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Research | 11 December 2019 | Open
Gender differences in the influence of obstructive sleep apnea on optic nerve head circulation
Scientific Reports 9 , 1–9

Rights & permissionsfor article Gender differences in the influence of obstructive sleep apnea on optic nerve head circulation . Opens in a new window.
Research | 29 November 2019 | Open
Influence of age and gender on the pulse waveform in optic nerve head circulation in healthy men and women
Scientific Reports 9 , 1–9

Rights & permissionsfor article Influence of age and gender on the pulse waveform in optic nerve head circulation in healthy men and women . Opens in a new window.
Research | 30 October 2019 | Open
The influences of gender and aging on optic nerve head microcirculation in healthy adults
Scientific Reports 9 , 1–8

Rights & permissionsfor article The influences of gender and aging on optic nerve head microcirculation in healthy adults . Opens in a new window.
Research | 29 May 2019
Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan
- Hiroyuki Mishima
- , Hisato Suzuki
- , Michiko Doi
- , Mutsuko Miyazaki
- , Satoshi Watanabe
- , Tadashi Matsumoto
- , Kanako Morifuji
- , Hiroyuki Moriuchi
- , Koh-ichiro Yoshiura
- , Tatsuro Kondoh
- & Kenjiro Kosaki
Journal of Human Genetics 64 , 789–794

Rights & permissionsfor article Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan . Opens in a new window.
Research | 10 August 2018
The neurorestorative effect of human amniotic fluid stem cells on the chronic phase of neonatal hypoxic–ischemic encephalopathy in mice
- Toshimitsu Otani
- , Daigo Ochiai
- , Hirotaka Masuda
- , Yushi Abe
- , Marie Fukutake
- , Tadashi Matsumoto
- , Kei Miyakoshi
- & Mamoru Tanaka
Pediatric Research 85 , 97–104

Rights & permissionsfor article The neurorestorative effect of human amniotic fluid stem cells on the chronic phase of neonatal hypoxic–ischemic encephalopathy in mice . Opens in a new window.
Research | 15 January 2018
A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome
- Midori Motokawa
- , Satoshi Watanabe
- , Akiko Nakatomi
- , Tatsuro Kondoh
- , Tadashi Matsumoto
- , Kanako Morifuji
- , Hirotake Sawada
- , Toyoki Nishimura
- , Hiroyuki Nunoi
- , Koh-ichiro Yoshiura
- , Hiroyuki Moriuchi
- & Sumito Dateki
Journal of Human Genetics 63 , 387–390

Rights & permissionsfor article A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome . Opens in a new window.
Research | 16 December 2004
Genotype-phenotype correlation of 5p- syndrome: pitfall of diagnosis
- Tatsuro Kondoh
- , Osamu Shimokawa
- , Naoki Harada
- , Tomoki Doi
- , Chyuns Yun
- , Yuji Gohda
- , Fumiko Kinoshita
- , Tadashi Matsumoto
- & Hiroyuki Moriuchi
Journal of Human Genetics 50 , 26–29

Rights & permissionsfor article Genotype-phenotype correlation of 5p- syndrome: pitfall of diagnosis . Opens in a new window.
1 January 1999
Autosomal dominant onychodystrophy and congenital sensorineural deafness
- T. Kondoh
- , Akira Tsuru
- , Tadashi Matsumoto
- , Tetsuo Matsuzaka
- & Yoshiro Tsuji
Journal of Human Genetics 44 , 60–62

Rights & permissionsfor article Autosomal dominant onychodystrophy and congenital sensorineural deafness . Opens in a new window.
Research | 1 December 1991
Rapid detection of a point mutation in thyroid-stimulating hormoneβ-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency
- Ryogo Mori
- , Tomoko Sawai
- , Ei-ichi Kinoshita
- , Tsuneyoshi Baba
- , Tadashi Matsumoto
- , Masaaki Yoshimoto
- , Yoshiro Tsuji
- , Yukishige Satake
- & Kei Sawada
Journal of Human Genetics 36 , 313–316

Rights & permissionsfor article Rapid detection of a point mutation in thyroid-stimulating hormoneβ-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency . Opens in a new window.
1 February 1998
A severe case of Moebius syndrome with calcification on the fourth ventricular floor
- Y. Matsunaga
- , Nagisa Amamoto
- , Tatsuro Kondoh
- , Yuichi Ohtsuka
- , Hatsuji Miyazoe
- , Naohisa Kamimura
- , Tadashi Matsumoto
- & Yoshiro Tsuji
Journal of Human Genetics 43 , 62–64

Rights & permissionsfor article A severe case of Moebius syndrome with calcification on the fourth ventricular floor . Opens in a new window.
Research | 1 September 1986
Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridization
- Yoshihiro Jinno
- , Tadashi Matsumoto
- , Tsutomu Kamei
- , Tatsuro Kondoh
- , Shuichiro Maeda
- , Shukuro Araki
- , Kazunori Shimada
- & Norio Niikawa
Journal of Human Genetics 31 , 243–248

Rights & permissionsfor article Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridization . Opens in a new window.
Research | 1 September 1994
A point mutation at ATP-binding region of the ALD gene in a family with X-linked adrenoleukodystrophy
- Tadashi Matsumoto
- , Tatsuro Kondoh
- , Hideaki Masuzaki
- , Naoki Harada
- , Tetsuo Matsusaka
- , Ei-ichi Kinoshita
- , Goh Takeo
- , Mitsuhiro Tsujihata
- , Yasuyuki Suzuki
- & Yoshiro Tsuji
Journal of Human Genetics 39 , 345–351

Rights & permissionsfor article A point mutation at ATP-binding region of the ALD gene in a family with X-linked adrenoleukodystrophy . Opens in a new window.
1 March 1994
A novelH19/HhaI RFLP and its allele frequency in the Japanese
Journal of Human Genetics 39 , 205–206

Rights & permissionsfor article A novelH19/HhaI RFLP and its allele frequency in the Japanese . Opens in a new window.
Research | 1 February 1998
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
- M. Fujimoto
- , Piranit Nik Kantaputra
- , Shiro Ikegawa
- , Yoshimitsu Fukushima
- , Shin-ichi Sonta
- , Masafumi Matsuo
- , Takafumi Ishida
- , Tadashi Matsumoto
- , Shinji Kondo
- , Hiroaki Tomita
- , Han-Xiang Deng
- , Michele D'urso
- , Maria Michela Rinaldi
- , Valerio Ventruto
- , Toshihisa Takagi
- , Yusuke Nakamura
- & Norio Niikawa
Journal of Human Genetics 43 , 32–36

Rights & permissionsfor article The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32 . Opens in a new window.
Research | 1 June 1994
Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma
- Tadashi Matsumoto
- , Ei-ichi Kinoshita
- , Hidenori Maeda
- , Norio Niikawa
- , Nobuko Kurosaki
- , Naoki Harada
- , Kankatsu Yun
- , Tomoko Sawai
- , Shigeru Aoki
- , Tatsuro Kondoh
- & Yoshiro Tsuji
Journal of Human Genetics 39 , 225–234

Rights & permissionsfor article Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma . Opens in a new window.
Research | 1 September 1997
A nager acrofacial dysostosis syndrome patient with severe respiratory distress syndrome (RDS)
- Tatsuro Kondoh
- , Masaki Ito
- , Akinori Ariyama
- , Takeshi Shitijoh
- , Tadashi Matsumoto
- & Yoshiro Tsuji
Journal of Human Genetics 42 , 445–449

Rights & permissionsfor article A nager acrofacial dysostosis syndrome patient with severe respiratory distress syndrome (RDS) . Opens in a new window.
Research | 1 February 1998
New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome
- Tatsuro Kondoh
- , Tadashi Matsumoto
- , Makoto Ochi
- , Kazuko Sukegawa
- & Y. Tsuji
Journal of Human Genetics 43 , 59–61

Rights & permissionsfor article New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome . Opens in a new window.
Research | 23 September 1982
Unique cell lines harbouring both Epstein–Barr virus and adult T-cell leukaemia virus, established from leukaemia patients
Nature 299 , 367–369

Rights & permissionsfor article Unique cell lines harbouring both Epstein–Barr virus and adult T-cell leukaemia virus, established from leukaemia patients . Opens in a new window.
Research | 1 December 1988
A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11–12 and on an atypical PWS patient with apparently normal karyotype
- Tsutomu Kamei
- , Jun-ichi Hamabe
- , Tadashi Matsumoto
- , Kyohko Abe
- , Naoki Harada
- , Satoshi Ishikiriyama
- , Tomoko Hasegawa
- , Kiyoshi Miyazaki
- , Seiji Mizuno
- , Kouji Narahara
- , Shigenori Yukizane
- & Norio Niikawa
Journal of Human Genetics 33 , 477–486

Rights & permissionsfor article A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11–12 and on an atypical PWS patient with apparently normal karyotype . Opens in a new window.
1 March 1994
Allele frequency ofHinfI restriction fragment length polymorphism (RFLP) and dinucleotide repeat polymorphism in the wilms tumor gene (WT1) among the Japanese
- Tadashi Matsumoto
- , Miho Okumura
- , Tomoko Sawai
- , Shigeru Aoki
- & Yoshiro Tsuji
Journal of Human Genetics 39 , 207–208

Rights & permissionsfor article Allele frequency ofHinfI restriction fragment length polymorphism (RFLP) and dinucleotide repeat polymorphism in the wilms tumor gene (WT1) among the Japanese . Opens in a new window.
Research | 3 April 2009
Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome
- Hideo Kuniba
- , Koh-ichiro Yoshiura
- , Tatsuro Kondoh
- , Hirofumi Ohashi
- , Kenji Kurosawa
- , Hidefumi Tonoki
- , Toshiro Nagai
- , Nobuhiko Okamoto
- , Mitsuhiro Kato
- , Yoshimitsu Fukushima
- , Tadashi Kaname
- , Kenji Naritomi
- , Tadashi Matsumoto
- , Hiroyuki Moriuchi
- , Tatsuya Kishino
- , Akira Kinoshita
- , Noriko Miyake
- , Naomichi Matsumoto
- & Norio Niikawa
Journal of Human Genetics 54 , 304–309

Rights & permissionsfor article Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome . Opens in a new window.
22 November 2004
Splenic transposition is superior to caudal shunt as a model of murine total hepatic ischemia
- Tadashi Matsumoto
- , Philip A Efron
- , Hironori Tsujimoto
- , Sven K Tschoeke
- , Ricardo Ungaro
- , Shiro Fujita
- , David P Foley
- , Alan Hemming
- & Lyle L Moldawer
Laboratory Investigation 85 , 90–98

Rights & permissionsfor article Splenic transposition is superior to caudal shunt as a model of murine total hepatic ischemia . Opens in a new window.
Research | 1 September 1989
Micro extraction of DNA from whole blood and amniocytes
Journal of Human Genetics 34 , 217–223

Rights & permissionsfor article Micro extraction of DNA from whole blood and amniocytes . Opens in a new window.

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Gender differences in the influence of obstructive sleep apnea on optic nerve head circulation

Influence of age and gender on the pulse waveform in optic nerve head circulation in healthy men and women

The influences of gender and aging on optic nerve head microcirculation in healthy adults

Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan

The neurorestorative effect of human amniotic fluid stem cells on the chronic phase of neonatal hypoxic–ischemic encephalopathy in mice

A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome

Genotype-phenotype correlation of 5p- syndrome: pitfall of diagnosis

Autosomal dominant onychodystrophy and congenital sensorineural deafness

Rapid detection of a point mutation in thyroid-stimulating hormoneβ-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency

A severe case of Moebius syndrome with calcification on the fourth ventricular floor

Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridization

A point mutation at ATP-binding region of the ALD gene in a family with X-linked adrenoleukodystrophy

A novelH19/HhaI RFLP and its allele frequency in the Japanese

The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32

Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma

A nager acrofacial dysostosis syndrome patient with severe respiratory distress syndrome (RDS)

New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome

Unique cell lines harbouring both Epstein–Barr virus and adult T-cell leukaemia virus, established from leukaemia patients

A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11–12 and on an atypical PWS patient with apparently normal karyotype

Allele frequency ofHinfI restriction fragment length polymorphism (RFLP) and dinucleotide repeat polymorphism in the wilms tumor gene (WT1) among the Japanese

Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome

Splenic transposition is superior to caudal shunt as a model of murine total hepatic ischemia

Micro extraction of DNA from whole blood and amniocytes

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