pathologies in Drosophila Models

E. Wanker, M. Sone, H. Okazawa, 2009, PloS one.

The hnRNP-Htt axis regulates necrotic cell death induced by transcriptional repression through impaired RNA splicing

S. Miyano, S. Imoto, Y. Tamada, 2016, Cell Death and Disease.

Systems biology analysis of Drosophila in vivo screen data elucidates core networks for DNA damage repair in SCA1.

S. Miyano, T. Shimamura, S. Imoto, 2014, Human molecular genetics.

Ku70 Alleviates Neurodegeneration in Drosophila Models of Huntington's Disease

E. Wanker, T. Iwatsubo, M. Sone, 2011, PloS one.

Ku 70 Alleviates Neurodegeneration in Drosophila Models of Huntington ’ s Disease

E. Wanker, T. Iwatsubo, M. Sone, 2011 .

Omi / HtrA2 is relevant to the selective vulnerability of striatal neurons in Huntington’s disease

I. Kanazawa, E. Wanker, S. Shimizu, 2008, The European journal of neuroscience.

HMGB1 facilitates repair of mitochondrial DNA damage and extends the lifespan of mutant ataxin-1 knock-in mice

S. Shimizu, S. Muramatsu, J. Shimizu, 2014, EMBO molecular medicine.

HMGB 1 facilitates repair of mitochondrial DNA damage and extends the lifespan of mutant ataxin-1 knockin mice

S. Shimizu, S. Muramatsu, J. Shimizu, 2014 .

Systematic Analysis of Fly Models with Multiple Drivers Reveals Different Effects of Ataxin-1 and Huntingtin in Neuron Subtype-Specific Expression

M. Sone, H. Okazawa, T. Tamura, 2014, PloS one.

Nerve-evoked synchronous release and high K+ -induced quantal events are regulated separately by synaptotagmin I at Drosophila neuromuscular junctions.

T. Tamura, Y. Kidokoro, N. Reist, 2007, Journal of neurophysiology.

Junctions Neuromuscular Drosophila by Synaptotagmin I at -Induced Quantal Events Are Regulated Separately + Nerve-Evoked Synchronous Release and High K

E. Chapman, T. Tamura, Y. Kidokoro, 2015 .

External Ca2+ dependency of synaptic transmission in drosophila synaptotagmin I mutants.

Kazuhiro Suzuki, T. Tamura, Y. Kidokoro, 2005, Journal of neurophysiology.

Delayed synaptic transmission in Drosophila cacophonynull embryos.

T. Tamura, Y. Kidokoro, Jiamei Hou, 2008, Journal of neurophysiology.

IN DROSOPHILA CACOPHONY NULL EMBRYOS

T. Tamura, Y. Kidokoro, Jiamei Hou, 2008 .

Glial Cell Lineage Expression of Mutant Ataxin-1 and Huntingtin Induces Developmental and Late-Onset Neuronal Pathologies in Drosophila Models

E. Wanker, M. Sone, H. Okazawa, 2009, Neuroscience Research.

Effect of specific inhibition of synaptic delivery of APP by loss-of-function of yata on the Drosophila Alzheimer's disease model.

M. Sone, H. Okazawa, T. Tamura, 2017 .

Suppression of the novel ER protein Maxer by mutant ataxin‐1 in Bergman glia contributes to non‐cell‐autonomous toxicity

M. Sone, S. Ogishima, K. Tagawa, 2010, The EMBO journal.

TRIAD (Transcriptional Repression-Induced Atypical Death)

H. Okazawa, T. Tamura, 2018, Apoptosis and Beyond.

A functional deficiency of TERA/VCP/p97 contributes to impaired DNA repair in multiple polyglutamine diseases

E. Wanker, G. Sobue, Y. Eishi, 2013, Nature Communications.

Mutant huntingtin impairs Ku70-mediated DNA repair

I. Kanazawa, R. Foulle, E. Wanker, 2010, Neuroscience Research.

Neutrophil Extracellular Traps Promote Metastases of Colorectal Cancers through Activation of ERK Signaling by Releasing Neutrophil Elastase

K. Obama, M. Okamoto, T. Tamura, 2023, International journal of molecular sciences.

Targeting TEAD/YAP-transcription-dependent necrosis, TRIAD, ameliorates Huntington's disease pathology.

S. Finkbeiner, M. Sudol, G. Blandino, 2016, Human molecular genetics.

The Induction Levels of Heat Shock Protein 70 Differentiate the Vulnerabilities to Mutant Huntingtin among Neuronal Subtypes

I. Kanazawa, E. Wanker, K. Tagawa, 2007, The Journal of Neuroscience.

Identification of hepta-histidine as a candidate drug for Huntington’s disease by in silico-in vitro- in vivo-integrated screens of chemical libraries

Kazunori D. Yamada, S. Finkbeiner, H. Okano, 2016, Scientific Reports.

Suppression of the synaptic localization of a subset of proteins including APP partially ameliorates phenotypes of the Drosophila Alzheimer's disease model

M. Sone, H. Okazawa, T. Tamura, 2018, PloS one.

HMGB1, a pathogenic molecule that induces neurite degeneration via TLR4-MARCKS, is a potential therapeutic target for Alzheimer’s disease

A. Miyawaki, G. Sobue, H. Hama, 2016, Scientific Reports.

A restricted level of PQBP1 is needed for the best longevity of Drosophila

S. Miyano, T. Shimamura, S. Imoto, 2013, Neurobiology of Aging.

Drosophila PQBP1 Regulates Learning Acquisition at Projection Neurons in Aversive Olfactory Conditioning

A. Chiang, M. Sone, T. Miyashita, 2010, The Journal of Neuroscience.

A clock gene, period, plays a key role in long-term memory formation in Drosophila.

T. Kitamoto, T. Sakai, T. Tamura, 2004, Proceedings of the National Academy of Sciences of the United States of America.

The Drosophila DCO mutation suppresses age-related memory impairment without affecting lifespan

D. Yamazaki, S. Nagano, M. Saitoe, 2007, Nature Neuroscience.

Drosophila as a Novel Animal Model for Studying the Genetics of Age-related Memory Impairment

M. Saitoe, T. Tamura, Naomi Ito, 2005, Reviews in the neurosciences.

Hepatoma‐derived growth factor, a new trophic factor for motor neurons, is up‐regulated in the spinal cord of PQBP‐1 transgenic mice before onset of degeneration

Y. Eishi, M. Shibata, K. Tagawa, 2006, Journal of neurochemistry.

Developmental YAPdeltaC determines adult pathology in a model of spinocerebellar ataxia type 1

M. Sudol, K. Tagawa, H. Okazawa, 2017, Nature Communications.

Delayed synaptic transmission in Drosophila cacophonynull embryos.

T. Tamura, Y. Kidokoro, Jiamei Hou, 2008, Journal of neurophysiology.

RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhance DNA damage repair

K. Tagawa, H. Okazawa, T. Tamura, 2016, Journal of the Neurological Sciences.