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Xuefang Zhao

Showing results (11-20 of 48) with videos related to

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Genome Biology|June 12, 2016
Resolving complex structural genomic rearrangements using a randomized approachXuefang Zhao, Sarah B Emery, Bridget Myers, et al.
Food Chemistry: X|June 1, 2026
Studies on the pure fermentation and aroma contributions of <i>Torulaspora delbrueckii</i> killer yeasts with high enzymatic activity in different white wine varietiesZhanzhan Jiang, Qinqin Liu, Xuefang Zhao, et al.
Food Chemistry|December 17, 2025
Effects of exogenous proline on malolactic fermentation by Oenococcus oeni and on volatiles, phenols, and antioxidant properties of Cabernet Sauvignon wineXuefang Zhao, Longxiang Liu, Akumawah Kyen Marie-Colette, et al.
Food Chemistry: X|March 21, 2025
From microbial communities to aroma profiles: A comparative study of spontaneous fermentation in merlot and cabernet sauvignon winesQinqin Liu, Nan Hao, Lan Mi, et al.
Frontiers in Plant Science|November 17, 2022
Evaluation of the resistance to Chinese predominant races of <i>Puccinia triticina</i> and analysis of effective leaf rust resistance genes in wheat accessions from the U.S. National Plant Germplasm SystemLin Zhang, Xuefang Zhao, Jingxian Liu, et al.
European Journal of Human Genetics : EJHG|June 29, 2022
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP geneBoxun Zhao, Jill A Madden, Jasmine Lin, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
Nature Genetics|January 24, 2024
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Nature Genetics|August 21, 2023
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadismMaria Stamou, Miranda Tompkins, Hannah Bow, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Genome Biology|June 12, 2016
Resolving complex structural genomic rearrangements using a randomized approachXuefang Zhao, Sarah B Emery, Bridget Myers, et al.
Food Chemistry: X|June 1, 2026
Studies on the pure fermentation and aroma contributions of <i>Torulaspora delbrueckii</i> killer yeasts with high enzymatic activity in different white wine varietiesZhanzhan Jiang, Qinqin Liu, Xuefang Zhao, et al.
Food Chemistry|December 17, 2025
Effects of exogenous proline on malolactic fermentation by Oenococcus oeni and on volatiles, phenols, and antioxidant properties of Cabernet Sauvignon wineXuefang Zhao, Longxiang Liu, Akumawah Kyen Marie-Colette, et al.
Food Chemistry: X|March 21, 2025
From microbial communities to aroma profiles: A comparative study of spontaneous fermentation in merlot and cabernet sauvignon winesQinqin Liu, Nan Hao, Lan Mi, et al.
Frontiers in Plant Science|November 17, 2022
Evaluation of the resistance to Chinese predominant races of <i>Puccinia triticina</i> and analysis of effective leaf rust resistance genes in wheat accessions from the U.S. National Plant Germplasm SystemLin Zhang, Xuefang Zhao, Jingxian Liu, et al.
European Journal of Human Genetics : EJHG|June 29, 2022
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP geneBoxun Zhao, Jill A Madden, Jasmine Lin, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
Nature Genetics|January 24, 2024
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Nature Genetics|August 21, 2023
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing dataMehrtash Babadi, Jack M Fu, Samuel K Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadismMaria Stamou, Miranda Tompkins, Hannah Bow, et al.
Pageof 5