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/vufind/Search/Results?lookfor=%22Chen%2C+Jian-Min%22&type=Person&sort=year
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PubPharm (559)
1
Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible
SPINK1
coding variants
enthalten in:
bioRxiv.org
| 2024
von
Wu, H.
|
Lin, J.
|
Tang, X.
| +8
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2
Alu
insertion-mediated dsRNA structure formation with pre-existing
Alu
elements as a novel disease-causing mechanism
enthalten in:
bioRxiv.org
| 2024
von
Masson, E.
|
Maestri, S.
|
Bordeau, V.
| +3
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3
Significant but partial lipoprotein lipase functional loss caused by a novel occurrence of rare LPL biallelic variants
enthalten in:
Lipids in health and disease
| 2024
von
Hu, Y.
|
Chen, J.
|
Zuo, H.
| +8
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4
Significant but partial lipoprotein lipase functional loss caused by a novel occurrence of rare LPL biallelic variants
enthalten in:
Lipids in health and disease
| 2024
von
Hu, Y.
|
Chen, J.
|
Zuo, H.
| +8
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5
Pancreas-directed AAV8-hSPINK1 gene therapy safely and effectively protects against pancreatitis in mice
enthalten in:
Gut
| 2024
von
Wang, Y.
|
Mao, X.
|
Sun, C.
| +12
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6
Construction and stability analysis of finite element model for spinal canal reconstruction with miniplates fixation
enthalten in:
Zhongguo gu shang = China journal of orthopaedics and traumatology
| 2024
von
Chen, J.
|
Liu, G.
|
Huang, W.
| +3
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7
Strengths and limitations of AlphaMissense in CPA1 missense variant classification
enthalten in:
Gut
| 2024
von
Wang, Y.
|
Masson, E.
|
Liao, Z.
| +3
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8
Exploring the enigmatic association between PNLIP variants and risk of chronic pancreatitis in a large Chinese cohort
enthalten in:
Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.
| 2024
von
Cassidy, B.
|
Jiang, F.
|
Lin, J.
| +10
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9
Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants
enthalten in:
Human genomics
| 2024
von
Wu, H.
|
Lin, J.
|
Tang, X.
| +10
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10
Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants
enthalten in:
Human genomics
| 2024
von
Wu, H.
|
Lin, J.
|
Tang, X.
| +10
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