ISHIKAWA, Kinya: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Fracture Strength on Fiber-Bonded Ceramic Composite Subjected to Static and Dynamic Bending.

SUGIYAMA, Fumiko, ISHIKAWA, Toshihiro, OGAWA, Kinya, NISHIDA, Toshihiko

Journal:

TRANSACTIONS OF THE JAPAN SOCIETY OF MECHANICAL ENGINEERS Series A

Year:

1997

File:

PDF, 939 KB

1997

2

Relationship between type 1 metabotropic glutamate receptors and cerebellar ataxia

Ishibashi, Kenji, Miura, Yoshiharu, Ishikawa, Kinya, Zhang, Ming-Rong, Toyohara, Jun, Ishiwata, Kiichi, Ishii, Kenji

Journal:

Journal of Neurology

Year:

2016

Language:

english

File:

PDF, 813 KB

english, 2016

3

Motor-dominant chronic inflammatory demyelinating polyradiculoneuropathy with uhthoff-like phenomenon is a distinct clinical entity?

Masaki Kobayashi, Takanori Yokota, Hiroyuki Tomimitsu, Satoru Ishibshi, Teruhiko Sekiguchi, Tadasi Kanouchi, Kinya Ishikawa, Hidehiro Mizusawa

Journal:

Year:

2012

Language:

english

File:

PDF, 264 KB

english, 2012

4

Effect of clinofibrate, a new hypelipidemic agent, on biliary and serum lipids in patients with hyperlipidemia

Nozomu Takeuchi, Hitoshi Kukita, Goro Kajiyama, Masamichi Fujiyama, Katsunori Ishikawa, Hitoshi Miki, Toshio Mishima, Kinya Murata, Takeo Asano

Journal:

Atherosclerosis

Year:

1982

Language:

english

File:

PDF, 654 KB

english, 1982

5

Calbindin-D 28k immunoreactivity in the cerebellum of spinocerebellar degeneration

Kinya Ishikawa, Hidehiro Mizusawa, Tsuneo Fujita, Norio Ohkoshi, Mikio Doi, Yasuko Komatsuzaki, Hiroyuki Iwamoto, Takesaburo Ogata, Shin'ichi Shoji

Journal:

Journal of the Neurological Sciences

Year:

1995

Language:

english

File:

PDF, 4.74 MB

english, 1995

6

Mutation of the EYA1 Gene in Patients with Branchio-oto Syndrome

Yashima, Takatoshi, Noguchi, Yoshihiro, Ishikawa, Kinya, Mizusawa, Hidehiro, Kitamura, Ken

Journal:

Acta Oto-Laryngologica

Year:

2003

Language:

english

File:

PDF, 358 KB

english, 2003

7

Fracture Strength of Fiber-Bonded Ceramic Composite Subjected to Static and Impact Bending.

SUGIYAMA, Fumiko, ISHIKAWA, Toshihiro, OGAWA, Kinya, NISHIDA, Toshihiko

Journal:

JSME International Journal Series A

Year:

1998

File:

PDF, 1.06 MB

1998

8

Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington’s Disease

Furukawa, Fumiko, Ishikawa, Kinya, Yokota, Takanori, Sanjo, Nobuo

Journal:

European Neurology

Year:

2019

Language:

english

File:

PDF, 344 KB

english, 2019

9

A case of dermatomyositis with rhabdomyolysis, rescued by intravenous immunoglobulin

Mizoguchi, Fumitaka, Takada, Kazuki, Ishikawa, Kinya, Mizusawa, Hidehiro, Kohsaka, Hitoshi, Miyasaka, Nobuyuki

Journal:

Modern Rheumatology

Year:

2015

Language:

english

File:

PDF, 249 KB

english, 2015

10

CADASIL with a Novel NOTCH3 Mutation (Cys478Tyr)

Ozaki, Kokoro, Irioka, Takashi, Ishikawa, Kinya, Mizusawa, Hidehiro

Journal:

Journal of Stroke and Cerebrovascular Diseases

Year:

2015

Language:

english

File:

PDF, 353 KB

english, 2015

11

Decreased metabotropic glutamate receptor type 1 availability in a patient with spinocerebellar ataxia type 6: A 11C-ITMM PET study

Ishibashi, Kenji, Miura, Yoshiharu, Ishikawa, Kinya, Ishii, Kenji, Ishiwata, Kiichi

Journal:

Journal of the Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 618 KB

english, 2015

12

A novel mutation of PDE8B Gene in a Japanese family with autosomal-dominant striatal degeneration

Azuma, Reo, Ishikawa, Kinya, Hirata, Kosei, Hashimoto, Yuji, Takahashi, Makoto, Ishii, Kenji, Inaba, Akira, Yokota, Takanori, Orimo, Satoshi

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 536 KB

english, 2015

13

The evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease

Yamashita, Chikara, Tomiyama, Hiroyuki, Funayama, Manabu, Inamizu, Saeko, Ando, Maya, Li, Yuanzhe, Yoshino, Hiroyo, Araki, Takehisa, Ichikawa, Tadashi, Ehara, Yoshiro, Ishikawa, Kinya, Mizusawa, Hideh

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 597 KB

english, 2014

14

Malignant Hidroacanthoma Simplex

Ishikawa, Kinya

Journal:

Archives of Dermatology

Year:

1971

Language:

english

File:

PDF, 5.22 MB

english, 1971

15

Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial

Masahisa Katsuno, Haruhiko Banno, Keisuke Suzuki, Yu Takeuchi, Motoshi Kawashima, Ichiro Yabe, Hidenao Sasaki, Masashi Aoki, Mitsuya Morita, Imaharu Nakano, Kazuaki Kanai, Shoichi Ito, Kinya Ishikawa,

Journal:

The Lancet Neurology

Year:

2010

Language:

english

File:

PDF, 232 KB

english, 2010

16

Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum

Makoto Takahashi, Kinya Ishikawa, Nozomu Sato, Masato Obayashi, Yusuke Niimi, Taro Ishiguro, Mitsunori Yamada, Yasuko Toyoshima, Hitoshi Takahashi, Takeo Kato, Masaki Takao, Shigeo Murayama, Osamu Mor

Journal:

Year:

2012

Language:

english

File:

PDF, 983 KB

english, 2012

17

Cell-type-specific alternative splicing in spinocerebellar ataxia type 6

Taiji Tsunemi, Kinya Ishikawa, Honglian Jin, Hidehiro Mizusawa

Journal:

Neuroscience Letters

Year:

2008

Language:

english

File:

PDF, 482 KB

english, 2008

18

Proteolytic cleavage and cellular toxicity of the human α1A calcium channel in spinocerebellar ataxia type 6

Takayuki Kubodera, Takanori Yokota, Kiyoshi Ohwada, Kinya Ishikawa, Hiroyuki Miura, Takeshi Matsuoka, Hidehiro Mizusawa

Journal:

Neuroscience Letters

Year:

2003

Language:

english

File:

PDF, 155 KB

english, 2003

19

A clinical, genetic, neuropathological study in a Japanese family with SCA 6 and a review of Japanese autopsy cases of autosomal dominant cortical cerebellar atrophy

Kuniaki Tsuchiya, Kinya Ishikawa, Sadakiyo Watabiki, Osamu Tone, Kazuhiro Taki, Chie Haga, Minoru Takashima, Umeo Ito, Riki Okeda, Hidehiro Mizusawa, Kenji Ikeda

Journal:

Journal of the Neurological Sciences

Year:

1998

Language:

english

File:

PDF, 888 KB

english, 1998

20

Establishing a New Methodology for Genome Mining and Biosynthesis of Polyketides and Peptides through Yeast Molecular Genetics

Dr. Kan'ichiro Ishiuchi, Dr. Takehito Nakazawa, Takashi Ookuma, Satoru Sugimoto, Dr. Michio Sato, Dr. Yuta Tsunematsu, Noriyasu Ishikawa, Prof. Hiroshi Noguchi, Dr. Kinya Hotta, Prof. Hisao Moriya, Pr

Journal:

Year:

2012

Language:

english

File:

PDF, 792 KB

english, 2012

21

Impaired Adaptive Motor Learning Is Correlated With Cerebellar Hemispheric Gray Matter Atrophy in Spinocerebellar Ataxia Patients: A Voxel-Based Morphometry Study

Bando, Kyota, Honda, Takeru, Ishikawa, Kinya, Takahashi, Yuji, Mizusawa, Hidehiro, Hanakawa, Takashi

Journal:

Frontiers in Neurology

Year:

2019

File:

PDF, 665 KB

2019

22

Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia

Takeshi Amino, Kinya Ishikawa, Shuta Toru, Taro Ishiguro, Nozomu Sato, Taiji Tsunemi, Miho Murata, Kazuhiro Kobayashi, Johji Inazawa, Tatsushi Toda, Hidehiro Mizusawa

Journal:

Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 292 KB

english, 2007

23

A −16C>T substitution in the 5′ UTR of thepuratrophin-1gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

Takako Ohata, Kunihiro Yoshida, Haruya Sakai, Haruka Hamanoue, Takeshi Mizuguchi, Yusaku Shimizu, Tomomi Okano, Fumio Takada, Kinya Ishikawa, Hidehiro Mizusawa, Ko-ichiro Yoshiura, Yoshimitsu Fukushim

Journal:

Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 233 KB

english, 2006

24

Loss of MyD88 alters neuroinflammatory response and attenuates early Purkinje cell loss in a spinocerebellar ataxia type 6 mouse model

Aikawa, Tomonori, Mogushi, Kaoru, Iijima-Tsutsui, Kumiko, Ishikawa, Kinya, Sakurai, Miyano, Tanaka, Hiroshi, Mizusawa, Hidehiro, Watase, Kei

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 899 KB

english, 2015

25

Spinocerebellar ataxia type 31

Ishikawa, Kinya, Sato, Nozomu, Niimi, Yusuke, Amino, Takeshi, Mizusawa, Hidehiro

Journal:

Rinsho Shinkeigaku

Year:

2010

File:

PDF, 338 KB

2010

26

Genetic diversity among perennial wild rice Oryza rufipogon Griff., in the Mekong Delta

Lam, Dinh T., Buu, Bui C., Lang, Nguyen T., Toriyama, Kinya, Nakamura, Ikuo, Ishikawa, Ryuji

Journal:

Ecology and Evolution

Year:

2019

Language:

english

File:

PDF, 853 KB

english, 2019

27

The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell : The 50th Anniversary of Japanese Society of Neuropathology

Kinya Ishikawa, Hidehiro Mizusawa

Journal:

Year:

2010

Language:

english

File:

PDF, 1.16 MB

english, 2010

28

Distinct mechanisms for spiro-carbon formation reveal biosynthetic pathway crosstalk

Tsunematsu, Yuta, Ishikawa, Noriyasu, Wakana, Daigo, Goda, Yukihiro, Noguchi, Hiroshi, Moriya, Hisao, Hotta, Kinya, Watanabe, Kenji

Journal:

Nature Chemical Biology

Year:

2013

Language:

english

File:

PDF, 1.52 MB

english, 2013

29

Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA) n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Niimi, Yusuke, Takahashi, Makoto, Sugawara, Emiko, Umeda, Shigeaki, Obayashi, Masato, Sato, Nozomu, Ishiguro, Taro, Higashi, Miwa, Eishi, Yoshinobu, Mizusawa, Hidehiro, Ishikawa, Kinya

Journal:

Year:

2013

Language:

english

File:

PDF, 1.56 MB

english, 2013

30

Relocation of p25α/tubulin polymerization promoting protein from the nucleus to the perinuclear cytoplasm in the oligodendroglia of sporadic andCOQ2mutant multiple system atrophy

Ota, Kiyobumi, Obayashi, Masato, Ozaki, Kokoro, Ichinose, Shizuko, Kakita, Akiyoshi, Tada, Mari, Takahashi, Hitoshi, Ando, Noboru, Eishi, Yoshinobu, Mizusawa, Hidehiro, Ishikawa, Kinya

Journal:

Acta Neuropathologica Communications

Year:

2014

Language:

english

File:

PDF, 6.20 MB

english, 2014

31

Signal loss in the motor cortex on magnetic resonance images in amyotrophic lateral sclerosis

Dr. Kinya Ishikawa, Hiroshi Nagura, Tsukasa Yokota, Hiroshi Yamanouchi

Journal:

Annals of Neurology

Year:

1993

Language:

english

File:

PDF, 1.39 MB

english, 1993

32

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6

Hiroki Takahashi, Kinya Ishikawa, Takeshi Tsutsumi, Hiroto Fujigasaki, Akihiro Kawata, Ryoichi Okiyama, Tsuneo Fujita, Kazuo Yoshizawa, Shigeki Yamaguchi, Hitoshi Tomiyasu, Fumihito Yoshii, Kazuko Mit

Journal:

Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 237 KB

english, 2004

33

Tandem internal models execute motor learning in the cerebellum

Honda, Takeru, Nagao, Soichi, Hashimoto, Yuji, Ishikawa, Kinya, Yokota, Takanori, Mizusawa, Hidehiro, Ito, Masao

Journal:

Proceedings of the National Academy of Sciences

Year:

2018

Language:

english

File:

PDF, 1.03 MB

english, 2018

34

SCA6 : cerebellar ataxia with characteristic neuro-otological features; 9. 特徴的なめまいを示す脊髄小脳変性症 SCA6;

Ishikawa, Kinya

Journal:

Equilibrium Research

Year:

2019

File:

PDF, 666 KB

2019

35

Non-Heme Dioxygenase Catalyzes Atypical Oxidations of 6,7-Bicyclic Systems To Form the 6,6-Quinolone Core of Viridicatin-Type Fungal Alkaloids

Ishikawa, Noriyasu, Tanaka, Hidenori, Koyama, Fumi, Noguchi, Hiroshi, Wang, Clay C. C., Hotta, Kinya, Watanabe, Kenji

Journal:

Angewandte Chemie International Edition

Year:

2014

Language:

english

File:

PDF, 606 KB

english, 2014

36

Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage

Obayashi, Masato, Ishikawa, Kinya, Izumi, Yuishin, Takahashi, Makoto, Niimi, Yusuke, Sato, Nozomu, Onodera, Osamu, Kaji, Ryuji, Nishizawa, Masatoyo, Mizusawa, Hidehiro

Journal:

Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 335 KB

english, 2012

37

A Commentary on Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3–q32.1

Ishikawa, Kinya

Journal:

Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 69 KB

english, 2012

38

A Case of Turner Syndrome with Congenital Hypothyroidism Untreated until Age 38 Years

Ishikawa, Norio, Tanaka, Toshiaki, Hashimoto, Kinya, Wada, Masaki

Journal:

Hormone Research

Year:

2003

Language:

english

File:

PDF, 138 KB

english, 2003

39

Gene dosage effect in spinocerebellar ataxia type 6 homozygotes: A clinical and neuropathological study

Soga, Kazumasa, Ishikawa, Kinya, Furuya, Tokuro, Iida, Tadatsune, Yamada, Tetsuo, Ando, Noboru, Ota, Kiyobumi, Kanno-Okada, Hiromi, Tanaka, Shinya, Shintaku, Masayuki, Eishi, Yoshinobu, Mizusawa, Hide

Journal:

Journal of the Neurological Sciences

Year:

2017

Language:

english

File:

PDF, 959 KB

english, 2017

40

Molecular genetic approach to spinocerebellar ataxias

Ishikawa, Kinya, Ishiguro, Taro, Takahashi, Makoto, Sato, Nozomu, Amino, Takeshi, Niimi, Yusuke, Mizusawa, Hidehiro

Journal:

Rinsho Shinkeigaku

Year:

2009

File:

PDF, 456 KB

2009

41

When should we test patients with familial ataxias for SCA31? A misdiagnosed condition outside Japan?

Pedroso, José Luiz, Abrahao, Agessandro, Ishikawa, Kinya, Raskin, Salmo, de Souza, Paulo Victor Sgobbi, de Rezende Pinto, Wladimir Bocca Vieira, Braga-Neto, Pedro, de Albuquerque, Marcus Vinicius Cris

Journal:

Journal of the Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 299 KB

english, 2015

42

SCA6: From gene identification to recent progress on pathogenesis

Watase, Kei, Ishikawa, Kinya, Mizusawa, Hidehiro

Journal:

Rinsho Shinkeigaku

Year:

2010

File:

PDF, 254 KB

2010

43

ENHANCED PLA2G3 EXPRESSION BY OXIDATIVE STRESS DECREASES THE IDE AND EXACERBATES AD

Nishida, Yoichiro, Yui, Daishi, Nishina, Tomoko, Mogushi, Kaoru, Ishibashi, Satoru, Ajioka, Itsuki, Ishikawa, Kinya, Mizusawa, Hidehiro, Murayama, Shigeo, Yokota, Takanori

Journal:

Alzheimer's & Dementia

Year:

2016

Language:

english

File:

PDF, 58 KB

english, 2016

44

Mechanisms for Facilitation of Nitric Oxide-Evoked [3H]GABA Release by Removal of Hydroxyl Radical

Seitaro Ohkuma, Masashi Katsura, Yasushi Hibino, Atsuo Hara, Kenji Shirotani, Emiko Ishikawa, Kinya Kuriyama

Journal:

Journal of Neurochemistry

Year:

1998

Language:

english

File:

PDF, 977 KB

english, 1998

45

On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA

Kinya Ishikawa, Hidehiro Mizusawa

Journal:

Year:

2006

Language:

english

File:

PDF, 965 KB

english, 2006

46

Donepezil-induced sleep spindle in a patient with dementia with Lewy bodies: a case report

OZAKI, Asami, NISHIDA, Masaki, KOYAMA, Keiko, ISHIKAWA, Kinya, NISHIKAWA, Toru

Journal:

Psychogeriatrics

Year:

2012

Language:

english

File:

PDF, 358 KB

english, 2012

47

Clinical features and MRI findings in spinocerebellar ataxia type 31 (SCA31) comparing with spinocerebellar ataxia type 6 (SCA6)

Sakakibara, Satoko, Aiba, Ikuko, Saito, Yufuko, Inukai, Akira, Ishikawa, Kinya, Mizusawa, Hidehiro

Journal:

Rinsho Shinkeigaku

Year:

2014

File:

PDF, 821 KB

2014

48

Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort

Ozaki, Kokoro, Ansai, Ayaka, Nobuhara, Kouji, Araki, Toshihiko, Kubodera, Takayuki, Ishii, Takashi, Higashi, Miwa, Sato, Nozomu, Soga, Kazumasa, Mizusawa, Hidehiro, Ishikawa, Kinya, Yokota, Takanori

Journal:

Parkinsonism & Related Disorders

Year:

2019

File:

PDF, 4.57 MB

2019

49

Tremor in Klinefelter’s syndrome improved by testosterone administration

Hiroyuki Kinoshita, Takuya Ohkubo, Masakazu Kaneko, Nozomu Satoh, Saneyuki Mizutani, Mutsuko Yasuda, Akira Machida, Kinya Ishikawa, Tomoyuki Kamata, Fumiatsu Yakushiji

Journal:

Journal of Neurology

Year:

2009

Language:

english

File:

PDF, 117 KB

english, 2009

50

An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains

Kinya Ishikawa, Shuta Toru, Taiji Tsunemi, Mingshun Li, Kazuhiro Kobayashi, Takanori Yokota, Takeshi Amino, Kiyoshi Owada, Hiroto Fujigasaki, Masaki Sakamoto, Hiroyuki Tomimitsu, Minoru Takashima, Jir

Journal:

The American Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 14.83 MB

english, 2005

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски