Hidenobu Soejima
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Explore the profile of Hidenobu Soejima including associated specialties, affiliations and a list of published articles.
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88
Citations
1761
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Recent Articles
1.
Nanri Y, Nunomura S, Honda Y, Yokomizo K, Takedomi H, Yamaguchi Y, et al.
J Invest Dermatol
. 2025 Jan;
PMID: 39884457
No abstract available.
2.
Hara S, Matsuhisa F, Kitajima S, Yatsuki H, Kubiura-Ichimaru M, Higashimoto K, et al.
Commun Biol
. 2024 Dec;
7(1):1605.
PMID: 39623082
Beckwith-Wiedemann syndrome (BWS) is caused by a gain of methylation (GOM) at the imprinting control region within the Igf2-H19 domain on the maternal allele (H19-ICR GOM). Mutations in the binding...
3.
Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
Urakawa T, Soejima H, Yamoto K, Hara-Isono K, Nakamura A, Kawashima S, et al.
Clin Epigenetics
. 2024 Oct;
16(1):138.
PMID: 39369220
Background: Multi-locus imprinting disturbance (MLID) with methylation defects in various differentially methylated regions (DMRs) has recently been identified in approximately 150 cases with imprinting disorders (IDs), and deleterious variants have...
4.
Higashimoto K, Sun F, Imagawa E, Saida K, Miyake N, Hara S, et al.
J Med Genet
. 2024 Jan;
61(6):590-594.
PMID: 38228391
Beckwith-Wiedemann syndrome (BWS) is an imprinting disorder caused by (epi)genetic alterations at 11p15. Because approximately 20% of patients test negative via molecular testing of peripheral blood leukocytes, the concept of...
5.
Yamamoto Y, Higashimoto K, Ohkawa Y, Soejima H, Kaneko K, Ohmi Y, et al.
Glycoconj J
. 2023 Mar;
40(3):323-332.
PMID: 36897478
Gangliosides are expressed in nervous systems and some neuroectoderm-derived tumors at high levels and play pivotal roles. However, mechanisms for the regulation of glycosyltransferase genes responsible for the ganglioside synthesis...
6.
Onizuka M, Imanishi T, Harada K, Aoyama Y, Amaki J, Toyosaki M, et al.
Sci Rep
. 2023 Feb;
13(1):2603.
PMID: 36788379
Cord blood stem cell transplantation is an important alternative for patients needing hematopoietic stem cell transplantation. However, it is unclear how cord blood cells, which are 0 years old, age...
7.
Soejima H, Hara S, Ohba T, Higashimoto K
Cancers (Basel)
. 2022 Nov;
14(22).
PMID: 36428656
Placental mesenchymal dysplasia (PMD) is characterized by placentomegaly, aneurysmally dilated chorionic plate vessels, thrombosis of the dilated vessels, and large grapelike vesicles, and is often mistaken for partial or complete...
8.
Higashimoto K, Hara S, Soejima H
Methods Mol Biol
. 2022 Sep;
2577:3-20.
PMID: 36173562
Pyrosequencing is a DNA sequencing-by-synthesis technique that can quantitatively detect single-nucleotide polymorphisms (SNPs). With pyrosequencing, the level of DNA methylation can be calculated according to the ratio of artificial cytosine/thymine...
9.
Hirata H, Kamohara A, Murayama M, Nishioka K, Honda H, Urano Y, et al.
J Cell Physiol
. 2022 Jul;
237(10):3912-3926.
PMID: 35908202
The basic helix-loop-helix transcriptional factor, Bhlhe40 has been shown as a crucial regulator of immune response, tumorigenesis, and circadian rhythms. We identified Bhlhe40 as a possible regulator of osteoclast differentiation...
10.
Aoki S, Higashimoto K, Hidaka H, Ohtsuka Y, Aoki S, Mishima H, et al.
Clin Epigenetics
. 2022 May;
14(1):64.
PMID: 35581658
Background: Placental mesenchymal dysplasia (PMD) is a morphological abnormality resembling partial hydatidiform moles. It is often associated with androgenetic/biparental mosaicism (ABM) and complicated by Beckwith-Wiedemann syndrome (BWS), an imprinting disorder....