日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Single-cell transcriptomic profiling reveals a novel signature of necrotizing granulomatous lesions in the lungs of Mycobacterium tuberculosis-infected C3HeB/FeJ mice

单细胞转录组分析揭示了结核分枝杆菌感染的C3HeB/FeJ小鼠肺部坏死性肉芽肿病变的新特征

Seto, Shintaro; Omori, Shiho; Nakamura, Hajime; Hijikata, Minako; Keicho, Naoto

Mafb deficiency in myeloid cells increases susceptibility to Mycobacterium tuberculosis infection in mice

小鼠髓系细胞中 Mafb 缺乏会增加其对结核分枝杆菌感染的易感性。

Hikichi, Haruka; Nakamura, Hajime; Omori, Shiho; Seto, Shintaro; Hijikata, Minako; Hamada, Michito; Takahashi, Satoru; Keicho, Naoto

Gene expression profiling of airway epithelium in Mycobacterium avium complex lung disease

鸟分枝杆菌复合群肺病气道上皮细胞的基因表达谱分析

Furuuchi, Koji; Hijikata, Minako; Seto, Shintaro; Miyabayashi, Akiko; Wakabayashi, Keiko; Nakagawa, Takayuki; Yoshida, Tsutomu; Shimoda, Kiyomi; Hiramatsu, Miyako; Shiraishi, Yuji; Morimoto, Kozo; Keicho, Naoto

Genetic investigation of sinopulmonary diseases in Vietnam: seeking specific causes from non-specific symptoms

越南鼻窦肺部疾病的基因研究:从非特异性症状中寻找特定病因

Phuong, Phan Thu; Hang, Nguyen Thi Le; Hijikata, Minako; Morimoto, Kozo; Chau, Ngo Quy; Dinh, Le Cong; Wakabayashi, Keiko; Miyabayashi, Akiko; Huyen, Nguyen Thu; Bich, Pham Thi Ngoc; Keicho, Naoto

Primary Ciliary Dyskinesia Due to Compound Heterozygous Variants in CFAP221 with Obstructive Azoospermia: Young's Syndrome May Be a Phenotype of Primary Ciliary Dyskinesia

CFAP221复合杂合变异引起的原发性纤毛运动障碍伴梗阻性无精子症:杨氏综合征可能是原发性纤毛运动障碍的一种表型

Ito, Masashi; Morimoto, Kozo; Ohashi, Masakazu; Wakabayashi, Keiko; Miyabayashi, Akiko; Yamada, Hiroyuki; Hijikata, Minako; Keicho, Naoto

Severe bronchiectasis and chronic rhinosinusitis due to homozygous WFDC2 Variants: The first three cases reported from Japan

由纯合WFDC2变异引起的严重支气管扩张和慢性鼻窦炎:日本报告的首批三例病例

Ito, Masashi; Morimoto, Kozo; Hijikata, Minako; Hasegawa, Hirotsugu; Wakabayashi, Keiko; Miyabayashi, Akiko; Keicho, Naoto

Primary Ciliary Dyskinesia Caused by Homozygous DNAAF1 Mutations Resulting from a Consanguineous Marriage: A Case Report from Japan

日本一例因近亲结婚导致的纯合DNAAF1突变引起的原发性纤毛运动障碍病例报告

Ito, Masashi; Morimoto, Kozo; Saotome, Mikio; Miyabayashi, Akiko; Wakabayashi, Keiko; Yamada, Hiroyuki; Hijikata, Minako; Keicho, Naoto; Ohta, Ken

FOXJ1 Variants Causing Primary Ciliary Dyskinesia with Hydrocephalus: A Case Report from Japan

日本一例因FOXJ1变异导致原发性纤毛运动障碍伴脑积水的病例报告

Ito, Masashi; Morimoto, Kozo; Ohfuji, Takashi; Miyabayashi, Akiko; Wakabayashi, Keiko; Yamada, Hiroyuki; Hijikata, Minako; Keicho, Naoto

Host-pathogen relationship in retreated tuberculosis with major rifampicin resistance-conferring mutations

携带主要利福平耐药突变的复发性结核病中的宿主-病原体关系

Hang, Nguyen Thi Le; Hijikata, Minako; Maeda, Shinji; Thuong, Pham Huu; Huan, Hoang Van; Hoang, Nguyen Phuong; Tam, Do Bang; Anh, Pham Thu; Huyen, Nguyen Thu; Cuong, Vu Cao; Kobayashi, Nobuyuki; Wakabayashi, Keiko; Miyabayashi, Akiko; Seto, Shintaro; Keicho, Naoto

Spatial multiomic profiling reveals the novel polarization of foamy macrophages within necrotic granulomatous lesions developed in lungs of C3HeB/FeJ mice infected with Mycobacterium tuberculosis

空间多组学分析揭示了感染结核分枝杆菌的C3HeB/FeJ小鼠肺部坏死性肉芽肿病变中泡沫巨噬细胞的新型极化现象

Seto, Shintaro; Nakamura, Hajime; Guo, Tz-Chun; Hikichi, Haruka; Wakabayashi, Keiko; Miyabayashi, Akiko; Nagata, Toshi; Hijikata, Minako; Keicho, Naoto