Username

Password

Forgot Password?

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Kenshi Hayashi

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Phenomena

Single-Stranded Conformational Polymorphism

Procedures

Genes & Molecular Sequences

Chemicals & Drugs

Geographic Areas

Japan

Concepts & Ideas

Physiology

Disorders

Loss of Heterozygosity

Sign-in to see full Profile

Network (preview)

Co-Publications
Name
31
Tahira, Tomoko
22
Kukita, Yoji
14
Higasa, Koichiro
14
Horiuchi, Takahiko
9
Tsukamoto, Hiroshi
6
Baba, Shingo
6
Harada, Mine
6
Inazuka, M
6
Iwaki, Toru
6
Nishizaka, Hiroaki
5
Sasaki, Tomio
4
Niho, Yoshiyuki
4
Mizoguchi, Masahiro
4
Nagasawa, Kohei
4
Nagata, Shinji

Sign-in to see all Coauthors

Publications

TOP 3
Higasa Koichiro; Kukita Yoji; Kato Kiyoko; Wake Norio; Tahira Tomoko; Hayashi Kenshi
Evaluation of haplotype inference using definitive haplotype data obtained from complete hydatidiform moles, and its significance for the analyses of positively selected regions.
Tahira Tomoko; Kukita Yoji; Higasa Koichiro; Okazaki Yuko; Yoshinaga Aki; Hayashi Kenshi
Estimation of SNP allele frequencies by SSCP analysis of pooled DNA.
Guan Yanlei; Hata Nobuhiro; Kuga Daisuke; Yoshimoto Koji; Mizoguchi Masahiro; Shono Tadahisa; Suzuki Satoshi O; Tahira Tomoko; Kukita Yoji; Higasa Koichiro; Yokoyama Nobuhiko; Nagata Shinji; Iwaki Toru; Sasaki Tomio; Hayashi Kenshi
Narrowing of the regions of allelic losses of chromosome 1p36 in meningioma tissues by an improved SSCP analysis.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Kenshi Hayashi (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2009: Higasa Koichiro; Kukita Yoji; Kato Kiyoko; Wake Norio; Tahira Tomoko; Hayashi Kenshi
Evaluation of haplotype inference using definitive haplotype data obtained from complete hydatidiform moles, and its significance for the analyses of positively selected regions.
PLoS genetics 2009;5(5):e1000468.
2009: Tahira Tomoko; Kukita Yoji; Higasa Koichiro; Okazaki Yuko; Yoshinaga Aki; Hayashi Kenshi
Estimation of SNP allele frequencies by SSCP analysis of pooled DNA.
Methods in molecular biology (Clifton, N.J.) 2009;578():193-207.
2008: Guan Yanlei; Hata Nobuhiro; Kuga Daisuke; Yoshimoto Koji; Mizoguchi Masahiro; Shono Tadahisa; Suzuki Satoshi O; Tahira Tomoko; Kukita Yoji; Higasa Koichiro; Yokoyama Nobuhiko; Nagata Shinji; Iwaki Toru; Sasaki Tomio; Hayashi Kenshi
Narrowing of the regions of allelic losses of chromosome 1p36 in meningioma tissues by an improved SSCP analysis.
International journal of cancer. Journal international du cancer 2008;122(8):1820-6.
2008: Miyagawa H; Yamai M; Sakaguchi D; Kiyohara C; Tsukamoto H; Kimoto Y; Nakamura T; Lee J-H; Tsai C-Y; Chiang B-L; Shimoda T; Harada M; Tahira T; Hayashi K; Horiuchi T
Association of polymorphisms in complement component C3 gene with susceptibility to systemic lupus erythematosus.
Rheumatology (Oxford, England) 2008;47(2):158-64.
2008: Qin Minghui; Kondo Hiroyuki; Tahira Tomoko; Hayashi Kenshi
Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy.
Human genetics 2008;122(6):615-23.
2007: Mitsuyasu Hiroshi; Kawasaki Hiroaki; Ninomiya Hideaki; Kinukawa Naoko; Yamanaka Takeharu; Tahira Tomoko; Stanton Vincent P; Springett Gregory M; Hayashi Kenshi; Tashiro Nobutada; Kanba Shigenobu
Genetic structure of the dopamine receptor D4 gene (DRD4) and lack of association with schizophrenia in Japanese patients.
Journal of psychiatric research 2007;41(9):763-75.
2007: Hata Nobuhiro; Shono Tadahisa; Mizoguchi Masahiro; Matsumoto Kenichi; Guan Yanlei; Nagata Shinji; Hayashi Kenshi; Iwaki Toru; Sasaki Tomio
Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy.
Neurological research 2007;29(7):723-6.
2007: Ju Myung-Jong; Yang Do-Hyeon; Takahara Naoki; Hayashi Kenshi; Toko Kiyoshi; Lee Seung-Woo; Kunitake Toyoki
Landmine detection: improved binding of 2,4-dinitrotoluene in a gamma-CD/metal oxide matrix and its sensitive detection via a cyclic surface polarization impedance (cSPI) method.
Chemical communications (Cambridge, England) 2007;(25):2630-2.
2007: Yanaru-Fujisawa Ritsuko; Matsumoto Takayuki; Kukita Yoji; Nakamura Shotaro; Yao Takashi; Hayashi Kenshi; Iida Mitsuo
Impact of Phospholipase A2 group IIa gene polymorphism on phenotypic features of patients with familial adenomatous polyposis.
Diseases of the colon and rectum 2007;50(2):223-31.
2007: Higasa Koichiro; Miyatake Katsuyuki; Kukita Yoji; Tahira Tomoko; Hayashi Kenshi
D-HaploDB: a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples.
Nucleic acids research 2007;35(Database issue):D685-9.
2006: Tahira Tomoko; Okazaki Yuko; Miura Kenichi; Yoshinaga Aki; Masumoto Kazumi; Higasa Koichiro; Kukita Yoji; Hayashi Kenshi
QSNPlite, a software system for quantitative analysis of SNPs based on capillary array SSCP analysis.
Electrophoresis 2006;27(19):3869-78.
2006: Hata Nobuhiro; Shono Tadahisa; Yoshimoto Koji; Mizoguchi Masahiro; Kawamura Tadao; Nagata Shinji; Matsumoto Kenichi; Hayashi Kenshi; Iwaki Toru; Sasaki Tomio
An astroblastoma case associated with loss of heterozygosity on chromosome 9p.
Journal of neuro-oncology 2006;80(1):69-73.
2006: Yang Do-Hyeon; Ju Myung-Jong; Maeda Aya; Hayashi Kenshi; Toko Kiyoshi; Lee Seung-Woo; Kunitake Toyoki
Design of highly efficient receptor sites by combination of cyclodextrin units and molecular cavity in TiO2 ultrathin layer.
Biosensors & bioelectronics 2006;22(3):388-92.
2006: Hata Nobuhiro; Yoshimoto Koji; Yokoyama Nobuhiko; Mizoguchi Masahiro; Shono Tadahisa; Guan Yanlei; Tahira Tomoko; Kukita Yoji; Higasa Koichiro; Nagata Shinji; Iwaki Toru; Sasaki Tomio; Hayashi Kenshi
Allelic losses of chromosome 10 in glioma tissues detected by quantitative single-strand conformation polymorphism analysis.
Clinical chemistry 2006;52(3):370-8.
2006: Qin Minghui; Kondo Hiroyuki; Uno Hideaki; Fujiwara Eriko; Uchio Eiichi; Tahira Tomoko; Hayashi Kenshi
Novel OPA1 mutations identified in Japanese pedigrees with optic atrophy.
Molecular vision 2006;12():485-91.
2006: Higasa Koichiro; Hayashi Kenshi
Periodicity of SNP distribution around transcription start sites.
BMC genomics 2006;7():66.
2005: Kukita Yoji; Miyatake Katsuyuki; Stokowski Renee; Hinds David; Higasa Koichiro; Wake Norio; Hirakawa Toshio; Kato Hidenori; Matsuda Takao; Pant Krishna; Cox David; Tahira Tomoko; Hayashi Kenshi
Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles.
Genome research 2005;15(11):1511-8.
2005: Qin Minghui; Hayashi Hideyuki; Oshima Kenji; Tahira Tomoko; Hayashi Kenshi; Kondo Hiroyuki
Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.
Human mutation 2005;26(2):104-12.
2005: Tahira Tomoko; Baba Shingo; Higasa Koichiro; Kukita Yoji; Suzuki Yutaka; Sugano Sumio; Hayashi Kenshi
dbQSNP: a database of SNPs in human promoter regions with allele frequency information determined by single-strand conformation polymorphism-based methods.
Human mutation 2005;26(2):69-77.
2005: Shikata Kentaro; Kukita Yoji; Matsumoto Takayuki; Esaki Motohiro; Yao Takashi; Mochizuki Yuichi; Hayashi Kenshi; Iida Mitsuo
Gastric juvenile polyposis associated with germline SMAD4 mutation.
American journal of medical genetics. Part A 2005;134(3):326-9.
2005: Horiuchi T; Gondo H; Miyagawa H; Otsuka J; Inaba S; Nagafuji K; Takase K; Tsukamoto H; Koyama T; Mitoma H; Tamimoto Y; Miyagi Y; Tahira T; Hayashi K; Hashimura C; Okamura S; Harada M
Association of MBL gene polymorphisms with major bacterial infection in patients treated with high-dose chemotherapy and autologous PBSCT.
Genes and immunity 2005;6(2):162-6.
2004: Horiuchi Takahiko; Tsukamoto Hiroshi; Mitoma Hiroki; Miyagawa Hiroshi; Tamimoto Yasuhiro; Yoshizawa Seiji; Harada Mine; Hayashi Kenshi; Hashimura Chinami; Oribe Motohiro; Okamura Seiichi
Novel mutations in TNFRSF1A in patients with typical tumor necrosis factor receptor-associated periodic syndrome and with systemic lupus erythematosus in Japanese.
International journal of molecular medicine 2004;14(5):813-8.
2004: Put-Ti-Noi Supawadee; Petmitr Songsak; Chanyavanich Voravut; Sangruji Tumtip; Theerapuncharoen Veerasak; Hayashi Kenshi; Thangnipon Wipawan
Chromosome 10 and 17 deletions and p53 gene mutations in Thai patients with astrocytomas.
Oncology reports 2004;11(1):207-11.
2003: Taniguchi Shuichi; Mochida Yasushi; Uchiumi Takeshi; Tahira Tomoko; Hayashi Kenshi; Takagi Koichi; Shimada Mitsuo; Maehara Yoshihiko; Kuwano Hiroyuki; Kono Suminori; Nakano Hitoo; Kuwano Michihiko; Wada Morimasa
Genetic polymorphism at the 5' regulatory region of multidrug resistance 1 (MDR1) and its association with interindividual variation of expression level in the colon.
Molecular cancer therapeutics 2003;2(12):1351-9.
2003: Koyama T; Tsukamoto H; Masumoto K; Himeji D; Hayashi K; Harada M; Horiuchi T
A novel polymorphism of the human APRIL gene is associated with systemic lupus erythematosus.
Rheumatology (Oxford, England) 2003;42(8):980-5.
2003: Baba S; Kukita Y; Higasa K; Tahira T; Hayashi K
Single-stranded conformational polymorphism analysis using automated capillary array electrophoresis apparatuses.
BioTechniques 2003;34(4):746-50.
2003: Tahira Tomoko; Suzuki Akari; Kukita Yoji; Hayashi Kenshi
SNP detection and allele frequency determination by SSCP.
Methods in molecular biology (Clifton, N.J.) 2003;212():37-46.
2002: Higasa Koichiro; Kukita Yoji; Baba Shingo; Hayashi Kenshi
Software for machine-independent quantitative interpretation of SSCP in capillary array electrophoresis (QUISCA).
BioTechniques 2002;33(6):1342-8.
2002: Kukita Yoji; Manago Sachi; Baba Shingo; Hayashi Kenshi
Hemi-stranded SSCP analysis of SNPs in short sequence-tagged sites.
BioTechniques 2002;33(5):1118-21.
2002: Horiuchi Takahiko; Nishimukai Hiroaki; Okiura Tatsuyuki; Nishimura Koji; Nishizaka Hiroaki; Kojima Takeshi; Tsukamoto Hiroshi; Hayashi Kenshi; Harada Mine
Molecular bases for human complement C7 polymorphisms, C7*3 and C7*4.
Biochemical and biophysical research communications 2002;298(3):450-5.
2002: Kukita Yoji; Hayashi Kenshi
Multicolor post-PCR labeling of DNA fragments with fluorescent ddNTPs.
BioTechniques 2002;33(3):502, 504, 506.
2002: Kukita Yoji; Higasa Koichiro; Baba Shingo; Nakamura Michihiro; Manago Sachi; Suzuki Akari; Tahira Tomoko; Hayashi Kenshi
A single-strand conformation polymorphism method for the large-scale analysis of mutations/polymorphisms using capillary array electrophoresis.
Electrophoresis 2002;23(14):2259-66.
2002: Himeji Daisuke; Horiuchi Takahiko; Tsukamoto Hiroshi; Hayashi Kenshi; Watanabe Takeshi; Harada Mine
Characterization of caspase-8L: a novel isoform of caspase-8 that behaves as an inhibitor of the caspase cascade.
Blood 2002;99(11):4070-8.
2002: Yoshimoto Koji; Iwaki Toru; Inamura Takanori; Fukui Masashi; Tahira Tomoko; Hayashi Kenshi
Multiplexed analysis of post-PCR fluorescence-labeled microsatellite alleles and statistical evaluation of their imbalance in brain tumors.
Japanese journal of cancer research : Gann 2002;93(3):284-90.
2002: Fukuda Shinji; Yamasaki Yuki; Iwaki Toru; Kawasaki Hiroaki; Akieda Shizuka; Fukuchi Naruhiko; Tahira Tomoko; Hayashi Kenshi
Characterization of the biological functions of a transcription factor, c-myc intron binding protein 1 (MIBP1).
Journal of biochemistry 2002;131(3):349-57.
2002: Higasa Koichiro; Hayashi Kenshi
Ordered catenation of sequence-tagged sites and multiplexed SNP genotyping by sequencing.
Nucleic acids research 2002;30(3):E11.
2001: Chawengchao B; Petmitr S; Ponglikitmongkol M; Chanyavanich V; Sangruji T; Theerapuncharoen V; Hayashi K; Thangnipon W
Detection of a novel point mutation in the p53 gene in grade II astrocytomas by PCR-SSCP analysis with additional Klenow treatment.
Anticancer research 2001;21(4A):2739-43.
2001: Kondo H; Ohno K; Tahira T; Hayashi H; Oshima K; Hayashi K
Delineation of the critical interval for the familial exudative vitreoretinopathy gene by linkage and haplotype analysis.
Human genetics 2001;108(5):368-75.
2001: Harashima S; Horiuchi T; Hatta N; Morita C; Higuchi M; Sawabe T; Tsukamoto H; Tahira T; Hayashi K; Fujita S; Niho Y
Outside-to-inside signal through the membrane TNF-alpha induces E-selectin (CD62E) expression on activated human CD4+ T cells.
Journal of immunology (Baltimore, Md. : 1950) 2001;166(1):130-6.
2001: Sasaki T; Tahira T; Suzuki A; Higasa K; Kukita Y; Baba S; Hayashi K
Precise estimation of allele frequencies of single-nucleotide polymorphisms by a quantitative SSCP analysis of pooled DNA.
American journal of human genetics 2001;68(1):214-8.
2001: Hayashi K; Wenz H M; Inazuka M; Tahira T; Sasaki T; Atha D H
SSCP analysis of point mutations by multicolor capillary electrophoresis.
Methods in molecular biology (Clifton, N.J.) 2001;163():109-26.
2000: Kondo H; Tahira T; Hayashi H; Oshima K; Hayashi K
Microsatellite genotyping of post-PCR fluorescently labeled markers.
BioTechniques 2000;29(4):868-72.
2000: Horiuchi T; Himeji D; Tsukamoto H; Harashima S; Hashimura C; Hayashi K
Dominant expression of a novel splice variant of caspase-8 in human peripheral blood lymphocytes.
Biochemical and biophysical research communications 2000;272(3):877-81.
2000: Inazuka M; Tahira T; Horiuchi T; Harashima S; Sawabe T; Kondo M; Miyahara H; Hayashi K
Analysis of p53 tumour suppressor gene somatic mutations in rheumatoid arthritis synovium.
Rheumatology (Oxford, England) 2000;39(3):262-6.
1999: Thangnipon W; Mizoguchi M; Kukita Y; Inazuka M; Iwaki T; Fukui M; Hayashi K
Distinct pattern of PCR-SSCP analysis of p53 mutations in human astrocytomas.
Cancer letters 1999;141(1-2):195-201.
1999: Horiuchi T; Nishizaka H; Yasunaga S; Higuchi M; Tsukamoto H; Hayashi K; Nagasawa K
Association of Fas/APO-1 gene polymorphism with systemic lupus erythematosus in Japanese.
Rheumatology (Oxford, England) 1999;38(6):516-20.
1998: Kojima T; Horiuchi T; Nishizaka H; Fukumori Y; Amano T; Nagasawa K; Niho Y; Hayashi K
Genetic basis of human complement C8 alpha-gamma deficiency.
Journal of immunology (Baltimore, Md. : 1950) 1998;161(7):3762-6.
1998: Higuchi M; Horiuchi T; Kojima T; Nishizaka H; Ishibashi H; Hayashi K; Niho Y; Nagasawa K
Analysis of CD40 ligand gene mutations in patients with primary biliary cirrhosis.
Scandinavian journal of clinical and laboratory investigation 1998;58(5):429-32.
1998: Horiuchi T; Nishizaka H; Kojima T; Sawabe T; Niho Y; Schneider P M; Inaba S; Sakai K; Hayashi K; Hashimura C; Fukumori Y
A non-sense mutation at Arg95 is predominant in complement 9 deficiency in Japanese.
Journal of immunology (Baltimore, Md. : 1950) 1998;160(3):1509-13.
1998: Sasaki T; Tian H; Kukita Y; Inazuka M; Tahira T; Imai T; Yamauchi M; Saito T; Hori T; Hashimoto-Tamaoki T; Komatsu K; Nikaido O; Hayashi K
ATM mutations in patients with ataxia telangiectasia screened by a hierarchical strategy.
Human mutation 1998;12(3):186-95.
1997: Inazuka M; Wenz H M; Sakabe M; Tahira T; Hayashi K
A streamlined mutation detection system: multicolor post-PCR fluorescence labeling and single-strand conformational polymorphism analysis by capillary electrophoresis.
Genome research 1997;7(11):1094-103.
1997: Furuya H; Kukita Y; Nagano S; Sakai Y; Yamashita Y; Fukuyama H; Inatomi Y; Saito Y; Koike R; Tsuji S; Fukumaki Y; Hayashi K; Kobayashi T
Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patients.
Human genetics 1997;100(3-4):450-6.
1997: Kukita Y; Furuya H; Kobayashi T; Sakai N; Hayashi K
Characterization of the GALC gene in three Japanese patients with adult-onset Krabbe disease.
Genetic testing 1997;1(3):217-23.
1997: Kukita Y; Tahira T; Sommer S S; Hayashi K
SSCP analysis of long DNA fragments in low pH gel.
Human mutation 1997;10(5):400-7.
1996: Inazuka M; Tahira T; Hayashi K
One-tube post-PCR fluorescent labeling of DNA fragments.
Genome research 1996;6(6):551-7.
1996: Nishizaka H; Horiuchi T; Zhu Z B; Fukumori Y; Nagasawa K; Hayashi K; Krumdieck R; Cobbs C G; Higuchi M; Yasunaga S; Niho Y; Volanakis J E
Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals.
Journal of immunology (Baltimore, Md. : 1950) 1996;156(6):2309-15.
1995: Shibata H; Tahira T; Hayashi K
RNA-primed PCR.
Genome research 1995;5(4):400-3.
1993: Hayashi K; Yandell D W
How sensitive is PCR-SSCP?
Human mutation 1993;2(5):338-46.

Sign-in to see more