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The Lancet. Infectious Diseases
|
April 25, 2024
The persistence of SARS-CoV-2 in tissues and its association with long COVID symptoms: a cross-sectional cohort study in China
Wenting Zuo, Di He, Chaoyang Liang, et al.
Cell Reports. Medicine
|
October 16, 2024
Modeling lung adenocarcinoma metastases using patient-derived organoids
Yuan Liu, Manendra Lankadasari, Joel Rosiene, et al.
Cancer Cell
|
April 21, 2023
Genomic mapping of metastatic organotropism in lung adenocarcinoma
Harry B Lengel, Brooke Mastrogiacomo, James G Connolly, et al.
JCI Insight
|
January 11, 2022
A congenital CMV infection model for follow-up studies of neurodevelopmental disorders, neuroimaging abnormalities, and treatment
Yue-Peng Zhou, Meng-Jie Mei, Xian-Zhang Wang, et al.
Nature Genetics
|
January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
Yaran Wen, Yang Liu, Yiming Xu, et al.
Nature Genetics
|
January 27, 2009
Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21
Xue-Jun Zhang, Wei Huang, Sen Yang, et al.
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Search research articles
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Showing results (421-430 of 426) with videos related to
Sort By:
Page
of 43
You have reached the last page of results.
This site can display upto 426 results.
The Lancet. Infectious Diseases
|
April 25, 2024
The persistence of SARS-CoV-2 in tissues and its association with long COVID symptoms: a cross-sectional cohort study in China
Wenting Zuo, Di He, Chaoyang Liang, et al.
Cell Reports. Medicine
|
October 16, 2024
Modeling lung adenocarcinoma metastases using patient-derived organoids
Yuan Liu, Manendra Lankadasari, Joel Rosiene, et al.
Cancer Cell
|
April 21, 2023
Genomic mapping of metastatic organotropism in lung adenocarcinoma
Harry B Lengel, Brooke Mastrogiacomo, James G Connolly, et al.
JCI Insight
|
January 11, 2022
A congenital CMV infection model for follow-up studies of neurodevelopmental disorders, neuroimaging abnormalities, and treatment
Yue-Peng Zhou, Meng-Jie Mei, Xian-Zhang Wang, et al.
Nature Genetics
|
January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
Yaran Wen, Yang Liu, Yiming Xu, et al.
Nature Genetics
|
January 27, 2009
Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21
Xue-Jun Zhang, Wei Huang, Sen Yang, et al.
Page
of 43