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1

Circulating steroids and mood disorders in patients with polycystic ovary syndrome

Yoshida, Tomoko, Saito, Kazuki, Kawamura, Toshihiro, Ishikawa, Tomonori, Kato, Tsuguhiko, Matsubara, Keiko, Miyasaka, Naoyuki, Miyado, Mami, Fukami, Maki

Journal:

Year:

2021

File:

PDF, 419 KB

2021

2

Milk Curdling by Rennet under High Pressure

KUNIO OHMIYA, KEIKO FUKAMI, SHOICHI SHIMIZU, KUNIHIKO GEKKO

Journal:

Journal of Food Science

Year:

1987

Language:

english

File:

PDF, 522 KB

english, 1987

3

Microglia-derived neuregulin expression in psychiatric disorders

Ikawa, Daisuke, Makinodan, Manabu, Iwata, Keiko, Ohgidani, Masahiro, Kato, Takahiro A., Yamashita, Yasunori, Yamamuro, Kazuhiko, Kimoto, Sohei, Toritsuka, Michihiro, Yamauchi, Takahira, Fukami, Shin-i

Journal:

Brain, Behavior, and Immunity

Year:

2017

Language:

english

File:

PDF, 1.17 MB

english, 2017

4

(Epi)genotype-Phenotype Analysis in 69 Japanese Patients With Pseudohypoparathyroidism Type I

Sano, Shinichiro, Nakamura, Akie, Matsubara, Keiko, Nagasaki, Keisuke, Fukami, Maki, Kagami, Masayo, Ogata, Tsutomu

Journal:

Journal of the Endocrine Society

Year:

2018

Language:

english

File:

PDF, 443 KB

english, 2018

5

Spatial distribution of activation energy in Bi2Sr2CaCu2O8+d single crystal

Ryuji Kondo, Takeshi Fukami, Keiko Nakashima, Takeshi Arai, Kazuya Shimakawa, Takafumi Aomine, Takashi Yasuda, Tsuyoshi Tamegai

Journal:

Physica B: Condensed Matter

Year:

2000

Language:

english

File:

PDF, 137 KB

english, 2000

6

Hydrogen peroxide induces Src family tyrosine kinase-dependent activation of Xenopus eggs

Ken-ichi Sato, Keiko Ogawa, Alexander A. Tokmakov, Tetsushi Iwasaki, Yasuo Fukami

Journal:

Development, Growth & Differentiation

Year:

2001

Language:

english

File:

PDF, 680 KB

english, 2001

7

Monozygotic female twins discordant for Silver–Russell syndrome and hypomethylation of theH19-DMR

Kazuki Yamazawa, Masayo Kagami, Maki Fukami, Keiko Matsubara, Tsutomu Ogata

Journal:

Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 274 KB

english, 2008

8

Evidence for the Involvement of a Src-Related Tyrosine Kinase inXenopusEgg Activation

Ken-ichi Sato, Yasuhiro Iwao, Tomoko Fujimura, Ikuo Tamaki, Keiko Ogawa, Tetsushi Iwasaki, Alexander A Tokmakov, Osamu Hatano, Yasuo Fukami

Journal:

Developmental Biology

Year:

1999

Language:

english

File:

PDF, 412 KB

english, 1999

9

A New Phase Transition of (NH 4 ) 3 H(SO 4 ) 2 at 190°C

Fukami, Takanori, Tobaru, Kazuyasu, Nakasone, Keiko

Journal:

Journal of the Physical Society of Japan

Year:

1994

File:

PDF, 196 KB

1994

10

Crystal Structure of (NH 4 ) 3 H(SO 4 ) 2 in Phase I

Fukami, Takanori, Horiuchi, Keizo, Nakasone, Keiko, Furukawa, Kazuo

Journal:

Japanese Journal of Applied Physics

Year:

1996

File:

PDF, 394 KB

1996

11

Backdoor pathway for dihydrotestosterone biosynthesis: Implications for normal and abnormal human sex development

Fukami, Maki, Homma, Keiko, Hasegawa, Tomonobu, Ogata, Tsutomu

Journal:

Developmental Dynamics

Year:

2013

Language:

english

File:

PDF, 663 KB

english, 2013

12

Birth seasonality in Prader-Willi syndrome resulting from chromosome 15 microdeletion

Ayabe, Tadayuki, Matsubara, Keiko, Ogata, Tsutomu, Ayabe, Atsuko, Murakami, Nobuyuki, Nagai, Toshiro, Fukami, Maki

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 102 KB

english, 2013

13

Mesenchymal stem cells ameliorate impaired wound healing through enhancing keratinocyte functions in diabetic foot ulcerations on the plantar skin of rats

Kato, Jiro, Kamiya, Hideki, Himeno, Tatsuhito, Shibata, Taiga, Kondo, Masaki, Okawa, Tetsuji, Fujiya, Atsushi, Fukami, Ayako, Uenishi, Eita, Seino, Yusuke, Tsunekawa, Shin, Hamada, Yoji, Naruse, Keiko

Journal:

Journal of Diabetes and its Complications

Year:

2014

Language:

english

File:

PDF, 400 KB

english, 2014

14

De novo Frameshift Mutation in Fibroblast Growth Factor 8 in a Male Patient with Gonadotropin Deficiency

Suzuki, Erina, Yatsuga, Shuichi, Igarashi, Maki, Miyado, Mami, Nakabayashi, Kazuhiko, Hayashi, Keiko, Hata, Kenichirou, Umezawa, Akihiro, Yamada, Gen, Ogata, Tsutomu, Fukami, Maki

Journal:

Hormone Research in Paediatrics

Year:

2014

Language:

english

File:

PDF, 425 KB

english, 2014

15

Physiology and gene expression of the rice landrace Horkuch under salt stress

Lisa, Laisa A., Elias, Sabrina M., Rahman, M. Sazzadur, Shahid, Saima, Iwasaki, Tetsushi, Hasan, A. K. M. Mahbub, Kosuge, Keiko, Fukami, Yasuo, Seraj, Zeba I.

Journal:

Functional Plant Biology

Year:

2011

Language:

english

File:

PDF, 326 KB

english, 2011

16

The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers

Kagami, Masayo, O'Sullivan, Maureen J., Green, Andrew J., Watabe, Yoshiyuki, Arisaka, Osamu, Masawa, Nobuhide, Matsuoka, Kentarou, Fukami, Maki, Matsubara, Keiko, Kato, Fumiko, Ferguson-Smith, Anne C.

Journal:

Year:

2010

Language:

english

File:

PDF, 4.31 MB

english, 2010

17

Cytochrome P450 Oxidoreductase Deficiency: Identification and Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients

Fukami, Maki, Nishimura, Gen, Homma, Keiko, Nagai, Toshiro, Hanaki, Keiichi, Uematsu, Ayumi, Ishii, Tomohiro, Numakura, Chikahiko, Sawada, Hirotake, Nakacho, Mariko, Kowase, Takanori, Motomura, Katsua

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 358 KB

english, 2009

18

Paternal uniparental disomy 14 and related disorders

Kagami, Masayo, Matsuoka, Kentaro, Nagai, Toshiro, Yamanaka, Michiko, Kurosawa, Kenji, Suzumori, Nobuhiro, Sekita, Yoichi, Miyado, Mami, Matsubara, Keiko, Fuke, Tomoko, Kato, Fumiko, Fukami, Maki, Oga

Journal:

Year:

2012

Language:

english

File:

PDF, 4.31 MB

english, 2012

19

Testicular Dysgenesis without Adrenal Insufficiency in a 46,XY Patient with a Heterozygous Inactive Mutation of Steroidogenic Factor-1

Hasegawa, Tomonobu, Fukami, Maki, Sato, Naoko, Katsumata, Noriyuki, Sasaki, Goro, Fukutani, Keiko, Morohashi, Ken-Ichirou, Ogata, Tsutomu

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2004

Language:

english

File:

PDF, 282 KB

english, 2004

20

Cytochrome P450 Oxidoreductase Deficiency in Three Patients Initially Regarded as Having 21-Hydroxylase Deficiency and/or Aromatase Deficiency: Diagnostic Value of Urine Steroid Hormone Analysis

Fukami, Maki, Hasegawa, Tomonobu, Horikawa, Reiko, Ohashi, Toya, Nishimura, Gen, Homma, Keiko, Ogata, Tsutomu

Journal:

Pediatric Research

Year:

2006

Language:

english

File:

PDF, 902 KB

english, 2006

21

Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver–Russell Syndrome-compatible phenotype

Kagami, Masayo, Mizuno, Seiji, Matsubara, Keiko, Nakabayashi, Kazuhiko, Sano, Shinichiro, Fuke, Tomoko, Fukami, Maki, Ogata, Tsutomu

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.21 MB

english, 2015

22

Growth and Yield Responses of Two Soybean Cultivars Grown under Controlled Groundwater Level in Southwestern Japan

Matsuo, Naoki, Takahashi, Motoki, Nakano, Hiroshi, Fukami, Koichiro, Tsuchiya, Shinori, Morita, Satoshi, Kitagawa, Hisashi, Nakano, Keiko, Nakamoto, Hiroaki, Tasaka, Kohei

Journal:

Plant Production Science

Year:

2013

Language:

english

File:

PDF, 734 KB

english, 2013

23

Beckwith–Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon?

Sano, Shinichiro, Matsubara, Keiko, Nagasaki, Keisuke, Kikuchi, Toru, Nakabayashi, Kazuhiko, Hata, Kenichiro, Fukami, Maki, Kagami, Masayo, Ogata, Tsutomu

Journal:

Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.11 MB

english, 2016

24

Exploration of hydroxymethylation in Kagami-Ogata syndrome caused by hypermethylation of imprinting control regions

Matsubara, Keiko, Kagami, Masayo, Nakabayashi, Kazuhiko, Hata, Kenichiro, Fukami, Maki, Ogata, Tsutomu, Yamazawa, Kazuki

Journal:

Clinical Epigenetics

Year:

2015

Language:

english

File:

PDF, 873 KB

english, 2015

25

Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome

Kagami, Masayo, Matsubara, Keiko, Nakabayashi, Kazuhiko, Nakamura, Akie, Sano, Shinichiro, Okamura, Kohji, Hata, Kenichiro, Fukami, Maki, Ogata, Tsutomu

Journal:

Genetics in Medicine

Year:

2016

Language:

english

File:

PDF, 4.01 MB

english, 2016

26

Uniparental disomy of chromosome 8 leading to homozygosity of a CYP11B1 mutation in a patient with congenital adrenal hyperplasia: Implication for a rare etiology of an autosomal recessive disorder

Matsubara, Keiko, Kataoka, Naoki, Ogita, Satoko, Sano, Shinichiro, Ogata, Tsutomu, Fukami, Maki, Katsumata, Noriyuki

Journal:

Endocrine Journal

Year:

2014

Language:

english

File:

PDF, 1.37 MB

english, 2014

27

Catastrophic Cellular Events Leading to Complex Chromosomal Rearrangements in the Germline

Fukami, Maki, Shima, Hitohito, Suzuki, Erina, Ogata, Tsutomu, Matsubara, Keiko, Kamimaki, Tsutomu

Journal:

Clinical Genetics

Year:

2016

Language:

english

File:

PDF, 846 KB

english, 2016

28

A Rare Case of Severe Acute Pancreatitis Complicated with Pancreatic Pseudocysts, Obstructive Jaundice and Intraperitoneal Hemorrhage.

FUJITA, Naoyuki, MATSUMOTO, Keiko, SHIGA, Nobuyuki, NONAKA, Akiko, KOYA, Yuji, OGAWA, Hidemi, TSUDA, Terutaka, TOMITA, Masato, FUKAMI, Takanori, ASAHARA, Masakyo, KINOSHITA, Yoshikazu, HATANI, Makoto

Journal:

Internal Medicine

Year:

1996

Language:

english

File:

PDF, 3.67 MB

english, 1996

29

Growth hormone deficiency in monozygotic twins with autosomal dominant pseudohypoparathyroidism type Ib

Sano, Shinichiro, Iwata, Hiromi, Matsubara, Keiko, Fukami, Maki, Kagami, Masayo, Ogata, Tsutomu

Journal:

Endocrine Journal

Year:

2015

Language:

english

File:

PDF, 1.08 MB

english, 2015

30

Detection of Campylobacters in Patients with Sporadic Diarrhea and Antibacterial Action of 37 Drugs against Campylobacter jejuni

FUKAMI, Toshie, KOUNOSU, Akiko, HIKOSAKA, Keiko, KASHIWA, Machiko, MIGITA, Takuo, NISHIKAWA, Yoshishige, MURATA, Misako, IMAGAWA, Yatsuka, SAITO, Makoto

Journal:

Kansenshogaku zasshi

Year:

1984

File:

PDF, 1.86 MB

1984

31

A 68-Year-Old Phenotypically Male Patient with 21-Hydroxylase Deficiency and Concomitant Adrenocortical Neoplasm Producing Testosterone and Cortisol

Hayashi, Masayuki, Kataoka, Yuko, Sugimura, Yoshihisa, Kato, Fumiko, Fukami, Maki, Ogata, Tsutomu, Homma, Keiko, Hasegawa, Tomonobu, Oiso, Yutaka, Sasano, Hironobu, Tanaka, Hiroshi

Journal:

The Tohoku Journal of Experimental Medicine

Year:

2013

Language:

english

File:

PDF, 1.91 MB

english, 2013

32

Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations

Suzuki, Erina, Shima, Hirohito, Toki, Machiko, Hanew, Kunihiko, Matsubara, Keiko, Kurahashi, Hiroki, Narumi, Satoshi, Ogata, Tsutomu, Kamimaki, Tsutomu, Fukami, Maki

Journal:

Cytogenetic and Genome Research

Year:

2016

Language:

english

File:

PDF, 479 KB

english, 2016

33

Maternally derived 15q11.2-q13.1 duplication and H19-DMR hypomethylation in a patient with Silver–Russell syndrome

Dateki, Sumito, Kagami, Masayo, Matsubara, Keiko, Izumi, Kei, Watanabe, Satoshi, Nakatomi, Akiko, Kondoh, Tatsuro, Fukami, Maki, Moriuchi, Hiroyuki

Journal:

Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 860 KB

english, 2017

34

Continuous hypomethylation of the KCNQ1OT1 :TSS-DMR in monochorionic twins discordant for Beckwith-Wiedemann syndrome

Inoue, Takanobu, Nakamura, Akie, Matsubara, Keiko, Nyuzuki, Hiromi, Nagasaki, Keisuke, Oka, Akira, Fukami, Maki, Kagami, Masayo

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 464 KB

english, 2017

35

Longitudinal Serum and Urine Steroid Metabolite Profiling in a 46,XY Infant with Prenatally Identified POR Deficiency

Ono, Hiroyuki, Numakura, Chikahiko, Homma, Keiko, Hasegawa, Tomonobu, Tsutsumi, Seiji, Kato, Fumiko, Fujisawa, Yasuko, Fukami, Maki, Ogata, Tsutomu

Journal:

The Journal of Steroid Biochemistry and Molecular Biology

Year:

2017

Language:

english

File:

PDF, 1.42 MB

english, 2017

36

A case of paternal uniparental isodisomy for chromosome 7 associated with overgrowth

Nakamura, Akie, Muroya, Koji, Ogata-Kawata, Hiroko, Nakabayashi, Kazuhiko, Matsubara, Keiko, Ogata, Tsutomu, Kurosawa, Kenji, Fukami, Maki, Kagami, Masayo

Journal:

Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 710 KB

english, 2018

37

TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia

Ogata, Tsutomu, Niihori, Tetsuya, Tanaka, Noriko, Kawai, Masahiko, Nagashima, Takeshi, Funayama, Ryo, Nakayama, Keiko, Nakashima, Shinichi, Kato, Fumiko, Fukami, Maki, Aoki, Yoko, Matsubara, Yoichi, V

Journal:

Year:

2014

Language:

english

File:

PDF, 893 KB

english, 2014

38

Phase Transition and Crystal Structure of CsHSeO4 and CsDSeO4 Crystals

Fukami, Takanori, Tahara, Shuta, Nakasone, Keiko, Seino, Mitsuhiro

Journal:

International Journal of Chemistry

Year:

2013

Language:

english

File:

PDF, 278 KB

english, 2013

39

Uniparental disomy as a cause of pediatric endocrine disorders

Matsubara, Keiko, Kagami, Masayo, Fukami, Maki

Journal:

Clinical Pediatric Endocrinology

Year:

2018

Language:

english

File:

PDF, 1.10 MB

english, 2018

40

Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology

Inoue, Takanobu, Yagasaki, Hideaki, Nishioka, Junko, Nakamura, Akie, Matsubara, Keiko, Narumi, Satoshi, Nakabayashi, Kazuhiko, Yamazawa, Kazuki, Fuke, Tomoko, Oka, Akira, Ogata, Tsutomu, Fukami, Maki,

Journal:

Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 2.21 MB

english, 2018

41

Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites

Koyama, Yuhei, Homma, Keiko, Fukami, Maki, Miwa, Masayuki, Ikeda, Kazushige, Ogata, Tsutomu, Murata, Mitsuru, Hasegawa, Tomonobu

Journal:

Clinical Pediatric Endocrinology

Year:

2016

Language:

english

File:

PDF, 613 KB

english, 2016

42

Crystal Structure of (NH 4 ) 3 H(SeO 4 ) 2 in Phase IV

Fukami, Takanori, Tobaru, Kazuyasu, Kaneda, Kazuhito, Nakasone, Keiko, Furukawa, Kazuo

Journal:

Journal of the Physical Society of Japan

Year:

1994

File:

PDF, 344 KB

1994

43

Structural Refinements and Thermal Properties of L(+)-Tartaric, D(–)-Tartaric, and Monohydrate Racemic Tartaric Acid

Fukami, Takanori, Tahara, Shuta, Yasuda, Chitoshi, Nakasone, Keiko

Journal:

International Journal of Chemistry

Year:

2016

Language:

english

File:

PDF, 532 KB

english, 2016

44

Assessing Correlation of High-Resolution NDVI with Fertilizer Application Level and Yield of Rice and Wheat Crops using Small UAVs

Guan, Senlin, Fukami, Koichiro, Matsunaka, Hitoshi, Okami, Midori, Tanaka, Ryo, Nakano, Hiroshi, Sakai, Tetsufumi, Nakano, Keiko, Ohdan, Hideki, Takahashi, Kimiyasu

Journal:

Year:

2019

File:

PDF, 5.98 MB

2019

45

Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR

Kagami, Masayo, Yanagisawa, Atsuhiro, Ota, Miyuki, Matsuoka, Kentaro, Nakamura, Akie, Matsubara, Keiko, Nakabayashi, Kazuhiko, Takada, Shuji, Fukami, Maki, Ogata, Tsutomu

Journal:

Clinical Epigenetics

Year:

2019

Language:

english

File:

PDF, 1.78 MB

english, 2019

46

Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells

Hattori, Atsushi, Okamura, Kohji, Terada, Yumiko, Tanaka, Rika, Katoh-Fukui, Yuko, Matsubara, Yoichi, Matsubara, Keiko, Kagami, Masayo, Horikawa, Reiko, Fukami, Maki

Journal:

BMC Medical Genomics

Year:

2019

Language:

english

File:

PDF, 1.46 MB

english, 2019

47

Design and evaluation of a one-operation shallow up-cut tillage sowing method for soybean production

Matsuo, Naoki, Tsuchiya, Shinori, Nakano, Keiko, Fukami, Koichiro

Journal:

Plant Production Science

Year:

2019

Language:

english

File:

PDF, 2.52 MB

english, 2019

48

Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men

Kinoshita, Takahiro, Mikami, Masashi, Ayabe, Tadayuki, Matsubara, Keiko, Ono, Hiromi, Ohki, Kentaro, Fukami, Maki, Katoh-Fukui, Yuko

Journal:

Cytogenetic and Genome Research

Year:

2019

Language:

english

File:

PDF, 359 KB

english, 2019

49

Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men

Kinoshita, Takahiro, Mikami, Masashi, Ayabe, Tadayuki, Matsubara, Keiko, Ono, Hiromi, Ohki, Kentaro, Fukami, Maki, Katoh-Fukui, Yuko

Journal:

Cytogenetic and Genome Research

Year:

2019

File:

PDF, 359 KB

2019

50

Identification of small molecule inhibitors of human COQ7

Tsuganezawa, Keiko, Sekimata, Katsuhiko, Nakagawa, Yukari, Utata, Rei, Nakamura, Kana, Ogawa, Naoko, Koyama, Hiroo, Shirouzu, Mikako, Fukami, Takehiro, Kita, Kiyoshi, Tanaka, Akiko

Journal:

Bioorganic & Medicinal Chemistry

Year:

2019

File:

PDF, 750 KB

2019

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