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Weilin Peng

Showing results (11-20 of 46) with videos related to

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Orphanet Journal of Rare Diseases|October 1, 2025
Clinical and genetic analysis of four Chinese patients with holocarboxylase synthetase deficiency and metabolic acidosisZhenzhu Zheng, Weilin Peng, Yiming Lin, et al.
International Journal of Neonatal Screening|March 27, 2026
Incorporating Next-Generation Sequencing in Newborn Screening for Organic AcidemiasYiming Lin, Jinping Zhong, Weilin Peng, et al.
Nature Communications|September 27, 2017
Noise reduction as an emergent property of single-cell agingPing Liu, Ruijie Song, Gregory L Elison, et al.
Frontiers in Pediatrics|December 6, 2021
Three Novel and One Potential Hotspot <i>CPT1A</i> Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A DeficiencyWeifeng Zhang, Yanru Chen, Chunmei Lin, et al.
Orphanet Journal of Rare Diseases|August 4, 2021
Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screeningYiming Lin, Wenjun Wang, Chunmei Lin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 5, 2022
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiencyYiming Lin, Wenwei Zheng, Yanru Chen, et al.
Orphanet Journal of Rare Diseases|March 24, 2021
Increased detection of primary carnitine deficiency through second-tier newborn genetic screeningYiming Lin, Weifeng Zhang, Chenggang Huang, et al.
Oncogene|October 24, 2024
PTPRZ1 dephosphorylates and stabilizes RNF26 to reduce the efficacy of TKIs and PD-1 blockade in ccRCCYongkang Ma, Wei Li, Xinlin Liu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 6, 2021
Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, ChinaYiming Lin, Weifeng Zhang, Zhixu Chen, et al.
Heliyon|January 8, 2024
Newborn screening for fatty acid oxidation disorders in a southern Chinese populationYiming Lin, Chunmei Lin, Bangbang Lin, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Orphanet Journal of Rare Diseases|October 1, 2025
Clinical and genetic analysis of four Chinese patients with holocarboxylase synthetase deficiency and metabolic acidosisZhenzhu Zheng, Weilin Peng, Yiming Lin, et al.
International Journal of Neonatal Screening|March 27, 2026
Incorporating Next-Generation Sequencing in Newborn Screening for Organic AcidemiasYiming Lin, Jinping Zhong, Weilin Peng, et al.
Nature Communications|September 27, 2017
Noise reduction as an emergent property of single-cell agingPing Liu, Ruijie Song, Gregory L Elison, et al.
Frontiers in Pediatrics|December 6, 2021
Three Novel and One Potential Hotspot <i>CPT1A</i> Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A DeficiencyWeifeng Zhang, Yanru Chen, Chunmei Lin, et al.
Orphanet Journal of Rare Diseases|August 4, 2021
Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screeningYiming Lin, Wenjun Wang, Chunmei Lin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 5, 2022
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiencyYiming Lin, Wenwei Zheng, Yanru Chen, et al.
Orphanet Journal of Rare Diseases|March 24, 2021
Increased detection of primary carnitine deficiency through second-tier newborn genetic screeningYiming Lin, Weifeng Zhang, Chenggang Huang, et al.
Oncogene|October 24, 2024
PTPRZ1 dephosphorylates and stabilizes RNF26 to reduce the efficacy of TKIs and PD-1 blockade in ccRCCYongkang Ma, Wei Li, Xinlin Liu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 6, 2021
Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, ChinaYiming Lin, Weifeng Zhang, Zhixu Chen, et al.
Heliyon|January 8, 2024
Newborn screening for fatty acid oxidation disorders in a southern Chinese populationYiming Lin, Chunmei Lin, Bangbang Lin, et al.
Pageof 5