R. Fujita

Publication List Details

Period

1994 - 2008

Number

34

Co-Authors

Modeling of the effect of friction in the temporomandibular joint on displacement of its disc during prolonged clenching (2008)

Tanaka, E., Hirose, M., Koolstra, J.H., Iwabuchi, Y., Fujita, R., ...

Purpose: The effect of the frictional coefficient in the temporomandibular joint on the disc during prolonged clenching was examined. Materials and Methods: For this purpose, a finite element model...

DECIGO pathfinder (2008)

Ando, M., Kawamura, Seiji, Nakamura, T., Tsubono, K., Tanaka, T., Funaki, I., ...

DECIGO pathfinder (DPF) is a milestone satellite mission for DECIGO (DECi-hertz Interferometer Gravitational wave Observatory) which is a future space gravitational wave antenna. DECIGO is expected...

The Japanese space gravitational wave antenna: DECIGO (2008)

Kawamura, Seiji, Ando, M., Nakamura, T., Tsubono, K., Tanaka, T., Funaki, I., ...

DECi-hertz Interferometer Gravitational wave Observatory (DECIGO) is the future Japanese space gravitational wave antenna. DECIGO is expected to open a new window of observation for gravitational...

The Japanese space gravitational wave antenna - DECIGO (2008)

Kawamura, Seiji, Ando, M., Nakamura, T., Tsubono, K., Tanaka, T., Funaki, I., ...

DECi-hertz Interferometer Gravitational wave Observatory (DECIGO) is the future Japanese space gravitational wave antenna. The goal of DECIGO is to detect gravitational waves from various kinds of...

Joint LIGO and TAMA300 search for gravitational waves from inspiralling neutron star binaries (2006)

Abbott, B., Abbott, R., Adhikari, R., Ageev, A., Agresti, J., Ajith, P., ...

We search for coincident gravitational wave signals from inspiralling neutron star binaries using LIGO and TAMA300 data taken during early 2003. Using a simple trigger exchange method, we perform an...

Joint LIGO and TAMA300 search for gravitational waves from inspiralling neutron star binaries (2006)

Abbott, B., Abbott, R., Adhikari, R., Ageev, A., Agresti, Juri, Ajith, P., ...

We search for coincident gravitational wave signals from inspiralling neutron star binaries using LIGO and TAMA300 data taken during early 2003. Using a simple trigger exchange method, we perform an...

Results of the search for inspiraling compact star binaries from TAMA300's observation in 2000-2004 (2006)

Akutsu, Tomomi, Akutsu, Tomotadu, Ando, Masaki, Arai, Koji, Araya, Akito, Asada, H., ...

We analyze the data of the TAMA300 detector to search for gravitational waves from inspiraling compact star binaries with masses of the component stars in the range 1M[sun]–3M[sun]. In this...

The Extent of Natural Cross-Pollination in Wild Soybean (Glycine soja) (1997)

Fujita, R., Ohara, M., Okazaki, K., Shimamoto, Y.

To evaluate the extent of natural cross-pollination in wild soybean (Glycine soja Sieb. and Zucc.), we analyzed the genetic structure of four populations along the Omono River in Akita Prefecture,...

Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia.

Fujita, R, Hanauer, A, Sirugo, G, Heilig, R, Mandel, J L

The gene for Friedreich ataxia (FA), a severe recessive neurodegenerative disease, has previously been shown to be tightly linked to the polymorphic markers D9S15 and D9S5 on human chromosome 9. In...

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.

Fujita, R, Buraczynska, M, Gieser, L, Wu, W, Forsythe, P, Abrahamson, M, ...

X-linked retinitis pigmentosa (XLRP) is a severe form of inherited progressive retinal degeneration. The RP3 (retinitis pigmentosa type 3) locus at Xp21.1 is believed to account for the disease in...

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.

Buraczynska, M, Wu, W, Fujita, R, Buraczynska, K, Phelps, E, Andréasson, S, ...

The RPGR (retinitis pigmentosa GTPase regulator) gene for RP3, the most frequent genetic subtype of X-linked retinitis pigmentosa (XLRP), has been shown to be mutated in 10%-15% of European XLRP...

A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

Gieser, L, Fujita, R, Göring, H H, Ott, J, Hoffman, D R, Cideciyan, A V, ...

Two genetic loci, RP2 and RP3, for X-linked retinitis pigmentosa (XLRP) have been localized to Xp11.3-11.23 and Xp21.1, respectively. RP3 appears to account for 70% of XLRP families; however,...

The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.

Hanauer, A, Chery, M, Fujita, R, Driesel, A J, Gilgenkrantz, S, Mandel, J L

Chamberlain et al. have assigned the gene for Friedreich ataxia (FA), a recessive neurodegenerative disorder, to chromosome 9, and have proposed a regional localization in the proximal short arm...

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes.

Sirugo, G, Keats, B, Fujita, R, Duclos, F, Purohit, K, Koenig, M, ...

Eleven Acadian families with Friedreich ataxia (FA) who were from southwest Louisiana were studied with a series of polymorphic markers spanning 310 kb in the D9S5-D9S15 region previously shown to be...

Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia.

Fujita, R, Hanauer, A, Sirugo, G, Heilig, R, Mandel, J L

The gene for Friedreich ataxia (FA), a severe recessive neurodegenerative disease, has previously been shown to be tightly linked to the polymorphic markers D9S15 and D9S5 on human chromosome 9. In...

A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

Gieser, L, Fujita, R, Göring, H H, Ott, J, Hoffman, D R, Cideciyan, A V, ...

Two genetic loci, RP2 and RP3, for X-linked retinitis pigmentosa (XLRP) have been localized to Xp11.3-11.23 and Xp21.1, respectively. RP3 appears to account for 70% of XLRP families; however,...

The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.

Hanauer, A, Chery, M, Fujita, R, Driesel, A J, Gilgenkrantz, S, Mandel, J L

Chamberlain et al. have assigned the gene for Friedreich ataxia (FA), a recessive neurodegenerative disorder, to chromosome 9, and have proposed a regional localization in the proximal short arm...

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes.

Sirugo, G, Keats, B, Fujita, R, Duclos, F, Purohit, K, Koenig, M, ...

Eleven Acadian families with Friedreich ataxia (FA) who were from southwest Louisiana were studied with a series of polymorphic markers spanning 310 kb in the D9S5-D9S15 region previously shown to be...

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.

Fujita, R, Buraczynska, M, Gieser, L, Wu, W, Forsythe, P, Abrahamson, M, ...

X-linked retinitis pigmentosa (XLRP) is a severe form of inherited progressive retinal degeneration. The RP3 (retinitis pigmentosa type 3) locus at Xp21.1 is believed to account for the disease in...

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.

Buraczynska, M, Wu, W, Fujita, R, Buraczynska, K, Phelps, E, Andréasson, S, ...

The RPGR (retinitis pigmentosa GTPase regulator) gene for RP3, the most frequent genetic subtype of X-linked retinitis pigmentosa (XLRP), has been shown to be mutated in 10%-15% of European XLRP...

A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Fujita, R., Bingham, E., Forsythe, P., McHenry, C., Aita, V., Navia, B. A., ...

Genetic loci for X-linked retinitis pigmentosa (XLRP) have been mapped between Xp11.22 and Xp22.13 (RP2, RP3, RP6, and RP15). The RP3 gene, which is responsible for the predominant form of XLRP in...