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Qin, Tingfeng
113  Ergebnisse:
Personensuche X
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1

Early Diagnosis of Syndromic Congenital Cataracts in a Larg..:

Wang, Qiwei ; Wang, Dongni ; Qin, Tingfeng...
American Journal of Ophthalmology.  263 (2024)  - p. 206-213 , 2024
Link: https://doi.org/10.1016/..
 
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2

A comprehensive evaluation of carbon capture technology in ..:

Li, Nan ; He, Yonglong ; Li, Jiqun...
Journal of Physics: Conference Series.  2474 (2023)  1 - p. 012007 , 2023
Link: https://doi.org/10.1088/..
 
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3

Novel compound heterozygous variants of the SEC23A gene in ..:

Wang, Qiwei ; Lin, Xiaoshan ; Lai, Kunbei...
BMC Medical Genomics.  16 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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4

Whole-Exome Sequencing and Copy Number Analysis in a Patien..:

Wang, Qiwei ; Qin, Tingfeng ; Wang, Xun...
Genes.  13 (2022)  12 - p. 2364 , 2022
Link: https://doi.org/10.3390/..
 
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5

Broadening the genotypic and phenotypic spectrum of MAF in ..:

Wang, Qiwei ; Qin, Tingfeng ; Tan, Haowen...
American Journal of Medical Genetics Part A.  188 (2022)  10 - p. 2888-2898 , 2022
Link: https://doi.org/10.1002/..
 
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6

Unusual Presentation in WAGR Syndrome: Expanding the Phenot..:

Wang, Qiwei ; Zhang, Xulin ; Qin, Tingfeng...
Genes.  13 (2022)  8 - p. 1431 , 2022
Link: https://doi.org/10.3390/..
 
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7

DOCK4 stimulates MUC2 production through its effect on gobl..:

Qin, Tingfeng ; Yang, Jie ; Huang, Dayin...
Journal of Cellular Physiology.  236 (2021)  9 - p. 6507-6519 , 2021
Link: https://doi.org/10.1002/..
 
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8

Overlap phenotypes of the left ventricular noncompaction an..:

Lin, Yubi ; Huang, Jiana ; Zhu, Zhiling...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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9

Interleukin-27 decreases ghrelin production through signal ..:

Zhang, Heng ; Li, Qingjie ; Teng, Yuxin...
Acta Pharmaceutica Sinica B.  10 (2020)  5 - p. 837-849 , 2020
Link: https://doi.org/10.1016/..
 
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10

Hepatic mTOR-AKT2-Insig2 signaling pathway contributes to t..:

Pan, Qinling ; Qin, Tingfeng ; Gao, Yuan...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.  1865 (2019)  3 - p. 525-534 , 2019
Link: https://doi.org/10.1016/..
 
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11

Takeda G Protein-Coupled Receptor 5-Mechanistic Target of R..:

Zhai, Hening ; Li, Zhi ; Peng, Miao...
EBioMedicine.  32 (2018)  - p. 201-214 , 2018
Link: https://doi.org/10.1016/..
 
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12

Novel compound heterozygous variants of the SEC23A gene in ..:

Wang, Qiwei ; Lin, Xiaoshan ; Lai, Kunbei...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568747/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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13

Whole-Exome Sequencing and Copy Number Analysis in a Patien..:

Wang, Qiwei ; Qin, Tingfeng ; Wang, Xun...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777746/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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14

Unusual Presentation in WAGR Syndrome: Expanding the Phenot..:

Wang, Qiwei ; Zhang, Xulin ; Qin, Tingfeng...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408430/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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15

Overlap phenotypes of the left ventricular noncompaction an..:

Lin, Yubi ; Huang, Jiana ; Zhu, Zhiling...
Lin, Yubi, Huang, Jiana, Zhu, Zhiling, Zhang, Zuoquan, Xian, Jianzhong, Yang, Zhe, Qin, Tingfeng, Chen, Linxi, Huang, Jingmin, Huang, Yin, Wu, Qiaoyun, Hu, Zhenyu, Lin, Xiufang, Xu, Geyang (2021-11-24). Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation. Orphanet Journal of Rare Diseases 16 (1) : 496. ScholarBank@NUS Repository. https://doi.org/10.1186/s13023-021-02112-9.  , 2021
Link: https://scholarbank.nus...
 
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