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Yanling Teng

Showing results (21-30 of 38) with videos related to

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RNA Biology|December 9, 2014
The survival motor neuron gene smn-1 interacts with the U2AF large subunit gene uaf-1 to regulate Caenorhabditis elegans lifespan and motor functionsXiaoyang Gao, Yanling Teng, Jintao Luo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 2022
Identification of four novel mutations in BTK from six Chinese families with X-linked agammaglobulinemiaQimin Zhou, Yanling Teng, Jianyan Pan, et al.
Medicine|May 18, 2019
Identification of pathogenic mutations in 6 Chinese families with multiple exostoses by whole-exome sequencing and multiplex ligation-dependent probe amplification: Case seriesXigui Long, Zhuo Li, Yanru Huang, et al.
Frontiers in Genetics|July 9, 2024
Application of whole exome sequencing in carrier screening for high-risk families without probandsQinlin Huang, Zhongjie Wang, Yanling Teng, et al.
Human Genomics|October 8, 2024
Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individualsQinlin Huang, Juan Wen, Hongyun Zhang, et al.
Scientific Reports|January 14, 2025
Oligogenic effect is associated with the clinical heterogeneity of autosomal dominant deafness-15Jianyan Pan, Hua Teng, Fang Liu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 2022
The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disabilityHongyun Zhang, Xin Chen, Hu Tan, et al.
Clinical Chemistry|June 17, 2022
Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read SequencingYingdi Liu, Miaomiao Chen, Jing Liu, et al.
Frontiers in Genetics|January 24, 2022
Noninvasive Prenatal Testing of Methylmalonic Acidemia cblC Type Using the cSMART Assay for <i>MMACHC</i> Gene MutationsWeigang Lv, Lili Liang, Xin Chen, et al.
Cell Death & Disease|November 9, 2024
PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiationSiyi Chen, Jiali You, Xiaowei Zhou, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
RNA Biology|December 9, 2014
The survival motor neuron gene smn-1 interacts with the U2AF large subunit gene uaf-1 to regulate Caenorhabditis elegans lifespan and motor functionsXiaoyang Gao, Yanling Teng, Jintao Luo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 2022
Identification of four novel mutations in BTK from six Chinese families with X-linked agammaglobulinemiaQimin Zhou, Yanling Teng, Jianyan Pan, et al.
Medicine|May 18, 2019
Identification of pathogenic mutations in 6 Chinese families with multiple exostoses by whole-exome sequencing and multiplex ligation-dependent probe amplification: Case seriesXigui Long, Zhuo Li, Yanru Huang, et al.
Frontiers in Genetics|July 9, 2024
Application of whole exome sequencing in carrier screening for high-risk families without probandsQinlin Huang, Zhongjie Wang, Yanling Teng, et al.
Human Genomics|October 8, 2024
Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individualsQinlin Huang, Juan Wen, Hongyun Zhang, et al.
Scientific Reports|January 14, 2025
Oligogenic effect is associated with the clinical heterogeneity of autosomal dominant deafness-15Jianyan Pan, Hua Teng, Fang Liu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 2022
The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disabilityHongyun Zhang, Xin Chen, Hu Tan, et al.
Clinical Chemistry|June 17, 2022
Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read SequencingYingdi Liu, Miaomiao Chen, Jing Liu, et al.
Frontiers in Genetics|January 24, 2022
Noninvasive Prenatal Testing of Methylmalonic Acidemia cblC Type Using the cSMART Assay for <i>MMACHC</i> Gene MutationsWeigang Lv, Lili Liang, Xin Chen, et al.
Cell Death & Disease|November 9, 2024
PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiationSiyi Chen, Jiali You, Xiaowei Zhou, et al.
Pageof 4