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Showing results (1241-1250 of 1,360) with videos related to

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Endoscopy International Open|February 29, 2024
The Bethesda ERCP Skills Assessment Tool (BESAT) can reliably differentiate endoscopists of different experience levelsKevin Liu, B Joseph Elmunzer, Sachin Wani, et al.
Pediatric Neurology|May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
Cell Host & Microbe|December 23, 2022
An epithelial-immune circuit amplifies inflammasome and IL-6 responses to SARS-CoV-2Katherine C Barnett, Yuying Xie, Takanori Asakura, et al.
NPJ Genomic Medicine|October 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline diseaseChristian R Marshall, Shimul Chowdhury, Ryan J Taft, et al.
Pharmaceuticals (Basel, Switzerland)|January 30, 2019
Identification of Potential Inhibitors from Pyriproxyfen with Insecticidal Activity by Virtual ScreeningRyan da Silva Ramos, Josivan da Silva Costa, Rai Campos Silva, et al.
NPJ Genomic Medicine|October 29, 2024
Clinical genome sequencing in patients with suspected rare genetic disease in PeruJeny Bazalar-Montoya, Mario Cornejo-Olivas, Milagros M Duenas-Roque, et al.
American Journal of Human Genetics|October 2, 2018
Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic EncephalopathyThi Tuyet Mai Nguyen, Yoshiko Murakami, Kristen M Wigby, et al.
Nature Genetics|November 25, 2014
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Science (New York, N.Y.)|June 16, 2022
Meteorin-like promotes heart repair through endothelial KIT receptor tyrosine kinaseMarc R Reboll, Stefanie Klede, Manuel H Taft, et al.
American Journal of Human Genetics|April 16, 2013
A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellumCas Simons, Nicole I Wolf, Nathan McNeil, et al.
Pageof 136

Showing results (1241-1250 of 1,360) with videos related to

Sort By:
Pageof 136
Endoscopy International Open|February 29, 2024
The Bethesda ERCP Skills Assessment Tool (BESAT) can reliably differentiate endoscopists of different experience levelsKevin Liu, B Joseph Elmunzer, Sachin Wani, et al.
Pediatric Neurology|May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
Cell Host & Microbe|December 23, 2022
An epithelial-immune circuit amplifies inflammasome and IL-6 responses to SARS-CoV-2Katherine C Barnett, Yuying Xie, Takanori Asakura, et al.
NPJ Genomic Medicine|October 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline diseaseChristian R Marshall, Shimul Chowdhury, Ryan J Taft, et al.
Pharmaceuticals (Basel, Switzerland)|January 30, 2019
Identification of Potential Inhibitors from Pyriproxyfen with Insecticidal Activity by Virtual ScreeningRyan da Silva Ramos, Josivan da Silva Costa, Rai Campos Silva, et al.
NPJ Genomic Medicine|October 29, 2024
Clinical genome sequencing in patients with suspected rare genetic disease in PeruJeny Bazalar-Montoya, Mario Cornejo-Olivas, Milagros M Duenas-Roque, et al.
American Journal of Human Genetics|October 2, 2018
Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic EncephalopathyThi Tuyet Mai Nguyen, Yoshiko Murakami, Kristen M Wigby, et al.
Nature Genetics|November 25, 2014
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Science (New York, N.Y.)|June 16, 2022
Meteorin-like promotes heart repair through endothelial KIT receptor tyrosine kinaseMarc R Reboll, Stefanie Klede, Manuel H Taft, et al.
American Journal of Human Genetics|April 16, 2013
A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellumCas Simons, Nicole I Wolf, Nathan McNeil, et al.
Pageof 136