Akiko Suga
Overview
Explore the profile of Akiko Suga 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
16
Citations
407
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Quinodoz M, Rodenburg K, Cvackova Z, Kaminska K, de Bruijn S, Iglesias-Romero A, et al.
medRxiv
. 2025 Jan;
PMID: 39830270
The U4 small nuclear RNA (snRNA) forms a duplex with the U6 snRNA and, together with U5 and ~30 proteins, is part of the U4/U6.U5 tri-snRNP complex, located at the...
2.
Suga A, Mizobuchi K, Inooka T, Yoshitake K, Minematsu N, Tsunoda K, et al.
Genet Med Open
. 2024 Dec;
2:101843.
PMID: 39669618
Purpose: Achromatopsia (ACHM) is an early-onset cone dysfunction caused by 5 genes with cone-specific functions (, , , and ) and by , a transcription factor with ubiquitous expression. To...
3.
Azuma K, Suzuki T, Kobayashi K, Nagahara M, Imai H, Suga A, et al.
Cell Death Dis
. 2024 Oct;
15(10):763.
PMID: 39426958
Age-related macular degeneration (AMD) is a leading cause of irreversible vision loss in the elderly population, particularly the late-stage of dry AMD known as geographic atrophy (GA), lacks effective treatment...
4.
Inooka T, Hayashi T, Tsunoda K, Kuniyoshi K, Kondo H, Mizobuchi K, et al.
Retina
. 2024 Sep;
44(10):1836-1844.
PMID: 39287548
Purpose: To ascertain the characteristics of achromatopsia (ACHM) in Japan by analyzing the genetic and phenotypic features of patients with ACHM. Methods: The medical records of 52 patients from 47...
5.
Suga A, Minegishi Y, Yamamoto M, Ueda K, Iwata T
Commun Biol
. 2024 Jun;
7(1):676.
PMID: 38830954
TRiC/CCT is a chaperonin complex required for the folding of cytoplasmic proteins. Although mutations in each subunit of TRiC/CCT are associated with various human neurodegenerative diseases, their impact in mammalian...
6.
Nakajima A, Kuniyoshi K, Iwahashi C, Mano F, Hayashi T, Kondo H, et al.
Front Med (Lausanne)
. 2023 Nov;
10:1280564.
PMID: 38034549
Introduction: Congenital X-linked retinoschisis (XLRS) presents as macular retinoschisis/degeneration in almost all patients and as peripheral retinoschisis in half the patients. Although the optical coherence tomography (OCT) findings of macular...
7.
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Fujinami K, Miyake Y, et al.
Hum Mutat
. 2022 Oct;
43(12):2251-2264.
PMID: 36284460
Inherited retinal diseases (IRDs) comprise a phenotypically and genetically heterogeneous group of ocular disorders that cause visual loss via progressive retinal degeneration. Here, we report the genetic characterization of 1210...
8.
Pan Y, Suga A, Kimura I, Kimura C, Minegishi Y, Nakayama M, et al.
J Clin Invest
. 2022 Sep;
132(21).
PMID: 36099048
Normal-tension glaucoma (NTG) is a heterogeneous disease characterized by retinal ganglion cell (RGC) death leading to cupping of the optic nerve head and visual field loss at normal intraocular pressure...
9.
Pan Y, Iejima D, Nakayama M, Suga A, Noda T, Kaur I, et al.
J Biol Chem
. 2021 Feb;
296:100456.
PMID: 33636181
The disease-initiating molecular events for age-related macular degeneration (AMD), a multifactorial retinal disease affecting many millions of elderly individuals worldwide, are still unknown. Of the over 30 risk and protective...
10.
Li H, Yuan S, Minegishi Y, Suga A, Yoshitake K, Sheng X, et al.
Hum Mol Genet
. 2020 Jan;
29(3):444-458.
PMID: 31915829
Inherited optic neuropathies are rare eye diseases of optic nerve dysfunction that present in various genetic forms. Previously, mutation in three genes encoding mitochondrial proteins has been implicated in autosomal...