Research output per year
Research output per year
- 47 results
Search results
-
2018
HER2 heterogeneity is associated with poor survival in HER2-positive breast cancer
Hosonaga, M., Arima, Y., Sampetrean, O., Komura, D., Koya, I., Sasaki, T., Sato, E., Okano, H., Kudoh, J., Ishikawa, S., Saya, H. & Ishikawa, T., 2018 Aug, In: International journal of molecular sciences. 19, 8, 2158.Research output: Contribution to journal › Article › peer-review
Open Access16 Citations (Scopus) -
2017
RNA Sequencing Analysis Reveals Interactions between Breast Cancer or Melanoma Cells and the Tissue Microenvironment during Brain Metastasis
Sato, R., Nakano, T., Hosonaga, M., Sampetrean, O., Harigai, R., Sasaki, T., Koya, I., Okano, H., Kudoh, J., Saya, H. & Arima, Y., 2017, In: BioMed Research International. 2017, 8032910.Research output: Contribution to journal › Article › peer-review
Open Access25 Citations (Scopus) -
2016
SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7
Narumi, S., Amano, N., Ishii, T., Katsumata, N., Muroya, K., Adachi, M., Toyoshima, K., Tanaka, Y., Fukuzawa, R., Miyako, K., Kinjo, S., Ohga, S., Ihara, K., Inoue, H., Kinjo, T., Hara, T., Kohno, M., Yamada, S., Urano, H., Kitagawa, Y., & 19 others, 2016 Jul 1, In: Nature genetics. 48, 7, p. 792-797 6 p.Research output: Contribution to journal › Article › peer-review
197 Citations (Scopus) -
2015
Pathological characterization of pachydermia in pachydermoperiostosis
Tanese, K., Niizeki, H., Seki, A., Otsuka, A., Kabashima, K., Kosaki, K., Kuwahara, M., Miyakawa, S. I., Miyasaka, M., Matsuoka, K., Okuyama, T., Shiohama, A., Sasaki, T., Kudoh, J., Amagai, M. & Ishiko, A., 2015 Jul 1, In: Journal of Dermatology. 42, 7, p. 710-714 5 p.Research output: Contribution to journal › Article › peer-review
Open Access25 Citations (Scopus) -
2013
Assessment of homozygosity levels in the mito-gynogenetic torafugu (Takifugu rubripes) by genome-wide SNP analyses
Zhang, H., Hirose, Y., Yoshino, R., Kinoshita, S., Saito, K., Tan, E., Suzuki, Y., Shimizu, A., Okano, H., Kudoh, J., Watabe, S. & Asakawa, S., 2013 Mar 4, In: Aquaculture. 380-383, p. 114-119 6 p.Research output: Contribution to journal › Article › peer-review
6 Citations (Scopus) -
2008
Binding sites on tau proteins as components for antimicrobial peptides
Kobayashi, N., Masuda, J., Kudoh, J., Shimizu, N. & Yoshida, T., 2008 Jun, In: Biocontrol Science. 13, 2, p. 49-56 8 p.Research output: Contribution to journal › Article › peer-review
Open Access23 Citations (Scopus) -
Sequence analysis of filaggrin gene by novel shotgun method in Japanese atopic dermatitis
Sasaki, T., Kudoh, J., Ebihara, T., Shiohama, A., Asakawa, S., Shimizu, A., Takayanagi, A., Dekio, I., Sadahira, C., Amagai, M. & Shimizu, N., 2008 Aug, In: Journal of Dermatological Science. 51, 2, p. 113-120 8 p.Research output: Contribution to journal › Article › peer-review
18 Citations (Scopus) -
2007
Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy associated with L29P and IVS9-1G>C compound heterozygous autoimmune regulator gene mutations
Nagafuchi, S., Umene, K., Yamanaka, F., Oohashi, S., Shindo, M., Kurisaki, H., Kudoh, J., Shimizu, N., Hara, T. & Harada, M., 2007 Jun, In: Journal of Internal Medicine. 261, 6, p. 605-610 6 p.Research output: Contribution to journal › Article › peer-review
12 Citations (Scopus) -
2004
Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
Shibuya, K., Kudoh, J., Obayashi, I., Shimizu, A., Sasaki, T., Minoshima, S. & Shimizu, N., 2004 Mar, In: Mammalian Genome. 15, 3, p. 179-192 14 p.Research output: Contribution to journal › Article › peer-review
9 Citations (Scopus) -
Subcellular expression of autoimmune regulator is organized in a spatiotemporal manner
Akiyoshi, H., Hatakeyama, S., Pitkänen, J., Mouri, Y., Doucas, V., Kudoh, J., Tsurugaya, K., Uchida, D., Matsushima, A., Oshikawa, K., Nakayama, K. I., Shimizu, N., Peterson, P. & Matsumoto, M., 2004 Aug 6, In: Journal of Biological Chemistry. 279, 32, p. 33984-33991 8 p.Research output: Contribution to journal › Article › peer-review
41 Citations (Scopus) -
2003
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I
Driss, A., Noguchi, S., Amouri, R., Kefi, M., Sasaki, T., Sugie, K., Souilem, S., Hayashi, Y. K., Shimizu, N., Minoshima, S., Kudoh, J., Hentati, F. & Nishino, I., 2003 Apr 22, In: Neurology. 60, 8, p. 1341-1344 4 p.Research output: Contribution to journal › Article › peer-review
17 Citations (Scopus) -
2002
Distinct clinical phenotype and immunoreactivity in Japanese siblings with autoimmune polyglandular syndrome type 1 (APS-1) associated with compound heterozygous novel AIRE gene mutations
Kogawa, K., Kudoh, J., Nagafuchi, S., Ohga, S., Katsuta, H., Ishibashi, H., Harada, M., Hara, T. & Shimizu, N., 2002, In: Clinical Immunology. 103, 3 I, p. 277-283 7 p.Research output: Contribution to journal › Article › peer-review
35 Citations (Scopus) -
Expression of AIRE gene in peripheral monocyte/dendritic cell lineage
Kogawa, K., Nagafuchi, S., Katsuta, H., Kudoh, J., Tamiya, S., Sakai, Y., Shimizu, N. & Harada, M., 2002 Mar 1, In: Immunology Letters. 80, 3, p. 195-198 4 p.Research output: Contribution to journal › Article › peer-review
52 Citations (Scopus) -
2000
Diagnosis and molecular analysis of an atypical case of holocarboxylase synthetase deficiency
Holme, E., Kudoh, J., Shimizu, N., Suzuki, Y., Sakamoto, O., Li, X., Aoki, Y., Hiratsuka, M. & Narisawa, K., 2000, In: European Journal of Pediatrics. 159, 1-2, p. 18-22 5 p.Research output: Contribution to journal › Article › peer-review
18 Citations (Scopus) -
Myocilin expression in the astrocytes of the optic nerve head
Noda, S., Mashima, Y., Obazawa, M., Kubota, R., Oguchi, Y., Kudoh, J., Minoshima, S. & Shimizu, N., 2000 Oct 5, In: Biochemical and Biophysical Research Communications. 276, 3, p. 1129-1135 7 p.Research output: Contribution to journal › Article › peer-review
27 Citations (Scopus) -
Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of Leber hereditary optic neuropathy who showed marked differences in clinical severity
Mashima, Y., Saga, M., Hiida, Y., Imamura, Y., Kudoh, J. & Shimizu, N., 2000 Sept, In: American Journal of Ophthalmology. 130, 3, p. 357-359 3 p.Research output: Contribution to journal › Article › peer-review
3 Citations (Scopus) -
The myocilin (MYOC) gene expression in the human trabecular meshwork
Takahashi, H., Noda, S., Mashima, Y., Kubota, R., Ohtake, Y., Tanino, T., Kudoh, J., Minoshima, S., Oguchi, Y. & Shimizu, N., 2000 Feb, In: Current Eye Research. 20, 2, p. 81-84 4 p.Research output: Contribution to journal › Article › peer-review
11 Citations (Scopus) -
1998
Molecular analysis of new Japanese patients with holocarboxylase synthetase deficiency
Sakamoto, O., Suzuki, Y., Aoki, Y., Li, X., Hiratsuka, M., Yanagihara, K., Inui, K., Okabe, T., Yamaguchi, S., Kudoh, J., Shimizu, N. & Narisawa, K., 1998, In: Journal of Inherited Metabolic Disease. 21, 8, p. 873-874 2 p.Research output: Contribution to journal › Article › peer-review
6 Citations (Scopus) -
Report of the sixth international workshop on human chromosome 21 mapping 1996
Korenberg, J. R., Aaltonen, J., Brahe, C., Cabin, D., Creau, N., Delabar, J. M., Doering, J., Gardiner, K., Hubert, R. S., Ives, J., Kessling, A., Kudoh, J., Lafrenière, R., Murakami, Y., Ohira, M., Ohki, M., Patterson, D., Potier, M. C., Quackenbush, J., Reeves, R. H., & 5 others, 1998, In: Cytogenetics and Cell Genetics. 79, 1-2, p. 21-52 32 p.Research output: Contribution to journal › Article › peer-review
9 Citations (Scopus) -
Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy
Mashima, Y., Yamada, K., Wakakura, M., Kigasawa, K., Kudoh, J., Shimizu, N. & Oguchi, Y., 1998 Apr, In: Current Eye Research. 17, 4, p. 403-408 6 p.Research output: Contribution to journal › Article › peer-review
97 Citations (Scopus) -
The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients
Konishi, M., Mashima, Y., Yamada, M., Kudoh, J. & Shimizu, N., 1998 Sept, In: American Journal of Ophthalmology. 126, 3, p. 450-452 3 p.Research output: Contribution to journal › Article › peer-review
4 Citations (Scopus) -
1997
A transcript map of the candidate genes in the down syndrome critical region of human chromosome 21
Shimizu, N., Shindoh, N., Maeda, H., Yamakf, A., Kawasaki, K., Asakawa, S., Osoegawa, K., Soeda, E., Shimizu, Y., Minoshima, S. & Kudoh, J., 1997 Dec 1, In: Japanese Journal of Human Genetics. 42, 1, 1 p.Research output: Contribution to journal › Article › peer-review
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Construction of bac/cosmid contigs for the cat eye syndrome chromosome region (22q11)
Minoshima, S., Asakawa, S., Kawasaki, K., Wang, Y., Kudoh, J. & Shimizu, N., 1997, In: Japanese Journal of Human Genetics. 42, 1, p. 84 1 p.Research output: Contribution to journal › Article › peer-review
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Human bac library: its application to mapping of 21q22.3 and isolation of disease genes
Asakawa, S., Abe, I., Kudoh, Y., Nagamine, K., Wang, Y., Kawasaki, K., Kudoh, J., Minoshima, S. & Shimizu, N., 1997 Dec 1, In: Japanese Journal of Human Genetics. 42, 1, 1 p.Research output: Contribution to journal › Article › peer-review
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Sixth International Workshop on Human Chromosome 21 Mapping 1996, New York, May 6-8 1996: Report
Korenberg, J. R., Aaltonen, J., Brahe, C., Cabin, D., Creau, N., Delabar, J. M., Doering, J., Gardiner, K., Hubert, R. S., Ives, J., Kessling, A., Kudoh, J., Lafreniere, R., Murakami, Y., Ohira, M., Ohki, M., Patterson, D., Potier, M. C., Quackenbush, J., Reeves, R. H., & 5 others, 1997, In: Cytogenetics and Cell Genetics. 79, 1-2, p. 22-34 13 p.Research output: Contribution to journal › Article › peer-review
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1996
Frequency of mitochondrial DNA mutations in Japanese families with Leber's Hereditary Optic Neuropathy(LHON)
Yamada, K., Mashima, Y., Saga, M., Kudoh, J., Shimizu, N. & Oguchi, Y., 1996 Feb 15, In: Investigative Ophthalmology and Visual Science. 37, 3, p. S998Research output: Contribution to journal › Article › peer-review
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1995
Molecular genetic analysis of Leber's hereditary optic neuropathy with the 3460 mutation in Japanese pedigrees
Hiida, Y., Mashima, Y., Saga, M., Shuu, M., Akiya, S., Kudoh, J., Shimizu, N. & Oguchi, Y., 1995, In: Journal of Japanese Ophthalmological Society. 99, 6, p. 728-734 7 p.Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism
Mashima, Y., Saga, M., Hiida, Y., Oguchi, Y., Wakakura, M., Kudoh, J. & Shimizu, N., 1995, In: Investigative Ophthalmology and Visual Science. 36, 8, p. 1714-1720 7 p.Research output: Contribution to journal › Article › peer-review
7 Citations (Scopus) -
Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy
Mashima, Y., Hiida, Y., Saga, M., Oguchi, Y., Kudoh, J. & Shimizu, N., 1995, In: American Journal of Ophthalmology. 119, 2, p. 245-246 2 p.Research output: Contribution to journal › Article › peer-review
1 Citation (Scopus) -
The organization of the human immunoglobulin λ gene locus
Kawasaki, K., Minoshima, S., Schooler, K., Kudoh, J., Asakawa, S., De Jong, P. J. & Shimizu, N., 1995, In: Genome Research. 5, 2, p. 125-135 11 p.Research output: Contribution to journal › Article › peer-review
46 Citations (Scopus) -
1994
Autosomal dominant retinitis pigmentosa: A mutation in codon 1 81 (Glu → Lys) of the rhodopsin gene in a Japanese family
Saga, M., Mashima, Y., Akeo, K., Oguchi, Y., Kudoh, J. & Shimizu, N., 1994, In: Ophthalmic Genetics. 15, 2, p. 61-67 7 p.Research output: Contribution to journal › Article › peer-review
4 Citations (Scopus) -
Isolated Growth Hormone Deficiency Type 1A without Apparent Growth Hormone 1 Gene Deletion
Tamai, S., Matsuo, N., Sato, S., Kudoh, J. & Shimizu, N., 1994, In: clinical pediatric endocrinology. 3, 2, p. 105-111 7 p.Research output: Contribution to journal › Article › peer-review
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1993
A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa
Saga, M., Mashima, Y., Akeo, K., Oguchi, Y., Kudoh, J. & Shimizu, N., 1993 Nov, In: Human genetics. 92, 5, p. 519-521 3 p.Research output: Contribution to journal › Article › peer-review
18 Citations (Scopus) -
Desmoyokin, a 680 kDa keratinocyte plasma membrane-associated protein, is homologous to the protein encoded by human gene AHNAK
Hashimoto, T., Amagai, M., Parry, D. A. D., Dixon, T. W., Tsukita, S., Tsukita, S., Miki, K., Sakai, K., Inokuchi, Y., Kudoh, J., Shimizu, N. & Nishikawa, T., 1993, In: Journal of Cell Science. 105, 2, p. 275-286 12 p.Research output: Contribution to journal › Article › peer-review
45 Citations (Scopus) -
High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy
Mashima, Y., Hiida, Y., Oguchi, Y., Kudoh, J. & Shimizu, N., 1993 Aug, In: Human genetics. 92, 1, p. 101-102 2 p.Research output: Contribution to journal › Article › peer-review
17 Citations (Scopus) -
Human Gene Mapping and Chromosome Sorting by Laser Technology
Shimizu, N., Minoshima, S., Kudoh, J., Kawasaki, K., Wang, Y., Sakai, K. & Shimizu, Y., 1993, In: the keio journal of medicine. 42, 4, p. 212-216 5 p.Research output: Contribution to journal › Article › peer-review
Open Access -
1992
Shotgun polymerase chain reaction: Construction of clone libraries specific to a NotI fragment of flow-sorted human chromosome 22
Kawasaki, K., Minoshima, S., Kudoh, J. & Shimizu, N., 1992 May, In: Genomics. 13, 1, p. 109-114 6 p.Research output: Contribution to journal › Article › peer-review
1 Citation (Scopus) -
1991
Linkage Analysis of Affective Disorder Using DNA Markers on Chromosomes 11 and X
Nanko, S., Kobayashi, M., Gamou, S., Kudoh, J., Shimizu, N., Takazawa, N., Kazamatsuri, H. & Furusho, T., 1991 Mar, In: Psychiatry and Clinical Neurosciences. 45, 1, p. 53-56 4 p.Research output: Contribution to journal › Article › peer-review
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Mitochondrial DNA analysis of Leber's hereditary optic neuropathy
Hiida, Y., Mashima, Y., Oguchi, Y., Uemura, Y., Kudoh, J., Sakai, K. & Shimizu, N., 1991, In: Japanese Journal of Ophthalmology. 35, 1, p. 102-106 5 p.Research output: Contribution to journal › Article › peer-review
1 Citation (Scopus) -
1990
A human testis-specific mRNA for phosphoribosylpyrophosphate synthetase that initiates from a non-AUG codon
Taira, M., Iizasa, T., Shimada, H., Kudoh, J., Shimizu, N. & Tatibana, M., 1990, In: Journal of Biological Chemistry. 265, 27, p. 16491-16497 7 p.Research output: Contribution to journal › Article › peer-review
43 Citations (Scopus) -
DNA diagnosis of Leber's hereditary optic neuropathy
Mashima, Y., Oguchi, Y., Uemura, Y., Kudoh, J., Sakai, K. & Shimizu, N., 1990, In: Journal of Japanese Ophthalmological Society. 94, 7, p. 683-687 5 p.Research output: Contribution to journal › Article › peer-review
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1989
A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressed
Li, K., Warner, C. K., Hodge, J. A., Minoshima, S., Kudoh, J., Fukuyama, R., Maekawa, M., Shimizu, Y., Shimizu, N. & Wallace, D. C., 1989, In: Journal of Biological Chemistry. 264, 24, p. 13998-14004 7 p.Research output: Contribution to journal › Article › peer-review
61 Citations (Scopus) -
Localization of human phosphoribosylpyrophosphate synthetase subunit I and II genes (PRPS1 and PRPS2) to different regions of the X chromosome and assignment of two PRPS1-related genes to autosomes
Taira, M., Kudoh, J., Minoshima, S., Iizasa, T., Shimada, H., Shimizu, Y., Tatibana, M. & Shimizu, N., 1989 Jan, In: Somatic Cell and Molecular Genetics. 15, 1, p. 29-37 9 p.Research output: Contribution to journal › Article › peer-review
6 Citations (Scopus) -
1988
Assignment of the myeloperoxidase gene MPO to human chromosome 17 using somatic cell hybrids and flow-sorted chromosomes
Kudoh, J., Minoshima, S., Hashinaka, K., Nishio, C., Yamada, M., Shimizu, Y. & Shimizu, N., 1988 Sept, In: The Japanese Journal of Human Genetics. 33, 3, p. 315-324 10 p.Research output: Contribution to journal › Article › peer-review
1 Citation (Scopus) -
1986
Amino-terminal structure of spoOA protein and sequence homology with spoOF and spoOB proteins
Ikeuchi, T., Kudoh, J. & Tsumasawa, S., 1986 Jun 1, In: MGG Molecular & General Genetics. 203, 3, p. 371-376 6 p.Research output: Contribution to journal › Article › peer-review
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1985
Genetic analysis of spo0A and spo0C mutants of Bacillus subtilis with a Φ105 prophage merodiploid system
Ikeuchi, T., Kudoh, J. & Kurahashi, K., 1985, In: Journal of Bacteriology. 163, 2, p. 411-416 6 p.Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
1983
Cloning of sporulation genes spo0A and spo0C of Bacillus subtilis onto ρ11 temperate bacteriophage
Ikeuchi, T., Kudoh, J. & Kurahashi, K., 1983 Jan 1, In: Journal of Bacteriology. 154, 2, p. 988-991 4 p.Research output: Contribution to journal › Article › peer-review