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Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.

Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K.

Sci Rep. 2020 Jan 14;10(1):270. doi: 10.1038/s41598-019-57149-5.


Inherited salt-losing tubulopathy: an old condition but a new category of tubulopathy.

Nozu K, Yamamura T, Horinouchi T, Nagano C, Sakakibara N, Ishikura K, Hamada R, Morisada N, Iijima K.

Pediatr Int. 2019 Dec 12. doi: 10.1111/ped.14089. [Epub ahead of print] Review.


Decreased electrodermal activity in patients with epilepsy.

Horinouchi T, Sakurai K, Munekata N, Kurita T, Takeda Y, Kusumi I.

Epilepsy Behav. 2019 Nov;100(Pt A):106517. doi: 10.1016/j.yebeh.2019.106517. Epub 2019 Sep 28.


Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay.

Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Morisada N, Ishiko S, Aoto Y, Nagase H, Takeda H, Rossanti R, Kaito H, Matsuo M, Iijima K.

Sci Rep. 2019 Sep 3;9(1):12696. doi: 10.1038/s41598-019-48990-9.


Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.

Yamamura T, Nozu K, Minamikawa S, Horinouchi T, Sakakibara N, Nagano C, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Morisada N, Kaito H, Iijima K.

Mol Genet Genomic Med. 2019 Sep;7(9):e883. doi: 10.1002/mgg3.883. Epub 2019 Jul 30.


Peripartum depression and infant care, sleep and growth.

Iwata S, Kinoshita M, Fujita F, Tsuda K, Unno M, Horinouchi T, Morokuma S, Saitoh S, Iwata O.

Sci Rep. 2019 Jul 15;9(1):10186. doi: 10.1038/s41598-019-46563-4.


Visual diagnosis in utero: Prenatal diagnosis of Treacher-Collins syndrome using a 3D/4D ultrasonography.

Kubo S, Horinouchi T, Kinoshita M, Yoshizato T, Kozuma Y, Shinagawa T, Ushijima K.

Taiwan J Obstet Gynecol. 2019 Jul;58(4):566-569. doi: 10.1016/j.tjog.2019.05.024.


Ca2+ signal is involved in endothelin-1-induced internalization of endothelin type A receptor expressed in Chinese hamster ovary cells.

Horinouchi T, Karki S, Terada K, Mazaki Y, Miwa S.

J Pharmacol Sci. 2019 May;140(1):102-105. doi: 10.1016/j.jphs.2019.03.008. Epub 2019 May 4.


Male CDPX2 patient with EBP mosaicism and asymmetrically lateralized skin lesions with strict midline demarcation.

Horinouchi T, Morisada N, Uemura H, Kobayashi D, Nozu K, Okamoto N, Iijima K.

Am J Med Genet A. 2019 Jul;179(7):1315-1318. doi: 10.1002/ajmg.a.61159. Epub 2019 Apr 29.


Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome.

Rossanti R, Shono A, Miura K, Hattori M, Yamamura T, Nakanishi K, Minamikawa S, Fujimura J, Horinouchi T, Nagano C, Sakakibara N, Kaito H, Nagase H, Morisada N, Asanuma K, Matsuo M, Nozu K, Iijima K.

J Hum Genet. 2019 Jul;64(7):673-679. doi: 10.1038/s10038-019-0606-4. Epub 2019 Apr 23.


Gestational age-related changes in shear wave speed of the uterine cervix in normal pregnancy at 12-35 weeks' gestation.

Horinouchi T, Yoshizato T, Muto M, Fujii M, Kozuma Y, Shinagawa T, Morokuma S, Kakuma T, Ushijima K.

J Perinat Med. 2019 May 27;47(4):393-401. doi: 10.1515/jpm-2018-0250.


Chinese herbal medicine Qing-Dai-induced pulmonary arterial hypertension in a patient with ulcerative colitis: A case report and experimental investigation.

Sato K, Ohira H, Horinouchi T, Nakaya T, Mazaki Y, Sugimoto A, Watanabe T, Tsujino I, Nishimura M.

Respir Med Case Rep. 2019 Feb 8;26:265-269. doi: 10.1016/j.rmcr.2019.02.007. eCollection 2019.


Endothelin type B receptor interacts with the 78-kDa glucose-regulated protein.

Mazaki Y, Higashi T, Onodera Y, Nam JM, Hashimoto A, Hashimoto S, Horinouchi T, Miwa S.

FEBS Lett. 2019 Mar;593(6):644-651. doi: 10.1002/1873-3468.13347. Epub 2019 Mar 5.


High-throughput identification of the sensitivities of an Escherichia coli ΔrecA mutant strain to various chemical compounds.

Maeda T, Horinouchi T, Sakata N, Sakai A, Furusawa C.

J Antibiot (Tokyo). 2019 Jul;72(7):566-573. doi: 10.1038/s41429-019-0160-5. Epub 2019 Feb 21.


Annexin A2 is involved in activation of extracellular signal-regulated kinase upon endothelin-1 stimulation.

Mazaki Y, Higashi T, Horinouchi T, Miwa S.

Biochem Biophys Res Commun. 2019 Mar 26;511(1):69-72. doi: 10.1016/j.bbrc.2019.02.040. Epub 2019 Feb 13.


Clinical and Genetic Characteristics in Patients With Gitelman Syndrome.

Fujimura J, Nozu K, Yamamura T, Minamikawa S, Nakanishi K, Horinouchi T, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Miyako K, Nozu Y, Morisada N, Nagase H, Ninchoji T, Kaito H, Iijima K.

Kidney Int Rep. 2018 Sep 28;4(1):119-125. doi: 10.1016/j.ekir.2018.09.015. eCollection 2019 Jan.


Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene.

Nakanishi K, Okamoto T, Nozu K, Hara S, Sato Y, Hayashi A, Takahashi T, Nagano C, Sakakibara N, Horinouchi T, Fujimura J, Minamikawa S, Yamamura T, Rossanti R, Nagase H, Kaito H, Ariga T, Iijima K.

Clin Exp Nephrol. 2019 May;23(5):669-675. doi: 10.1007/s10157-018-1682-z. Epub 2018 Dec 24.


The utility of urinary CD80 as a diagnostic marker in patients with renal diseases.

Minamikawa S, Nozu K, Maeta S, Yamamura T, Nakanishi K, Fujimura J, Horinouchi T, Nagano C, Sakakibara N, Nagase H, Shima H, Noda K, Ninchoji T, Kaito H, Iijima K.

Sci Rep. 2018 Nov 23;8(1):17322. doi: 10.1038/s41598-018-35798-2.


Seizure manifesting as a reaching/grasping movement in a patient with post-traumatic epilepsy.

Horinouchi T, Sakurai K, Kurita T, Takeda Y, Yoshida Y, Akiyama H, Fukushima K, Kusumi I.

Clin Case Rep. 2018 Oct 17;6(11):2271-2275. doi: 10.1002/ccr3.1872. eCollection 2018 Nov.


Clinical spectrum of male patients with OFD1 mutations.

Sakakibara N, Morisada N, Nozu K, Nagatani K, Ohta T, Shimizu J, Wada T, Shima Y, Yamamura T, Minamikawa S, Fujimura J, Horinouchi T, Nagano C, Shono A, Ye MJ, Nozu Y, Nakanishi K, Iijima K.

J Hum Genet. 2019 Jan;64(1):3-9. doi: 10.1038/s10038-018-0532-x. Epub 2018 Nov 6.


Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry.

Nakanishi K, Kaito H, Ogi M, Takai D, Fujimura J, Horinouchi T, Yamamura T, Minamikawa S, Ninchoji T, Nozu K, Imadome KI, Iijima K.

Case Rep Nephrol Dial. 2018 Sep 25;8(3):198-206. doi: 10.1159/000493092. eCollection 2018 Sep-Dec.


Understanding and engineering alcohol-tolerant bacteria using OMICS technology.

Horinouchi T, Maeda T, Furusawa C.

World J Microbiol Biotechnol. 2018 Oct 19;34(11):157. doi: 10.1007/s11274-018-2542-4. Review.


Raman spectral signature reflects transcriptomic features of antibiotic resistance in Escherichia coli.

Germond A, Ichimura T, Horinouchi T, Fujita H, Furusawa C, Watanabe TM.

Commun Biol. 2018 Jul 2;1:85. doi: 10.1038/s42003-018-0093-8. eCollection 2018.


Enhancement of K-strategy evolution in histidine utilization using a container with compartments.

Komori T, Shibai A, Saito H, Akeno Y, Germond A, Horinouchi T, Furusawa C, Tsuru S.

Genes Cells. 2018 Oct;23(10):893-903. doi: 10.1111/gtc.12640. Epub 2018 Sep 26.


A review of clinical characteristics and genetic backgrounds in Alport syndrome.

Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K.

Clin Exp Nephrol. 2019 Feb;23(2):158-168. doi: 10.1007/s10157-018-1629-4. Epub 2018 Aug 20. Review.


TGFBI-associated corneal dystrophy and nephropathy: a novel syndrome?

Nagano C, Nozu K, Yamamura T, Minamikawa S, Fujimura J, Sakakibara N, Nakanishi K, Horinouchi T, Iwafuchi Y, Kusuhara S, Matsumiya W, Yoshikawa N, Iijima K.

CEN Case Rep. 2019 Feb;8(1):14-17. doi: 10.1007/s13730-018-0356-8. Epub 2018 Aug 7.


Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.

Jia X, Horinouchi T, Hitomi Y, Shono A, Khor SS, Omae Y, Kojima K, Kawai Y, Nagasaki M, Kaku Y, Okamoto T, Ohwada Y, Ohta K, Okuda Y, Fujimaru R, Hatae K, Kumagai N, Sawanobori E, Nakazato H, Ohtsuka Y, Nakanishi K, Shima Y, Tanaka R, Ashida A, Kamei K, Ishikura K, Nozu K, Tokunaga K, Iijima K; Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan.

J Am Soc Nephrol. 2018 Aug;29(8):2189-2199. doi: 10.1681/ASN.2017080859. Epub 2018 Jul 16.


Approaches to suicide prevention: Ideas and models presented by Japanese and international early career psychiatrists.

Saito S, Horinouchi T, Nakagami Y, Ii T, Sarkar S, McSweeney A, Yoshida L, Aniwattanapong D, Xin LM, Segrec N, Varbanov SV, Shams SF, Suzuki K, Mariano MPV, Tomlin SC, Kuno K, Freedman R, Riba MB, Akiyama T, Kawanishi C.

Psychiatry Clin Neurosci. 2018 Sep;72(9):741. doi: 10.1111/pcn.12737. Epub 2018 Aug 6. No abstract available.


Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.

Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Omori T, Nakanishi K, Fujimura J, Ashida A, Kitamura M, Kawano M, Shimabukuro W, Kitabayashi C, Imafuku A, Tamagaki K, Kamei K, Okamoto K, Fujinaga S, Oka M, Igarashi T, Miyazono A, Sawanobori E, Fujimaru R, Nakanishi K, Shima Y, Matsuo M, Ye MJ, Nozu Y, Morisada N, Kaito H, Iijima K.

J Am Soc Nephrol. 2018 Aug;29(8):2244-2254. doi: 10.1681/ASN.2018030228. Epub 2018 Jun 29.


Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome.

Matsunoshita N, Nozu K, Yoshikane M, Kawaguchi A, Fujita N, Morisada N, Ishimori S, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Ninchoji T, Morioka I, Nagase H, Taniguchi-Ikeda M, Kaito H, Iijima K.

J Hum Genet. 2018 Jul;63(8):887-892. doi: 10.1038/s10038-018-0470-7. Epub 2018 May 30.


[Molecular mechanism for ET-1-induced insulin resistance in skeletal muscle cells].

Horinouchi T, Mazaki Y, Terada K, Miwa S.

Nihon Yakurigaku Zasshi. 2018;151(4):140-147. doi: 10.1254/fpj.151.140. Japanese.


Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease.

Minamikawa S, Nozu K, Nozu Y, Yamamura T, Taniguchi-Ikeda M, Nakanishi K, Fujimura J, Horinouchi T, Shima Y, Nakanishi K, Hattori M, Kanda K, Tanaka R, Morisada N, Nagano C, Sakakibara N, Nagase H, Morioka I, Kaito H, Iijima K.

J Hum Genet. 2018 May;63(5):589-595. doi: 10.1038/s10038-018-0415-1. Epub 2018 Feb 19.


Application of adaptive laboratory evolution to overcome a flux limitation in an Escherichia coli production strain.

Tokuyama K, Toya Y, Horinouchi T, Furusawa C, Matsuda F, Shimizu H.

Biotechnol Bioeng. 2018 Jun;115(6):1542-1551. doi: 10.1002/bit.26568. Epub 2018 Mar 8.


Toward prediction and control of antibiotic-resistance evolution.

Furusawa C, Horinouchi T, Maeda T.

Curr Opin Biotechnol. 2018 Dec;54:45-49. doi: 10.1016/j.copbio.2018.01.026. Epub 2018 Feb 14. Review.


Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases.

Nagano C, Nozu K, Morisada N, Yazawa M, Ichikawa D, Numasawa K, Kourakata H, Matsumura C, Tazoe S, Tanaka R, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Sakakibara N, Nozu Y, Ye MJ, Kaito H, Iijima K.

Clin Exp Nephrol. 2018 Aug;22(4):881-888. doi: 10.1007/s10157-018-1534-x. Epub 2018 Jan 25.


Prediction of histological chorioamnionitis and neonatal and infantile outcomes using procalcitonin in the umbilical cord blood and amniotic fluid at birth.

Horinouchi T, Yoshizato T, Kozuma Y, Shinagawa T, Muto M, Yamasaki T, Hori D, Ushijima K.

J Obstet Gynaecol Res. 2018 Apr;44(4):630-636. doi: 10.1111/jog.13573. Epub 2018 Jan 5.


An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis.

Yamamura T, Nozu K, Miyoshi Y, Nakanishi K, Fujimura J, Horinouchi T, Minamikawa S, Mori N, Fujimaru R, Nakanishi K, Ninchoji T, Kaito H, Mariko TI, Morioka I, Matsuo M, Iijima K.

BMC Nephrol. 2017 Dec 4;18(1):353. doi: 10.1186/s12882-017-0774-4.


Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits.

Tsuji Y, Nozu K, Sofue T, Hara S, Nakanishi K, Yamamura T, Minamikawa S, Nozu Y, Kaito H, Fujimura J, Horinouchi T, Morisada N, Morioka I, Taniguchi-Ikeda M, Matsuo M, Iijima K.

Nephron. 2018;138(2):166-171. doi: 10.1159/000484209. Epub 2017 Nov 3.


Cigarette Smoke Extract Inhibits Platelet Aggregation by Suppressing Cyclooxygenase Activity.

Kashiwagi H, Yuhki KI, Imamichi Y, Kojima F, Kumei S, Higashi T, Horinouchi T, Miwa S, Narumiya S, Ushikubi F.

TH Open. 2017 Oct 30;1(2):e122-e129. doi: 10.1055/s-0037-1607979. eCollection 2017 Jul.


Prediction of Cross-resistance and Collateral Sensitivity by Gene Expression profiles and Genomic Mutations.

Horinouchi T, Suzuki S, Kotani H, Tanabe K, Sakata N, Shimizu H, Furusawa C.

Sci Rep. 2017 Oct 25;7(1):14009. doi: 10.1038/s41598-017-14335-7.


ARF1 recruits RAC1 to leading edge in neutrophil chemotaxis.

Mazaki Y, Onodera Y, Higashi T, Horinouchi T, Oikawa T, Sabe H.

Cell Commun Signal. 2017 Oct 2;15(1):36. doi: 10.1186/s12964-017-0193-y.


Learning About the Management of Physical Illness During the Postgraduate Training to Become a Good Psychiatrist.

Horinouchi T, Nishida K, Nakagami Y, Nakamura I, Aoki N, Tanaka M, Suzuki M, Kuga H, Takeda M, Bhugra D, Sartorius N.

Acad Psychiatry. 2018 Feb;42(1):173-175. doi: 10.1007/s40596-017-0782-5. Epub 2017 Sep 5. No abstract available.


A comparison of splicing assays to detect an intronic variant of the OCRL gene in Lowe syndrome.

Nakanishi K, Nozu K, Hiramoto R, Minamikawa S, Yamamura T, Fujimura J, Horinouchi T, Ninchoji T, Kaito H, Morisada N, Ishimori S, Nakanishi K, Morioka I, Awano H, Matsuo M, Iijima K.

Eur J Med Genet. 2017 Dec;60(12):631-634. doi: 10.1016/j.ejmg.2017.08.001. Epub 2017 Aug 9.


Eye movement activity in normal human fetuses between 24 and 39 weeks of gestation.

Okawa H, Morokuma S, Maehara K, Arata A, Ohmura Y, Horinouchi T, Konishi Y, Kato K.

PLoS One. 2017 Jul 12;12(7):e0178722. doi: 10.1371/journal.pone.0178722. eCollection 2017.


Improvement of isopropanol tolerance of Escherichia coli using adaptive laboratory evolution and omics technologies.

Horinouchi T, Sakai A, Kotani H, Tanabe K, Furusawa C.

J Biotechnol. 2017 Aug 10;255:47-56. doi: 10.1016/j.jbiotec.2017.06.408. Epub 2017 Jun 20.


Time-programmable drug dosing allows the manipulation, suppression and reversal of antibiotic drug resistance in vitro.

Yoshida M, Reyes SG, Tsuda S, Horinouchi T, Furusawa C, Cronin L.

Nat Commun. 2017 Jun 8;8:15589. doi: 10.1038/ncomms15589.


Acceleration and suppression of resistance development by antibiotic combinations.

Suzuki S, Horinouchi T, Furusawa C.

BMC Genomics. 2017 Apr 26;18(1):328. doi: 10.1186/s12864-017-3718-2.


Dependence of nighttime sleep duration in one-month-old infants on alterations in natural and artificial photoperiod.

Iwata S, Fujita F, Kinoshita M, Unno M, Horinouchi T, Morokuma S, Iwata O.

Sci Rep. 2017 Mar 17;7:44749. doi: 10.1038/srep44749.


Diagnostic strategy for inherited hypomagnesemia.

Horinouchi T, Nozu K, Kamiyoshi N, Kamei K, Togawa H, Shima Y, Urahama Y, Yamamura T, Minamikawa S, Nakanishi K, Fujimura J, Morioka I, Ninchoji T, Kaito H, Nakanishi K, Iijima K.

Clin Exp Nephrol. 2017 Dec;21(6):1003-1010. doi: 10.1007/s10157-017-1396-7. Epub 2017 Mar 1.


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