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Journal of Applied Microbiology
|
September 12, 2024
Heterologous expression of sulfur: quinone oxidoreductase (Sqr) to improve Thioalkalivibrio versutus D301 desulfurization performance
Zhuang Tian, Chenxi Yu, He Li, et al.
Journal of Chromatography. A
|
June 18, 2026
Fragmentation property identity card-assisted reliable structural annotation of calycosin metabolites in vivo: A strategy for isomer discrimination using mass spectrometry
Rui Wang, Yang Liu, Wenhan Song, et al.
Frontiers in Genetics
|
July 2, 2024
Deciphering the pathogenic role of rare <i>RAF1</i> heterozygous missense mutation in the late-presenting DDH
Yuzhao Liu, Xuesong Fan, Kun Qian, et al.
BMC Medical Genetics
|
May 29, 2020
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia
Jiashen Shao, Sen Zhao, Zihui Yan, et al.
Orphanet Journal of Rare Diseases
|
March 29, 2022
Delineation of dual molecular diagnosis in patients with skeletal deformity
Lian Liu, Liying Sun, Yujun Chen, et al.
Prostate Cancer and Prostatic Diseases
|
April 1, 2026
Cytoplasmic versus nuclear localization of androgen receptor splice variant 7 as a predictor of benefit from androgen receptor pathway inhibitors in metastatic castration-resistant prostate cancer (PROPHECY trial)
Santosh Gupta, Siyuan Guo, Susan Halabi, et al.
Nature Biotechnology
|
October 31, 2025
High-plex spatial RNA imaging in one round with conventional microscopes using color-intensity barcodes
Tianyi Chang, Shihui Zhao, Kunyue Deng, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
November 29, 2025
HPD is an m<sup>6</sup>A Methyltransferase that Protects Colorectal Cancer Cells from Ferroptotic Cell Death by m<sup>6</sup>A Methylating SLC7A11/GPX4
Jiyan Wang, Xintong Dai, Huanle Liu, et al.
Orphanet Journal of Rare Diseases
|
September 16, 2020
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Zefu Chen, Zihui Yan, Chenxi Yu, et al.
American Journal of Human Genetics
|
January 22, 2022
PhenoApt leverages clinical expertise to prioritize candidate genes via machine learning
Zefu Chen, Yu Zheng, Yongxin Yang, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 71) with videos related to
Sort By:
Page
of 8
Journal of Applied Microbiology
|
September 12, 2024
Heterologous expression of sulfur: quinone oxidoreductase (Sqr) to improve Thioalkalivibrio versutus D301 desulfurization performance
Zhuang Tian, Chenxi Yu, He Li, et al.
Journal of Chromatography. A
|
June 18, 2026
Fragmentation property identity card-assisted reliable structural annotation of calycosin metabolites in vivo: A strategy for isomer discrimination using mass spectrometry
Rui Wang, Yang Liu, Wenhan Song, et al.
Frontiers in Genetics
|
July 2, 2024
Deciphering the pathogenic role of rare <i>RAF1</i> heterozygous missense mutation in the late-presenting DDH
Yuzhao Liu, Xuesong Fan, Kun Qian, et al.
BMC Medical Genetics
|
May 29, 2020
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia
Jiashen Shao, Sen Zhao, Zihui Yan, et al.
Orphanet Journal of Rare Diseases
|
March 29, 2022
Delineation of dual molecular diagnosis in patients with skeletal deformity
Lian Liu, Liying Sun, Yujun Chen, et al.
Prostate Cancer and Prostatic Diseases
|
April 1, 2026
Cytoplasmic versus nuclear localization of androgen receptor splice variant 7 as a predictor of benefit from androgen receptor pathway inhibitors in metastatic castration-resistant prostate cancer (PROPHECY trial)
Santosh Gupta, Siyuan Guo, Susan Halabi, et al.
Nature Biotechnology
|
October 31, 2025
High-plex spatial RNA imaging in one round with conventional microscopes using color-intensity barcodes
Tianyi Chang, Shihui Zhao, Kunyue Deng, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
November 29, 2025
HPD is an m<sup>6</sup>A Methyltransferase that Protects Colorectal Cancer Cells from Ferroptotic Cell Death by m<sup>6</sup>A Methylating SLC7A11/GPX4
Jiyan Wang, Xintong Dai, Huanle Liu, et al.
Orphanet Journal of Rare Diseases
|
September 16, 2020
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis
Zefu Chen, Zihui Yan, Chenxi Yu, et al.
American Journal of Human Genetics
|
January 22, 2022
PhenoApt leverages clinical expertise to prioritize candidate genes via machine learning
Zefu Chen, Yu Zheng, Yongxin Yang, et al.
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of 8