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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 3, 2024
[Clinical phenotype, genetic characteristics, and creation of immortalized cell lines for patients from a pedigree affected with Hunter syndrome]
Benchang Li, Fengyu Che, Lidangzhi Mo, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2024
Insights From a Novel Splicing Variant and Recurrent Arginine Variants in the CHD3 Gene Causing Snijders Blok-Campeau Syndrome
Xiaoling Tie, Fengyu Che, Siting Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
November 11, 2024
[Clinical features and genetic analysis of a child with Congenital disorder of glycosylation due to novel variants of COG6 gene]
Liyu Zhang, Ying Yang, Fengyu Che, et al.
Pediatric Neurology
|
February 2, 2024
A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients
Lidangzhi Mo, Xiaoling Tie, Fengyu Che, et al.
Stem Cell Research
|
July 21, 2023
Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient
Benchang Li, Yafei Zhou, Fengyu Che, et al.
Human Cell
|
October 7, 2022
Hedgehog pathway is negatively regulated during the development of Drosophila melanogaster PheRS-m (Drosophila homologs gene of human FARS2) mutants
Lidangzhi Mo, Rui Li, Chunxia He, et al.
Journal of Applied Genetics
|
February 28, 2024
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
Fengyu Che, Chenhao Li, Liyu Zhang, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
March 19, 2026
Aptamer-targeted hybrid nanoparticles based on human exosomes and LXR agonist-loaded liposomes for enhanced anti-AML therapy
Liyu Zhang, Ying Yang, Lidangzhi Mo, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
September 10, 2025
Visualizing NEK9 in action: aptamer-based fluorescent probes for real-time live-cell imaging
Liyu Zhang, Ying Yang, Lidangzhi Mo, et al.
Frontiers in Endocrinology
|
November 3, 2022
Aberrant activation of TGF-β1 induces high bone turnover <i>via</i> Rho GTPases-mediated cytoskeletal remodeling in Camurati-Engelmann disease
Qi Chen, Yan Yao, Kun Chen, et al.
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Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 3, 2024
[Clinical phenotype, genetic characteristics, and creation of immortalized cell lines for patients from a pedigree affected with Hunter syndrome]
Benchang Li, Fengyu Che, Lidangzhi Mo, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2024
Insights From a Novel Splicing Variant and Recurrent Arginine Variants in the CHD3 Gene Causing Snijders Blok-Campeau Syndrome
Xiaoling Tie, Fengyu Che, Siting Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
November 11, 2024
[Clinical features and genetic analysis of a child with Congenital disorder of glycosylation due to novel variants of COG6 gene]
Liyu Zhang, Ying Yang, Fengyu Che, et al.
Pediatric Neurology
|
February 2, 2024
A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients
Lidangzhi Mo, Xiaoling Tie, Fengyu Che, et al.
Stem Cell Research
|
July 21, 2023
Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient
Benchang Li, Yafei Zhou, Fengyu Che, et al.
Human Cell
|
October 7, 2022
Hedgehog pathway is negatively regulated during the development of Drosophila melanogaster PheRS-m (Drosophila homologs gene of human FARS2) mutants
Lidangzhi Mo, Rui Li, Chunxia He, et al.
Journal of Applied Genetics
|
February 28, 2024
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
Fengyu Che, Chenhao Li, Liyu Zhang, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
March 19, 2026
Aptamer-targeted hybrid nanoparticles based on human exosomes and LXR agonist-loaded liposomes for enhanced anti-AML therapy
Liyu Zhang, Ying Yang, Lidangzhi Mo, et al.
Nucleosides, Nucleotides & Nucleic Acids
|
September 10, 2025
Visualizing NEK9 in action: aptamer-based fluorescent probes for real-time live-cell imaging
Liyu Zhang, Ying Yang, Lidangzhi Mo, et al.
Frontiers in Endocrinology
|
November 3, 2022
Aberrant activation of TGF-β1 induces high bone turnover <i>via</i> Rho GTPases-mediated cytoskeletal remodeling in Camurati-Engelmann disease
Qi Chen, Yan Yao, Kun Chen, et al.
Page
of 1