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NPJ Biofilms and Microbiomes
|
December 15, 2025
Maternal health status is associated with paired maternal and cord blood virome and mother-to-infant transmission
Xiaofei Song, Yutong Fu, Hui Xu, et al.
Human Genetics
|
November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype
Przemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
Human Genetics
|
July 27, 2018
Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis
Renqian Du, Nuriye Dinckan, Xiaofei Song, et al.
American Journal of Medical Genetics. Part A
|
November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)
Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
American Journal of Human Genetics
|
July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles
Zeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
August 9, 2024
Rapid Autopsy to Define Dendritic Cell Spatial Distribution and T Cell Association in Lung Adenocarcinoma
Hilal Ozakinci, Xiaofei Song, Gina S Nazario, et al.
Journal for Immunotherapy of Cancer
|
November 13, 2024
Differences in the pathological, transcriptomic, and prognostic implications of lymphoid structures between primary and metastatic cutaneous melanomas
Lilit Karapetyan, Aofei Li, Danielle Vargas De Stefano, et al.
Cancer Cell
|
October 10, 2025
Developing SEMA4A-directed CAR T cells to overcome low BCMA antigen density in multiple myeloma
Francesco Di Meo, Francesca Albano, Annamaria Cesarano, et al.
Genetics in Medicine Open
|
December 13, 2024
The impact of the Turkish population variome on the genomic architecture of rare disease traits
Zeynep Coban-Akdemir, Xiaofei Song, Francisco C Ceballos, et al.
Journal of Human Genetics
|
August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)
Kun Wang, Sen Zhao, Qianqian Zhang, et al.
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Search research articles
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Showing results (141-150 of 173) with videos related to
Sort By:
Page
of 18
NPJ Biofilms and Microbiomes
|
December 15, 2025
Maternal health status is associated with paired maternal and cord blood virome and mother-to-infant transmission
Xiaofei Song, Yutong Fu, Hui Xu, et al.
Human Genetics
|
November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype
Przemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
Human Genetics
|
July 27, 2018
Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis
Renqian Du, Nuriye Dinckan, Xiaofei Song, et al.
American Journal of Medical Genetics. Part A
|
November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)
Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
American Journal of Human Genetics
|
July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles
Zeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
August 9, 2024
Rapid Autopsy to Define Dendritic Cell Spatial Distribution and T Cell Association in Lung Adenocarcinoma
Hilal Ozakinci, Xiaofei Song, Gina S Nazario, et al.
Journal for Immunotherapy of Cancer
|
November 13, 2024
Differences in the pathological, transcriptomic, and prognostic implications of lymphoid structures between primary and metastatic cutaneous melanomas
Lilit Karapetyan, Aofei Li, Danielle Vargas De Stefano, et al.
Cancer Cell
|
October 10, 2025
Developing SEMA4A-directed CAR T cells to overcome low BCMA antigen density in multiple myeloma
Francesco Di Meo, Francesca Albano, Annamaria Cesarano, et al.
Genetics in Medicine Open
|
December 13, 2024
The impact of the Turkish population variome on the genomic architecture of rare disease traits
Zeynep Coban-Akdemir, Xiaofei Song, Francisco C Ceballos, et al.
Journal of Human Genetics
|
August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)
Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Page
of 18