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Yongjun Song

Showing results (21-30 of 41) with videos related to

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Molecular Genetics & Genomic Medicine|July 27, 2023
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature reviewAtefeh Mir, Yongjun Song, Hane Lee, et al.
Scientific Reports|November 21, 2025
Creep acoustic emission characteristics and failure precursor identification of double-fissured red sandstone under freeze-thaw actionDengke Yang, Xiaoxiao Duan, Keyan Cheng, et al.
Environmental Research|February 1, 2024
Activated carbon fiber as an efficient co-catalyst toward accelerating Fe<sup>2+</sup>/Fe<sup>3+</sup> cycling for improved removal of antibiotic cefaclor via electro-Fenton process using a gas diffusion electrodeYue Zhao, Aimin Wang, Songyu Ren, et al.
BMC Medical Genomics|October 11, 2023
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literatureAtefeh Mir, Yongjun Song, Hane Lee, et al.
Molecular Genetics & Genomic Medicine|March 4, 2024
A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE-1 insertion in LDLRYongjun Song, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, et al.
BMC Medical Genomics|February 27, 2025
Correction: whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literatureAtefeh Mir, Yongjun Song, Hane Lee, et al.
ACS Applied Materials & Interfaces|January 24, 2019
Temperature-Driven Precise Control of Biological Droplet's Adhesion on a Slippery SurfaceJinhua Wang, Yu Huang, Ke You, et al.
Gene|January 23, 2022
Whole genome re-sequencing and transcriptome reveal an alteration in hormone signal transduction in a more-branching mutant of appleHongjuan Ge, Guofang Li, Shuwei Wan, et al.
Gene|March 16, 2023
Erratum to "Whole genome re-sequencing and transcriptome reveal an alteration in hormone signal transduction in a more branching mutant of apple" [Gene 818 (2022) 146214]Hongjuan Ge, Guofang Li, Shuwei Wan, et al.
Journal of Medical Case Reports|May 2, 2026
A de novo start-loss variant in the NIPBL gene causing mild type 1 Cornelia de Lange syndrome in an Iranian family: A Case ReportAtefeh Mir, Zahra Abbasi, Yongjun Song, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Molecular Genetics & Genomic Medicine|July 27, 2023
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature reviewAtefeh Mir, Yongjun Song, Hane Lee, et al.
Scientific Reports|November 21, 2025
Creep acoustic emission characteristics and failure precursor identification of double-fissured red sandstone under freeze-thaw actionDengke Yang, Xiaoxiao Duan, Keyan Cheng, et al.
Environmental Research|February 1, 2024
Activated carbon fiber as an efficient co-catalyst toward accelerating Fe<sup>2+</sup>/Fe<sup>3+</sup> cycling for improved removal of antibiotic cefaclor via electro-Fenton process using a gas diffusion electrodeYue Zhao, Aimin Wang, Songyu Ren, et al.
BMC Medical Genomics|October 11, 2023
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literatureAtefeh Mir, Yongjun Song, Hane Lee, et al.
Molecular Genetics & Genomic Medicine|March 4, 2024
A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE-1 insertion in LDLRYongjun Song, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, et al.
BMC Medical Genomics|February 27, 2025
Correction: whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literatureAtefeh Mir, Yongjun Song, Hane Lee, et al.
ACS Applied Materials & Interfaces|January 24, 2019
Temperature-Driven Precise Control of Biological Droplet's Adhesion on a Slippery SurfaceJinhua Wang, Yu Huang, Ke You, et al.
Gene|January 23, 2022
Whole genome re-sequencing and transcriptome reveal an alteration in hormone signal transduction in a more-branching mutant of appleHongjuan Ge, Guofang Li, Shuwei Wan, et al.
Gene|March 16, 2023
Erratum to "Whole genome re-sequencing and transcriptome reveal an alteration in hormone signal transduction in a more branching mutant of apple" [Gene 818 (2022) 146214]Hongjuan Ge, Guofang Li, Shuwei Wan, et al.
Journal of Medical Case Reports|May 2, 2026
A de novo start-loss variant in the NIPBL gene causing mild type 1 Cornelia de Lange syndrome in an Iranian family: A Case ReportAtefeh Mir, Zahra Abbasi, Yongjun Song, et al.
Pageof 5