Works matching AU Shigeo Kure

Results: 185

Rapid Detection of CYP2C18 Genotypes by Real-time Fluorescence Polymerase Chain Reaction.

Published in:

Journal of Pharmacy & Pharmacology, 2000, v. 52, n. 2, p. 199, doi. 10.1211/0022357001773850

By:

MIZUGAKI, MICHINAO;
HIRATSUKA, MASAHIRO;
AGATSUMA, YASUYUKI;
MATSUBARA, YOICHI;
FUJII, KUNIHIRO;
KURE, SHIGEO;
NARISAWA, KUNIAKI

Publication type:

Article

Comprehensive Targeted Sequencing Identifies Monogenic Disorders in Patients With Early-onset Refractory Diarrhea.

Published in:

2020

By:

Takashi Uchida;
Tasuku Suzuki;
Atsuo Kikuchi;
Fumihiko Kakuta;
Takashi Ishige;
Yoshiko Nakayama;
Hirokazu Kanegane;
Yuri Etani;
Tatsuki Mizuochi;
Shin-ichi Fujiwara;
Ryusuke Nambu;
Kazuhide Suyama;
Masanori Tanaka;
Atsushi Yoden;
Daiki Abukawa;
Yoji Sasahara;
Shigeo Kure;
Uchida, Takashi;
Suzuki, Tasuku;
Kikuchi, Atsuo

Publication type:

journal article

Omics research project on prospective cohort studies from the Tohoku Medical Megabank Project.

Published in:

Genes to Cells, 2018, v. 23, n. 6, p. 406, doi. 10.1111/gtc.12588

By:

Koshiba, Seizo;
Motoike, Ikuko;
Saigusa, Daisuke;
Inoue, Jin;
Shirota, Matsuyuki;
Katoh, Yasutake;
Katsuoka, Fumiki;
Danjoh, Inaho;
Hozawa, Atsushi;
Kuriyama, Shinichi;
Minegishi, Naoko;
Nagasaki, Masao;
Takai‐Igarashi, Takako;
Ogishima, Soichi;
Fuse, Nobuo;
Kure, Shigeo;
Tamiya, Gen;
Tanabe, Osamu;
Yasuda, Jun;
Kinoshita, Kengo

Publication type:

Article

Successful Treatment of an Infant with Left Ventricular Noncompaction Presenting with Fatal Ventricular Arrhythmia Treated with Cardiac Resynchronization Therapy and an Implantable Cardioverter Defibrillator.

Published in:

Case Reports in Cardiology, 2018, p. 1, doi. 10.1155/2018/9562326

By:

Kimura, Masato;
Kawano, Kengo;
Yaoita, Hisao;
Kure, Shigeo

Publication type:

Article

The Onset of Interictal Spike-Related Ripples Facilitates Detection of the Epileptogenic Zone.

Published in:

Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.724417

By:

Numata-Uematsu, Yurika;
Uematsu, Mitsugu;
Sakuraba, Rie;
Iwasaki, Masaki;
Osawa, Shinichiro;
Jin, Kazutaka;
Nakasato, Nobukazu;
Kure, Shigeo

Publication type:

Article

NR0B1 Frameshift Mutation in a Boy with Idiopathic Central Precocious Puberty.

Published in:

Sexual Development, 2016, v. 10, n. 4, p. 205, doi. 10.1159/000448726

By:

Shima, Hirohito;
Yatsuga, Shuichi;
Nakamura, akie;
Sano, Shinichiro;
Sasaki, Takako;
Katsumata, Noriyuki;
Suzuki, Erina;
Hata, Kenichiro;
Nakabayashi, Kazuhiko;
Momozawa, Yukihide;
Kubo, Michiaki;
Okamura, Kohji;
Kure, Shigeo;
Matsubara, Yoichi;
Ogata, Tsutomu;
Narumi, Satoshi;
Fukami, Maki

Publication type:

Article

Association between maternal psychological distress and children's neurodevelopment in offspring aged 4 years in Japan: The Tohoku Medical Megabank Project Birth and Three‐Generation Cohort Study.

Published in:

Journal of Paediatrics & Child Health, 2023, v. 59, n. 3, p. 548, doi. 10.1111/jpc.16353

By:

Takahashi, Ippei;
Obara, Taku;
Kikuchi, Saya;
Kobayashi, Mika;
Ishikuro, Mami;
Murakami, Keiko;
Ueno, Fumihiko;
Noda, Aoi;
Onuma, Tomomi;
Matsuzaki, Fumiko;
Kobayashi, Natsuko;
Hamada, Hirotaka;
Iwama, Noriyuki;
Saito, Masatoshi;
Sugawara, Junichi;
Tomita, Hiroaki;
Kure, Shigeo;
Yaegashi, Nobuo;
Kuriyama, Shinichi

Publication type:

Article

A Prevalent TMEM260 Deletion Causes Conotruncal Heart Defects, Including Truncus Arteriosus.

Published in:

American Journal of Medical Genetics. Part A, 2025, v. 197, n. 3, p. 1, doi. 10.1002/ajmg.a.63906

By:

Saijo, Naoya;
Yaoita, Hisao;
Takayama, Jun;
Ota, Chiharu;
Kawai, Eiichiro;
Kimura, Masato;
Ozawa, Akira;
Tamiya, Gen;
Kure, Shigeo;
Kikuchi, Atsuo

Publication type:

Article

Long‐term clinical observation of patients with heterozygous KIF1A variants.

Published in:

American Journal of Medical Genetics. Part A, 2024, v. 194, n. 10, p. 1, doi. 10.1002/ajmg.a.63656

By:

Kawashima, Aritomo;
Kodama, Kaori;
Okubo, Yukimune;
Endo, Wakaba;
Inui, Takehiko;
Ikeda, Miki;
Katata, Yu;
Togashi, Noriko;
Ohba, Chihiro;
Imagawa, Eri;
Iwama, Kazuhiro;
Mizuguchi, Takeshi;
Kitami, Masahiro;
Aihara, Yu;
Takayama, Jun;
Tamiya, Gen;
Kikuchi, Atsuo;
Kure, Shigeo;
Saitsu, Hirotomo;
Matsumoto, Naomichi

Publication type:

Article

Increased Cerebrospinal Fluid Glycine: A Biochemical Marker for a Leukoencephalopathy With...

Published in:

Journal of Child Neurology, 1999, v. 14, n. 11, p. 728

By:

van der Knaap, Marjo S.;
Wevers, Ron A.;
Kure, Shigeo;
Gabreels, Fons J.M.;
Verhoeven, Nanda M.;
Raaij-Selten, Bertie van;
Jaeken, Jaak

Publication type:

Article

Atypical Nonketotic Hyperglycinemia With Normal Cerebrospinal Fluid to Plasma Glycine Ratio.

Published in:

Journal of Child Neurology, 1999, v. 14, n. 7, p. 464

By:

Jackson, Anthony H.;
Applegarth, Derrek A.;
Toone, Jennifer R.;
Kure, Shigeo;
Levy, Harvey L.

Publication type:

Article

Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia-telangiectasia caused by novel compound heterozygous variants in ATM.

Published in:

2021

By:

Sato, Daichi;
Moriya, Kunihiko;
Nakano, Tomohiro;
Miyagawa, Chihiro;
Katayama, Saori;
Niizuma, Hidetaka;
Sasahara, Yoji;
Kure, Shigeo

Publication type:

journal article

Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation.

Published in:

International Journal of Hematology, 2020, v. 112, n. 2, p. 258, doi. 10.1007/s12185-020-02860-7

By:

Moriya, Kunihiko;
Suzuki, Tasuku;
Uchida, Nao;
Nakano, Tomohiro;
Katayama, Saori;
Irie, Masahiro;
Rikiishi, Takeshi;
Niizuma, Hidetaka;
Okada, Satoshi;
Imai, Kohsuke;
Sasahara, Yoji;
Kure, Shigeo

Publication type:

Article

Successful treatment with rituximab of an infant with refractory autoimmune hemolytic anemia.

Published in:

2013

By:

Moriya, Kunihiko;
Matsuhashi, Tetsuro;
Onuma, Masaei;
Niizuma, Hidetaka;
Rikiishi, Takeshi;
Asada, Hiroshi;
Suzuki, Jun;
Sasahara, Yoji;
Kure, Shigeo

Publication type:

Report

De novo GABRA1 mutations in Ohtahara and West syndromes.

Published in:

Epilepsia (Series 4), 2016, v. 57, n. 4, p. 566, doi. 10.1111/epi.13344

By:

Kodera, Hirofumi;
Ohba, Chihiro;
Kato, Mitsuhiro;
Maeda, Toshiyuki;
Araki, Kaoru;
Tajima, Daisuke;
Matsuo, Muneaki;
Hino‐Fukuyo, Naomi;
Kohashi, Kosuke;
Ishiyama, Akihiko;
Takeshita, Saoko;
Motoi, Hirotaka;
Kitamura, Taro;
Kikuchi, Atsuo;
Tsurusaki, Yoshinori;
Nakashima, Mitsuko;
Miyake, Noriko;
Sasaki, Masayuki;
Kure, Shigeo;
Haginoya, Kazuhiro

Publication type:

Article

Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy.

Published in:

Epilepsia (Series 4), 2008, v. 49, n. 9, p. 1528, doi. 10.1111/j.1528-1167.2008.01609.x

By:

Wang, Ji-wen;
Kurahashi, Hirokazu;
Ishii, Atsushi;
Kojima, Toshio;
Ohfu, Masaharu;
Inoue, Takahito;
Ogawa, Atsushi;
Yasumoto, Sawa;
Oguni, Hirokazu;
Kure, Shigeo;
Fujii, Tatsuya;
Ito, Masatoshi;
Okuno, Takehiko;
Shirasaka, Yukiyoshi;
Natsume, Jun;
Hasegawa, Aki;
Konagaya, Akihiko;
Kaneko, Sunao;
Hirose, Shinichi

Publication type:

Article

Impacts of the urinary sodium-to-potassium ratio, sleep efficiency, and conventional risk factors on home hypertension in a general Japanese population.

Published in:

Hypertension Research, 2021, v. 44, n. 7, p. 858, doi. 10.1038/s41440-021-00628-y

By:

Hirata, Takumi;
Kogure, Mana;
Tsuchiya, Naho;
Miyagawa, Ken;
Narita, Akira;
Nochioka, Kotaro;
Uruno, Akira;
Obara, Taku;
Nakamura, Tomohiro;
Nakaya, Naoki;
Metoki, Hirohito;
Kikuya, Masahiro;
Sugawara, Junichi;
Kuriyama, Shinichi;
Tsuji, Ichiro;
Kure, Shigeo;
Hozawa, Atsushi

Publication type:

Article

Hypertensive disorders of pregnancy, obesity, and hypertension in later life by age group: a cross-sectional analysis.

Published in:

Hypertension Research, 2020, v. 43, n. 11, p. 1277, doi. 10.1038/s41440-020-0463-8

By:

Wagata, Maiko;
Kogure, Mana;
Nakaya, Naoki;
Tsuchiya, Naho;
Nakamura, Tomohiro;
Hirata, Takumi;
Narita, Akira;
Metoki, Hirohito;
Ishikuro, Mami;
Kikuya, Masahiro;
Tanno, Kozo;
Fukushima, Akimune;
Yaegashi, Nobuo;
Kure, Shigeo;
Yamamoto, Masayuki;
Kuriyama, Shinichi;
Hozawa, Atsushi;
Sugawara, Junichi

Publication type:

Article

Multiple measurements of the urinary sodium-to-potassium ratio strongly related home hypertension: TMM Cohort Study.

Published in:

Hypertension Research, 2020, v. 43, n. 1, p. 62, doi. 10.1038/s41440-019-0335-2

By:

Kogure, Mana;
Hirata, Takumi;
Nakaya, Naoki;
Tsuchiya, Naho;
Nakamura, Tomohiro;
Narita, Akira;
Miyagawa, Ken;
Koshimizu, Hiroshi;
Obara, Taku;
Metoki, Hirohito;
Uruno, Akira;
Kikuya, Masahiro;
Sugawara, Junichi;
Kuriyama, Shinichi;
Tsuji, Ichiro;
Kure, Shigeo;
Hozawa, Atsushi

Publication type:

Article

Reduced sleep efficiency, measured using an objective device, was related to an increased prevalence of home hypertension in Japanese adults.

Published in:

Hypertension Research, 2020, v. 43, n. 1, p. 23, doi. 10.1038/s41440-019-0329-0

By:

Hirata, Takumi;
Nakamura, Tomohiro;
Kogure, Mana;
Tsuchiya, Naho;
Narita, Akira;
Miyagawa, Ken;
Nochioka, Kotaro;
Uruno, Akira;
Obara, Taku;
Nakaya, Naoki;
Metoki, Hirohito;
Kikuya, Masahiro;
Sugawara, Junichi;
Kuriyama, Shinichi;
Tsuji, Ichiro;
Kure, Shigeo;
Hozawa, Atsushi

Publication type:

Article

IDH2 and TP53 mutations are correlated with gliomagenesis in a patient with Maffucci syndrome.

Published in:

Cancer Science, 2014, v. 105, n. 3, p. 359, doi. 10.1111/cas.12337

By:

Moriya, Kunihiko;
Kaneko, Mika K.;
Liu, Xing;
Hosaka, Masami;
Fujishima, Fumiyoshi;
Sakuma, Jun;
Ogasawara, Satoshi;
Watanabe, Mika;
Sasahara, Yoji;
Kure, Shigeo;
Kato, Yukinari

Publication type:

Article

The guanylate cyclase C agonist linaclotide ameliorates the gut–cardio–renal axis in an adenine-induced mouse model of chronic kidney disease.

Published in:

Nephrology Dialysis Transplantation, 2020, v. 35, n. 2, p. 250, doi. 10.1093/ndt/gfz126

By:

Nanto-Hara, Fumika;
Kanemitsu, Yoshitomi;
Fukuda, Shinji;
Kikuchi, Koichi;
Asaji, Kei;
Saigusa, Daisuke;
Iwasaki, Tomoyuki;
Ho, Hsin-Jung;
Mishima, Eikan;
Suzuki, Takehiro;
Suzuki, Chitose;
Tsukimi, Tomoya;
Matsuhashi, Tetsuro;
Oikawa, Yoshitsugu;
Akiyama, Yukako;
Kure, Shigeo;
Owada, Yuji;
Tomioka, Yoshihisa;
Soga, Tomoyoshi;
Ito, Sadayoshi

Publication type:

Article

The Discovery of GALM Deficiency (Type IV Galactosemia) and Newborn Screening System for Galactosemia in Japan.

Published in:

International Journal of Neonatal Screening (IJNS), 2021, v. 7, n. 4, p. 68, doi. 10.3390/ijns7040068

By:

Kikuchi, Atsuo;
Wada, Yoichi;
Ohura, Toshihiro;
Kure, Shigeo

Publication type:

Article

Oral Microbiome Analysis in Prospective Genome Cohort Studies of the Tohoku Medical Megabank Project.

Published in:

Frontiers in Cellular & Infection Microbiology, 2021, p. N.PAG, doi. 10.3389/fcimb.2020.604596

By:

Saito, Sakae;
Aoki, Yuichi;
Tamahara, Toru;
Goto, Maki;
Matsui, Hiroyuki;
Kawashima, Junko;
Danjoh, Inaho;
Hozawa, Atsushi;
Kuriyama, Shinichi;
Suzuki, Yoichi;
Fuse, Nobuo;
Kure, Shigeo;
Yamashita, Riu;
Tanabe, Osamu;
Minegishi, Naoko;
Kinoshita, Kengo;
Tsuboi, Akito;
Shimizu, Ritsuko;
Yamamoto, Masayuki

Publication type:

Article

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 1, p. 34, doi. 10.1038/jhg.2010.132

By:

Kamada, Fumiaki;
Aoki, Yoko;
Narisawa, Ayumi;
Abe, Yu;
Komatsuzaki, Shoko;
Kikuchi, Atsuo;
Kanno, Junko;
Niihori, Tetsuya;
Ono, Masao;
Ishii, Naoto;
Owada, Yuji;
Fujimura, Miki;
Mashimo, Yoichi;
Suzuki, Yoichi;
Hata, Akira;
Tsuchiya, Shigeru;
Tominaga, Teiji;
Matsubara, Yoichi;
Kure, Shigeo

Publication type:

Article

Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 12, p. 801, doi. 10.1038/jhg.2010.116

By:

Komatsuzaki, Shoko;
Aoki, Yoko;
Niihori, Tetsuya;
Okamoto, Nobuhiko;
Hennekam, Raoul C M;
Hopman, Saskia;
Ohashi, Hirofumi;
Mizuno, Seiji;
Watanabe, Yoriko;
Kamasaki, Hotaka;
Kondo, Ikuko;
Moriyama, Nobuko;
Kurosawa, Kenji;
Kawame, Hiroshi;
Okuyama, Ryuhei;
Imaizumi, Masue;
Rikiishi, Takeshi;
Tsuchiya, Shigeru;
Kure, Shigeo;
Matsubara, Yoichi

Publication type:

Article

A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 5, p. 455, doi. 10.1007/s10038-006-0384-7

By:

Kamada, Fumiaki;
Kure, Shigeo;
Kudo, Takayuki;
Suzuki, Yoichi;
Oshima, Takeshi;
Ichinohe, Akiko;
Kojima, Kanako;
Niihori, Tetsuya;
Kanno, Junko;
Narumi, Yoko;
Narisawa, Ayumi;
Kato, Kumi;
Aoki, Yoko;
Ikeda, Katsuhisa;
Kobayashi, Toshimitsu;
Matsubara, Yoichi

Publication type:

Article

A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 5, p. 230, doi. 10.1007/s10038-005-0243-y

By:

Boneh, Avihu;
Korman, Stanley H.;
Sato, Kenichi;
Kanno, Junko;
Matsubara, Yoichi;
Lerer, Israela;
Ben-Neriah, Ziva;
Kure, Shigeo

Publication type:

Article

Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 4, p. 192, doi. 10.1007/s10038-005-0239-7

By:

Tetsuya Niihori;
Yoko Aoki;
Hirofumi Ohashi;
Kenji Kurosawa;
Tatsuro Kondoh;
Satoshi Ishikiriyama;
Hiroshi Kawame;
Hotaka Kamasaki;
Tsutomu Yamanaka;
Fumio Takada;
Kimio Nishio;
Masahiro Sakurai;
Hiroshi Tamai;
Tatsuro Nagashima;
Yoichi Suzuki;
Shigeo Kure;
Kunihiro Fujii;
Masue Imaizumi;
Yoichi Matsubara

Publication type:

Article

Linkage and association of childhood asthma with the chromosome 12 genes.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 3, p. 115

By:

Shao, Chenchen;
Suzuki, Yoichi;
Kamada, Fumiaki;
Kanno, Kiyoshi;
Tamari, Mayumi;
Hasegawa, Koichi;
Aoki, Yoko;
Kure, Shigeo;
Yang, Xue;
Endo, Hiroko;
Takayanagi, Reiko;
Nakazawa, Chifuyu;
Morikawa, Toshio;
Morikawa, Miki;
Miyabayashi, Shigeaki;
Chiba, Yasushi;
Karahashi, Minoru;
Saito, Seichi;
Tamura, Gen;
Shirakawa, Taro

Publication type:

Article

Novel IRF6 mutations in Japanese patients with Van der Woude Syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion.

Published in:

Journal of Human Genetics, 2003, v. 48, n. 12, p. 622, doi. 10.1007/s10038-003-0089-0

By:

Kayano, Shuji;
Kure, Shigeo;
Suzuki, Yoichi;
Kanno, Kiyoshi;
Aoki, Yoko;
Kondo, Shinji;
Schutte, Brian C.;
Murray, Jeffrey C.;
Yamada, Atsushi;
Matsubara, Yoichi

Publication type:

Article

Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut[sup 0] patients.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 35, doi. 10.1007/s100380050103

By:

Mikami, Hitoshi;
Ogasawara, Masahito;
Matsubara, Y.;
Kikuchi, Masahiro;
Miyabayashi, Shigeaki;
Kure, Shigeo;
Narisawa, Kuniaki

Publication type:

Article

Neurofibromatosis Type 1 Complicated by Atypical Coarctation of the Thoracic Aorta.

Published in:

Case Reports in Pediatrics, 2013, p. 1, doi. 10.1155/2013/458543

By:

Masato Kimura;
Shuhei Kakizaki;
Kengo Kawano;
Shinichi Sato;
Shigeo Kure

Publication type:

Article

Association between fat mass index, fat‐free mass index and hemoglobin A1c in a Japanese population: The Tohoku Medical Megabank Community‐based Cohort Study.

Published in:

Journal of Diabetes Investigation, 2022, v. 13, n. 5, p. 858, doi. 10.1111/jdi.13729

By:

Takase, Masato;
Nakamura, Tomohiro;
Hirata, Takumi;
Tsuchiya, Naho;
Kogure, Mana;
Itabashi, Fumi;
Nakaya, Naoki;
Hamanaka, Yohei;
Sugawara, Junichi;
Suzuki, Kichiya;
Fuse, Nobuo;
Uruno, Akira;
Kodama, Eiichi N;
Kuriyama, Shinichi;
Tsuji, Ichiro;
Kure, Shigeo;
Hozawa, Atsushi

Publication type:

Article

Development of icterus gravis in a preterm infant with G71R UGT1A1 polymorphism.

Published in:

BMC Research Notes, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1756-0500-6-51

By:

Kaga, Akimune;
Ohkubo, Yukimune;
Watanabe, Yohei;
Saito, Sachiko;
Matsuki, Takuma;
Usuda, Haruo;
Kanda, Susumu;
Suzuki, Yutaka;
Tanabu, Muneyuki;
Kure, Shigeo

Publication type:

Article

Catecholamine-induced paralytic ileus controlled by phentolamine in a child with giant differentiating neuroblastoma.

Published in:

2021

By:

Hagiwara, Motomi;
Niizuma, Hidetaka;
Kazama, Takuro;
Sasahara, Yoji;
Kure, Shigeo

Publication type:

Letter

A pediatric case of osteosarcoma and tuberous sclerosis complex with a novel germline mutation in the TSC2 gene and a somatic mutation in the TP53 gene.

Published in:

2021

By:

Kuroda, Kaoru;
Moriya, Kunihiko;
Nakano, Tomohiro;
Saito, Ryoko;
Sato, Daichi;
Katayama, Saori;
Niizuma, Hidetaka;
Watanuki, Munenori;
Uematsu, Mitsugu;
Sasahara, Yoji;
Kure, Shigeo

Publication type:

Case Study

Utility of a bridged nucleic acid clamp for liquid biopsy: Detecting BRAF V600E in the cerebrospinal fluid of a patient with brain tumor.

Published in:

2020

By:

Nakano, Yoshiko;
Watanabe, Yuko;
Honda‐Kitahara, Mai;
Yamagishi, Yuki;
Niizuma, Hidetaka;
Niihori, Tetsuya;
Sasahara, Yoji;
Sonoda, Yukihiko;
Narita, Yoshitaka;
Nagane, Motoo;
Kure, Shigeo;
Ichimura, Koichi;
Honda-Kitahara, Mai

Publication type:

Case Study

Novel Compound Heterozygous RTEL1 Gene Mutations in a Patient With Hoyeraal-Hreidarsson Syndrome.

Published in:

2016

By:

Moriya, Kunihiko;
Niizuma, Hidetaka;
Rikiishi, Takeshi;
Yamaguchi, Hiroki;
Sasahara, Yoji;
Kure, Shigeo

Publication type:

Case Study

Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.

Published in:

2015

By:

Ouchi‐Uchiyama, Meri;
Sasahara, Yoji;
Kikuchi, Atsuo;
Goi, Kumiko;
Nakane, Takaya;
Ikeno, Mitsuru;
Noguchi, Yasushi;
Uike, Naokuni;
Miyajima, Yuji;
Matsubara, Kousaku;
Koh, Katsuyoshi;
Sugita, Kanji;
Imaizumi, Masue;
Kure, Shigeo

Publication type:

journal article

Germline mutations in HRAS proto-oncogene cause Costello syndrome.

Published in:

Nature Genetics, 2005, v. 37, n. 10, p. 1038, doi. 10.1038/ng1641

By:

Aoki, Yoko;
Niihori, Tetsuya;
Kawame, Hiroshi;
Kurosawa, Kenji;
Ohashi, Hirofumi;
Tanaka, Yukichi;
Filocamo, Mirella;
Kato, Kumi;
Suzuki, Yoichi;
Kure, Shigeo;
Matsubara, Yoichi

Publication type:

Article

Association of achondroplasia with Down syndrome: Difficulty in prenatal diagnosis by sonographic and 3- D helical computed tomographic analyses.

Published in:

Congenital Anomalies, 2015, v. 55, n. 2, p. 116, doi. 10.1111/cga.12097

By:

Kaga, Akimune;
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Kimura, Masato;
Saito-Hakoda, Akiko;
Kanno, Junko;
Hoshi, Kazuhiko;
Kure, Shigeo;
Fujiwara, Ikuma

Publication type:

Article

Inherited risk factors for deep venous thrombosis following total hip arthroplasty in Japanese patients: matched control study.

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Journal of Orthopaedic Science, 2007, v. 12, n. 2, p. 118, doi. 10.1007/s00776-006-1100-3

By:

Yoshiro Kiyoshige;
Shigeo Kure;
Kaoru Goto;
Masaji Ishii;
Junko Kanno

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Article

Methionine Enkephalin Suppresses Osteocyte Apoptosis Induced by Compressive Force through Regulation of Nuclear Translocation of NFATc1.

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JBMR Plus, 2020, v. 4, n. 7, p. 1, doi. 10.1002/jbm4.10369

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Sogi, Chisumi;
Takeshita, Nobuo;
Jiang, Wei;
Kim, Siyoung;
Maeda, Toshihiro;
Yoshida, Michiko;
Oyanagi, Toshihito;
Ito, Arata;
Kimura, Seiji;
Seki, Daisuke;
Takano, Ikuko;
Sakai, Yuichi;
Fujiwara, Ikuma;
Kure, Shigeo;
Takano‐Yamamoto, Teruko

Publication type:

Article

Methionine Enkephalin Suppresses Osteocyte Apoptosis Induced by Compressive Force through Regulation of Nuclear Translocation of NFATc1.

Published in:

JBMR Plus, 2020, v. 4, n. 7, p. 1, doi. 10.1002/jbm4.10369

By:

Sogi, Chisumi;
Takeshita, Nobuo;
Jiang, Wei;
Kim, Siyoung;
Maeda, Toshihiro;
Yoshida, Michiko;
Oyanagi, Toshihito;
Ito, Arata;
Kimura, Seiji;
Seki, Daisuke;
Takano, Ikuko;
Sakai, Yuichi;
Fujiwara, Ikuma;
Kure, Shigeo;
Takano‐Yamamoto, Teruko

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Article

Risk of Major Congenital Malformations Associated with the Use of Japanese Traditional (Kampo) Medicine Containing Ephedra During the First Trimester of Pregnancy.

Published in:

Drugs - Real World Outcomes, 2024, v. 11, n. 2, p. 263, doi. 10.1007/s40801-023-00411-0

By:

Noda, Aoi;
Obara, Taku;
Matsuzaki, Fumiko;
Suzuki, Satoko;
Arita, Ryutaro;
Ohsawa, Minoru;
Obara, Ryo;
Morishita, Kei;
Ueno, Fumihiko;
Shinoda, Genki;
Orui, Masatsugu;
Murakami, Keiko;
Ishikuro, Mami;
Kikuchi, Akiko;
Takayama, Shin;
Ishii, Tadashi;
Kawame, Hiroshi;
Kure, Shigeo;
Kuriyama, Shinichi

Publication type:

Article

Effectiveness of third vaccine dose for coronavirus disease 2019 during the Omicron variant pandemic: a prospective observational study in Japan.

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Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-17990-7

By:

Akaishi, Tetsuya;
Kushimoto, Shigeki;
Katori, Yukio;
Sugawara, Noriko;
Egusa, Hiroshi;
Igarashi, Kaoru;
Fujita, Motoo;
Kure, Shigeo;
Takayama, Shin;
Abe, Michiaki;
Kikuchi, Akiko;
Ohsawa, Minoru;
Ishizawa, Kota;
Abe, Yoshiko;
Imai, Hiroyuki;
Inaba, Yohei;
Iwamatsu-Kobayashi, Yoko;
Nishioka, Takashi;
Onodera, Ko;
Ishii, Tadashi

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Article

Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome.

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International Immunology, 2020, v. 32, n. 4, p. 283, doi. 10.1093/intimm/dxz081

By:

Niitsuma, Sou;
Kudo, Hiroki;
Kikuchi, Atsuo;
Hayashi, Takaya;
Kumakura, Satoshi;
Kobayashi, Shuhei;
Okuyama, Yuko;
Kumagai, Naonori;
Niihori, Tetsuya;
Aoki, Yoko;
So, Takanori;
Funayama, Ryo;
Nakayama, Keiko;
Shirota, Matsuyuki;
Kondo, Shuji;
Kagami, Shoji;
Tsukaguchi, Hiroyasu;
Iijima, Kazumoto;
Kure, Shigeo;
Ishii, Naoto

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Article

The open conformation of WASP regulates its nuclear localization and gene transcription in myeloid cells.

Published in:

International Immunology, 2014, v. 26, n. 6, p. 341, doi. 10.1093/intimm/dxt072

By:

Looi, Chung Yeng;
Sasahara, Yoji;
Watanabe, Yuko;
Satoh, Miki;
Hakozaki, Ikuko;
Uchiyama, Meri;
Wong, Won Fen;
Du, Wei;
Uchiyama, Toru;
Kumaki, Satoru;
Tsuchiya, Shigeru;
Kure, Shigeo

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Article

Mutation detection of GJB2 using IsoCode and real-time quantitative polymerase chain reaction with SYBR green I dye for newborn hearing screening.

Published in:

2004

By:

Kudo, Takayuki;
Oshima, Takeshi;
Kure, Shigeo;
Matsubara, Yoichi;
Ikeda, Katsuhisa

Publication type:

journal article