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Showing results (291-300 of 329) with videos related to

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BMC Medicine|December 4, 2020
Cisplatin and carboplatin result in similar gonadotoxicity in immature human testis with implications for fertility preservation in childhood cancerMelissa D Tharmalingam, Gabriele Matilionyte, William H B Wallace, et al.
Journal of Hematology & Oncology|October 25, 2021
Predictors of neutralizing antibody response to BNT162b2 vaccination in allogeneic hematopoietic stem cell transplant recipientsLorenzo Canti, Stéphanie Humblet-Baron, Isabelle Desombere, et al.
Mucosal Immunology|May 30, 2020
The RNA-binding protein tristetraprolin regulates RALDH2 expression by intestinal dendritic cells and controls local Treg homeostasisCaroline La, Bérengère de Toeuf, Laure B Bindels, et al.
Physical Review Letters|August 29, 2014
Plumbing neutron stars to new depths with the binding energy of the exotic nuclide 82ZnR N Wolf, D Beck, K Blaum, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 3, 2016
Solution-Grown Monocrystalline Hybrid Perovskite Films for Hole-Transporter-Free Solar CellsWei Peng, Lingfei Wang, Banavoth Murali, et al.
Cell Reports|February 14, 2026
In vivo modeling of human γδ T cell ontogeny reveals terminal deoxynucleotidyl transferase as a key regulator of type 3 Vδ2 T cell developmentCéline La, Aurélie Detavernier, Maria Papadopoulou, et al.
JCI Insight|January 26, 2021
Tristetraprolin expression by keratinocytes protects against skin carcinogenesisAssiya Assabban, Ingrid Dubois-Vedrenne, Laurye Van Maele, et al.
Journal of Hepatology|July 13, 2024
Infection history imprints prolonged changes to the epigenome, transcriptome and function of Kupffer cellsMohamed Amer Musrati, Benoit Stijlemans, Abdulkader Azouz, et al.
American Journal of Human Genetics|May 11, 2006
The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier malesStephen R F Twigg, Kazuya Matsumoto, Alexa M J Kidd, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2013
Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germlineEleni Giannoulatou, Gilean McVean, Indira B Taylor, et al.
Pageof 33

Showing results (291-300 of 329) with videos related to

Sort By:
Pageof 33
BMC Medicine|December 4, 2020
Cisplatin and carboplatin result in similar gonadotoxicity in immature human testis with implications for fertility preservation in childhood cancerMelissa D Tharmalingam, Gabriele Matilionyte, William H B Wallace, et al.
Journal of Hematology & Oncology|October 25, 2021
Predictors of neutralizing antibody response to BNT162b2 vaccination in allogeneic hematopoietic stem cell transplant recipientsLorenzo Canti, Stéphanie Humblet-Baron, Isabelle Desombere, et al.
Mucosal Immunology|May 30, 2020
The RNA-binding protein tristetraprolin regulates RALDH2 expression by intestinal dendritic cells and controls local Treg homeostasisCaroline La, Bérengère de Toeuf, Laure B Bindels, et al.
Physical Review Letters|August 29, 2014
Plumbing neutron stars to new depths with the binding energy of the exotic nuclide 82ZnR N Wolf, D Beck, K Blaum, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 3, 2016
Solution-Grown Monocrystalline Hybrid Perovskite Films for Hole-Transporter-Free Solar CellsWei Peng, Lingfei Wang, Banavoth Murali, et al.
Cell Reports|February 14, 2026
In vivo modeling of human γδ T cell ontogeny reveals terminal deoxynucleotidyl transferase as a key regulator of type 3 Vδ2 T cell developmentCéline La, Aurélie Detavernier, Maria Papadopoulou, et al.
JCI Insight|January 26, 2021
Tristetraprolin expression by keratinocytes protects against skin carcinogenesisAssiya Assabban, Ingrid Dubois-Vedrenne, Laurye Van Maele, et al.
Journal of Hepatology|July 13, 2024
Infection history imprints prolonged changes to the epigenome, transcriptome and function of Kupffer cellsMohamed Amer Musrati, Benoit Stijlemans, Abdulkader Azouz, et al.
American Journal of Human Genetics|May 11, 2006
The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier malesStephen R F Twigg, Kazuya Matsumoto, Alexa M J Kidd, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2013
Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germlineEleni Giannoulatou, Gilean McVean, Indira B Taylor, et al.
Pageof 33