Y. Matsushima

Y. Matsushima, H. Inagaki, Y. Kitagawa, 1997, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Mitochondrial Lon protease is a gatekeeper for proteins newly imported into the matrix

S. Fukuchi, T. Uchiumi, D. Kang, 2019, Communications biology.

Functional Domains of Chicken Mitochondrial Transcription Factor A for the Maintenance of Mitochondrial DNA Copy Number in Lymphoma Cell Line DT40*

Y. Matsuda, K. Beck, Y. Matsushima, 2003, Journal of Biological Chemistry.

The manner in which DNA is packaged with TFAM has an impact on transcription activation and inhibition

H. Harashima, Yuma Yamada, Y. Matsushima, 2012, FEBS open bio.

Differential Phenotypes of Active Site and Human Autosomal Dominant Progressive External Ophthalmoplegia Mutations in Drosophila Mitochondrial DNA Helicase Expressed in Schneider Cells*

Y. Matsushima, L. Kaguni, 2007, Journal of Biological Chemistry.

Drosophila Mitochondrial Transcription Factor B2 Regulates Mitochondrial DNA Copy Number and Transcription in Schneider Cells*

Y. Matsushima, R. Garesse, L. Kaguni, 2004, Journal of Biological Chemistry.

Within-host evolution of a Klebsiella pneumoniae clone: selected mutations associated with the alteration of outer membrane protein expression conferred multidrug resistance.

Tetsuya Hayashi, T. Uchiumi, D. Kang, 2020, The Journal of antimicrobial chemotherapy.

Mitochondrial Complex III Deficiency Caused by a Homozygous UQCRC2 Mutation Presenting with Neonatal‐Onset Recurrent Metabolic Decompensation

N. Matsumoto, M. Shiina, K. Ogata, 2013, Human mutation.

Modeling Pathogenic Mutations of Human Twinkle in Drosophila Suggests an Apoptosis Role in Response to Mitochondrial Defects

A. Whitworth, Y. Matsushima, R. Garesse, 2012, PloS one.

Drosophila mitochondrial transcription factor A (d-TFAM) is dispensable for the transcription of mitochondrial DNA in Kc167 cells.

Y. Matsushima, A. Goto, T. Kadowaki, 2001, The Biochemical journal.

Neural-specific deletion of mitochondrial p32/C1qbp leads to leukoencephalopathy due to undifferentiated oligodendrocyte and axon degeneration

T. Uchiumi, D. Kang, Y. Matsushima, 2017, Scientific Reports.

Selective Suppression of Endogenous Gene Expression Using RNAi in Drosophila Schneider S2 Cells.

Y. Matsushima, 2021, Methods in molecular biology.

Functional analysis by inducible RNA interference in Drosophila melanogaster.

Y. Matsushima, R. Garesse, L. Kaguni, 2007, Methods in molecular biology.

Mitochondrial Lon protease regulates mitochondrial DNA copy number and transcription by selective degradation of mitochondrial transcription factor A (TFAM)

Yuichi Matsushima, Y. Matsushima, Yu-ichi Goto, 2010, Proceedings of the National Academy of Sciences.

A Large DNA-binding Nuclear Protein with RNA Recognition Motif and Serine/Arginine-rich Domain (*)

Y. Matsushima, K. Nakamura, T. Kadowaki, 1996, The Journal of Biological Chemistry.

1 Modeling pathogenic mutations of human Twinkle in Drosophila melanogaster suggests that apoptosis plays a critical role in mitochondrial intergenomic communication defects

A. Whitworth, Y. Matsushima, R. Garesse, 2013 .

Coiled Coil Domain-containing Protein 56 (CCDC56) Is a Novel Mitochondrial Protein Essential for Cytochrome c Oxidase Function*

Y. Matsushima, C. Ugalde, R. Garesse, 2012, The Journal of Biological Chemistry.

Serum depletion induced cancer stem cell-like phenotype due to nitric oxide synthesis in oncogenic HRas transformed cells

T. Uchiumi, Takashi Matsumoto, Y. Matsushima, 2016, Oncotarget.

Isolation of Rat Mitochondrial Transcription Factor A (r-Tfam) cDNA

Takao Saito, Toshihiko Hayashi, Y. Matsushima, 2000, DNA sequence : the journal of DNA sequencing and mapping.

Matrix proteases in mitochondrial DNA function.

Y. Matsushima, L. Kaguni, 2012, Biochimica et biophysica acta.

Neural-specific deletion of mitochondrial p32/C1qbp leads to leukoencephalopathy due to undifferentiated oligodendrocyte and axon degeneration

T. Uchiumi, D. Kang, Y. Matsushima, 2017, Scientific Reports.

Physiological and Biochemical Defects in Functional Interactions of Mitochondrial DNA Polymerase and DNA-binding Mutants of Single-stranded DNA-binding Protein*

C. Farr, Y. Matsushima, A. Lagina, 2004, Journal of Biological Chemistry.

Mitochondrial Transcription Factor B2 Is Essential for Metabolic Function in Drosophila melanogaster Development*

Raquel Marco-Ferreres, J. J. Aragón, Y. Matsushima, 2008, Journal of Biological Chemistry.

Targeted Disruption of a Mitochondrial Transcription Factor a in the Chicken DT40 Cell Lines

Y. Matsushima, Y. Kitagawa, K. Matsumura, 2002 .

Functional importance of the conserved N-terminal domain of the mitochondrial replicative DNA helicase.

Y. Matsushima, L. Kaguni, 2009, Biochimica et Biophysica Acta.

ECHS1 Mutations Cause Combined Respiratory Chain Deficiency Resulting in Leigh Syndrome

Yuichi Matsushima, Masayuki Sasaki, Seiji Yamaguchi, 2015, Human mutation.

NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy

Y. Goto, I. Nishino, C. Sakai, 2018, Clinical genetics.

Drosophila nuclear factor DREF regulates the expression of the mitochondrial DNA helicase and mitochondrial transcription factor B2 but not the mitochondrial translation factor B1.

Y. Matsushima, R. Garesse, M. Roberti, 2013, Biochimica et biophysica acta.

Mitochondrial Lon protease is a gatekeeper for proteins newly imported into the matrix

S. Fukuchi, T. Uchiumi, D. Kang, 2021, Communications Biology.

Tor and the Sin3–Rpd3 complex regulate expression of the mitophagy receptor protein Atg32 in yeast

T. Saigusa, T. Uchiumi, D. Kang, 2014, Journal of Cell Science.

Drosophila protease ClpXP specifically degrades DmLRPPRC1 controlling mitochondrial mRNA and translation

T. Uchiumi, D. Kang, Y. Matsushima, 2017, Scientific Reports.

IBA57 mutations abrogate iron-sulfur cluster assembly leading to cavitating leukoencephalopathy

Y. Goto, I. Nonaka, Y. Hayashi, 2017, Neurology: Genetics.

Zinc finger-like motif conserved in a family of RNA binding proteins.

Y. Matsushima, Y. Kitagawa, K. Matsumura, 1997, Bioscience, biotechnology, and biochemistry.

A family of novel DNA-binding nuclear proteins having polypyrimidine tract-binding motif and arginine/serine-rich motif.

Y. Matsushima, Y. Kitagawa, M. Sonoda, 1996, Biochemical and biophysical research communications.

Tor and the Sin3–Rpd3 complex regulate expression of the mitophagy receptor protein Atg32 in yeast

T. Saigusa, T. Uchiumi, D. Kang, 2014, Journal of Cell Science.