Chie Kobayashi
Overview
Explore the profile of Chie Kobayashi including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
47
Citations
306
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Sawai T, Ishida S, Kobayashi C, Murase Y, Nakao G, Nakamura T, et al.
EMBO Rep
. 2025 Mar;
PMID: 40087470
No abstract available.
2.
Kataoka M, Ishida S, Kobayashi C, Lee T, Sawai T
Trends Biotechnol
. 2024 Sep;
43(3):491-493.
PMID: 39306492
Neuroprivacy, or the privacy of neural data, has attracted considerable interest. Here, we explore the implications of neuroprivacy in human brain organoid research, detailing different interpretations of this right. Findings...
3.
Kobayashi C, Miura M, Yamasaki Y, Taniguchi K, Miyaishi S
Leg Med (Tokyo)
. 2024 Aug;
71:102496.
PMID: 39154432
It is reported that immunostaining of Myoglobin (Mb) is useful for forensic diagnosis. In this study, we investigated the condition of fixation of striated muscle in 10 % neutral-buffered formalin...
4.
Asano F, Tanigaki S, Sato Y, Kobayashi C, Kobayashi Y
Cureus
. 2023 Mar;
15(2):e34627.
PMID: 36891020
Some studies have reported increased severe coronavirus disease (COVID-19) infection in the third trimester of pregnancy. Therefore, prenatal care in the third trimester requires careful judgment. It has been reported...
5.
Hasegawa M, Fukushima H, Suzuki R, Yamaki Y, Hosaka S, Inaba M, et al.
Oncology
. 2022 May;
100(7):376-383.
PMID: 35551132
Introduction: MEFV is the gene responsible for familial Mediterranean fever. It encodes pyrin, which controls inflammation. Besides, previous studies have reported that some germline MEFV variants were associated with tumour...
6.
Tomomasa D, Booth C, Bleesing J, Isoda T, Kobayashi C, Koike K, et al.
Clin Immunol
. 2022 Apr;
237:108993.
PMID: 35367395
Few reports have examined whether prophylactic allogeneic hematopoietic cell transplantation (HCT) for X-linked lymphoproliferative syndrome type 1 (XLP1) improves the prognosis. We compared the prognosis of symptomatic probands and affected...
7.
Toyofuku E, Takeshita K, Ohnishi H, Kiridoshi Y, Masuoka H, Kadowaki T, et al.
Front Cell Infect Microbiol
. 2022 Feb;
11:787667.
PMID: 35155270
Introduction: Haploinsufficiency of A20 (HA20) is a form of inborn errors of immunity (IEI). IEIs are genetically occurring diseases, some of which cause intestinal dysbiosis. Due to the dysregulation of...
8.
Takemori S, Tanigaki S, Nozu K, Yoshihashi H, Uchiumi Y, Sakaguchi K, et al.
Eur J Med Genet
. 2021 Aug;
64(10):104308.
PMID: 34400373
Transient antenatal Bartter syndrome due to melanoma-associated antigen D2 gene mutation is a newly reported type of Bartter syndrome. Its characteristics include an X-linked inheritance pattern, early-onset hydramnios, and spontaneous...
9.
Tanaka R, Fukushima F, Motoyama K, Kobayashi C, Izumi I
Pediatr Int
. 2021 Jul;
63(8):973-974.
PMID: 34245199
No abstract available.
10.
Kadowaki T, Ohnishi H, Kawamoto N, Kadowaki S, Hori T, Nishimura K, et al.
Clin Immunol
. 2020 Apr;
216:108441.
PMID: 32335289
Haploinsufficiency of A20 (HA20) causes inflammatory disease resembling Behçet's disease; many cases have been reported, including some that are complicated with autoimmune diseases. This study aims to clarify the immunophenotype...