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American Journal of Medical Genetics. Part A
|
February 6, 2019
Isolated vocal cord paralysis in two siblings with compound heterozygous variants in MUSK: Expanding the phenotypic spectrum
Chaya Murali, Dong Li, Katheryn Grand, et al.
Genes
|
April 28, 2023
RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic Target
Brian E White, Yichuan Liu, Hakon Hakonarson, et al.
Nature Methods
|
May 23, 2024
Dependency-aware deep generative models for multitasking analysis of spatial omics data
Tian Tian, Jie Zhang, Xiang Lin, et al.
Discovery Medicine
|
July 29, 2011
Convergent mechanisms of somatic mutations in polycythemia vera
Kai Wang, Sabina Swierczek, Kimberly Hickman, et al.
Nucleic Acids Research
|
August 5, 2011
SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data
Zhi Wei, Wei Wang, Pingzhao Hu, et al.
World Journal of Gastroenterology
|
November 5, 2013
Impact of exome sequencing in inflammatory bowel disease
Christopher J Cardinale, Judith R Kelsen, Robert N Baldassano, et al.
Scientific Reports
|
September 13, 2024
Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children
Jelte Kelchtermans, Michael E March, Hakon Hakonarson, et al.
European Journal of Human Genetics : EJHG
|
November 21, 2013
Making the genomic leap in HCT: application of second-generation sequencing to clinical advances in hematopoietic cell transplantation
Yun R Li, John E Levine, Hakon Hakonarson, et al.
American Journal of Human Genetics
|
August 14, 2012
Phasing of many thousands of genotyped samples
Amy L Williams, Nick Patterson, Joseph Glessner, et al.
Viruses
|
October 21, 2020
Expression Pattern of the SARS-CoV-2 Entry Genes <i>ACE2</i> and <i>TMPRSS2</i> in the Respiratory Tract
Yichuan Liu, Hui-Qi Qu, Jingchun Qu, et al.
Page
of 95
Search research articles
Search
Showing results (81-90 of 950) with videos related to
Sort By:
Page
of 95
American Journal of Medical Genetics. Part A
|
February 6, 2019
Isolated vocal cord paralysis in two siblings with compound heterozygous variants in MUSK: Expanding the phenotypic spectrum
Chaya Murali, Dong Li, Katheryn Grand, et al.
Genes
|
April 28, 2023
RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic Target
Brian E White, Yichuan Liu, Hakon Hakonarson, et al.
Nature Methods
|
May 23, 2024
Dependency-aware deep generative models for multitasking analysis of spatial omics data
Tian Tian, Jie Zhang, Xiang Lin, et al.
Discovery Medicine
|
July 29, 2011
Convergent mechanisms of somatic mutations in polycythemia vera
Kai Wang, Sabina Swierczek, Kimberly Hickman, et al.
Nucleic Acids Research
|
August 5, 2011
SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data
Zhi Wei, Wei Wang, Pingzhao Hu, et al.
World Journal of Gastroenterology
|
November 5, 2013
Impact of exome sequencing in inflammatory bowel disease
Christopher J Cardinale, Judith R Kelsen, Robert N Baldassano, et al.
Scientific Reports
|
September 13, 2024
Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children
Jelte Kelchtermans, Michael E March, Hakon Hakonarson, et al.
European Journal of Human Genetics : EJHG
|
November 21, 2013
Making the genomic leap in HCT: application of second-generation sequencing to clinical advances in hematopoietic cell transplantation
Yun R Li, John E Levine, Hakon Hakonarson, et al.
American Journal of Human Genetics
|
August 14, 2012
Phasing of many thousands of genotyped samples
Amy L Williams, Nick Patterson, Joseph Glessner, et al.
Viruses
|
October 21, 2020
Expression Pattern of the SARS-CoV-2 Entry Genes <i>ACE2</i> and <i>TMPRSS2</i> in the Respiratory Tract
Yichuan Liu, Hui-Qi Qu, Jingchun Qu, et al.
Page
of 95