Yifei Xu
Tsu, Japan
Last Updated: 09/26/2026
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Found 12 publications
A 3000-year-old founder variant in the DRC1 gene causes primary ciliary dyskinesia in Japan and Korea.
Journal: Journal of human genetics
Published: June 12, 2024
Immunohistochemical analyses reveal FoxP3 expressions in spleen and colorectal cancer in mice treated with AOM/DSS, and their suppression by glycyrrhizin.
Journal: PloS one
Published: April 14, 2024
Two Pediatric Cases of Primary Ciliary Dyskinesia Caused by Loss-of-Function Variants in Oral-Facial-Digital Syndrome Gene, OFD1.
Journal: Case reports in genetics
Published: December 11, 2023
Characteristic genetic spectrum of primary ciliary dyskinesia in Japanese patients and global ethnic heterogeneity: population-based genomic variation database analysis.
Journal: Journal of human genetics
Published: October 03, 2022
A Novel Homozygous Variant in GAS2L2 in Two Sisters with Primary Ciliary Dyskinesia.
Journal: Internal medicine (Tokyo, Japan)
Published: September 14, 2022
Analysis of the clinical features of Japanese patients with primary ciliary dyskinesia.
Journal: Auris, nasus, larynx
Published: January 21, 2021
A pediatric case of primary ciliary dyskinesia caused by novel copy number variation in PIH1D3.
Journal: Auris, nasus, larynx
Published: December 01, 2020
A pediatric case of productive cough caused by novel variants in DNAH9.
Journal: Human genome variation
Published: October 19, 2020
Multicellular modeling of ciliopathy by combining iPS cells and microfluidic airway-on-a-chip technology.
Journal: Science translational medicine
Published: February 05, 2020
Copy number variation in DRC1 is the major cause of primary ciliary dyskinesia in the Japanese population.
Journal: Molecular genetics & genomic medicine
Published: August 02, 2019
Showing 1-12 of 12
Last Updated: 09/26/2026