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K Dale

Showing results (251-260 of 283) with videos related to

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Developmental Cell|February 27, 2025
Deletion of a single CTCF motif at the boundary of a chromatin domain with three FGF genes disrupts gene expression and embryonic developmentShreeta Chakraborty, Nina Wenzlitschke, Matthew J Anderson, et al.
Nature|September 28, 2002
Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiencyHyung J Chun, Lixin Zheng, Manzoor Ahmad, et al.
American Journal of Human Genetics|March 26, 1999
Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetranceC E Jackson, R E Fischer, A P Hsu, et al.
Pediatrics|October 15, 2014
Reducing mortality and infections after congenital heart surgery in the developing worldKathy J Jenkins, Aldo R Castañeda, K M Cherian, et al.
Nature Communications|September 14, 2023
Multimodal spatiotemporal transcriptomic resolution of embryonic palate osteogenesisJeremie Oliver Piña, Resmi Raju, Daniela M Roth, et al.
Biomarker Research|February 1, 2023
Identification of cerebral spinal fluid protein biomarkers in Niemann-Pick disease, type C1Kiersten Campbell, Niamh X Cawley, Rachel Luke, et al.
The American Journal of Pathology|November 12, 1998
Pathological findings in human autoimmune lymphoproliferative syndromeM S Lim, S E Straus, J K Dale, et al.
Nature Communications|October 31, 2025
Young KRAB-zinc finger gene clusters are highly dynamic incubators of ERV-driven genetic heterogeneity in miceMelania Bruno, Sharaf M Farhana, Apratim Mitra, et al.
AIDS Patient Care and Stds|May 19, 2023
<i>Viv Byen</i> (Live Well): A Qualitative Pilot Study to Assess Telehealth Use for HIV Care Among People of Haitian DescentCandice A Sternberg, Camille Jackyvens, Raema Mimrod Jean, et al.
The Journal of Experimental Medicine|April 2, 2020
Somatic SMAD3-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathwayHeeseog Kang, Smita Jha, Aleksandra Ivovic, et al.
Pageof 29

Showing results (251-260 of 283) with videos related to

Sort By:
Pageof 29
Developmental Cell|February 27, 2025
Deletion of a single CTCF motif at the boundary of a chromatin domain with three FGF genes disrupts gene expression and embryonic developmentShreeta Chakraborty, Nina Wenzlitschke, Matthew J Anderson, et al.
Nature|September 28, 2002
Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiencyHyung J Chun, Lixin Zheng, Manzoor Ahmad, et al.
American Journal of Human Genetics|March 26, 1999
Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetranceC E Jackson, R E Fischer, A P Hsu, et al.
Pediatrics|October 15, 2014
Reducing mortality and infections after congenital heart surgery in the developing worldKathy J Jenkins, Aldo R Castañeda, K M Cherian, et al.
Nature Communications|September 14, 2023
Multimodal spatiotemporal transcriptomic resolution of embryonic palate osteogenesisJeremie Oliver Piña, Resmi Raju, Daniela M Roth, et al.
Biomarker Research|February 1, 2023
Identification of cerebral spinal fluid protein biomarkers in Niemann-Pick disease, type C1Kiersten Campbell, Niamh X Cawley, Rachel Luke, et al.
The American Journal of Pathology|November 12, 1998
Pathological findings in human autoimmune lymphoproliferative syndromeM S Lim, S E Straus, J K Dale, et al.
Nature Communications|October 31, 2025
Young KRAB-zinc finger gene clusters are highly dynamic incubators of ERV-driven genetic heterogeneity in miceMelania Bruno, Sharaf M Farhana, Apratim Mitra, et al.
AIDS Patient Care and Stds|May 19, 2023
<i>Viv Byen</i> (Live Well): A Qualitative Pilot Study to Assess Telehealth Use for HIV Care Among People of Haitian DescentCandice A Sternberg, Camille Jackyvens, Raema Mimrod Jean, et al.
The Journal of Experimental Medicine|April 2, 2020
Somatic SMAD3-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathwayHeeseog Kang, Smita Jha, Aleksandra Ivovic, et al.
Pageof 29