Kitakado相关文献与解析，生知库 | 链接生命科学的每一步

Sakakibara, Nana; Ishiko, Shinya; Tanaka, Yu; Inoki, Yuta; Ichikawa, Yuta; Kitakado, Hideaki; Ueda, Chika; Kondo, Atsushi; Aoto, Yuya; Horinouchi, Tomoko; Yamamura, Tomohiko; Ishimori, Shingo; Onodera, Chinatsu; Inaba, Aya; Hamada, Riku; Harita, Yutaka; Nagano, China; Nozu, Kandai

发表日期：2026

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COL4A5 Intronic Variants at Third to Fifth Nucleotides Cause Alport Syndrome

COL4A5基因内含子第三至第五核苷酸的变异导致阿尔波特综合征

期刊:Kidney International Reports

影响因子:5.7

doi:10.1016/j.ekir.2024.11.016

Kitakado, Hideaki; Horinouchi, Tomoko; Aoyama, Shuhei; Kimura, Yuka; Inoki, Yuta; Tanaka, Yu; Ueda, Chika; Aoto, Yuya; Sakakibara, Nana; Nagano, China; Yamamura, Tomohiko; Ishimori, Shingo; Rossanti, Rini; Matsuo, Masafumi; Nozu, Kandai

COL

发表日期：2025

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Impact of Age-3 Urine Screening on Diagnosis and Treatment Timing in Alport Syndrome

3岁尿液筛查对阿尔波特综合征诊断和治疗时机的影响

期刊:Kidney International Reports

影响因子:5.7

doi:10.1016/j.ekir.2025.09.022

Kitakado, Hideaki; Ishimori, Shingo; Aoyama, Shuhei; Kimura, Yuka; Inoki, Yuta; Ueda, Chika; Tanaka, Yu; Horinouchi, Tomoko; Yamamura, Tomohiko; Sakakibara, Nana; Nagano, China; Nozu, Kandai

发表日期：2025

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Comprehensive Splice Pattern Analysis for Previously Reported OCRL Splicing Variants and Their Phenotypic Contributions

对先前报道的OCRL剪接变体及其表型贡献进行全面的剪接模式分析

期刊:Kidney International Reports

影响因子:5.7

doi:10.1016/j.ekir.2025.02.023.

Rini Rossanti,Eri Okada,Nana Sakakibara,Ryota Suzuki,Yuta Inoki,Yuta Ichikawa,Yu Tanaka,Hideaki Kitakado,Chika Ueda,Atsushi Kondo,Yuya Aoto,China Nagano,Tomoko Horinouchi,Tomohiko Yamamura,Shingo Ishimori,Kandai Nozu

OCRL

发表日期：2025

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Differences in kidney prognosis between congenital and infantile nephrotic syndrome

先天性肾病综合征和婴儿肾病综合征肾脏预后的差异

期刊:Pediatric Nephrology

影响因子:2.6

doi:10.1007/s00467-025-06735-z

Inoki, Yuta; Horinouchi, Tomoko; Aoyama, Shuhei; Kimura, Yuka; Ichikawa, Yuta; Tanaka, Yu; Ueda, Chika; Kitakado, Hideaki; Kondo, Atsushi; Sakakibara, Nana; Kamei, Koichi; Hamada, Riku; Fujita, Naoya; Gotoh, Yoshimitsu; Kaku, Yoshitsugu; Nishiyama, Kei; Okamoto, Takayuki; Toya, Yukiko; Yamamura, Tomohiko; Ishimori, Shingo; Nagano, China; Nozu, Kandai

发表日期：2025

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Latent Intrarenal Renin-Angiotensin-Aldosterone System Activation Could Persist Until Early School-Aged in Children with a History of Low Birth Weight

低出生体重儿童的肾内肾素-血管紧张素-醛固酮系统潜在激活可能持续到学龄早期。

期刊:Biomarker Insights

影响因子:2.6

doi:10.1177/11772719251379198

Ishimori, Shingo; Ishiko, Shinya; Fujimura, Junya; Aoyama, Shuhei; Kimura, Yuka; Kitakado, Hideaki; Ueda, Chika; Inoki, Yuta; Tanaka, Yu; Horinouchi, Tomoko; Yamamura, Tomohiko; Sakakibara, Nana; Nagano, China; Nozu, Kandai

发表日期：2025

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Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort

日本人群中常染色体显性遗传性肾小管间质性肾病的表型和基因型

期刊:Clinical and Experimental Nephrology

影响因子:1.7

doi:10.1007/s10157-025-02629-4

Tanaka, Yu; Nagano, China; Sakakibara, Nana; Okada, Eri; Aoyama, Shuhei; Kimura, Yuka; Inoki, Yuta; Ichikawa, Yuta; Ueda, Chika; Kitakado, Hideaki; Horinouchi, Tomoko; Yamamura, Tomohiko; Ishimori, Shingo; Iijima, Kazumoto; Nozu, Kandai; Morisada, Naoya

发表日期：2025

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Clinical use of the VNtyper-Kestrel pipeline for MUC1 variant detection in autosomal-dominant tubulointerstitial kidney disease

VNtyper-Kestrel流程在常染色体显性遗传性肾小管间质性疾病中MUC1变异检测的临床应用

期刊:Clinical and Experimental Nephrology

影响因子:1.7

doi:10.1007/s10157-025-02675-y

Nagano, China; Morisada, Naoya; Inoki, Yuta; Tanaka, Yu; Ichikawa, Yuta; Ueda, Chika; Kitakado, Hideaki; Aoto, Yuya; Sakakibara, Nana; Horinouchi, Tomoko; Yamamura, Tomohiko; Ishimori, Shingo; Nozu, Kandai

MUC1

发表日期：2025

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Potential involvement of abnormal splicing in severe WT1-related disorders

异常剪接可能与严重的WT1相关疾病有关

期刊:Clinical and Experimental Nephrology

影响因子:1.7

doi:10.1007/s10157-025-02715-7

Nagano, China; Matuso, Masafumi; Inoki, Yuta; Tanaka, Yu; Ichikawa, Yuta; Ueda, Chika; Kitakado, Hideaki; Sakakibara, Nana; Horinouchi, Tomoko; Yamamura, Tomohiko; Ishimori, Shingo; Nozu, Kandai

WT1

发表日期：2025

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Prolonged hypokalemia long after causative factor elimination in pseudo-Bartter/Gitelman syndrome

假性巴特/吉特曼综合征中，病因消除后仍持续存在低钾血症

期刊:Clinical and Experimental Nephrology

影响因子:1.7

doi:10.1007/s10157-025-02734-4

Kondo, Atsushi; Horinouchi, Tomoko; Inoki, Yuta; Ichikawa, Yuta; Tanaka, Yu; Kitakado, Hideaki; Ueda, Chika; Sakakibara, Nana; Nagano, China; Nozu, Kandai

Clinical and Genetic Insights Into Isolated Proteinuria With CUBN Variants

CUBN变异引起的孤立性蛋白尿的临床和遗传学见解

COL4A5 Intronic Variants at Third to Fifth Nucleotides Cause Alport Syndrome

COL4A5基因内含子第三至第五核苷酸的变异导致阿尔波特综合征

Impact of Age-3 Urine Screening on Diagnosis and Treatment Timing in Alport Syndrome

3岁尿液筛查对阿尔波特综合征诊断和治疗时机的影响

Comprehensive Splice Pattern Analysis for Previously Reported OCRL Splicing Variants and Their Phenotypic Contributions

对先前报道的OCRL剪接变体及其表型贡献进行全面的剪接模式分析

Differences in kidney prognosis between congenital and infantile nephrotic syndrome

先天性肾病综合征和婴儿肾病综合征肾脏预后的差异

Latent Intrarenal Renin-Angiotensin-Aldosterone System Activation Could Persist Until Early School-Aged in Children with a History of Low Birth Weight

低出生体重儿童的肾内肾素-血管紧张素-醛固酮系统潜在激活可能持续到学龄早期。

Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort

日本人群中常染色体显性遗传性肾小管间质性肾病的表型和基因型

Clinical use of the VNtyper-Kestrel pipeline for MUC1 variant detection in autosomal-dominant tubulointerstitial kidney disease

VNtyper-Kestrel流程在常染色体显性遗传性肾小管间质性疾病中MUC1变异检测的临床应用

Potential involvement of abnormal splicing in severe WT1-related disorders

异常剪接可能与严重的WT1相关疾病有关

Prolonged hypokalemia long after causative factor elimination in pseudo-Bartter/Gitelman syndrome

假性巴特/吉特曼综合征中，病因消除后仍持续存在低钾血症