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A Borja

Showing results (41-50 of 54) with videos related to

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JCO Precision Oncology|January 23, 2026
Impact of Hereditary Cancer Susceptibility in Solid-Organ Transplant RecipientsNicholas Khuu, Marie Jeanjean, Talia Donenberg, et al.
Medicina|October 18, 2025
[Electrotonic modulation as a differential diagnosis of negative T wave]Ana C Pires, Gonzalo R Voboril, Juan M Iroulart, et al.
Medicina|April 10, 2026
[Terminological accuracy in the diagnosis of electrical memory]Ana C Pires, Gonzalo R Voboril, Juan M Iroulart, et al.
Pediatric Blood & Cancer|March 18, 2026
Biallelic Inactivation of NSD1 Associated With Carcinogenesis in Sotos SyndromeNicholas A Borja, Anuja Sule, Katie Ann McMullen, et al.
Journal of Medical Genetics|December 31, 2024
Congenital urinary tract anomalies are a variable finding associated with nevoid basal cell carcinoma syndromeIsha Harshe, Talia Donenberg, Marie Jeanjean, et al.
Oncotarget|July 10, 2015
Selective impact of CDK4/6 suppression on patient-derived models of pancreatic cancerAgnieszka K Witkiewicz, Nicholas A Borja, Jorge Franco, et al.
American Journal of Medical Genetics. Part A|October 14, 2024
Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease NetworkNicholas A Borja, Rory J Tinker, Stephanie A Bivona, et al.
Molecular Genetics and Metabolism|August 5, 2025
Institutional readiness for novel therapeutics: A framework for multidisciplinary integrationElizabeth G Ames, Nicholas A Borja, Russell J Butterfield, et al.
Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Ophthalmic Genetics|May 29, 2025
Novel <i>KMT2D</i> pathogenic variant causing Kabuki Syndrome with associated macular abnormalities and retinopathy of prematurityFrancisco J López-Font, Sofia De Arrigunaga, Natasha F Santos da Cruz, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
JCO Precision Oncology|January 23, 2026
Impact of Hereditary Cancer Susceptibility in Solid-Organ Transplant RecipientsNicholas Khuu, Marie Jeanjean, Talia Donenberg, et al.
Medicina|October 18, 2025
[Electrotonic modulation as a differential diagnosis of negative T wave]Ana C Pires, Gonzalo R Voboril, Juan M Iroulart, et al.
Medicina|April 10, 2026
[Terminological accuracy in the diagnosis of electrical memory]Ana C Pires, Gonzalo R Voboril, Juan M Iroulart, et al.
Pediatric Blood & Cancer|March 18, 2026
Biallelic Inactivation of NSD1 Associated With Carcinogenesis in Sotos SyndromeNicholas A Borja, Anuja Sule, Katie Ann McMullen, et al.
Journal of Medical Genetics|December 31, 2024
Congenital urinary tract anomalies are a variable finding associated with nevoid basal cell carcinoma syndromeIsha Harshe, Talia Donenberg, Marie Jeanjean, et al.
Oncotarget|July 10, 2015
Selective impact of CDK4/6 suppression on patient-derived models of pancreatic cancerAgnieszka K Witkiewicz, Nicholas A Borja, Jorge Franco, et al.
American Journal of Medical Genetics. Part A|October 14, 2024
Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease NetworkNicholas A Borja, Rory J Tinker, Stephanie A Bivona, et al.
Molecular Genetics and Metabolism|August 5, 2025
Institutional readiness for novel therapeutics: A framework for multidisciplinary integrationElizabeth G Ames, Nicholas A Borja, Russell J Butterfield, et al.
Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Ophthalmic Genetics|May 29, 2025
Novel <i>KMT2D</i> pathogenic variant causing Kabuki Syndrome with associated macular abnormalities and retinopathy of prematurityFrancisco J López-Font, Sofia De Arrigunaga, Natasha F Santos da Cruz, et al.
Pageof 6