C. Iwahashi

发表

Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.

P. Hagerman, A. Beilina, F. Tassone, 2005, Human molecular genetics.

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).

J Grigsby, B. Trapp, J. Brunberg, 2006, Brain : a journal of neurology.

Decreased Fragile X Mental Retardation Protein Expression Underlies Amygdala Dysfunction in Carriers of the Fragile X Premutation

Andrea Schneider, Kami Koldewyn, Flora Tassone, 2011, Biological Psychiatry.

CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS.

P. Hagerman, F. Tassone, C. Iwahashi, 2011, Human molecular genetics.

Isolation of pathology-associated intranuclear inclusions.

P. Hagerman, C. Iwahashi, Christine Iwahashi, 2008, Methods in molecular biology.

A quantitative ELISA assay for the fragile x mental retardation 1 protein.

D. Nguyen, P. Hagerman, F. Tassone, 2009, The Journal of molecular diagnostics : JMD.

Stimulation of epithelial cell growth by the neuropeptide substance P

C. Murphy, B. Foster, M. Mannis, 1993, Journal of cellular biochemistry.

Autism phenotype in fragile X premutation males is not associated with FMR1 expression: a preliminary evaluation

D. Nguyen, P. Hagerman, F. Tassone, 2018 .

High-throughput screening of FDA-approved drugs using oxygen biosensor plates reveals secondary mitofunctional effects.

G. Cortopassi, A. Tomilov, C. Iwahashi, 2014, Mitochondrion.

Clinical and molecular implications of mosaicism in FMR1 full mutations

Dalyir I. Pretto, Flora Tassone, Blythe Durbin-Johnson, 2014, Front. Genet..

FMR1 RNA within the Intranuclear Inclusions of Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)

P. Hagerman, F. Tassone, C. Iwahashi, 2004, RNA biology.

Protein composition of the intranuclear inclusions of FXTAS.

P. Hagerman, C. Lebrilla, F. Tassone, 2006, Brain : a journal of neurology.

Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome.

Sarah Wong, P. Hagerman, C. Giulivi, 2010, The Biochemical journal.

Fibroblast phenotype in male carriers of FMR1 premutation alleles.

C. Goetz, D. Nguyen, P. Hagerman, 2010, Human molecular genetics.

Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome.

Sarah Wong, P. Hagerman, C. Giulivi, 2011, Human molecular genetics.

Effects of Dexamethasone on DNA Synthesis in Lens Epithelial Cells Are Dependent on Cell Type and Growth Factor

T. Reid, C. Iwahashi, J. Kopel, 2022, Current eye research.

Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles

Andrea Schneider, Jun Yi Wang, David Hessl, 2013, NeuroImage.