Higashimoto K - Search Results

1

Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.

Hara S, Matsuhisa F, Kitajima S, Yatsuki H, Kubiura-Ichimaru M, Higashimoto K, Soejima H. Hara S, et al. Among authors: higashimoto k. Commun Biol. 2024 Dec 2;7(1):1605. doi: 10.1038/s42003-024-07323-x. Commun Biol. 2024. PMID: 39623082 Free PMC article.

2

Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.

Higashimoto K, Sun F, Imagawa E, Saida K, Miyake N, Hara S, Yatsuki H, Kubiura-Ichimaru M, Fujita A, Mizuguchi T, Matsumoto N, Soejima H. Higashimoto K, et al. J Med Genet. 2024 May 21;61(6):590-594. doi: 10.1136/jmg-2023-109621. J Med Genet. 2024. PMID: 38228391

3

Possible regulation of ganglioside GD3 synthase gene expression with DNA methylation in human glioma cells.

Yamamoto Y, Higashimoto K, Ohkawa Y, Soejima H, Kaneko K, Ohmi Y, Furukawa K, Furukawa K. Yamamoto Y, et al. Among authors: higashimoto k. Glycoconj J. 2023 Jun;40(3):323-332. doi: 10.1007/s10719-023-10108-9. Epub 2023 Mar 10. Glycoconj J. 2023. PMID: 36897478

4

Donor cord blood aging accelerates in recipients after transplantation.

Onizuka M, Imanishi T, Harada K, Aoyama Y, Amaki J, Toyosaki M, Machida S, Kikkawa E, Yamada S, Nakabayashi K, Hata K, Higashimoto K, Soejima H, Ando K. Onizuka M, et al. Among authors: higashimoto k. Sci Rep. 2023 Feb 14;13(1):2603. doi: 10.1038/s41598-023-29912-2. Sci Rep. 2023. PMID: 36788379 Free PMC article.

5

Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome.

Soejima H, Hara S, Ohba T, Higashimoto K. Soejima H, et al. Among authors: higashimoto k. Cancers (Basel). 2022 Nov 12;14(22):5563. doi: 10.3390/cancers14225563. Cancers (Basel). 2022. PMID: 36428656 Free PMC article. Review.

6

DNA Methylation Analysis Using Bisulfite Pyrosequencing.

Higashimoto K, Hara S, Soejima H. Higashimoto K, et al. Methods Mol Biol. 2023;2577:3-20. doi: 10.1007/978-1-0716-2724-2_1. Methods Mol Biol. 2023. PMID: 36173562

7

Bipedicled SIEA Flap with Deep Inferior Epigastric Artery and Vein Grafts for Breast Reconstruction.

Nakamura R, Tomita K, Omura N, Nishimura E, Higashimoto K, Kubo T, Hikasa H. Nakamura R, et al. Among authors: higashimoto k. Plast Reconstr Surg Glob Open. 2022 Aug 24;10(8):e4484. doi: 10.1097/GOX.0000000000004484. eCollection 2022 Aug. Plast Reconstr Surg Glob Open. 2022. PMID: 36032370 Free PMC article.

8

Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.

Aoki S, Higashimoto K, Hidaka H, Ohtsuka Y, Aoki S, Mishima H, Yoshiura KI, Nakabayashi K, Hata K, Yatsuki H, Hara S, Ohba T, Katabuchi H, Soejima H. Aoki S, et al. Among authors: higashimoto k. Clin Epigenetics. 2022 May 17;14(1):64. doi: 10.1186/s13148-022-01280-0. Clin Epigenetics. 2022. PMID: 35581658 Free PMC article.

9

Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.

Sun F, Hara S, Tomita C, Tanoue Y, Yatsuki H, Higashimoto K, Soejima H. Sun F, et al. Among authors: higashimoto k. Am J Med Genet A. 2021 Oct;185(10):3062-3067. doi: 10.1002/ajmg.a.62364. Epub 2021 May 26. Am J Med Genet A. 2021. PMID: 34037318

10

TYK2 Promoter Variant Is Associated with Impaired Insulin Secretion and Lower Insulin Resistance in Japanese Type 2 Diabetes Patients.

Mori H, Takahashi H, Mine K, Higashimoto K, Inoue K, Kojima M, Kuroki S, Eguchi T, Ono Y, Inuzuka S, Soejima H, Nagafuchi S, Anzai K. Mori H, et al. Among authors: higashimoto k. Genes (Basel). 2021 Mar 11;12(3):400. doi: 10.3390/genes12030400. Genes (Basel). 2021. PMID: 33799705 Free PMC article. Clinical Trial.

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