Y. Fukuda

发表

Comparative study of overlapping genes in the genomes of Mycoplasma genitalium and Mycoplasma pneumoniae.

M. Tomita, T. Washio, Y. Fukuda, 1999, Nucleic acids research.

On dynamics of overlapping genes in bacterial genomes.

Masaru Tomita, Yoichi Nakayama, Yoko Fukuda, 2003, Gene.

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

S. Tsuji, H. Shimazaki, Y. Fukuda, 2012, Journal of Medical Genetics.

Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation

S. Tsuji, Kunihiro Yoshida, S. Ikeda, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Mutations in COQ2 in familial and sporadic multiple-system atrophy.

J. Trojanowski, S. Gilman, K. Shirahige, 2013, The New England journal of medicine.

Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.

S. Tsuji, Y. Fukuda, H. Sasaki, 2010, Archives of neurology.

Cutting Edge: The Transcription Factor Bob1 Counteracts B Cell Activation and Regulates miR-146a in B Cells

John M. Lindner, Y. Fukuda, P. Nielsen, 2014, The Journal of Immunology.

ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.

Robert H. Brown, A. Fujiyama, A. Toyoda, 2013, American journal of human genetics.

Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1

S. Tsuji, Y. Fukuda, H. Ishiura, 2011, neurogenetics.

Mutations for Gaucher disease confer high susceptibility to Parkinson disease.

A. Toyoda, S. Tsuji, N. Hattori, 2009, Archives of neurology.

An Evolutionarily Conserved Mechanism for MicroRNA-223 Expression Revealed by MicroRNA Gene Profiling

Yoko Fukuda, Kimihiro Hino, Yutaka Enomoto, 2007, Cell.

Construction of microRNA-containing vectors for expression in mammalian cells.

Yoko Fukuda, Hiroaki Kawasaki, Kazunari Taira, 2006, Methods in molecular biology.

Suppression of Gene Expression via Chromatin Remodeling and the siRNA-Induced Silencing of Transcription

K. Morris, K. Taira, Y. Fukuda, 2005 .

A mutation database for amyotrophic lateral sclerosis

Asako Koike, Yoko Fukuda, Yuji Takahashi, 2010, Human mutation.

SNP Haplotype Mapping in a Small ALS Family

S. Tsuji, Michael B. Miller, Y. Fukuda, 2009, PloS one.

Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.

H. Morita, Y. Kuroiwa, S. Tsuji, 2011, American journal of human genetics.

Dominant mutations in RP1L1 are responsible for occult macular dystrophy.

S. Tsuji, K. Tsunoda, Makoto Nakamura, 2010, American journal of human genetics.

Are Responsible for Occult Macular Dystrophy

S. Tsuji, K. Tsunoda, Makoto Nakamura, 2010 .

Characterization of a heat-stable enzyme possessing GTP-dependent RNA ligase activity from a hyperthermophilic archaeon, Pyrococcus furiosus.

M. Tomita, S. Yokoyama, A. Kanai, 2009, RNA.

Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5

A. Hida, S. Aoki, T. Matsukawa, 2011, neurogenetics.

Exploration of human miRNA target genes in neuronal differentiation.

Yoko Fukuda, Hiroaki Kawasaki, Kazunari Taira, 2005, Nucleic acids symposium series.

Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer

S. Tsuji, Y. Fukuda, H. Ishiura, 2010, Journal of Human Genetics.

SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data

Yuji Takahashi, Jun Goto, Yoko Fukuda, 2009, BMC Bioinformatics.

Corrigendum to “On dynamics of overlapping genes in bacterial genomes” [Gene 323 (2003) 181–187]

Y. Nakayama, M. Tomita, Y. Fukuda, 2004 .

Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.

H. Morita, Y. Kuroiwa, S. Tsuji, 2011, American journal of human genetics.

Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.

S. Tsuji, Y. Fukuda, H. Sasaki, 2010, Archives of neurology.