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Items: 1 to 50 of 452


Amplicon Sequencing-Based Noninvasive Fetal Genotyping for RHD-Positive D Antigen-Negative Alleles.

Takahashi K, Migita O, Sasaki A, Nasu M, Kawashima A, Sekizawa A, Sato T, Ito Y, Sago H, Okamoto A, Nakabayashi K, Hata K.

Clin Chem. 2019 Oct;65(10):1307-1316. doi: 10.1373/clinchem.2019.307074. Epub 2019 Sep 5.


Genome-wide single nucleotide polymorphism array analysis unveils the origin of heterozygous androgenetic complete moles.

Usui H, Nakabayashi K, Maehara K, Hata K, Shozu M.

Sci Rep. 2019 Aug 29;9(1):12542. doi: 10.1038/s41598-019-49047-7.


Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2.

Yamaguchi Y, Tayama C, Tomikawa J, Akaishi R, Kamura H, Matsuoka K, Wake N, Minakami H, Kato K, Yamada T, Nakabayashi K, Hata K.

Clin Epigenetics. 2019 Aug 1;11(1):113. doi: 10.1186/s13148-019-0712-3.


Acute promyelocytic leukemia with a cryptic insertion of RARA into TBL1XR1.

Osumi T, Watanabe A, Okamura K, Nakabayashi K, Yoshida M, Tsujimoto SI, Uchiyama M, Takahashi H, Tomizawa D, Hata K, Kiyokawa N, Kato M.

Genes Chromosomes Cancer. 2019 Nov;58(11):820-823. doi: 10.1002/gcc.22791. Epub 2019 Aug 10.


DNA methylation changes involved in the tumor increase in F2 males born to gestationally arsenite-exposed F1 male mice.

Okamura K, Nakabayashi K, Kawai T, Suzuki T, Sano T, Hata K, Nohara K.

Cancer Sci. 2019 Aug;110(8):2629-2642. doi: 10.1111/cas.14104. Epub 2019 Jul 25.


Clonal Expansion of Second-Hit Cells with Somatic Recombinations or C>T Transitions Form Porokeratosis in MVD or MVK Mutant Heterozygotes.

Kubo A, Sasaki T, Suzuki H, Shiohama A, Aoki S, Sato S, Fujita H, Ono N, Umegaki-Arao N, Kawai T, Nakabayashi K, Hata K, Yamada D, Matsubara Y, Kosaki K, Amagai M.

J Invest Dermatol. 2019 Jun 15. pii: S0022-202X(19)31762-2. doi: 10.1016/j.jid.2019.05.020. [Epub ahead of print]


Photoluminescent Lanthanide(III) Single-Molecule Magnets in Three-Dimensional Polycyanidocuprate(I)-Based Frameworks.

Zakrzewski JJ, Chorazy S, Nakabayashi K, Ohkoshi SI, Sieklucka B.

Chemistry. 2019 Sep 12;25(51):11820-11825. doi: 10.1002/chem.201902420. Epub 2019 Jul 11.


Combined Use of Excimer Laser and High-Speed Rotational Atherectomy to Overcome a Severely Calcified Lesion in Endovascular Therapy.

Nakabayashi K, Hata S, Kaneko N, Matsui A, Tanaka K, Ando H, Shimizu M.

Case Rep Vasc Med. 2019 Apr 16;2019:1719035. doi: 10.1155/2019/1719035. eCollection 2019.


A novel KMT2A-ACTN2 fusion in infant B-cell acute lymphoblastic leukemia.

Yoshida M, Nakabayashi K, Ogata-Kawata H, Osumi T, Tsujimoto SI, Shirai R, Yoshida K, Okamura K, Matsumoto K, Kiyokawa N, Tomizawa D, Hata K, Kato M.

Pediatr Blood Cancer. 2019 Aug;66(8):e27821. doi: 10.1002/pbc.27821. Epub 2019 May 21. No abstract available.


Donor-Acceptor Core-Shell Nanoparticles and Their Application in Non-Volatile Transistor Memory Devices.

Lo CT, Watanabe Y, Murakami D, Shih CC, Nakabayashi K, Mori H, Chen WC.

Macromol Rapid Commun. 2019 Jun;40(12):e1900115. doi: 10.1002/marc.201900115. Epub 2019 Apr 25.


In Situ Ligand Transformation for Two-Step Spin Crossover in FeII[MIV(CN)8]4- (M = Mo, Nb) Cyanido-Bridged Frameworks.

Kawabata S, Chorazy S, Zakrzewski JJ, Imoto K, Fujimoto T, Nakabayashi K, Stanek J, Sieklucka B, Ohkoshi SI.

Inorg Chem. 2019 May 6;58(9):6052-6063. doi: 10.1021/acs.inorgchem.9b00361. Epub 2019 Apr 19.


Effect of Noble Metals on Luminescence and Single-Molecule Magnet Behavior in the Cyanido-Bridged Ln-Ag and Ln-Au (Ln = Dy, Yb, Er) Complexes.

Kumar K, Stefańczyk O, Chorazy S, Nakabayashi K, Sieklucka B, Ohkoshi SI.

Inorg Chem. 2019 May 6;58(9):5677-5687. doi: 10.1021/acs.inorgchem.8b03634. Epub 2019 Apr 18.


Germline-Derived Gain-of-Function Variants of Gsα-Coding GNAS Gene Identified in Nephrogenic Syndrome of Inappropriate Antidiuresis.

Miyado M, Fukami M, Takada S, Terao M, Nakabayashi K, Hata K, Matsubara Y, Tanaka Y, Sasaki G, Nagasaki K, Shiina M, Ogata K, Masunaga Y, Saitsu H, Ogata T.

J Am Soc Nephrol. 2019 May;30(5):877-889. doi: 10.1681/ASN.2018121268. Epub 2019 Apr 8.


Synthesis and Optoelectronic Properties of Block and Random Copolymers Containing Pendant Carbazole and (Di)phenylanthracene.

Lo CT, Abiko Y, Kosai J, Watanabe Y, Nakabayashi K, Mori H.

Polymers (Basel). 2018 Jul 1;10(7). pii: E721. doi: 10.3390/polym10070721.


The desmosome is a mesoscale lipid raft-like membrane domain.

Lewis JD, Caldara AL, Zimmer SE, Stahley SN, Seybold A, Strong NL, Frangakis AS, Levental I, Wahl JK 3rd, Mattheyses AL, Sasaki T, Nakabayashi K, Hata K, Matsubara Y, Ishida-Yamamoto A, Amagai M, Kubo A, Kowalczyk AP.

Mol Biol Cell. 2019 Jun 1;30(12):1390-1405. doi: 10.1091/mbc.E18-10-0649. Epub 2019 Apr 3.


Whole transcriptome sequencing reveals a KMT2A-USP2 fusion in infant acute myeloid leukemia.

Ikeda J, Shiba N, Tsujimoto SI, Yoshida M, Nakabayashi K, Ogata-Kawata H, Okamura K, Takeuchi M, Osumi T, Tomizawa D, Hata K, Kiyokawa N, Ito S, Kato M.

Genes Chromosomes Cancer. 2019 Sep;58(9):669-672. doi: 10.1002/gcc.22751. Epub 2019 Apr 8.


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 M, Yanagisawa A, Ota M, Matsuoka K, Nakamura A, Matsubara K, Nakabayashi K, Takada S, Fukami M, Ogata T.

Clin Epigenetics. 2019 Mar 7;11(1):42. doi: 10.1186/s13148-019-0640-2.


Synthesis, Assembled Structures, and DNA Complexation of Thermoresponsive Lysine-Based Zwitterionic and Cationic Block Copolymers.

Kanto R, Qiao Y, Masuko K, Furusawa H, Yano S, Nakabayashi K, Mori H.

Langmuir. 2019 Apr 2;35(13):4646-4659. doi: 10.1021/acs.langmuir.8b04303. Epub 2019 Mar 19.


Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.

Matsubara K, Itoh M, Shimizu K, Saito S, Enomoto K, Nakabayashi K, Hata K, Kurosawa K, Ogata T, Fukami M, Kagami M.

Clin Epigenetics. 2019 Feb 28;11(1):36. doi: 10.1186/s13148-019-0633-1.


Epitope recognized by anti-glomerular basement membrane (GBM) antibody in a patient with repeated relapse of anti-GBM disease.

Nishibata Y, Masuda S, Nakazawa D, Tanaka S, Tomaru U, Nergui M, Jia X, Cui Z, Zhao MH, Nakabayashi K, Ishizu A.

Exp Mol Pathol. 2019 Apr;107:165-170. doi: 10.1016/j.yexmp.2019.02.005. Epub 2019 Feb 25.


Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures.

Nakashima M, Tohyama J, Nakagawa E, Watanabe Y, Siew CG, Kwong CS, Yamoto K, Hiraide T, Fukuda T, Kaname T, Nakabayashi K, Hata K, Ogata T, Saitsu H, Matsumoto N.

J Hum Genet. 2019 Apr;64(4):313-322. doi: 10.1038/s10038-018-0559-z. Epub 2019 Jan 17.


The Wire Rendezvous and Chasing Wire Technique in the Bidirectional Approach for the Percutaneous Coronary Intervention for Chronic Total Occlusion with a Single Guiding Catheter.

Nakabayashi K, Sunaga D, Kaneko N, Matsui A, Tanaka K, Ando H, Shimizu M.

Case Rep Cardiol. 2018 Oct 30;2018:7162949. doi: 10.1155/2018/7162949. eCollection 2018.


Variations in the eicosapentaenoic acid-arachidonic acid ratio associated with age in acute myocardial infarction patients undergoing primary percutaneous coronary intervention.

Nakabayashi K, Jujo K, Furuki Y, Ishida I, Ando H, Shimizu M, Hagiwara N, Saito K.

Heart Vessels. 2019 May;34(5):755-762. doi: 10.1007/s00380-018-1302-6. Epub 2018 Nov 14.


Simple percutaneous coronary interventions using the modification of complex coronary lesion with excimer laser.

Nakabayashi K, Sunaga D, Kaneko N, Matsui A, Tanaka K, Ando H, Shimizu M.

Cardiovasc Revasc Med. 2019 Apr;20(4):293-302. doi: 10.1016/j.carrev.2018.10.022. Epub 2018 Oct 26. Review.


Dehydration-Triggered Charge Transfer and High Proton Conductivity in (H3O)[NiIII(cyclam)][MII(CN)6] (M = Ru, Os) Cyanide-Bridged Chains.

Reczyński M, Nowicka B, Näther C, Kozieł M, Nakabayashi K, Ohkoshi SI, Sieklucka B.

Inorg Chem. 2018 Nov 5;57(21):13415-13422. doi: 10.1021/acs.inorgchem.8b01992. Epub 2018 Oct 19.


Novel SIN3A mutation identified in a Japanese patient with Witteveen-Kolk syndrome.

Narumi-Kishimoto Y, Araki N, Migita O, Kawai T, Okamura K, Nakabayashi K, Kaname T, Ozawa Y, Ozawa H, Takada F, Hata K.

Eur J Med Genet. 2019 Sep;62(9):103547. doi: 10.1016/j.ejmg.2018.09.014. Epub 2018 Sep 26. No abstract available.


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 T, Yagasaki H, Nishioka J, Nakamura A, Matsubara K, Narumi S, Nakabayashi K, Yamazawa K, Fuke T, Oka A, Ogata T, Fukami M, Kagami M.

J Med Genet. 2019 Jun;56(6):413-418. doi: 10.1136/jmedgenet-2018-105463. Epub 2018 Sep 21.


Reciprocal changes of H3K27ac and H3K27me3 at the promoter regions of the critical genes for endometrial decidualization.

Katoh N, Kuroda K, Tomikawa J, Ogata-Kawata H, Ozaki R, Ochiai A, Kitade M, Takeda S, Nakabayashi K, Hata K.

Epigenomics. 2018 Sep;10(9):1243-1257. doi: 10.2217/epi-2018-0006. Epub 2018 Sep 13.


Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion.

Ohki K, Kiyokawa N, Saito Y, Hirabayashi S, Nakabayashi K, Ichikawa H, Momozawa Y, Okamura K, Yoshimi A, Ogata-Kawata H, Sakamoto H, Kato M, Fukushima K, Hasegawa D, Fukushima H, Imai M, Kajiwara R, Koike T, Komori I, Matsui A, Mori M, Moriwaki K, Noguchi Y, Park MJ, Ueda T, Yamamoto S, Matsuda K, Yoshida T, Matsumoto K, Hata K, Kubo M, Matsubara Y, Takahashi H, Fukushima T, Hayashi Y, Koh K, Manabe A, Ohara A; Tokyo Children’s Cancer Study Group (TCCSG).

Haematologica. 2019 Jan;104(1):128-137. doi: 10.3324/haematol.2017.186320. Epub 2018 Aug 31.


Congenital nail clubbing.

Nakazawa S, Niizeki H, Nakabayashi K, Tanese K, Tokura Y.

J Dermatol. 2019 Mar;46(3):e101-e102. doi: 10.1111/1346-8138.14614. Epub 2018 Aug 27. No abstract available.


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.


Recurrent RARB Translocations in Acute Promyelocytic Leukemia Lacking RARA Translocation.

Osumi T, Tsujimoto SI, Tamura M, Uchiyama M, Nakabayashi K, Okamura K, Yoshida M, Tomizawa D, Watanabe A, Takahashi H, Hori T, Yamamoto S, Hamamoto K, Migita M, Ogata-Kawata H, Uchiyama T, Kizawa H, Ueno-Yokohata H, Shirai R, Seki M, Ohki K, Takita J, Inukai T, Ogawa S, Kitamura T, Matsumoto K, Hata K, Kiyokawa N, Goyama S, Kato M.

Cancer Res. 2018 Aug 15;78(16):4452-4458. doi: 10.1158/0008-5472.CAN-18-0840. Epub 2018 Jun 19.


Elucidation of the developmental mechanism of ovarian mature cystic teratomas using B allele-frequency plots of single nucleotide polymorphism array data.

Usui H, Nakabayashi K, Kaku H, Maehara K, Hata K, Shozu M.

Genes Chromosomes Cancer. 2018 Aug;57(8):409-419. doi: 10.1002/gcc.1.


The DNA methylation profile of liver tumors in C3H mice and identification of differentially methylated regions involved in the regulation of tumorigenic genes.

Matsushita J, Okamura K, Nakabayashi K, Suzuki T, Horibe Y, Kawai T, Sakurai T, Yamashita S, Higami Y, Ichihara G, Hata K, Nohara K.

BMC Cancer. 2018 Mar 22;18(1):317. doi: 10.1186/s12885-018-4221-0.


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 Aug;55(8):567-570. doi: 10.1136/jmedgenet-2017-104986. Epub 2018 Feb 17.


Identification of G-quadruplex clusters by high-throughput sequencing of whole-genome amplified products with a G-quadruplex ligand.

Yoshida W, Saikyo H, Nakabayashi K, Yoshioka H, Bay DH, Iida K, Kawai T, Hata K, Ikebukuro K, Nagasawa K, Karube I.

Sci Rep. 2018 Feb 15;8(1):3116. doi: 10.1038/s41598-018-21514-7.


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.


The 0.035-Inch Wire Externalization Technique for Overcoming a Severely Angled and Calcified Aortic Bifurcation.

Nakabayashi K, Kaneko N, Ando H, Shimizu M.

JACC Cardiovasc Interv. 2018 May 14;11(9):e75-e76. doi: 10.1016/j.jcin.2017.11.011. Epub 2018 Jan 17. No abstract available.


Somatic MECOM mosaicism in a patient with congenital bone marrow failure without a radial abnormality.

Osumi T, Tsujimoto SI, Nakabayashi K, Taniguchi M, Shirai R, Yoshida M, Uchiyama T, Nagasawa J, Goyama S, Yoshioka T, Tomizawa D, Kurokawa M, Matsubara Y, Kiyokawa N, Matsumoto K, Hata K, Kato M.

Pediatr Blood Cancer. 2018 Jun;65(6):e26959. doi: 10.1002/pbc.26959. Epub 2018 Jan 22. No abstract available.


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.


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.


Acid-Responsive Conductive Nanofiber of Tetrabenzoporphyrin Made by Solution Processing.

Zhen Y, Inoue K, Wang Z, Kusamoto T, Nakabayashi K, Ohkoshi SI, Hu W, Guo Y, Harano K, Nakamura E.

J Am Chem Soc. 2018 Jan 10;140(1):62-65. doi: 10.1021/jacs.7b10575. Epub 2017 Dec 13.


Ionic Conductivity and Assembled Structures of Imidazolium Salt-Based Block Copolymers with Thermoresponsive Segments.

Nakabayashi K, Sato Y, Isawa Y, Lo CT, Mori H.

Polymers (Basel). 2017 Nov 15;9(11). pii: E616. doi: 10.3390/polym9110616.


Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum.

Nakamura Y, Togawa Y, Okuno Y, Muramatsu H, Nakabayashi K, Kuroki Y, Ieda D, Hori I, Negishi Y, Togawa T, Hattori A, Kojima S, Saitoh S.

Brain Dev. 2018 Feb;40(2):134-139. doi: 10.1016/j.braindev.2017.08.003. Epub 2017 Oct 12.


CTCF deletion syndrome: clinical features and epigenetic delineation.

Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S.

J Med Genet. 2017 Dec;54(12):836-842. doi: 10.1136/jmedgenet-2017-104854. Epub 2017 Aug 28.


Successful Catheter Ablation as a Substitute for Cardiac Resynchronization Therapy in Patient with an Accessory Pathway-induced Cardiomyopathy.

Nakabayashi K, Sugiura R, Mizuno Y, Kato H, Nakazawa N, Suzuki T, Saito H, Kawakatsu N, Goto M, Isomura D, Okada H, Oka T.

Intern Med. 2017 Aug 15;56(16):2165-2169. doi: 10.2169/internalmedicine.8205-16. Epub 2017 Aug 1.


Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature.

Hattori A, Katoh-Fukui Y, Nakamura A, Matsubara K, Kamimaki T, Tanaka H, Dateki S, Adachi M, Muroya K, Yoshida S, Ida S, Mitani M, Nagasaki K, Ogata T, Suzuki E, Hata K, Nakabayashi K, Matsubara Y, Narumi S, Tanaka T, Fukami M.

Endocr J. 2017 Oct 28;64(10):947-954. doi: 10.1507/endocrj.EJ17-0150. Epub 2017 Aug 3.


Molecular characteristics of the KCNJ5 mutated aldosterone-producing adenomas.

Murakami M, Yoshimoto T, Nakabayashi K, Nakano Y, Fukaishi T, Tsuchiya K, Minami I, Bouchi R, Okamura K, Fujii Y, Hashimoto K, Hata KI, Kihara K, Ogawa Y.

Endocr Relat Cancer. 2017 Oct;24(10):531-541. doi: 10.1530/ERC-17-0117. Epub 2017 Jul 26.


Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.

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

Andrology. 2017 Jul;5(4):824-831. doi: 10.1111/andr.12378.

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