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Nucleic Acids Research
|
June 8, 2024
iSuRe-HadCre is an essential tool for effective conditional genetics
Irene Garcia-Gonzalez, Susana F Rocha, Anahita Hamidi, et al.
Vaccines
|
June 28, 2023
Sulfated Lactosyl Archaeol Archaeosome-Adjuvanted Vaccine Formulations Targeting Rabbit Hemorrhagic Disease Virus Are Immunogenic and Efficacious
Bassel Akache, Andrew J Read, Renu Dudani, et al.
The Journal of Experimental Medicine
|
May 14, 2021
Upregulation of VCAM-1 in lymphatic collectors supports dendritic cell entry and rapid migration to lymph nodes in inflammation
Jorge Arasa, Victor Collado-Diaz, Ioannis Kritikos, et al.
Frontiers in Physiology
|
February 23, 2023
Mapping the lymphatic system across body scales and expertise domains: A report from the 2021 National Heart, Lung, and Blood Institute workshop at the Boston Lymphatic Symposium
Dhruv Singhal, Katy Börner, Elliot L Chaikof, et al.
Scientific Reports
|
June 13, 2022
Intranasal immunization with a proteosome-adjuvanted SARS-CoV-2 spike protein-based vaccine is immunogenic and efficacious in mice and hamsters
Felicity C Stark, Bassel Akache, Lise Deschatelets, et al.
JCI Insight
|
August 17, 2021
Mutations in EPHB4 cause human venous valve aplasia
Oliver Lyons, James Walker, Christopher Seet, et al.
Nature Genetics
|
September 6, 2011
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
Pia Ostergaard, Michael A Simpson, Fiona C Connell, et al.
The Journal of Experimental Medicine
|
July 21, 2017
Human venous valve disease caused by mutations in FOXC2 and GJC2
Oliver Lyons, Prakash Saha, Christopher Seet, et al.
Genes & Development
|
April 19, 2011
Vascular endothelial growth factor receptor 3 directly regulates murine neurogenesis
Charles-Félix Calvo, Romain H Fontaine, Jihane Soueid, et al.
The Journal of Clinical Investigation
|
July 12, 2016
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis
Silvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 204) with videos related to
Sort By:
Page
of 21
Nucleic Acids Research
|
June 8, 2024
iSuRe-HadCre is an essential tool for effective conditional genetics
Irene Garcia-Gonzalez, Susana F Rocha, Anahita Hamidi, et al.
Vaccines
|
June 28, 2023
Sulfated Lactosyl Archaeol Archaeosome-Adjuvanted Vaccine Formulations Targeting Rabbit Hemorrhagic Disease Virus Are Immunogenic and Efficacious
Bassel Akache, Andrew J Read, Renu Dudani, et al.
The Journal of Experimental Medicine
|
May 14, 2021
Upregulation of VCAM-1 in lymphatic collectors supports dendritic cell entry and rapid migration to lymph nodes in inflammation
Jorge Arasa, Victor Collado-Diaz, Ioannis Kritikos, et al.
Frontiers in Physiology
|
February 23, 2023
Mapping the lymphatic system across body scales and expertise domains: A report from the 2021 National Heart, Lung, and Blood Institute workshop at the Boston Lymphatic Symposium
Dhruv Singhal, Katy Börner, Elliot L Chaikof, et al.
Scientific Reports
|
June 13, 2022
Intranasal immunization with a proteosome-adjuvanted SARS-CoV-2 spike protein-based vaccine is immunogenic and efficacious in mice and hamsters
Felicity C Stark, Bassel Akache, Lise Deschatelets, et al.
JCI Insight
|
August 17, 2021
Mutations in EPHB4 cause human venous valve aplasia
Oliver Lyons, James Walker, Christopher Seet, et al.
Nature Genetics
|
September 6, 2011
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
Pia Ostergaard, Michael A Simpson, Fiona C Connell, et al.
The Journal of Experimental Medicine
|
July 21, 2017
Human venous valve disease caused by mutations in FOXC2 and GJC2
Oliver Lyons, Prakash Saha, Christopher Seet, et al.
Genes & Development
|
April 19, 2011
Vascular endothelial growth factor receptor 3 directly regulates murine neurogenesis
Charles-Félix Calvo, Romain H Fontaine, Jihane Soueid, et al.
The Journal of Clinical Investigation
|
July 12, 2016
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis
Silvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, et al.
Page
of 21