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K Morgan

Showing results (1001-1010 of 1,112) with videos related to

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Oncotarget|February 26, 2013
Dual EGFR inhibition in combination with anti-VEGF treatment: a phase I clinical trial in non-small cell lung cancerGerald S Falchook, Aung Naing, David S Hong, et al.
NAR Cancer|April 24, 2023
Deletion of the mRNA stability factor <i>ELAVL1</i> (HuR) in pancreatic cancer cells disrupts the tumor microenvironment integrityGrace A McCarthy, Roberto Di Niro, Jennifer M Finan, et al.
American Journal of Obstetrics and Gynecology|October 10, 2020
To the Point: advising students applying to Obstetrics and Gynecology residency in 2020 and beyondCeleste S Royce, Elise N Everett, LaTasha B Craig, et al.
JACC. Cardiovascular Imaging|December 15, 2012
Ultrasound-mediated vascular gene transfection by cavitation of endothelial-targeted cationic microbubblesAris Xie, Todd Belcik, Yue Qi, et al.
Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.
American Journal of Obstetrics and Gynecology|August 16, 2022
Placental pathology is necessary to understand common pregnancy complications and achieve an improved taxonomy of obstetrical diseaseRaymond W Redline, Drucilla J Roberts, Mana M Parast, et al.
Immunity|April 15, 2025
Acute exposure to high-fat diet impairs ILC3 functions and gut homeostasisLe Xiong, Shanti Diwakarla, Roxanne Chatzis, et al.
Environmental Science & Technology|March 2, 2019
Comparative Analyses of the 12 Most Abundant PCB Congeners Detected in Human Maternal Serum for Activity at the Thyroid Hormone Receptor and Ryanodine ReceptorSunjay Sethi, Rhianna K Morgan, Wei Feng, et al.
The Journal of Clinical Investigation|July 3, 1998
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complexS M Mulders, D G Bichet, J P Rijss, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Bowen-Conradi syndrome: a clinical and genetic studyR B Lowry, A M Innes, F P Bernier, et al.
Pageof 112

Showing results (1001-1010 of 1,112) with videos related to

Sort By:
Pageof 112
Oncotarget|February 26, 2013
Dual EGFR inhibition in combination with anti-VEGF treatment: a phase I clinical trial in non-small cell lung cancerGerald S Falchook, Aung Naing, David S Hong, et al.
NAR Cancer|April 24, 2023
Deletion of the mRNA stability factor <i>ELAVL1</i> (HuR) in pancreatic cancer cells disrupts the tumor microenvironment integrityGrace A McCarthy, Roberto Di Niro, Jennifer M Finan, et al.
American Journal of Obstetrics and Gynecology|October 10, 2020
To the Point: advising students applying to Obstetrics and Gynecology residency in 2020 and beyondCeleste S Royce, Elise N Everett, LaTasha B Craig, et al.
JACC. Cardiovascular Imaging|December 15, 2012
Ultrasound-mediated vascular gene transfection by cavitation of endothelial-targeted cationic microbubblesAris Xie, Todd Belcik, Yue Qi, et al.
Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.
American Journal of Obstetrics and Gynecology|August 16, 2022
Placental pathology is necessary to understand common pregnancy complications and achieve an improved taxonomy of obstetrical diseaseRaymond W Redline, Drucilla J Roberts, Mana M Parast, et al.
Immunity|April 15, 2025
Acute exposure to high-fat diet impairs ILC3 functions and gut homeostasisLe Xiong, Shanti Diwakarla, Roxanne Chatzis, et al.
Environmental Science & Technology|March 2, 2019
Comparative Analyses of the 12 Most Abundant PCB Congeners Detected in Human Maternal Serum for Activity at the Thyroid Hormone Receptor and Ryanodine ReceptorSunjay Sethi, Rhianna K Morgan, Wei Feng, et al.
The Journal of Clinical Investigation|July 3, 1998
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complexS M Mulders, D G Bichet, J P Rijss, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Bowen-Conradi syndrome: a clinical and genetic studyR B Lowry, A M Innes, F P Bernier, et al.
Pageof 112