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Lu Xia

Showing results (521-530 of 528) with videos related to

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Computational and Structural Biotechnology Journal|April 19, 2021
GPCards: An integrated database of genotype-phenotype correlations in human genetic diseasesBin Li, Zheng Wang, Qian Chen, et al.
Journal of Medical Genetics|June 4, 2014
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopiaHui Guo, Xuemin Jin, Tengfei Zhu, et al.
Science Advances|June 17, 2026
Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorderLu Xia, Hailiang Guo, Ruiting Liu, et al.
Nature Communications|November 9, 2016
De novo genic mutations among a Chinese autism spectrum disorder cohortTianyun Wang, Hui Guo, Bo Xiong, et al.
Nature Materials|February 28, 2025
Operando-informed precatalyst programming towards reliable high-current-density electrolysisLu Xia, Bruna Ferreira Gomes, Wulyu Jiang, et al.
Global Change Biology|July 6, 2021
Ambient climate determines the directional trend of community stability under warming and grazingPeipei Liu, Wangwang Lv, Jianping Sun, et al.
Human Genetics|October 13, 2020
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathyAshfaque Ahmed, Meng Wang, Gaber Bergant, et al.
Molecular Autism|December 20, 2018
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial modelHui Guo, Tianyun Wang, Huidan Wu, et al.
Pageof 53

Showing results (521-530 of 528) with videos related to

Sort By:
Pageof 53
You have reached the last page of results.This site can display upto 528 results.
Computational and Structural Biotechnology Journal|April 19, 2021
GPCards: An integrated database of genotype-phenotype correlations in human genetic diseasesBin Li, Zheng Wang, Qian Chen, et al.
Journal of Medical Genetics|June 4, 2014
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopiaHui Guo, Xuemin Jin, Tengfei Zhu, et al.
Science Advances|June 17, 2026
Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorderLu Xia, Hailiang Guo, Ruiting Liu, et al.
Nature Communications|November 9, 2016
De novo genic mutations among a Chinese autism spectrum disorder cohortTianyun Wang, Hui Guo, Bo Xiong, et al.
Nature Materials|February 28, 2025
Operando-informed precatalyst programming towards reliable high-current-density electrolysisLu Xia, Bruna Ferreira Gomes, Wulyu Jiang, et al.
Global Change Biology|July 6, 2021
Ambient climate determines the directional trend of community stability under warming and grazingPeipei Liu, Wangwang Lv, Jianping Sun, et al.
Human Genetics|October 13, 2020
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathyAshfaque Ahmed, Meng Wang, Gaber Bergant, et al.
Molecular Autism|December 20, 2018
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial modelHui Guo, Tianyun Wang, Huidan Wu, et al.
Pageof 53