SHIMOZAWA, Nobuyuki: search on Z-Library

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1

Takashi Hashimoto, Professor Emeritus at the Department of Biochemistry, Shinshu University Graduate School of Medicine, Matsumoto, Japan (b 14 March 1933; q 1962 at the University of Tokyo; d 18 April 2019; Japan)

Fukao, Toshiyuki, Yamaguchi, Seiji, Suzuki, Yasuyuki, Shimozawa, Nobuyuki, Orii, Tadao, Wanders, Ronald J. A.

Journal:

Journal of Inherited Metabolic Disease

Year:

2020

Language:

english

File:

PDF, 286 KB

english, 2020

2

Highly asymmetric and subacutely progressive motor weakness with unilateral T2-weighted high intensities along the pyramidal tract in the brainstem in adrenomyeloneuropathy

Tsuboi, Takashi, Tanaka, Yasuhiro, Yoshida, Yusuke, Nakamura, Tomohiko, Shimozawa, Nobuyuki, Katsuno, Masahisa

Journal:

Journal of the Neurological Sciences

Year:

2017

Language:

english

File:

PDF, 352 KB

english, 2017

3

Biallelic mutation of HSD17B4 induces middle age–onset spinocerebellar ataxia

Matsuda, Yukiko, Morino, Hiroyuki, Miyamoto, Ryosuke, Kurashige, Takashi, Kume, Kodai, Mizuno, Noriyoshi, Kanaya, Yuhei, Tada, Yui, Ohsawa, Ryosuke, Yokota, Kazunori, Shimozawa, Nobuyuki, Maruyama, Hi

Journal:

Neurology: Genetics

Year:

2020

Language:

english

File:

PDF, 1013 KB

english, 2020

4

Rapid diagnosis of peroxisome biogenesis disorders through immunofluorescence staining of buccal smears

Zhongyi Zhang, Yasuyuki Suzuki, Nobuyuki Shimozawa, Naomi Kondo

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 542 KB

english, 2000

5

Proliferative responses towards native, heat-denatured and pepsin-treated ovalbumin by peripheral blood mononuclear cells from patients with hen's egg-sensitive atopic dermatitis

Takashi Nishida, Naomi Kondo, Hiroatsu Agata, Osamu Fukutomi, Shinji Shinoda, Yasuyuki Suzuki, Nobuyuki Shimozawa, Shunji Tomatsu, Tadao Orii

Journal:

Year:

1994

Language:

english

File:

PDF, 775 KB

english, 1994

6

Very-long-chain fatty acid metabolism in adrenoleukodystrophy protein-deficient mice

Takeshi Yamada, Nobue Shinnoh, Akira Kondo, Atsushi Uchiyama, Nobuyuki Shimozawa, Jun-ichi Kira, Takuro Kobayashi

Journal:

Cell Biochemistry and Biophysics

Year:

2000

Language:

english

File:

PDF, 297 KB

english, 2000

7

Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1

Imamura, Atsushi, Shimozawa, Nobuyuki, Suzuki, Yasuyuki, Zhang, Zhongyi, Tsukamoto, Toshiro, Fujiki, Yukio, Orii, Tadao, Osumi, Takashi, Wanders, Ronald J A, Kondo, Naomi

Journal:

Pediatric Research

Year:

2000

Language:

english

File:

PDF, 381 KB

english, 2000

8

Major Peroxisomal Membrane Polypeptides Are Synthesized in Cultured Skin Fibroblasts from Patients with Zellweger Syndrome

Suzuki, Yasuyuki, Shimozawa, Nobuyuki, Orii, Tada, Hashimoto, Takashi

Journal:

Pediatric Research

Year:

1989

Language:

english

File:

PDF, 461 KB

english, 1989

9

Phenotype–genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p–Pex6p interaction

TAMURA, Shigehiko, MATSUMOTO, Naomi, IMAMURA, Atsushi, SHIMOZAWA, Nobuyuki, SUZUKI, Yasuyuki, KONDO, Naomi, FUJIKI, Yukio

Journal:

Biochemical Journal

Year:

2001

Language:

english

File:

PDF, 430 KB

english, 2001

10

Incidence of peroxisomal disorders in Japan

Yasuyuki Suzuki, Nobuyuki Shimozawa, Shigehiro Yajima, Kyoko Inoue, Tadao Orii, Naomi Kondo

Journal:

Journal of Human Genetics

Year:

1996

Language:

english

File:

PDF, 465 KB

english, 1996

11

A Comparative Study on Endoscopic Ulcer Healing of Omeprazole Versus Rabeprazole with Respect to CYP2C19 Genotypic Differences

Takashi Ando, Haruki Kato, Naohito Sugimoto, Yasuyuki Nagao, Nobuyuki Seto, Hitoshi Hongo, Hirokazu Kajikawa, Yutaka Isozaki, Makoto Shimozawa, Yuji Naito, Norimasa Yoshida, Takashi Ishizaki, Toshikaz

Journal:

Digestive Diseases and Sciences

Year:

2005

Language:

english

File:

PDF, 292 KB

english, 2005

12

A Novel Aberrant Splicing Mutation of the PEX16 Gene in Two Patients with Zellweger Syndrome

Nobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto, Yasuyuki Suzuki, Yukio Fujiki, Ronald J.A. Wanders, Naomi Kondo

Journal:

Biochemical and Biophysical Research Communications

Year:

2002

Language:

english

File:

PDF, 153 KB

english, 2002

13

The syndrome of the absence of a septum pellucidum with porencephaly

Shimozawa, Nobuyuki, Ohno, Kousaku, Takashima, Sachio, Takakura, Hiroki, Sugitani, Akitoshi

Journal:

Brain and Development

Year:

1986

Language:

english

File:

PDF, 659 KB

english, 1986

14

Human PEX19: cDNA Cloning by Functional Complementation, Mutation Analysis in a Patient with Zellweger Syndrome, and Potential Role in Peroxisomal Membrane Assembly

Yuji Matsuzono, Naohiko Kinoshita, Shigehiko Tamura, Nobuyuki Shimozawa, Maho Hamasaki, Kamran Ghaedi, Ronald J. A. Wanders, Yasuyuki Suzuki, Naomi Kondo and Yukio Fujiki

Journal:

Proceedings of the National Academy of Sciences

Year:

1999

Language:

english

File:

PDF, 1.82 MB

english, 1999

15

ABC Subfamily D Proteins and Very Long Chain Fatty Acid Metabolism as Novel Targets in Adrenoleukodystrophy

Morita, Masashi, Shimozawa, Nobuyuki, Kashiwayama, Yoshinori, Suzuki, Yasuyuki, Imanaka, Tsuneo

Journal:

Current Drug Targets

Year:

2011

Language:

english

File:

PDF, 532 KB

english, 2011

16

Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defect

YASUYUKI SUZUKI, NOBUYUKI SHIMOZAWA, ATSUSHI IMAMURA, YUKO FUKUDA, HIROSHI ICHIHASHI, TADAO ORII, NAOMI KONDO

Journal:

Pediatrics International

Year:

1996

Language:

english

File:

PDF, 309 KB

english, 1996

17

Correlations Between Serum Immunoglobulin Concentrations and Immunoglobulin Secreting Cells in Healthy Peripheral Blood

KONDO, NAOMI, AGATA, HIROATSU, LI, GENG PAI, TOMATSU, SHUNJI, SHIMOZAWA, NOBUYUKI, SUZUKI, YASUYUKI, NAKASHIMA, YOSHIHIRO, HORI, TOSHINORI, YAMAGISHI, ATSUSHI, OGAWA, TATSUYA, IWATA, HIDEKI, ORII, TAD

Journal:

Pediatric Asthma Allergy & Immunology

Year:

1993

Language:

english

File:

PDF, 342 KB

english, 1993

18

Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis

Yamada, Kenichiro, Naiki, Misako, Hoshino, Shin, Kitaura, Yasuyuki, Kondo, Yusuke, Nomura, Noriko, Kimura, Reiko, Fukushi, Daisuke, Yamada, Yasukazu, Shimozawa, Nobuyuki, Yamaguchi, Seiji, Shimomura,

Journal:

Molecular Genetics and Metabolism Reports

Year:

2014

Language:

english

File:

PDF, 531 KB

english, 2014

19

A 29-year-old patient with adrenoleukodystrophy presenting with Addisonâs disease

Tanaka, Hajime, Amano, Naoko, Tanaka, Kumiko, Katsuki, Takeshi, Adachi, Tomohide, Shimozawa, Nobuyuki, Kawai, Toshihide

Journal:

Endocrine Journal

Year:

2020

Language:

english

File:

PDF, 870 KB

english, 2020

20

Isolation of a New Peroxisome-Deficient CHO Cell Mutant Defective in Peroxisome Targeting Signal-1 Receptor

Toshiro Tsukamoto, Akemi Bogaki, Kanji Okumoto, Keita Tateishi, Yukio Fujiki, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Takashi Osumi

Journal:

Biochemical and Biophysical Research Communications

Year:

1997

Language:

english

File:

PDF, 256 KB

english, 1997

21

Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy

Atsushi Imamura, Yasunaga Komori, Osamu Fukutomi, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Tadao Orii

Journal:

Brain and Development

Year:

1994

Language:

english

File:

PDF, 339 KB

english, 1994

22

A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents

Annick Raas-Rothschild, Ronald J.A. Wanders, Petra A.W. Mooijer, Jeannette Gootjes, Hans R. Waterham, Alisa Gutman, Yasuyuki Suzuki, Nobuyuki Shimozawa, Naomi Kondo, Gideon Eshel, Marc Espeel, Frank R

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 293 KB

english, 2002

23

Genetic and molecular bases of peroxisome biogenesis disorders

Suzuki, Yasuyuki, Shimozawa, Nobuyuki, Orii, Tadao, Tsukamoto, Toshiro, Osumi, Takashi, Fujiki, Yukio, Kondo, Naomi

Journal:

Genetics in Medicine

Year:

2001

Language:

english

File:

PDF, 610 KB

english, 2001

24

Dynein Dysfunction Reproduces Age-Dependent Retromer Deficiency

Kimura, Nobuyuki, Samura, Eriko, Suzuki, Keiko, Okabayashi, Sachi, Shimozawa, Nobuhiro, Yasutomi, Yasuhiro

Journal:

The American Journal of Pathology

Year:

2016

Language:

english

File:

PDF, 3.59 MB

english, 2016

25

Positional determination of the carbonâcarbon double bonds in unsaturated fatty acids mediated by solvent plasmatization using LCâMS

Takashima, Shigeo, Toyoshi, Kayoko, Yamamoto, Takuhei, Shimozawa, Nobuyuki

Journal:

Scientific Reports

Year:

2020

File:

PDF, 3.71 MB

2020

26

Adrenoleukodystrophy: subcellular localization and degradation of adrenoleukodystrophy protein (ALDP/ABCD1) with naturally occurring missense mutations

Norimasa Takahashi, Masashi Morita, Takanori Maeda, Yuta Harayama, Nobuyuki Shimozawa, Yasuyuki Suzuki, Hirokazu Furuya, Ryuichiro Sato, Yoshinori Kashiwayama, Tsuneo Imanaka

Journal:

Journal of Neurochemistry

Year:

2007

Language:

english

File:

PDF, 1011 KB

english, 2007

27

Molecular Mechanism of Detectable Catalase-Containing Particles, Peroxisomes, in Fibroblasts from a PEX2-Defective Patient

Nobuyuki Shimozawa, Zhongyi Zhang, Atsushi Imamura, Yasuyuki Suzuki, Yukio Fujiki, Toshiro Tsukamoto, Takashi Osumi, Patrick Aubourg, Ronald J.A Wanders, Naomi Kondo

Journal:

Biochemical and Biophysical Research Communications

Year:

2000

Language:

english

File:

PDF, 458 KB

english, 2000

28

Assignment of the Human Peroxisome Assembly Factor-1 Gene (PXMP3) Responsible for Zellweger Syndrome to Chromosome 8q21.1 by Fluorescence in Situ Hybridization

Mitsuo Masuno, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Tadao Orii, Toshiro Tsukamoto, Takashi Osumi, Yukio Fujiki, Kiyoshi Imaizumi, Yoshikazu Kuroki

Journal:

Year:

1994

File:

PDF, 94 KB

1994

29

Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases

Yasuyuki Suzuki, Nobuyuki Shimozawa, Shigehiro Yajima, Seiji Yamaguchi, Tadao Orii, Takashi Hashimoto

Journal:

Biochemical Pharmacology

Year:

1991

Language:

english

File:

PDF, 379 KB

english, 1991

30

Congenital myotonic dystrophy: report of paternal transmission

Yoko Tanaka, Yasuyuki Suzuki, Nobuyuki Shimozawa, Eiji Nanba, Naomi Kondo

Journal:

Brain and Development

Year:

2000

Language:

english

File:

PDF, 181 KB

english, 2000

31

Retinal Ganglion Cell Loss in X-linked Adrenoleukodystrophy with an ABCD1 Mutation (Gly266Arg)

Ohkuma, Yasuhiro, Hayashi, Takaaki, Yoshimine, Syouyou, Tsuneoka, Hiroshi, Terao, Yoko, Akiyama, Masaharu, Ida, Hiroyuki, Ohashi, Toya, Okumura, Akihisa, Ebihara, Nobuyuki, Murakami, Akira, Shimozawa,

Journal:

Neuro-Ophthalmology

Year:

2014

Language:

english

File:

PDF, 1.12 MB

english, 2014

32

Induction of peroxisomal lipid metabolism in mice fed a high-fat diet

Shimozawa, Nobuyuki

Journal:

Molecular Medicine Reports

Year:

2011

Language:

english

File:

PDF, 554 KB

english, 2011

33

Urinary organic acids in peroxisomal disorders: a simple screening method

Seiji Yamaguchi, Misako Iga, Masahiko Kimura, Yasuyuki Suzuki, Nobuyuki Shimozawa, Toshiyuki Fukao, Naomi Kondo, Yusaku Tazawa, Tadao Orii

Journal:

Journal of Chromatography B: Biomedical Sciences and Applications

Year:

2001

Language:

english

File:

PDF, 137 KB

english, 2001

34

Two novel missense mutations in the ATP-binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients

Atsushi Imamura, Yasuyuki Suzuki, Xiang-Qian Song, Toshiyuki Fukao, Atsushi Uchiyama, Nobuyuki Shimozawa, Keiju Kamijo, Takashi Hashimoto, Tadao Orii, Naomi Kondo

Journal:

Clinical Genetics

Year:

1997

Language:

english

File:

PDF, 571 KB

english, 1997

35

Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case

Mitsuaki Iwasa, Takanori Yamagata, Masashi Mizuguchi, Masayuki Itoh, Ayumi Matsumoto, Mitsugu Hironaka, Ayako Honda, Mariko Y. Momoi, Nobuyuki Shimozawa

Journal:

Year:

2012

Language:

english

File:

PDF, 787 KB

english, 2012

36

Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene

Ogawa, Tatsuya, Tomatsu, Shunji, Fukuda, Seiji, Yamagishi, Atsushi, Rezvi, Golam Md. Maruf, Sukegawa, Kazuko, Kondo, Neomi, Suzuki, Yasuyuki, Shimozawa, Nobuyuki, Orii, Tadao

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 800 KB

english, 1995

37

First Japanese case of Zellweger syndrome with a mutation in PEX14

Komatsuzaki, Shoko, Ogawa, Eishin, Shimozawa, Nobuyuki, Sakamoto, Osamu, Haginoya, Kazuhiro, Uematsu, Mitsugu, Hasegawa, Yuki, Matsubara, Yoichi, Ohura, Toshihiro

Journal:

Pediatrics International

Year:

2015

Language:

english

File:

PDF, 1.37 MB

english, 2015

38

Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II

Tomomi Kato, Zenichiro Kato, Izumi Kuratsubo, Noboru Tanaka, Tabito Ishigami, Jun-ichi Kajihara, Kazuko Sukegawa-Hayasaka, Koji Orii, Koji Isogai, Toshiyuki Fukao, Nobuyuki Shimozawa, Tadao Orii, Naom

Journal:

Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 356 KB

english, 2005

39

Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies

Michinori Funato, Nobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto, Yasuyuki Suzuki, Yoshihiko Imamura, Tadashi Matsumoto, Toshiro Tsukamoto, Tomoko Kojidani, Takashi Osumi, Toshiyuki Fukao, Naomi

Journal:

Brain and Development

Year:

2006

Language:

english

File:

PDF, 366 KB

english, 2006

40

Temperature-Sensitive Phenotype of Chinese Hamster Ovary Cells Defective in PEX5 Gene

Ritsu Ito, Yuan Huang, Can Yao, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Tsuneo Imanaka, Nobuteru Usuda, Masaki Ito

Journal:

Biochemical and Biophysical Research Communications

Year:

2001

Language:

english

File:

PDF, 460 KB

english, 2001

41

Infantile Refsum Disease Associated with Hypobetalipoproteinemia

Matsuo, Muneaki, Akutsu, Tsugio, Kanazawa, Naomi, Shimozawa, Nobuyuki

Journal:

Journal of Pediatric Neurology

Year:

2019

File:

PDF, 184 KB

2019

42

Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene

Nobuyuki Shimozawa, Toshiro Tsukamoto, Tomoko Nagase, Yasuhiko Takemoto, Naoki Koyama, Yasuyuki Suzuki, Masayuki Komori, Takashi Osumi, Gootjes Jeannette, Ronald J.A. Wanders, Naomi Kondo

Journal:

Year:

2004

Language:

english

File:

PDF, 292 KB

english, 2004

43

Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells

Zhongyi Zhang, Yasuyuki Suzuki, Nobuyuki Shimozawa, Ichiro Kawabata, Teruhiko Tamaya, Kodo Sato, Naomi Kondo

Journal:

Clinical Genetics

Year:

1999

Language:

english

File:

PDF, 118 KB

english, 1999

44

Mucopolysaccharidosis IVA: polymorphic haplotypes and informative RFLPs in the Japanese population

Hideki Iwata, Shunji Tomatsu, Seiji Fukuda, Atsushi Uchiyama, G. M. M. Rezvi, Tatsuya Ogawa, Toshinori Hori, Yoshihiro Nakashima, Atsushi Yamagishi, Kazuko Sukegawa, Nobuyuki Shimozawa, Yasuyuki Suzuk

Journal:

Year:

1995

Language:

english

File:

PDF, 1.10 MB

english, 1995

45

Peroxisome assembly factor–2, a putative ATPase cloned by functional complementation on a peroxisome–deficient mammalian cell mutant

Tsukamoto, Toshiro, Miura, Satoshi, Nakai, Toshiki, Yokota, Sadaki, Shimozawa, Nobuyuki, Suzuki, Yasuyuki, Orii, Tadao, Fujiki, Yukio, Sakai, Fumie, Bogaki, Akemi

Journal:

Nature Genetics

Year:

1995

File:

PDF, 908 KB

1995

46

Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders

Yasuhiko Takemoto, Yasuyuki Suzuki, Ryoko Horibe, Nobuyuki Shimozawa, Ronald J.A. Wanders, Naomi Kondo

Journal:

Brain and Development

Year:

2003

Language:

english

File:

PDF, 154 KB

english, 2003

47

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L

Naohide Shiroma, Naomi Kanazawa, Zenichiro Kato, Nobuyuki Shimozawa, Atsushi Imamura, Masayuki Ito, Kyoich Ohtani, Akira Oka, Kazuyo Wakabayashi, Mizue Iai, Kenji Sugai, Masayuki Sasaki, Makiko Kaga,

Journal:

Brain and Development

Year:

2003

Language:

english

File:

PDF, 288 KB

english, 2003

48

Chediak-Higashi syndrome with cerebellar cortical atrophy detected by MRI

Naomi Kondo, Nobuyuki Shimozawa, Junichi Asano, Atsushi Imamura, Tadao Orii

Journal:

Clinical Genetics

Year:

1994

Language:

english

File:

PDF, 120 KB

english, 1994

49

Diagnosis of Zellweger syndrome by rectal biopsy: immunoblot of peroxisomal β-oxidation enzyme and activity of dihydroxyacetone phosphate acyltransferase in rectal mucosa

Nobuyuki Shimozawa, Yasuyuki Suzuki, Tadao Orii, Takashi Hashimoto

Journal:

Clinica Chimica Acta

Year:

1988

Language:

english

File:

PDF, 239 KB

english, 1988

50

d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder

Yasuyuki Suzuki, Ling Ling Jiang, Masayoshi Souri, Shoko Miyazawa, Seiji Fukuda, Zhongyi Zhang, Mizuho Une, Nobuyuki Shimozawa, Naomi Kondo, Tadao Orii, Takashi Hashimoto

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 3.15 MB

english, 1997

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