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N Robinson

Showing results (1131-1140 of 1,318) with videos related to

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European Journal of Human Genetics : EJHG|October 9, 2014
Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patientDenise Emmerich, Tomasz Zemojtel, Jochen Hecht, et al.
Archives of Psychiatric Nursing|October 9, 2023
A scoping review of the concept of resilience among African American womenCheryl L Woods-Giscombe, Karen Patricia Williams, Jamie Conklin, et al.
Human-Computer Interaction|April 19, 2021
<i>Screenomics</i>: A Framework to Capture and Analyze Personal Life Experiences and the Ways that Technology Shapes ThemByron Reeves, Nilam Ram, Thomas N Robinson, et al.
NAR Genomics and Bioinformatics|December 10, 2021
Supervised learning with word embeddings derived from PubMed captures latent knowledge about protein kinases and cancerVida Ravanmehr, Hannah Blau, Luca Cappelletti, et al.
Stem Cells (Dayton, Ohio)|June 23, 2009
Noninvasive bioluminescent imaging demonstrates long-term multilineage engraftment of ex vivo-expanded CD34-selected umbilical cord blood cellsDavid Steiner, Juri Gelovani, Barbara Savoldo, et al.
Journal of Virology|April 6, 2007
Effective T-cell responses select human immunodeficiency virus mutants and slow disease progressionA J Frater, H Brown, A Oxenius, et al.
American Journal of Human Genetics|August 7, 2020
Interpretable Clinical Genomics with a Likelihood Ratio ParadigmPeter N Robinson, Vida Ravanmehr, Julius O B Jacobsen, et al.
Bioinformatics Advances|July 7, 2025
Leveraging generative AI to assist biocuration of medical actions for rare diseaseEnock Niyonkuru, J Harry Caufield, Leigh C Carmody, et al.
Scientific Data|February 8, 2025
An ontology-based rare disease common data model harmonising international registries, FHIR, and PhenopacketsAdam S L Graefe, Miriam R Hübner, Filip Rehburg, et al.
Nature Communications|June 12, 2021
E2F6 initiates stable epigenetic silencing of germline genes during embryonic developmentThomas Dahlet, Matthias Truss, Ute Frede, et al.
Pageof 132

Showing results (1131-1140 of 1,318) with videos related to

Sort By:
Pageof 132
European Journal of Human Genetics : EJHG|October 9, 2014
Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patientDenise Emmerich, Tomasz Zemojtel, Jochen Hecht, et al.
Archives of Psychiatric Nursing|October 9, 2023
A scoping review of the concept of resilience among African American womenCheryl L Woods-Giscombe, Karen Patricia Williams, Jamie Conklin, et al.
Human-Computer Interaction|April 19, 2021
<i>Screenomics</i>: A Framework to Capture and Analyze Personal Life Experiences and the Ways that Technology Shapes ThemByron Reeves, Nilam Ram, Thomas N Robinson, et al.
NAR Genomics and Bioinformatics|December 10, 2021
Supervised learning with word embeddings derived from PubMed captures latent knowledge about protein kinases and cancerVida Ravanmehr, Hannah Blau, Luca Cappelletti, et al.
Stem Cells (Dayton, Ohio)|June 23, 2009
Noninvasive bioluminescent imaging demonstrates long-term multilineage engraftment of ex vivo-expanded CD34-selected umbilical cord blood cellsDavid Steiner, Juri Gelovani, Barbara Savoldo, et al.
Journal of Virology|April 6, 2007
Effective T-cell responses select human immunodeficiency virus mutants and slow disease progressionA J Frater, H Brown, A Oxenius, et al.
American Journal of Human Genetics|August 7, 2020
Interpretable Clinical Genomics with a Likelihood Ratio ParadigmPeter N Robinson, Vida Ravanmehr, Julius O B Jacobsen, et al.
Bioinformatics Advances|July 7, 2025
Leveraging generative AI to assist biocuration of medical actions for rare diseaseEnock Niyonkuru, J Harry Caufield, Leigh C Carmody, et al.
Scientific Data|February 8, 2025
An ontology-based rare disease common data model harmonising international registries, FHIR, and PhenopacketsAdam S L Graefe, Miriam R Hübner, Filip Rehburg, et al.
Nature Communications|June 12, 2021
E2F6 initiates stable epigenetic silencing of germline genes during embryonic developmentThomas Dahlet, Matthias Truss, Ute Frede, et al.
Pageof 132