Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 430

1.

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 Jan 17. doi: 10.1038/s10038-018-0559-z. [Epub ahead of print]

PMID:
30655572
2.

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.

3.

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. 2018 Nov 14. doi: 10.1007/s00380-018-1302-6. [Epub ahead of print]

PMID:
30430295
4.

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. 2018 Oct 26. pii: S1553-8389(18)30462-7. doi: 10.1016/j.carrev.2018.10.022. [Epub ahead of print] Review.

PMID:
30413345
5.

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.

PMID:
30338994
6.

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. 2018 Sep 26. pii: S1769-7212(18)30312-4. doi: 10.1016/j.ejmg.2018.09.014. [Epub ahead of print] No abstract available.

7.

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. 2018 Sep 21. pii: jmedgenet-2018-105463. doi: 10.1136/jmedgenet-2018-105463. [Epub ahead of print]

8.

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.

PMID:
30212243
9.

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.

10.

Congenital nail clubbing.

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

J Dermatol. 2018 Aug 27. doi: 10.1111/1346-8138.14614. [Epub ahead of print] No abstract available.

PMID:
30151908
11.

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
12.

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.

PMID:
29921692
13.

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.

PMID:
29700881
14.

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.

15.

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.

PMID:
29455159
16.

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.

18.

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.

19.

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.

PMID:
29361443
20.

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.

PMID:
29356389
21.

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
22.

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
23.

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.

PMID:
29205033
24.

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.

PMID:
28893434
25.

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.

PMID:
28848059
26.

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.

27.

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.

28.

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.

PMID:
28747387
29.

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.

30.

External revascularisation for pseudochronic total occlusion of the dorsal pedis artery due to foot drop with severe diabetes mellitus.

Nakabayashi K, Matsui A, Ando H, Shimizu M.

BMJ Case Rep. 2017 Jul 14;2017. pii: bcr-2017-220633. doi: 10.1136/bcr-2017-220633. No abstract available.

PMID:
28710243
31.

DELAY OF GERMINATION1 requires PP2C phosphatases of the ABA signalling pathway to control seed dormancy.

Née G, Kramer K, Nakabayashi K, Yuan B, Xiang Y, Miatton E, Finkemeier I, Soppe WJJ.

Nat Commun. 2017 Jul 13;8(1):72. doi: 10.1038/s41467-017-00113-6.

32.

An Alpha-kinase 2 Gene Variant Disrupts Filamentous Actin Localization in the Surface Cells of Colorectal Cancer Spheroids.

Nishi K, Luo H, Nakabayashi K, Doi K, Ishikura S, Iwaihara Y, Yoshida Y, Tanisawa K, Arai T, Mori S, Sawabe M, Muramatsu M, Tanaka M, Sakata T, Shirasawa S, Tsunoda T.

Anticancer Res. 2017 Jul;37(7):3855-3862.

33.

Evaluation of the association between sleep apnea and polyunsaturated fatty acids profiles in patients after percutaneous coronary intervention.

Nakabayashi K, Jujo K, Saito K, Oka T, Hagiwara N.

Heart Vessels. 2017 Nov;32(11):1296-1303. doi: 10.1007/s00380-017-1010-7. Epub 2017 Jun 19.

PMID:
28631078
34.

Comprehensive screening for monogenic diabetes in 89 Japanese children with insulin-requiring antibody-negative type 1 diabetes.

Ushijima K, Fukami M, Ayabe T, Narumi S, Okuno M, Nakamura A, Takahashi T, Ihara K, Ohkubo K, Tachikawa E, Nakayama S, Arai J, Kikuchi N, Kikuchi T, Kawamura T, Urakami T, Hata K, Nakabayashi K, Matsubara Y, Amemiya S, Ogata T, Yokota I, Sugihara S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes.

Pediatr Diabetes. 2018 Mar;19(2):243-250. doi: 10.1111/pedi.12544. Epub 2017 Jun 9.

PMID:
28597946
35.

Salvage of fetal karyotype information from SNP array data obtained from products of conception with maternal cell contamination.

Sasaki K, Abe K, Mori T, Hashimoto K, Nakabayashi K.

Prenat Diagn. 2017 Aug;37(8):781-787. doi: 10.1002/pd.5082. Epub 2017 Jul 19.

PMID:
28591488
36.

Utility of a 0.035″ compatible rapid-exchange balloon (Metacross RX™) as a perfusion balloon in endovascular therapy compared with conventional percutaneous coronary intervention: A mini-review.

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

Cardiovasc Revasc Med. 2017 Dec;18(8):619-622. doi: 10.1016/j.carrev.2017.05.016. Epub 2017 May 18. Review.

PMID:
28551422
37.

A novel lesion crossing technique: Balloon deployment using FORcible Manner (BADFORM) technique.

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

Catheter Cardiovasc Interv. 2017 Dec 1;90(7):1161-1165. doi: 10.1002/ccd.27119. Epub 2017 May 4.

PMID:
28471016
38.

Fine Tuning of Multicolored Photoluminescence in Crystalline Magnetic Materials Constructed of Trimetallic EuxTb1-x[Co(CN)6] Cyanido-Bridged Chains.

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

Inorg Chem. 2017 May 1;56(9):5239-5252. doi: 10.1021/acs.inorgchem.7b00369. Epub 2017 Apr 18.

PMID:
28418260
39.

GNG11 (G-protein subunit γ 11) suppresses cell growth with induction of reactive oxygen species and abnormal nuclear morphology in human SUSM-1 cells.

Takauji Y, Kudo I, En A, Matsuo R, Hossain MN, Nakabayashi K, Miki K, Fujii M, Ayusawa D.

Biochem Cell Biol. 2017 Aug;95(4):517-523. doi: 10.1139/bcb-2016-0248. Epub 2017 Apr 5.

PMID:
28380310
40.

Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty.

Fukami M, Suzuki E, Izumi Y, Torii T, Narumi S, Igarashi M, Miyado M, Katsumi M, Fujisawa Y, Nakabayashi K, Hata K, Umezawa A, Matsubara Y, Yamauchi J, Ogata T.

J Cell Mol Med. 2017 Oct;21(10):2623-2626. doi: 10.1111/jcmm.13146. Epub 2017 Mar 24.

41.

Antifibrotic effect of pirfenidone in a mouse model of human nonalcoholic steatohepatitis.

Komiya C, Tanaka M, Tsuchiya K, Shimazu N, Mori K, Furuke S, Miyachi Y, Shiba K, Yamaguchi S, Ikeda K, Ochi K, Nakabayashi K, Hata KI, Itoh M, Suganami T, Ogawa Y.

Sci Rep. 2017 Mar 17;7:44754. doi: 10.1038/srep44754.

42.

Somatic HRAS p.G12S mosaic mutation causes unilaterally distributed epidermal nevi, woolly hair and palmoplantar keratosis.

Honda A, Umegaki-Arao N, Sasaki T, Nakabayashi K, Hata K, Matsubara Y, Tanikawa A, Amagai M, Kubo A.

J Dermatol. 2017 Jun;44(6):e109-e110. doi: 10.1111/1346-8138.13801. Epub 2017 Mar 11. No abstract available.

PMID:
28295558
43.

Infiltration of mast cells in pachydermia of pachydermoperiostosis.

Tanese K, Niizeki H, Seki A, Nakabayashi K, Nakazawa S, Tokura Y, Kawashima Y, Kubo A, Ishiko A.

J Dermatol. 2017 Nov;44(11):1320-1321. doi: 10.1111/1346-8138.13770. Epub 2017 Feb 13. No abstract available.

44.

Potential roles of DNA methylation in the initiation and establishment of replicative senescence revealed by array-based methylome and transcriptome analyses.

Sakaki M, Ebihara Y, Okamura K, Nakabayashi K, Igarashi A, Matsumoto K, Hata K, Kobayashi Y, Maehara K.

PLoS One. 2017 Feb 3;12(2):e0171431. doi: 10.1371/journal.pone.0171431. eCollection 2017.

45.

Bis(aminoaryl) Carbon-Bridged Oligo(phenylenevinylene)s Expand the Limits of Electronic Couplings.

Burrezo PM, Lin NT, Nakabayashi K, Ohkoshi SI, Calzado EM, Boj PG, Díaz García MA, Franco C, Rovira C, Veciana J, Moos M, Lambert C, López Navarrete JT, Tsuji H, Nakamura E, Casado J.

Angew Chem Int Ed Engl. 2017 Mar 6;56(11):2898-2902. doi: 10.1002/anie.201610921. Epub 2017 Jan 31.

PMID:
28140501
46.

Complete type of pachydermoperiostosis with a novel mutation c.510G>A of the SLCO2A1 gene.

Nakazawa S, Mori T, Niizeki H, Nakabayashi K, Tokura Y.

J Dermatol. 2017 Dec;44(12):1411-1412. doi: 10.1111/1346-8138.13728. Epub 2016 Dec 27. No abstract available.

PMID:
28026033
47.

Changeability of the fully methylated status of the 15q11.2 region in induced pluripotent stem cells derived from a patient with Prader-Willi syndrome.

Okuno H, Nakabayashi K, Abe K, Ando T, Sanosaka T, Kohyama J, Akamatsu W, Ohyama M, Takahashi T, Kosaki K, Okano H.

Congenit Anom (Kyoto). 2017 Jul;57(4):96-103. doi: 10.1111/cga.12206. Epub 2017 Mar 22.

PMID:
28004416
48.

External and internal compressions to retrieve a kinked catheter in the right brachial artery.

Nakabayashi K, Kawakatsu N, Nakazawa N, Suzuki T, Okada H, Oka T.

Cardiovasc Interv Ther. 2017 Oct;32(4):416-419. doi: 10.1007/s12928-016-0446-5. Epub 2016 Nov 28.

PMID:
27896704
49.

Nucleotide substitutions in CD101, the human homolog of a diabetes susceptibility gene in non-obese diabetic mouse, in patients with type 1 diabetes.

Okuno M, Kasahara Y, Onodera M, Takubo N, Okajima M, Suga S, Watanabe N, Suzuki J, Ayabe T, Urakami T, Kawamura T, Kikuchi N, Yokota I, Kikuchi T, Amemiya S, Nakabayashi K, Hayashi K, Hata K, Matsubara Y, Ogata T, Fukami M, Sugihara S.

J Diabetes Investig. 2017 May;8(3):286-294. doi: 10.1111/jdi.12586. Epub 2016 Nov 25.

50.

Photo-induced magnetization and first-principles calculations of a two-dimensional cyanide-bridged Co-W bimetal assembly.

Miyamoto Y, Nasu T, Ozaki N, Umeta Y, Tokoro H, Nakabayashi K, Ohkoshi S.

Dalton Trans. 2016 Dec 6;45(48):19249-19256.

PMID:
27883131

Supplemental Content

Loading ...
Support Center