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Items: 1 to 50 of 1540

1.

Prostate Cancer Detection with Multiparametric MRI: A Comparison of 1 M-Concentration Gadobutrol with 0.5 M-Concentration Gadolinium-Based Contrast Agents.

Hara T, Ogata T, Wada H, Yabuki T, Kanazawa S.

Curr Urol. 2018 Jun;11(4):201-205. doi: 10.1159/000447219. Epub 2018 Mar 30.

2.

Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform.

Hernandez Mora JR, Tayama C, Sánchez-Delgado M, Monteagudo-Sánchez A, Hata K, Ogata T, Medrano J, Poo-Llanillo ME, Simón C, Moran S, Esteller M, Tenorio J, Lapunzina P, Kagami M, Monk D, Nakabayashi K.

Epigenomics. 2018 Jul;10(7):941-954. doi: 10.2217/epi-2017-0172. Epub 2018 Jul 2.

PMID:
29962238
3.

Endovascular Treatment for Very Early Hepatic Artery Stenosis Following Living-Donor Liver Transplantation: Report of Two Cases.

Goto Y, Shirahama N, Sasaki S, Kawahara R, Sakai H, Ishikawa H, Hisaka T, Ogata T, Yasunaga M, Akagi Y, Tanaka H, Okuda K.

Transplant Proc. 2018 Jun;50(5):1457-1460. doi: 10.1016/j.transproceed.2018.02.074. Epub 2018 Mar 10.

PMID:
29880370
4.

Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients.

Kawashima S, Nakamura A, Inoue T, Matsubara K, Horikawa R, Wakui K, Takano K, Fukushima Y, Tatematsu T, Mizuno S, Tsubaki J, Kure S, Matsubara Y, Ogata T, Fukami M, Kagami M.

J Clin Endocrinol Metab. 2018 Jun 1;103(6):2083-2088. doi: 10.1210/jc.2017-02780.

PMID:
29878129
5.

Whole-brain low-intensity pulsed ultrasound therapy markedly improves cognitive dysfunctions in mouse models of dementia - Crucial roles of endothelial nitric oxide synthase.

Eguchi K, Shindo T, Ito K, Ogata T, Kurosawa R, Kagaya Y, Monma Y, Ichijo S, Kasukabe S, Miyata S, Yoshikawa T, Yanai K, Taki H, Kanai H, Osumi N, Shimokawa H.

Brain Stimul. 2018 May 22. pii: S1935-861X(18)30159-1. doi: 10.1016/j.brs.2018.05.012. [Epub ahead of print]

6.
7.

The Negative Survival Impact of Infectious Complications After Surgery is Canceled Out by the Response of Neoadjuvant Chemotherapy in Patients with Esophageal Cancer.

Kano K, Aoyama T, Yoshikawa T, Maezawa Y, Nakajima T, Hayashi T, Yamada T, Sato T, Oshima T, Rino Y, Masuda M, Cho H, Ogata T.

Ann Surg Oncol. 2018 Jul;25(7):2034-2043. doi: 10.1245/s10434-018-6504-8. Epub 2018 May 10.

PMID:
29748890
8.

GATA4 mutations are uncommon in patients with 46,XY disorders of sex development without heart anomaly.

Igarashi M, Mizuno K, Kon M, Narumi S, Kojima Y, Hayashi Y, Ogata T, Fukami M.

Asian J Androl. 2018 May 4. doi: 10.4103/aja.aja_20_18. [Epub ahead of print] No abstract available.

9.

Effects of glucosamine in patients with osteoarthritis of the knee: a systematic review and meta-analysis.

Ogata T, Ideno Y, Akai M, Seichi A, Hagino H, Iwaya T, Doi T, Yamada K, Chen AZ, Li Y, Hayashi K.

Clin Rheumatol. 2018 Apr 30. doi: 10.1007/s10067-018-4106-2. [Epub ahead of print]

PMID:
29713967
10.

Metagenome-based diversity analyses suggest a strong locality signal for bacterial communities associated with oyster aquaculture farms in Ofunato Bay.

Kobiyama A, Ikeo K, Reza MS, Rashid J, Yamada Y, Ikeda Y, Ikeda D, Mizusawa N, Sato S, Ogata T, Jimbo M, Kudo T, Kaga S, Watanabe S, Naiki K, Kaga Y, Mineta K, Bajic V, Gojobori T, Watabe S.

Gene. 2018 Jul 30;665:149-154. doi: 10.1016/j.gene.2018.04.073. Epub 2018 Apr 30.

PMID:
29709640
11.

Seasonal changes in the communities of photosynthetic picoeukaryotes in Ofunato Bay as revealed by shotgun metagenomic sequencing.

Rashid J, Kobiyama A, Reza MS, Yamada Y, Ikeda Y, Ikeda D, Mizusawa N, Ikeo K, Sato S, Ogata T, Kudo T, Kaga S, Watanabe S, Naiki K, Kaga Y, Mineta K, Bajic V, Gojobori T, Watabe S.

Gene. 2018 Jul 30;665:127-132. doi: 10.1016/j.gene.2018.04.071. Epub 2018 Apr 30.

PMID:
29709637
12.

Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature.

Montalbano A, Juergensen L, Fukami M, Thiel CT, Hauer NH, Roeth R, Weiss B, Naiki Y, Ogata T, Hassel D, Rappold GA.

Eur J Hum Genet. 2018 Apr 30. doi: 10.1038/s41431-018-0148-9. [Epub ahead of print]

PMID:
29706635
13.

Transplantation of periaortic adipose tissue inhibits atherosclerosis in apoE-/- mice by evoking TGF-β1-mediated anti-inflammatory response in transplanted graft.

Terada K, Yamada H, Kikai M, Wakana N, Yamamoto K, Wada N, Motoyama S, Saburi M, Sugimoto T, Irie D, Kato T, Kawahito H, Kami D, Ogata T, Matoba S.

Biochem Biophys Res Commun. 2018 Jun 18;501(1):145-151. doi: 10.1016/j.bbrc.2018.04.196. Epub 2018 May 5.

PMID:
29705699
14.

Seasonal changes in the abundance of bacterial genes related to dimethylsulfoniopropionate catabolism in seawater from Ofunato Bay revealed by metagenomic analysis.

Kudo T, Kobiyama A, Rashid J, Reza MS, Yamada Y, Ikeda Y, Ikeda D, Mizusawa N, Ikeo K, Sato S, Ogata T, Jimbo M, Kaga S, Watanabe S, Naiki K, Kaga Y, Segawa S, Mineta K, Bajic V, Gojobori T, Watabe S.

Gene. 2018 Jul 30;665:174-184. doi: 10.1016/j.gene.2018.04.072. Epub 2018 Apr 26.

PMID:
29705130
15.

Basin-scale seasonal changes in marine free-living bacterioplankton community in the Ofunato Bay.

Reza MS, Kobiyama A, Yamada Y, Ikeda Y, Ikeda D, Mizusawa N, Ikeo K, Sato S, Ogata T, Jimbo M, Kudo T, Kaga S, Watanabe S, Naiki K, Kaga Y, Mineta K, Bajic V, Gojobori T, Watabe S.

Gene. 2018 Jul 30;665:185-191. doi: 10.1016/j.gene.2018.04.074. Epub 2018 Apr 26.

PMID:
29705129
16.

Taxonomic profiles in metagenomic analyses of free-living microbial communities in the Ofunato Bay.

Reza MS, Kobiyama A, Yamada Y, Ikeda Y, Ikeda D, Mizusawa N, Ikeo K, Sato S, Ogata T, Jimbo M, Kudo T, Kaga S, Watanabe S, Naiki K, Kaga Y, Mineta K, Bajic V, Gojobori T, Watabe S.

Gene. 2018 Jul 30;665:192-200. doi: 10.1016/j.gene.2018.04.075. Epub 2018 Apr 27.

PMID:
29705124
17.

Association between the gait pattern characteristics of older people and their two-step test scores.

Kobayashi Y, Ogata T.

BMC Geriatr. 2018 Apr 27;18(1):101. doi: 10.1186/s12877-018-0784-5.

18.

Hyperprogressive Disease in the Irradiation Field after a Single Dose of Nivolumab for Gastric Cancer: A Case Report.

Ogata T, Satake H, Ogata M, Hatachi Y, Yasui H.

Case Rep Oncol. 2018 Mar 7;11(1):143-150. doi: 10.1159/000487477. eCollection 2018 Jan-Apr.

19.

Augmented neutrophil extracellular traps formation promotes atherosclerosis development in socially defeated apoE-/- mice.

Yamamoto K, Yamada H, Wakana N, Kikai M, Terada K, Wada N, Motoyama S, Saburi M, Sugimoto T, Kami D, Ogata T, Ibi M, Yabe-Nishimura C, Matoba S.

Biochem Biophys Res Commun. 2018 Jun 2;500(2):490-496. doi: 10.1016/j.bbrc.2018.04.115. Epub 2018 Apr 19.

PMID:
29673593
20.

Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations.

Kurata K, Hosono K, Hikoya A, Kato A, Saitsu H, Minoshima S, Ogata T, Hotta Y.

Jpn J Ophthalmol. 2018 Jul;62(4):458-466. doi: 10.1007/s10384-018-0591-8. Epub 2018 Apr 17.

PMID:
29666954
21.

[A Case of Unresectable Advanced Gastric Cancer Treated by Seven Courses of Chemotherapy with Docetaxel, Cisplatin, and S-1Followed by Conversion Surgery Achieved Five Year Relapse Free Survival].

Nakajima T, Cho H, Okubo Y, Kano K, Maezawa Y, Ikeda K, Yamada T, Ogata T, Yoshikawa T.

Gan To Kagaku Ryoho. 2018 Apr;45(4):755-757. Japanese.

PMID:
29650858
22.

A double-blind, randomized comparative study to investigate the morphine to hydromorphone conversion ratio in Japanese cancer patients.

Inoue S, Saito Y, Tsuneto S, Aruga E, Ogata T, Uemori M.

Jpn J Clin Oncol. 2018 May 1;48(5):442-449. doi: 10.1093/jjco/hyy046.

23.

Impact of RUNX2 gene silencing on the gemcitabine sensitivity of p53‑mutated pancreatic cancer MiaPaCa‑2 spheres.

Sang M, Nakamura M, Ogata T, Sun D, Shimozato O, Nikaido T, Ozaki T.

Oncol Rep. 2018 Jun;39(6):2749-2758. doi: 10.3892/or.2018.6344. Epub 2018 Mar 30.

PMID:
29620279
24.

Variations in mating-type-like (MTL) loci direct PCR-based tracking of Zygosaccharomyces strains formed by mating.

Ogata T, Kuroki K, Ito K, Kondo A, Nakamura K.

J Gen Appl Microbiol. 2018 Mar 31. doi: 10.2323/jgam.2017.11.001. [Epub ahead of print]

25.

STX2 is a causative gene for nonobstructive azoospermia.

Nakamura S, Kobori Y, Ueda Y, Tanaka Y, Ishikawa H, Yoshida A, Katsumi M, Saito K, Nakamura A, Ogata T, Okada H, Nakai H, Miyado M, Fukami M.

Hum Mutat. 2018 Jun;39(6):830-833. doi: 10.1002/humu.23423. Epub 2018 Apr 10.

PMID:
29570232
26.

Multiple Thrombi in the Heart in Trousseau Syndrome Caused by Pancreatic Carcinoma.

Takeshita S, Ogata T, Mera H, Tsugawa J, Aoki M, Takeshita M, Tsuboi Y.

J Stroke Cerebrovasc Dis. 2018 May;27(5):e75-e77. doi: 10.1016/j.jstrokecerebrovasdis.2017.12.005. Epub 2018 Mar 2.

PMID:
29503168
27.

Adrenergic receptor-mediated activation of FGF-21-adiponectin axis exerts atheroprotective effects in brown adipose tissue-transplanted apoE-/- mice.

Kikai M, Yamada H, Wakana N, Terada K, Yamamoto K, Wada N, Motoyama S, Saburi M, Sugimoto T, Irie D, Kato T, Kawahito H, Ogata T, Matoba S.

Biochem Biophys Res Commun. 2018 Mar 18;497(4):1097-1103. doi: 10.1016/j.bbrc.2018.02.185. Epub 2018 Feb 26.

PMID:
29496444
28.

Effects of goal-directed fluid therapy on enhanced postoperative recovery: An interventional comparative observational study with a historical control group on oesophagectomy combined with ERAS program.

Taniguchi H, Sasaki T, Fujita H, Kobayashi H, Kawasaki R, Ogata T, Cho H, Yoshikawa T, Ushigome K, Tanaka A, Takano O.

Clin Nutr ESPEN. 2018 Feb;23:184-193. doi: 10.1016/j.clnesp.2017.10.002. Epub 2017 Nov 7.

29.

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

Nakamura A, Muroya K, Ogata-Kawata H, Nakabayashi K, Matsubara K, Ogata T, Kurosawa K, Fukami M, Kagami M.

J Med Genet. 2018 Feb 17. pii: jmedgenet-2017-104986. doi: 10.1136/jmedgenet-2017-104986. [Epub ahead of print]

PMID:
29455159
30.

Repercussions of the Great East Japan Earthquake tsunami on ellipsoidal Alexandrium cysts (Dinophyceae) in Ofunato Bay, Japan.

Matsuoka K, Ikeda Y, Kaga S, Kaga Y, Ogata T.

Mar Environ Res. 2018 Apr;135:123-135. doi: 10.1016/j.marenvres.2018.01.001. Epub 2018 Jan 4.

PMID:
29449069
31.

Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene.

Ono H, Saitsu H, Horikawa R, Nakashima S, Ohkubo Y, Yanagi K, Nakabayashi K, Fukami M, Fujisawa Y, Ogata T.

Sci Rep. 2018 Feb 2;8(1):2287. doi: 10.1038/s41598-018-20691-9.

32.

Safety and Feasibility of Carotid Artery Stenting with Dual-Echo Technique to Minimize Iodinated Contrast Dose.

Okawa M, Higashi T, Fukuda K, Ogata T, Yoshioka T, Inoue T.

J Stroke Cerebrovasc Dis. 2018 Apr;27(4):825-830. doi: 10.1016/j.jstrokecerebrovasdis.2017.08.030. Epub 2018 Feb 1.

PMID:
29395639
33.

[A Long-Term Survivor Who Are Responding to Sunitinib Treatment for Recurrent Imatinib-Resistant Gastrointestinal Stromal Tumor(GIST)of the Stomach].

Kano K, Cho H, Maezawa Y, Aoyama T, Hayashi T, Yamada T, Sato T, Oshima T, Yukawa N, Rino Y, Masuda M, Ogata T, Yoshikawa T.

Gan To Kagaku Ryoho. 2017 Nov;44(12):1898-1900. Japanese.

PMID:
29394813
34.

Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature Review.

Takasawa K, Igarashi M, Ono M, Takemoto A, Takada S, Yamataka A, Ogata T, Morio T, Fukami M, Kashimada K.

Sex Dev. 2017;11(5-6):284-288. doi: 10.1159/000485868. Epub 2018 Jan 24.

PMID:
29393271
35.

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

Sano S, Nakamura A, Matsubara K, Nagasaki K, Fukami M, Kagami M, Ogata T.

J Endocr Soc. 2017 Nov 21;2(1):9-23. doi: 10.1210/js.2017-00293. eCollection 2018 Jan 1.

36.

Mosaic upd(14)pat in a patient with mild features of Kagami-Ogata syndrome.

Haug MG, Brendehaug A, Houge G, Kagami M, Ogata T.

Clin Case Rep. 2017 Nov 28;6(1):91-95. doi: 10.1002/ccr3.1300. eCollection 2018 Jan.

37.

Age independency of mobility decrease assessed using the Locomotive Syndrome Risk Test in elderly with disability: a cross-sectional study.

Yamada K, Muranaga S, Shinozaki T, Nakamura K, Tanaka S, Ogata T.

BMC Geriatr. 2018 Jan 26;18(1):28. doi: 10.1186/s12877-017-0698-7.

38.

NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy.

Ishiyama A, Muramatsu K, Uchino S, Sakai C, Matsushima Y, Makioka N, Ogata T, Suzuki E, Komaki H, Sasaki M, Mimaki M, Goto YI, Nishino I.

Clin Genet. 2018 May;93(5):1103-1106. doi: 10.1111/cge.13215. Epub 2018 Feb 11.

PMID:
29344937
39.

Biofeedback effect of hybrid assistive limb in stroke rehabilitation: A proof of concept study using functional near infrared spectroscopy.

Saita K, Morishita T, Arima H, Hyakutake K, Ogata T, Yagi K, Shiota E, Inoue T.

PLoS One. 2018 Jan 16;13(1):e0191361. doi: 10.1371/journal.pone.0191361. eCollection 2018.

40.

Effects of Treadmill Training Combined with Serotonergic Interventions on Spasticity after Contusive Spinal Cord Injury.

Ryu Y, Ogata T, Nagao M, Sawada Y, Nishimura R, Fujita N.

J Neurotrauma. 2018 Jun 15;35(12):1358-1366. doi: 10.1089/neu.2017.5400. Epub 2018 Apr 5.

PMID:
29336209
41.

De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism.

Hiraide T, Nakashima M, Yamoto K, Fukuda T, Kato M, Ikeda H, Sugie Y, Aoto K, Kaname T, Nakabayashi K, Ogata T, Matsumoto N, Saitsu H.

Hum Genet. 2018 Jan;137(1):95-104. doi: 10.1007/s00439-017-1863-y. Epub 2018 Jan 10.

PMID:
29322246
42.

Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D, a Gene Associated with Kabuki Syndrome: A Case Report.

Sakata S, Okada S, Aoyama K, Hara K, Tani C, Kagawa R, Utsunomiya-Nakamura A, Miyagawa S, Ogata T, Mizuno H, Kobayashi M.

Front Genet. 2017 Dec 11;8:210. doi: 10.3389/fgene.2017.00210. eCollection 2017.

43.

A de novo 50-bp GNAS Intragenic Duplication in a Patient with Pseudohypoparathyroidism Type 1a.

Suzuki E, Bo R, Sue K, Awano H, Ogata T, Narumi S, Kagami M, Sano S, Fukami M.

Cytogenet Genome Res. 2017;153(3):125-130. doi: 10.1159/000485644. Epub 2018 Jan 11.

PMID:
29320763
44.

Representation Learning of Logic Words by an RNN: From Word Sequences to Robot Actions.

Yamada T, Murata S, Arie H, Ogata T.

Front Neurorobot. 2017 Dec 22;11:70. doi: 10.3389/fnbot.2017.00070. eCollection 2017.

45.

Longitudinal serum and urine steroid metabolite profiling in a 46,XY infant with prenatally identified POR deficiency.

Ono H, Numakura C, Homma K, Hasegawa T, Tsutsumi S, Kato F, Fujisawa Y, Fukami M, Ogata T.

J Steroid Biochem Mol Biol. 2018 Apr;178:177-184. doi: 10.1016/j.jsbmb.2017.12.008. Epub 2017 Dec 28.

PMID:
29289577
46.

Does cerebral large-artery disease contribute to cognitive impairment?

Kimura S, Ogata T, Watanabe J, Inoue T, Tsuboi Y.

eNeurologicalSci. 2017 Jun 13;8:5-8. doi: 10.1016/j.ensci.2017.06.003. eCollection 2017 Sep.

47.

Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes.

Okuno M, Ayabe T, Yokota I, Musha I, Shiga K, Kikuchi T, Kikuchi N, Ohtake A, Nakamura A, Nakabayashi K, Okamura K, Momozawa Y, Kubo M, Suzuki J, Urakami T, Kawamura T, Amemiya S, Ogata T, Sugihara S, Fukami M; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes.

Diabet Med. 2018 Mar;35(3):376-380. doi: 10.1111/dme.13566. Epub 2018 Jan 3.

PMID:
29247561
48.

Cardiac-Specific Bdh1 Overexpression Ameliorates Oxidative Stress and Cardiac Remodeling in Pressure Overload-Induced Heart Failure.

Uchihashi M, Hoshino A, Okawa Y, Ariyoshi M, Kaimoto S, Tateishi S, Ono K, Yamanaka R, Hato D, Fushimura Y, Honda S, Fukai K, Higuchi Y, Ogata T, Iwai-Kanai E, Matoba S.

Circ Heart Fail. 2017 Dec;10(12). pii: e004417. doi: 10.1161/CIRCHEARTFAILURE.117.004417.

PMID:
29242353
49.

Prediction of postoperative inflammatory complications after esophageal cancer surgery based on early changes in the C-reactive protein level in patients who received perioperative steroid therapy and enhanced recovery after surgery care: a retrospective analysis.

Kano K, Aoyama T, Nakajima T, Maezawa Y, Hayashi T, Yamada T, Sato T, Oshima T, Rino Y, Masuda M, Cho H, Yoshikawa T, Ogata T.

BMC Cancer. 2017 Dec 4;17(1):812. doi: 10.1186/s12885-017-3831-2.

50.

Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations.

Shima H, Koehler K, Nomura Y, Sugimoto K, Satoh A, Ogata T, Fukami M, Jühlen R, Schuelke M, Mohnike K, Huebner A, Narumi S.

J Med Genet. 2018 Feb;55(2):81-85. doi: 10.1136/jmedgenet-2017-105020. Epub 2017 Nov 24.

PMID:
29175836

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