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/vufind/Search/Results?lookfor=%22Qu%2C+Yujin%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Qu%2C+Yujin%22&type=Person&sort=year
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PubPharm (20)
1
Variants located in intron 6 of SMN1 lead to misdiagnosis in genetic detection and screening for SMA
enthalten in:
Heliyon
| 2024
von
Qu, Y.
|
Bai, J.
|
Jiao, H.
| +7
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2
A high-fidelity long-read sequencing-based approach enables accurate and effective genetic diagnosis of spinal muscular atrophy
enthalten in:
Clinica chimica acta; international journal of clinical chemistry
| 2024
von
Bai, J.
|
Qu, Y.
|
Huang, W.
| +7
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3
Novel Alu-mediated deletions of the SMN1 gene were identified by ultra-long read sequencing technology in patients with spinal muscular atrophy
enthalten in:
Neuromuscular disorders : NMD
| 2023
von
Bai, J.
|
Qu, Y.
|
OuYang, S.
| +10
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4
Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model
enthalten in:
Human molecular genetics
| 2022
von
Wang, J.
|
Bai, J.
|
OuYang, S.
| +10
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5
Bone mineral density and its influencing factors in Chinese children with spinal muscular atrophy types 2 and 3
enthalten in:
BMC musculoskeletal disorders
| 2021
von
Peng, X.
|
Qu, Y.
|
Li, X.
| +4
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6
Bone mineral density and its influencing factors in Chinese children with spinal muscular atrophy types 2 and 3
enthalten in:
BMC musculoskeletal disorders
| 2021
von
Peng, X.
|
Qu, Y.
|
Li, X.
| +4
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7
Factors associated with delayed diagnosis of spinal muscular atrophy in China and changes in diagnostic delay
enthalten in:
Neuromuscular disorders : NMD
| 2021
von
Cao, Y.
|
Cheng, M.
|
Qu, Y.
| +6
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8
Bone Mineral Density and its Influencing Factors in Chinese Children with Spinal Muscular Atrophy types 2 and 3
enthalten in:
ResearchSquare.com
| 2021
von
Peng, X.
|
Qu, Y.
|
Li, X.
| +4
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9
Dual Mechanism of a New SMN1 Variant (c.835G>C, p.Gly279Arg) by Interrupting Exon 7 Skipping and YG Oligomerization in Causation of Spinal Muscular Atrophy
enthalten in:
Journal of molecular neuroscience : MN
| 2021
von
Bai, J.
|
Qu, Y.
|
Song, F.
| +5
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10
Dual Mechanism of a New SMN1 Variant (c.835G>C, p.Gly279Arg) by Interrupting Exon 7 Skipping and YG Oligomerization in Causation of Spinal Muscular Atrophy
enthalten in:
Journal of molecular neuroscience
| 2020
von
Bai, J.
|
Qu, Y.
|
Song, F.
| +5
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Thema
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SMN1 protein, human
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Survival motor neuron gene-1
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Survival of Motor Neuron 2 Protein
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