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1

BQ788, an endothelin ETB receptor antagonist, attenuates stab wound injury-induced reactive astrocytes in rat brain

Yutaka Koyama, Motohide Takemura, Keiko Fujiki, Nobue Ishikawa, Yoshio Shigenaga, Akemichi Baba

Journal:

Year:

1999

Language:

english

File:

PDF, 104 KB

english, 1999

2

Genetic epidemiology of duchenne muscular dystrophy in Japan: Classical segregation analysis

Masao Kanamori, Newton E. Morton, Keiko Fujiki, Kiyotaro Kondo, D. C. Rao, I. B. Borecki

Journal:

Genetic Epidemiology

Year:

1987

Language:

english

File:

PDF, 421 KB

english, 1987

3

Interleukin 6 receptor expression by human cord blood- or peripheral blood-derived primitive haematopoietic progenitors implies acquisition of different functional properties

Hitoshi Minamiguchi, Naoyuki Yahata, Takafumi Kimura, Hiroshi Fujiki, Sachio Harada, Jianfeng Wang, Keiko Okuda, Hiroto Kaneko, Keiko Hodohara, Tadao Banba, Kiyoshi Yasukawa, Junko H. Ohyashiki, Kazum

Journal:

British Journal of Haematology

Year:

2000

Language:

english

File:

PDF, 601 KB

english, 2000

4

A hemizygous A to CC base change of theCHMgene causing choroideremia associated with pinealoma

Yoshihiro Hotta, Keiko Fujiki, Mutsuko Hayakawa, Nao Kohno, Hitoshi Kitagawa, Rie Doi, Atsushi Kanai

Journal:

Graefe's Archive for Clinical and Experimental Ophthalmology

Year:

1997

Language:

english

File:

PDF, 292 KB

english, 1997

5

Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa

Keiko Fujiki, Yoshihiro Hotta, Akira Murakami, Masaru Yoshii, Mutsuko Hayakawa, Takafumi Ichikawa, Misako Takeda, Kiyoshi Akeo, Shigekuni Okisaka, Atsushi Kanai

Journal:

Journal of Human Genetics

Year:

1995

Language:

english

File:

PDF, 1.72 MB

english, 1995

6

A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathy

Keiko Fujiki, Yoshihiro Hotta, Mutsuko Hayakawa, Kimiko Saito, Fumino Ara, Syunsuke Ueda, Toshiko Goto, Misako Ishida, Kenji Yanashima, Takashi Shiono, Jo Sakai, Atsushi Kanai, Akira Nakajima

Journal:

Journal of Human Genetics

Year:

1991

Language:

english

File:

PDF, 332 KB

english, 1991

7

A research of consanguinity in Japanese young couples

Yuri Hosoda, Keiko Fujiki, Akira Nakajima

Journal:

Journal of Human Genetics

Year:

1983

Language:

english

File:

PDF, 124 KB

english, 1983

8

Effects of parental age and birth order in motor neuron disease

Kiyotaro Kondo, Keiko Fujiki

Journal:

Journal of Human Genetics

Year:

1984

Language:

english

File:

PDF, 310 KB

english, 1984

9

Frequencies of polymorphisms in the rhodopsin gene of Japanese retinitis pigmentosa and normal individuals

Keiko Fujiki, Hiroyuki Kawano, Yoshihiro Hotta, Mutsuko Hayakawa, Marilou G. Nicolas, Misako Takeda, Fumino Iwata, Naohiro Ohta, Atsushi Kanai, Tomoko Hashimoto, Jun-ichi Furuyama

Journal:

Journal of Human Genetics

Year:

1995

Language:

english

File:

PDF, 344 KB

english, 1995

10

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)

Keiko Fujiki, Yoshihiro Hotta, Mutsuko Hayakawa, Hitoshi Sakuma, Takashi Shiono, Michiru Noro, Takehiko Sakuma, Makoto Tamai, Kazumasa Hikiji, Ryuji Kawaguchi, Akihiko Hoshi, Akira Nakajima, Atsushi K

Journal:

Journal of Human Genetics

Year:

1992

Language:

english

File:

PDF, 827 KB

english, 1992

11

Is risk to motor neuron disease influenced by the season of birth?

Kiyotaro Kondo, Keiko Fujiki

Journal:

Journal of Human Genetics

Year:

1989

Language:

english

File:

PDF, 178 KB

english, 1989

12

Japanese juvenile retinoschisis is caused by mutations of theXLRS1gene

Y. Hotta, Keiko Fujiki, Mutsuko Hayakawa, Takashi Ohta, Takuro Fujimaki, Kouichi Tamaki, Toshiyuki Yokoyama, Atsushi Kanai, Akito Hirakata, Tetsuo Hida, Sachiko Nishina, Noriyuki Azuma

Journal:

Year:

1998

Language:

english

File:

PDF, 64 KB

english, 1998

13

Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778

M. Matsumoto, Seiji Hayasaka, Yoshihiro Hotta, Keiko Fujiki, Takuro Fujimaki, Misako Takeda, Nobuo Ishida, Shin-ichiro Endo, Atsushi Kanai

Journal:

Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 106 KB

english, 1998

14

Mutation Analysis of theTGFBIGene in Vietnamese with Granular and Avellino Corneal Dystrophy

Le Xuan Cung, Nguyen Thanh Ha, Hoang Minh Chau, Ton Kim Thanh, Keiko Fujiki, Akira Murakami, Yoshimune Hiratsuka, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2004

Language:

english

File:

PDF, 304 KB

english, 2004

15

Mutations in the Membrane Component, Chromosome 1, Surface Marker 1 (M1S1) Gene in Gelatinous Drop-like Corneal Dystrophy

Akira Murakami, Shunsuke Kimura, Keiko Fujiki, Takuro Fujimaki, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2004

Language:

english

File:

PDF, 219 KB

english, 2004

16

Analysis ofCOL8A2Gene Mutation in Japanese Patients with Fuchs’ Endothelial Dystrophy and Posterior Polymorphous Dystrophy

Akira Kobayashi, Keiko Fujiki, Akira Murakami, Takuji Kato, Li-Zhong Chen, Hitoshi Onoe, Kiyoo Nakayasu, Mayumi Sakurai, Mami Takahashi, Kazuhisa Sugiyama, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2004

Language:

english

File:

PDF, 249 KB

english, 2004

17

Novel mutation (V505D) of theTGFBIgene found in a Chinese family with lattice corneal dystrophy, type I

Xin Tian, Keiko Fujiki, Wei Wang, Akira Murakami, Peiying Xie, Atsushi Kanai, Zuguo Liu

Journal:

Japanese Journal of Ophthalmology

Year:

2005

Language:

english

File:

PDF, 267 KB

english, 2005

18

Long-term Follow-up of Two Sisters with Leber's Hereditary Optic Neuropathy

Toshiyuki Yokoyama, Keiko Fujiki, Akira Murakami, Yoshihiro Hotta

Journal:

Japanese Journal of Ophthalmology

Year:

2006

Language:

english

File:

PDF, 216 KB

english, 2006

19

A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy

Takahiko Seto, Keiko Fujiki, Hitoshi Kishishita, Takuro Fujimaki, Akira Murakami, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2008

Language:

english

File:

PDF, 173 KB

english, 2008

20

Expression and Distribution of Junctional Adhesion Molecule-1 in the Human Cornea

Lizhong Chen, Nobuyuki Ebihara, Keiko Fujiki, Akira Murakami

Journal:

Japanese Journal of Ophthalmology

Year:

2007

Language:

english

File:

PDF, 241 KB

english, 2007

21

A novel mutation (967−970+2)delAAAGGT in the choroideremia gene found in a Japanese family and related clinical findings

Yutaka Iino, Takuro Fujimaki, Keiko Fujiki, Akira Murakami

Journal:

Japanese Journal of Ophthalmology

Year:

2008

Language:

english

File:

PDF, 778 KB

english, 2008

22

A case of oculodentodigital dysplasia syndrome with novelGJA1gene mutation

Momoko Himi, Takuro Fujimaki, Toshiyuki Yokoyama, Keiko Fujiki, Toshiaki Takizawa, Akira Murakami

Journal:

Japanese Journal of Ophthalmology

Year:

2009

Language:

english

File:

PDF, 299 KB

english, 2009

23

Clinical findings in a choroideremia patient who underwent vitrectomy for retinal detachment associated with macular hole

Hajime Shinoda, Takashi Koto, Keiko Fujiki, Akira Murakami, Kazuo Tsubota, Yoko Ozawa

Journal:

Japanese Journal of Ophthalmology

Year:

2011

Language:

english

File:

PDF, 376 KB

english, 2011

24

OPA1mutations in Japanese patients suspected to have autosomal dominant optic atrophy

Tetsuya Hamahata, Takuro Fujimaki, Keiko Fujiki, Ai Miyazaki, Atsushi Mizota, Akira Murakami

Journal:

Japanese Journal of Ophthalmology

Year:

2012

Language:

english

File:

PDF, 511 KB

english, 2012

25

WT1235, a Ninemer Peptide Derived from Wilms’ Tumor Gene Product, Is a Candidate Peptide for the Vaccination of HLA-A*0201-Positive Patients with Hematopoietic Malignancies

Zheyu Li, Yoshihiro Oka, Akihiro Tsuboi, Tomoki Masuda, Naoko Tatsumi, Manabu Kawakami, Tatsuya Fujioka, Nao Sakaguchi, Hiroko Nakajima, Fumihiro Fujiki, Keiko Udaka, Yusuke Oji, Ichiro Kawase, Haruo

Journal:

International Journal of Hematology

Year:

2005

Language:

english

File:

PDF, 74 KB

english, 2005

26

A Case of Juvenile Retinoschisis Diagnosed by Analysis of the XLRS 1 Gene

Ryo Taketani, Toshiyuki Yokoyama, Yoshihiro Hotta, Fumino Iwata, Kouji Yazawa, Keiko Fujiki, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2000

Language:

english

File:

PDF, 36 KB

english, 2000

27

Transferrin-Polyethylenimine Conjugate, FuGENE6 and TransIT-LT as Nonviral Vectors for Gene Transfer to the Corneal Endothelium

Ha Nguyen Thanh, Akira Murakami, Keiko Fujiki, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2002

Language:

english

File:

PDF, 667 KB

english, 2002

28

Mutation Analysis of Membrane Component, Chromosome 1, Surface Marker 1

Toshihiro Yajima, Keiko Fujiki, Akira Murakami, Kiyoo Nakayasu

Journal:

Japanese Journal of Ophthalmology

Year:

2002

Language:

english

File:

PDF, 50 KB

english, 2002

29

Estimation of Patient Visit Rate and Incidence of Keratoconus in the 23 Wards of Tokyo

Rika Ota, Keiko Fujiki, Kiyoo Nakayasu

Journal:

Japanese Journal of Ophthalmology

Year:

2002

Language:

english

File:

PDF, 32 KB

english, 2002

30

Multiplex Polymerase Chain Reaction for Detection of Herpes Simplex Virus Type 1, Type 2, Cytomegalovirus, and Varicella-Zoster Virus in Ocular Viral Infections

Yan Zhang, Tairo Kimura, Keiko Fujiki, Hitoshi Sakuma, Akira Murakami, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2003

Language:

english

File:

PDF, 168 KB

english, 2003

31

A Novel Mutation of the TGFBI Gene Found in a Vietnamese Family with Atypical Granular Corneal Dystrophy

Nguyen Thanh Ha, Le Xuan Cung, Hoang Minh Chau, Ton Kim Thanh, Keiko Fujiki, Akira Murakami, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2003

Language:

english

File:

PDF, 127 KB

english, 2003

32

OPA1 Gene Mutations in Japanese Patients with Bilateral Optic Atrophy Unassociated with Mitochondrial DNA Mutations at nt 11778, 3460, and 14484

Tetsuya Yamada, Seiji Hayasaka, Masayuki Matsumoto, Budu, Tenri Esa, Yoriko Hayasaka, Machi Endo, Yasunori Nagaki, Keiko Fujiki, Akira Murakami, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2003

Language:

english

File:

PDF, 144 KB

english, 2003

33

Multicenter genetic study of retinitis pigmentosa in Japan: II. Prevalence of autosomal recessive retinitis pigmentosa

Mutsuko Hayakawa, Keiko Fujiki, Atsushi Kanai, Miyo Matsumura, Yoshihito Honda, Hiroshi Sakaue, Makoto Tamai, Takehiko Sakuma, Takashi Tokoro, Tomotsugu Yura, Nobue Kubota, Shinichiro Kawano, Mizuo Ma

Journal:

Japanese Journal of Ophthalmology

Year:

1997

Language:

english

File:

PDF, 453 KB

english, 1997

34

Gene transfer into corneal endothelial cells by helios gene gun

Wen Nan Lu, Nobuyuki Ebihara, Keiko Fujiki, Hitoshi Sakuma, Shinji Nakamura, Yasuo Watanabe, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

2003

Language:

english

File:

PDF, 45 KB

english, 2003

35

Plus/minus screening of rabbit corneal endothelial cDNA library

Yoshihiro Hotta, Hitoshi Kitagawa, Keiko Fujiki, Takuro Fujimaki, Hisashi Ohnuki, Hitoshi Sakuma, Fumino Iwata, Michifumi Watanabe, Kiyoo Nakayasu, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

1997

Language:

english

File:

PDF, 822 KB

english, 1997

36

Multicenter genetic study of retinitis pigmentosa in Japan: I. Genetic heterogeneity in typical retinitis pigmentosa

Mutsuko Hayakawa, Keiko Fujiki, Atsushi Kanai, Miyo Matsumura, Yoshihito Honda, Hiroshi Sakaue, Makoto Tamai, Takehiko Sakuma, Takashi Tokoro, Tomotsugu Yura, Nobue Kubota, Shinichiro Kawano, Mizuo Ma

Journal:

Japanese Journal of Ophthalmology

Year:

1997

Language:

english

File:

PDF, 580 KB

english, 1997

37

Analysis of Peripherin/Rds Gene for Japanese Retinal Dystrophies

Keiko Fujiki, Yoshihiro Hotta, Mutsuko Hayakawa, Takuro Fujimaki, Misako Takeda, Yasushi Isashiki, Norio Ohba, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

1998

Language:

english

File:

PDF, 264 KB

english, 1998

38

Arg124Cys Mutation of the βig-h3 Gene in a Japanese Family With Lattice Corneal Dystrophy Type I

Yoshihiro Hotta, Keiko Fujiki, Ono, Takuro Fujimaki, Kiyoo Nakayasu, Tatsuo Yamaguchi, Atsushi Kanai

Journal:

Japanese Journal of Ophthalmology

Year:

1999

Language:

english

File:

PDF, 304 KB

english, 1999

39

Age of Onset and Progress by Ageing in High Myopia

Keiko FUJIKI, Kuniko MOROTOMI, Kazuyuki KABASAWA, Tsunehiko AKAMATSU, Akira NAKAJIMA

Journal:

Congenital Anomalies

Year:

1985

Language:

english

File:

PDF, 79 KB

english, 1985

40

Hydrogen Peroxide Is an Endothelium-Derived Hyperpolarizing Factor in Human Mesenteric Arteries

Tetsuya Matoba, Hiroaki Shimokawa, Hiroshi Kubota, Keiko Morikawa, Takako Fujiki, Ikuko Kunihiro, Yasushi Mukai, Yoji Hirakawa, Akira Takeshita

Journal:

Biochemical and Biophysical Research Communications

Year:

2002

Language:

english

File:

PDF, 96 KB

english, 2002

41

Studies on the Mechanism of Early Onset Macular Degeneration in Cynomolgus (Macaca fascicularis) Monkeys. I. Abnormal Concentrations of Two Proteins in the Retina

MARILOU G. NICOLAS, KEIKO FUJIKI, KIMIE MURAYAMA, MICHIHIRO T. SUZUKI, REIKO MINEKI, MUTSUKO HAYAKAWA, YASUHIRO YOSHIKAWA, FUMIAKI CHO, ATSUSHI KANAI

Journal:

Experimental Eye Research

Year:

1996

Language:

english

File:

PDF, 907 KB

english, 1996

42

Studies on the Mechanism of Early Onset Macular Degeneration in Cynomolgus Monkeys. II. Suppression of Metallothionein Synthesis in the Retina in Oxidative Stress

MARILOU G. NICOLAS, KEIKO FUJIKI, KIMIE MURAYAMA, MICHIHIRO T. SUZUKI, NORIKO SHINDO, YOSHIHIRO HOTTA, FUMINO IWATA, TSUTOMU FUJIMURA, YASUHIRO YOSHIKAWA, FUMIAKI CHO, ATSUSHI KANAI

Journal:

Experimental Eye Research

Year:

1996

Language:

english

File:

PDF, 496 KB

english, 1996

43

A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa

Hitoshi Sakuma, George Inana, Akira Murakami, Toshihiro Yajima, Richard G. Weleber, William H. Murphey, J.Donald M. Gass, Yoshihiro Hotta, Mutsuko Hayakawa, Keiko Fujiki, Yong Qing Gao, Michael Dancig

Journal:

Year:

1995

File:

PDF, 187 KB

1995

44

Incidence of congenital malformations in Tokyo Metropolitan Hospitals, 1979–1993

Kyoko Kato, Keiko Fujiki

Journal:

Brain and Development

Year:

1996

Language:

english

File:

PDF, 388 KB

english, 1996

45

Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy

Xin Tian, Keiko Fujiki, Qin Li, Akira Murakami, Peiying Xie, Atsushi Kanai, Wei Wang, Zuguo Liu

Journal:

American Journal of Ophthalmology

Year:

2004

Language:

english

File:

PDF, 234 KB

english, 2004

46

A Novel Variant Lattice Corneal Dystrophy Caused by Association of Mutation (V625D) in TGFBI Gene

Xin Tian, Keiko Fujiki, Yan Zhang, Akira Murakami, Qin Li, Atsushi Kanai, Wei Wang, Yansheng Hao, Zhizhong Ma

Journal:

American Journal of Ophthalmology

Year:

2007

Language:

english

File:

PDF, 493 KB

english, 2007

47

Distribution of goblet cells and MUC5AC mRNA in the canine nictitating membrane

Yasuyoshi Umeda, Sinji Nakamura, Keiko Fujiki, Hiroshi Toshida, Akihiko Saito, Akira Murakami

Journal:

Experimental Eye Research

Year:

2010

Language:

english

File:

PDF, 1.02 MB

english, 2010

48

In Vivo Laser Confocal Microscopy Findings and Mutational Analysis for Schnyder's Crystalline Corneal Dystrophy

Akira Kobayashi, Keiko Fujiki, Akira Murakami, Kazuhisa Sugiyama

Journal:

Year:

2009

Language:

english

File:

PDF, 2.91 MB

english, 2009

49

Author reply

Akira Kobayashi, Kazuhisa Sugiyama, Akira Murakami, Keiko Fujiki

Journal:

Year:

2009

Language:

english

File:

PDF, 98 KB

english, 2009

50

Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy: the p501t of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophy

Nguyen Thanh Ha, Keiko Fujiki, Yoshihiro Hotta, Kiyoo Nakayasu, Atsushi Kanai

Journal:

American Journal of Ophthalmology

Year:

2000

Language:

english

File:

PDF, 238 KB

english, 2000

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