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Human Genomics
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November 13, 2015
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments
Yichuan Liu, Yun Li, Michael E March, et al.
Human Genomics
|
September 17, 2015
Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma
Xiaoyu Wang, Xiaohong Li, Yichen Cheng, et al.
Human Genomics
|
May 20, 2016
Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population
Li An, Yingxiang Lin, Ting Yang, et al.
Human Genomics
|
April 6, 2016
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry
Adalgisa Pietropolli, Maria Vittoria Capogna, Raffaella Cascella, et al.
Human Genomics
|
July 21, 2017
Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome
Benjamin M Helm, Jason R Willer, Azita Sadeghpour, et al.
Human Genomics
|
September 15, 2019
lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cells
Qian Li, Jing Zhang, Dong-Mei Su, et al.
Human Genomics
|
February 24, 2021
cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVF
Jianjiang Zhu, Feng Hui, Xuequn Mao, et al.
Human Genomics
|
March 18, 2017
Transcriptome analysis of bronchoalveolar lavage fluid from children with severe Mycoplasma pneumoniae pneumonia reveals novel gene expression and immunodeficiency
Kuo Wang, Man Gao, Mingyue Yang, et al.
Human Genomics
|
December 17, 2004
Genomic and proteomic approaches for studying human cancer: prospects for true patient-tailored therapy
Kristen M Carr, Kevin Rosenblatt, Emanuel F Petricoin, et al.
Human Genomics
|
April 9, 2005
Cosmopolitan linkage disequilibrium maps
Jane Gibson, William Tapper, Weihua Zhang, et al.
Page
of 111
Search research articles
Search
Showing results (831-840 of 1,110) with videos related to
Sort By:
Page
of 111
Human Genomics
|
November 13, 2015
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments
Yichuan Liu, Yun Li, Michael E March, et al.
Human Genomics
|
September 17, 2015
Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma
Xiaoyu Wang, Xiaohong Li, Yichen Cheng, et al.
Human Genomics
|
May 20, 2016
Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population
Li An, Yingxiang Lin, Ting Yang, et al.
Human Genomics
|
April 6, 2016
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry
Adalgisa Pietropolli, Maria Vittoria Capogna, Raffaella Cascella, et al.
Human Genomics
|
July 21, 2017
Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome
Benjamin M Helm, Jason R Willer, Azita Sadeghpour, et al.
Human Genomics
|
September 15, 2019
lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cells
Qian Li, Jing Zhang, Dong-Mei Su, et al.
Human Genomics
|
February 24, 2021
cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVF
Jianjiang Zhu, Feng Hui, Xuequn Mao, et al.
Human Genomics
|
March 18, 2017
Transcriptome analysis of bronchoalveolar lavage fluid from children with severe Mycoplasma pneumoniae pneumonia reveals novel gene expression and immunodeficiency
Kuo Wang, Man Gao, Mingyue Yang, et al.
Human Genomics
|
December 17, 2004
Genomic and proteomic approaches for studying human cancer: prospects for true patient-tailored therapy
Kristen M Carr, Kevin Rosenblatt, Emanuel F Petricoin, et al.
Human Genomics
|
April 9, 2005
Cosmopolitan linkage disequilibrium maps
Jane Gibson, William Tapper, Weihua Zhang, et al.
Page
of 111