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Daniel Greene

Showing results (21-30 of 53) with videos related to

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Nucleic Acids Research|August 24, 2021
MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseasesThiloka E Ratnaike, Daniel Greene, Wei Wei, et al.
Journal of Economic Entomology|May 17, 2024
Exploring market-available pheromone lures and traps for monitoring Anthonomus testaceosquamosus (Coleoptera: Curculionidae)Livia M S Ataide, A Daniel Greene, Kevin R Cloonan, et al.
Journal of Educational Psychology|August 16, 2016
Using Design Thinking to Improve Psychological Interventions: The Case of the Growth Mindset During the Transition to High SchoolDavid S Yeager, Carissa Romero, Dave Paunesku, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
The Journal of Allergy and Clinical Immunology|February 3, 2018
Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndromeJessica Heremans, Josselyn E Garcia-Perez, Ernest Turro, et al.
Medrxiv : the Preprint Server for Health Sciences|September 5, 2025
Biallelic variants in <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Blood|June 23, 2017
Expanded repertoire of <i>RASGRP2</i> variants responsible for platelet dysfunction and severe bleedingSarah K Westbury, Matthias Canault, Daniel Greene, et al.
Bioinformatics (Oxford, England)|March 24, 2017
Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic dataNikolas Pontikos, Jing Yu, Ismail Moghul, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 11, 2024
A Deep Intronic PKHD1 Variant Identified by SpliceAI in a Deceased Neonate With Autosomal Recessive Polycystic Kidney DiseaseFelix Richter, Kayleigh D Rutherford, Anisha J Cooke, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Nucleic Acids Research|August 24, 2021
MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseasesThiloka E Ratnaike, Daniel Greene, Wei Wei, et al.
Journal of Economic Entomology|May 17, 2024
Exploring market-available pheromone lures and traps for monitoring Anthonomus testaceosquamosus (Coleoptera: Curculionidae)Livia M S Ataide, A Daniel Greene, Kevin R Cloonan, et al.
Journal of Educational Psychology|August 16, 2016
Using Design Thinking to Improve Psychological Interventions: The Case of the Growth Mindset During the Transition to High SchoolDavid S Yeager, Carissa Romero, Dave Paunesku, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
The Journal of Allergy and Clinical Immunology|February 3, 2018
Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndromeJessica Heremans, Josselyn E Garcia-Perez, Ernest Turro, et al.
Medrxiv : the Preprint Server for Health Sciences|September 5, 2025
Biallelic variants in <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Blood|June 23, 2017
Expanded repertoire of <i>RASGRP2</i> variants responsible for platelet dysfunction and severe bleedingSarah K Westbury, Matthias Canault, Daniel Greene, et al.
Bioinformatics (Oxford, England)|March 24, 2017
Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic dataNikolas Pontikos, Jing Yu, Ismail Moghul, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 11, 2024
A Deep Intronic PKHD1 Variant Identified by SpliceAI in a Deceased Neonate With Autosomal Recessive Polycystic Kidney DiseaseFelix Richter, Kayleigh D Rutherford, Anisha J Cooke, et al.
Pageof 6