FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Hisao Ueyama

Research Profile

Disorders

Color Vision Defects

Chemicals & Drugs

Concepts & Ideas

Molecular Sequence Data

Procedures

Co-author Network

Publications

TOP 3
Hisao Ueyama; Shinichi Yamade; Takahiro Yamashita; Sanae Muraki-Oda; Yoshinori Shichida; Shoko Tanabe; Hisakazu Ogita
Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect.
Wei-Guang Ding; Futoshi Toyoda; Hisao Ueyama; Hiroshi Matsuura
Lysophosphatidylcholine enhances I(Ks) currents in cardiac myocytes through activation of G protein, PKC and Rho signaling pathways.
Kosei Ando; Shinji Imai; Eiji Isoya; Mitsuhiko Kubo; Tomohiro Mimura; Suguru Shioji; Hisao Ueyama; Yoshitaka Matsusue
Effect of dynamic compressive loading and its combination with a growth factor on the chondrocytic phenotype of 3-dimensional scaffold-embedded chondrocytes.

Register for free to view:

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 research activity
of experts around the globe

Geonetwork of Hisao Ueyama (preview)

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

Flash Player Required

All Publications

2012: Hisao Ueyama; Shinichi Yamade; Takahiro Yamashita; Sanae Muraki-Oda; Yoshinori Shichida; Shoko Tanabe; Hisakazu Ogita
Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect.
Biochemical and biophysical research communications 2012;424(1):152-7.
2011: Wei-Guang Ding; Futoshi Toyoda; Hisao Ueyama; Hiroshi Matsuura
Lysophosphatidylcholine enhances I(Ks) currents in cardiac myocytes through activation of G protein, PKC and Rho signaling pathways.
Journal of molecular and cellular cardiology 2011;50(1):58-65.
2009: Kosei Ando; Shinji Imai; Eiji Isoya; Mitsuhiko Kubo; Tomohiro Mimura; Suguru Shioji; Hisao Ueyama; Yoshitaka Matsusue
Effect of dynamic compressive loading and its combination with a growth factor on the chondrocytic phenotype of 3-dimensional scaffold-embedded chondrocytes.
Acta orthopaedica 2009;80(6):724-33.
2009: Hisao Ueyama; Shoko Tanabe; Sanae Muraki-Oda; Shinichi Yamade; Masahito Ohji; Iwao Ohkubo
Analysis of introns and promoters of L/M visual pigment genes in relation to deutan color-vision deficiency with an array of normal gene orders.
Journal of human genetics 2009;54(9):525-30.
2007: Sanae Muraki-Oda; Futoshi Toyoda; Akira Okada; Shoko Tanabe; Shinichi Yamade; Hisao Ueyama; Hiroshi Matsuura; Masahito Ohji
Functional analysis of rod monochromacy-associated missense mutations in the CNGA3 subunit of the cone photoreceptor cGMP-gated channel.
Biochemical and biophysical research communications 2007;362(1):88-93.
2006: Futoshi Toyoda; Hisao Ueyama; Wei-Guang Ding; Hiroshi Matsuura
Modulation of functional properties of KCNQ1 channel by association of KCNE1 and KCNE2.
Biochemical and biophysical research communications 2006;344(3):814-20.
2006: Hisao Ueyama; Shoko Tanabe; Sanae Muraki-Oda; Shinichi Yamade; Iwao Ohkubo
Protan color vision deficiency with a unique order of green-red as the first two genes of a visual pigment array.
Journal of human genetics 2006;51(8):686-94.
2004: Akira Okada; Hisao Ueyama; Futoshi Toyoda; Sanae Oda; Wei-Guang Ding; Shoko Tanabe; Shinichi Yamade; Hiroshi Matsuura; Iwao Ohkubo; Kazutaka Kani
Functional role of hCngb3 in regulation of human cone cng channel: effect of rod monochromacy-associated mutations in hCNGB3 on channel function.
Investigative ophthalmology & visual science 2004;45(7):2324-32.
2004: Hisao Ueyama; Ryuzo Torii; Shoko Tanabe; Sanae Oda; Shinichi Yamade
An insertion/deletion TEX28 polymorphism and its application to analysis of red/green visual pigment gene arrays.
Journal of human genetics 2004;49(10):548-57.
2004: Hisao Ueyama; Shigeki Kuwayama; Hiroo Imai; Sanae Oda; Yasuhiro Nishida; Shoko Tanabe; Yoshinori Shichida; Shinichi Yamade
Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency.
Vision research 2004;44(19):2241-52.
2003: Hisao Ueyama; Yao-Hua Li; Gui-Lian Fu; Patcharee Lertrit; La-ongsri Atchaneeyasakul; Sanae Oda; Shoko Tanabe; Yasuhiro Nishida; Shinichi Yamade; Iwao Ohkubo
An A-71C substitution in a green gene at the second position in the red/green visual-pigment gene array is associated with deutan color-vision deficiency.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(6):3357-62.
2003: Sanae Oda; Hisao Ueyama; Yasuhiro Nishida; Shoko Tanabe; Shinichi Yamade
Analysis of L-cone/M-cone visual pigment gene arrays in females by long-range PCR.
Vision research 2003;43(5):489-95.
2002: Hisao Ueyama; Shigeki Kuwayama; Hiroo Imai; Shoko Tanabe; Sanae Oda; Yasuhiro Nishida; Akimori Wada; Yoshinori Shichida; Shinichi Yamade
Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies.
Biochemical and biophysical research communications 2002;294(2):205-9.
2001: S Hayashi; Hisao Ueyama; Shoko Tanabe; Shinichi Yamade; Kazutaka Kani
Number and variations of the red and green visual pigment genes in Japanese men with normal color vision.
Japanese journal of ophthalmology 2001;45(1):60-7.
2000: Sanae Oda; Hisao Ueyama; Shoko Tanabe; Y Tanaka; Shinichi Yamade; Kazutaka Kani
Detection of female carriers of congenital color-vision deficiencies by visual pigment gene analysis.
Current eye research 2000;21(4):767-73.
1999: Hisao Ueyama; Iwao Ohkubo
[Regulation of prostate gland-specific gene expression].
Seikagaku. The Journal of Japanese Biochemical Society 1999;71(3):210-4.
1998: Hisao Ueyama; Iwao Ohkubo
The expression of beta-microseminoprotein gene is regulated by cAMP.
Biochemical and biophysical research communications 1998;248(3):852-7.
1996: Hisao Ueyama; J Inazawa; H Nishino; Iwao Ohkubo; T Miwa
FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenes.
Cytogenetics and cell genetics 1996;74(3):221-4.
1995: Iwao Ohkubo; T Tada; Y Ochiai; Hisao Ueyama; T Eimoto; M Sasaki
Human seminal plasma beta-microseminoprotein: its purification, characterization, and immunohistochemical localization.
The international journal of biochemistry & cell biology 1995;27(6):603-11.
1995: Hisao Ueyama; J Inazawa; H Nishino; D Han-Xiang; Y Ochiai; I Ohkubo
Chromosomal mapping of the human smooth muscle actin gene (enteric type, ACTA3) to 2p13.1 and molecular nature of the hindIII polymorphism.
Genomics 1995;25(3):720-3.
1995: Y Ochiai; J Inazawa; Hisao Ueyama; Iwao Ohkubo
Human gene for beta-microseminoprotein: its promoter structure and chromosomal localization.
Journal of biochemistry 1995;117(2):346-52.
1994: Hisao Ueyama; H Naitoh; Iwao Ohkubo
Structure and expression of rat and mouse mRNAs for Zn-alpha 2-glycoprotein.
Journal of biochemistry 1994;116(3):677-81.
1993: Hisao Ueyama; H X Deng; Iwao Ohkubo
Molecular cloning and chromosomal assignment of the gene for human Zn-alpha 2-glycoprotein.
Biochemistry 1993;32(48):12968-76.
1991: Hisao Ueyama; M Niwa; T Tada; M Sasaki; Iwao Ohkubo
Cloning and nucleotide sequence of a human Zn-alpha 2-glycoprotein cDNA and chromosomal assignment of its gene.
Biochemical and biophysical research communications 1991;177(2):696-703.
1991: Hisao Ueyama
A HindIII DNA polymorphism in the human enteric type smooth muscle actin gene (ACTSG).
Nucleic acids research 1991;19(2):411.
1990: Hisao Ueyama; G Bruns; N Kanda
Assignment of the vascular smooth muscle actin gene ACTSA to human chromosome 10.
Jinrui idengaku zasshi. The Japanese journal of human genetics 1990;35(2):145-50.
1990: Hisao Ueyama; R Ohsugi
TaqI polymorphism in the 3' flanking region of the human aortic smooth muscle actin gene.
Nucleic acids research 1990;18(5):1318.