Gen Kurosawa: search on Z-Library

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1

Heterozygous C-propeptide mutations in COL1A1: Osteogenesis imperfecta type IIC and dense bone variant

Masaki Takagi, Naoaki Hori, Yasutsugu Chinen, Kenji Kurosawa, Yukichi Tanaka, Kikuko Oku, Hitomi Sakata, Ryuji Fukuzawa, Gen Nishimura, Jürgen Spranger, Tomonobu Hasegawa

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 692 KB

english, 2011

2

Amplitude of circadian oscillations entrained by 24-h light–dark cycles

Gen Kurosawa, Albert Goldbeter

Journal:

Journal of Theoretical Biology

Year:

2006

Language:

english

File:

PDF, 673 KB

english, 2006

3

Paternal UPD14 is responsible for a distinctive malformation complex

Kenji Kurosawa, Hiroyuki Sasaki, Yoshiaki Sato, Michiko Yamanaka, Mitsumasa Shimizu, Yuji Ito, Torayuki Okuyama, Mari Matsuo, Kiyoshi Imaizumi, Yoshikazu Kuroki, Gen Nishimura

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 206 KB

english, 2002

4

Newly recognized syndrome of metaphyseal undermodeling, spondylar dysplasia, and overgrowth: Report of two adolescents and a child

Gen Nishimura, Tomonobu Hasegawa, Eiichi Kinoshita, Yoko Tanaka, Kenzi Kurosawa, Masaaki Yoshimoto

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 184 KB

english, 2004

5

Congenital anomaly of cervical vertebrae is a major complication of Rubinstein–Taybi syndrome

Toshiyuki Yamamoto, Kenji Kurosawa, Mitsuo Masuno, Shigeharu Okuzumi, Soichi Kondo, Sahoko Miyama, Nobuhiko Okamoto, Noriko Aida, Gen Nishimura

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 148 KB

english, 2005

6

Segmental and full paternal isodisomy for chromosome 14 in three patients: Narrowing the critical region and implication for the clinical features

Masayo Kagami, Gen Nishimura, Torayuki Okuyama, Michiko Hayashidani, Toshio Takeuchi, Shinya Tanaka, Fumitoshi Ishino, Kenji Kurosawa, Tsutomu Ogata

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 158 KB

english, 2005

7

Prenatal findings of paternal uniparental disomy 14: Report of four patients

Michiko Yamanaka, Hiroshi Ishikawa, Keisuke Saito, Yasuyo Maruyama, Katsuske Ozawa, Jun Shibasaki, Gen Nishimura, Kenji Kurosawa

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 82 KB

english, 2010

8

Ruvalcaba syndrome revisited

Masanori Adachi, Koji Muroya, Yumi Asakura, Kenji Kurosawa, Gen Nishimura, Satoshi Narumi, Tomonobu Hasegawa

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 106 KB

english, 2010

9

Comparative Study of Circadian Clock Models, in Search of Processes Promoting Oscillation

GEN KUROSAWA, ATSUSHI MOCHIZUKI, YOH IWASA

Journal:

Journal of Theoretical Biology

Year:

2002

Language:

english

File:

PDF, 344 KB

english, 2002

10

Temperature compensation in circadian clock models

Gen Kurosawa, Yoh Iwasa

Journal:

Journal of Theoretical Biology

Year:

2005

Language:

english

File:

PDF, 388 KB

english, 2005

11

A temperature-compensated model for circadian rhythms that can be entrained by temperature cycles

Tsutomu Takeuchi, Takamichi Hinohara, Gen Kurosawa, Kenko Uchida

Journal:

Journal of Theoretical Biology

Year:

2007

Language:

english

File:

PDF, 671 KB

english, 2007

12

Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein

Bauer, Peter O, Goswami, Anand, Wong, Hon Kit, Okuno, Misako, Kurosawa, Masaru, Yamada, Mizuki, Miyazaki, Haruko, Matsumoto, Gen, Kino, Yoshihiro, Nagai, Yoshitaka

Journal:

Nature Biotechnology

Year:

2010

Language:

english

File:

PDF, 1.20 MB

english, 2010

13

First case of a Japanese girl with Myhre syndrome due to a heterozygous SMAD4 mutation

Yumi Asakura, Koji Muroya, Takeshi Sato, Kenji Kurosawa, Gen Nishimura, Masanori Adachi

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 144 KB

english, 2012

14

Long-term Assessment of Mitral Valve Reconstruction With Resection of the Leaflets: Triangular and Quadrangular Resection

Yoshimasa Sakamoto, Kazuhiro Hashimoto, Hiroshi Okuyama, Shinichi Ishii, Makoto Hanai, Takahiro Inoue, Gen Shinohara, Kiyozo Morita, Hiromi Kurosawa

Journal:

The Annals of Thoracic Surgery

Year:

2005

Language:

english

File:

PDF, 117 KB

english, 2005

15

Serine 403 Phosphorylation of p62/SQSTM1 Regulates Selective Autophagic Clearance of Ubiquitinated Proteins

Gen Matsumoto, Koji Wada, Misako Okuno, Masaru Kurosawa, Nobuyuki Nukina

Journal:

Year:

2011

Language:

english

File:

PDF, 1.66 MB

english, 2011

16

A Model for the Circadian Rhythm of Cyanobacteria that Maintains Oscillation without Gene Expression

Kurosawa, Gen, Aihara, Kazuyuki, Iwasa, Yoh

Journal:

Biophysical Journal

Year:

2006

Language:

english

File:

PDF, 139 KB

english, 2006

17

Dynamics and control at feedback vertex sets. II: A faithful monitor to determine the diversity of molecular activities in regulatory networks

Mochizuki, Atsushi, Fiedler, Bernold, Kurosawa, Gen, Saito, Daisuke

Journal:

Journal of Theoretical Biology

Year:

2013

Language:

english

File:

PDF, 4.29 MB

english, 2013

18

[IEEE 2006 IEEE/NLM Life Science Systems and Applications Workshop - Bethesda, MD (2006.7.13-2006.7.13)] 2006 IEEE/NLM Life Science Systems and Applications Workshop - Effects of Light Waveforms on a Circadian Oscillation of Clock Genes

Tsumoto, Kunichika, Kurosawa, Gen, Aihara, Kazuyuki

Year:

2006

Language:

english

File:

PDF, 2.35 MB

english, 2006

19

[IEEE 2006 IEEE/NLM Life Science Systems and Applications Workshop - Bethesda, MD (2006.7.13-2006.7.13)] 2006 IEEE/NLM Life Science Systems and Applications Workshop - Bifurcation analyses in the cyanobacterial circadian clock model

Kurosawa, Gen, Aihara, Kazuyuki, Iwasa, Yoh

Year:

2006

Language:

english

File:

PDF, 2.41 MB

english, 2006

20

NF-Y inactivation causes atypical neurodegeneration characterized by ubiquitin and p62 accumulation and endoplasmic reticulum disorganization

Yamanaka, Tomoyuki, Tosaki, Asako, Kurosawa, Masaru, Matsumoto, Gen, Koike, Masato, Uchiyama, Yasuo, Maity, Sankar N., Shimogori, Tomomi, Hattori, Nobutaka, Nukina, Nobuyuki

Journal:

Nature Communications

Year:

2014

Language:

english

File:

PDF, 2.92 MB

english, 2014

21

Serine 403-phosphorylated p62/SQSTM1 immunoreactivity in inclusions of neurodegenerative diseases

Kurosawa, Masaru, Matsumoto, Gen, Sumikura, Hiroyuki, Hatsuta, Hiroyuki, Murayama, Shigeo, Sakurai, Takashi, Shimogori, Tomomi, Hattori, Nobutaka, Nukina, Nobuyuki

Journal:

Neuroscience Research

Year:

2015

Language:

english

File:

PDF, 2.70 MB

english, 2015

22

FUS/TLS acts as an aggregation-dependent modifier of polyglutamine disease model mice

Kino, Yoshihiro, Washizu, Chika, Kurosawa, Masaru, Yamada, Mizuki, Doi, Hiroshi, Takumi, Toru, Adachi, Hiroaki, Katsuno, Masahisa, Sobue, Gen, Hicks, Geoffrey G., Hattori, Nobutaka, Shimogori, Tomomi,

Journal:

Scientific Reports

Year:

2016

Language:

english

File:

PDF, 2.17 MB

english, 2016

23

Time-lapse imaging of microRNA activity reveals the kinetics of microRNA activation in single living cells

Ando, Hideaki, Hirose, Matsumi, Kurosawa, Gen, Impey, Soren, Mikoshiba, Katsuhiko

Journal:

Scientific Reports

Year:

2017

Language:

english

File:

PDF, 10.84 MB

english, 2017

24

1P-058 Cross-seeding fibrillation of Q/N-rich proteins offers new pathomechanism of polyglutamine diseases(Protein:Property, The 47th Annual Meeting of the Biophysical Society of Japan)

Furukawa, Yoshiaki, Kaneko, Kumi, Kurosawa, Masaru, Matsumoto, Gen, Nukina, Nobuyuki

Journal:

Seibutsu Butsuri

Year:

2009

Language:

english

File:

PDF, 204 KB

english, 2009

25

Two Ck1δ transcripts regulated by m6A methylation code for two antagonistic kinases in the control of the circadian clock

Fustin, Jean-Michel, Kojima, Rika, Itoh, Kakeru, Chang, Hsin-Yi, Shiqi, Ye, Zhuang, Bowen, Oji, Asami, Gibo, Shingo, Narasimamurthy, Rajesh, Virshup, David, Kurosawa, Gen, Doi, Masao, Manabe, Ichiro,

Journal:

Proceedings of the National Academy of Sciences

Year:

2018

Language:

english

File:

PDF, 1.24 MB

english, 2018

26

Positive Autoregulation Delays the Expression Phase of Mammalian Clock Gene Per2

Ogawa, Yukino, Koike, Nobuya, Kurosawa, Gen, Soga, Tomoyoshi, Tomita, Masaru, Tei, Hajime, Bartell, Paul A.

Journal:

Year:

2011

Language:

english

File:

PDF, 463 KB

english, 2011

27

Circadian Regulation of Food-Anticipatory Activity in Molecular Clock–Deficient Mice

Takasu, Nana N., Kurosawa, Gen, Tokuda, Isao T., Mochizuki, Atsushi, Todo, Takeshi, Nakamura, Wataru, Schwartz, William

Journal:

Year:

2012

Language:

english

File:

PDF, 847 KB

english, 2012

28

1YP1-08 Cross-seeding fibrillation of Q/N-rich proteins offers new pathomechanism of polyglutamine diseases(1YP1 Early Research in Biophysics Award Candidate Presentations,The 47th Annual Meeting of the Biophysical Society of Japan)

Furukawa, Yoshiaki, Kaneko, Kumi, Kurosawa, Masaru, Matsumoto, Gen, Nukina, Nobuyuki

Journal:

Seibutsu Butsuri

Year:

2009

Language:

english

File:

PDF, 198 KB

english, 2009

29

Non-sinusoidal Waveform in Temperature-Compensated Circadian Oscillations

Gibo, Shingo, Kurosawa, Gen

Journal:

Biophysical Journal

Year:

2019

File:

PDF, 1.13 MB

2019

30

A novel gene ( FAM20B encoding glycosaminoglycan xylosylkinase) for neonatal short limb dysplasia resembling Desbuquois dysplasia

Kuroda, Yukiko, Murakami, Hiroaki, Enomoto, Yumi, Tsurusaki, Yoshinori, Takahashi, Kazumi, Mitsuzuka, Kanako, Ishimoto, Hitoshi, Nishimura, Gen, Kurosawa, Kenji

Journal:

Clinical Genetics

Year:

2019

Language:

english

File:

PDF, 4.70 MB

english, 2019

31

A severe form of Ellis-van Creveld syndrome caused by novel mutations in EVC2

Ohashi, Ikuko, Enomoto, Yumi, Naruto, Takuya, Tsurusaki, Yoshinori, Kuroda, Yukiko, Ishikawa, Hiroshi, Ohyama, Makiko, Aida, Noriko, Nishimura, Gen, Kurosawa, Kenji

Journal:

Human Genome Variation

Year:

2019

Language:

english

File:

PDF, 689 KB

english, 2019

32

A severe form of Ellis-van Creveld syndrome caused by novel mutations in EVC2

Ohashi, Ikuko, Enomoto, Yumi, Naruto, Takuya, Tsurusaki, Yoshinori, Kuroda, Yukiko, Ishikawa, Hiroshi, Ohyama, Makiko, Aida, Noriko, Nishimura, Gen, Kurosawa, Kenji

Journal:

Human Genome Variation

Year:

2019

File:

PDF, 689 KB

2019

33

Novel CUL7 biallelic mutations alter the skeletal phenotype of 3M syndrome

Takizaki, Nao, Tsurusaki, Yoshinori, Katsumata, Kaoru, Enomoto, Yumi, Murakami, Hiroaki, Muroya, Koji, Ishikawa, Hiroshi, Aida, Noriko, Nishimura, Gen, Kurosawa, Kenji

Journal:

Human Genome Variation

Year:

2020

Language:

english

File:

PDF, 637 KB

english, 2020

34

Unique skeletal manifestations in patients with Primrose syndrome

Arora, Veronica, Leon, Eyby, Diaz, Jullianne, Hove, Hanne Buciek, Carvalho, Daniel Rocha, Kurosawa, Kenji, Nishimura, Naoto, Nishimura, Gen, Saxena, Renu, Ferreira, Carlos, Puri, Ratna Dua, Verma, Ish

Journal:

European Journal of Medical Genetics

Year:

2020

File:

PDF, 4.24 MB

2020

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