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Showing results (301-310 of 307) with videos related to

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Science Bulletin|December 10, 2021
Reprogramming of Ovarian Granulosa Cells by YAP1 Leads to Development of High-Grade Cancer with Mesenchymal Lineage and Serous FeaturesXiangmin Lv, Chunbo He, Cong Huang, et al.
Human Mutation|August 11, 2018
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVarErin R Riggs, Tristan Nelson, Andrew Merz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Circulation|June 21, 2019
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating VariantsChristopher M Haggerty, Scott M Damrauer, Michael G Levin, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Nature Neuroscience|April 18, 2023
Author Correction: A consensus protocol for functional connectivity analysis in the rat brainJoanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
Nature Neuroscience|March 27, 2023
A consensus protocol for functional connectivity analysis in the rat brainJoanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
Pageof 31

Showing results (301-310 of 307) with videos related to

Sort By:
Pageof 31
You have reached the last page of results.This site can display upto 307 results.
Science Bulletin|December 10, 2021
Reprogramming of Ovarian Granulosa Cells by YAP1 Leads to Development of High-Grade Cancer with Mesenchymal Lineage and Serous FeaturesXiangmin Lv, Chunbo He, Cong Huang, et al.
Human Mutation|August 11, 2018
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVarErin R Riggs, Tristan Nelson, Andrew Merz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Circulation|June 21, 2019
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating VariantsChristopher M Haggerty, Scott M Damrauer, Michael G Levin, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Nature Neuroscience|April 18, 2023
Author Correction: A consensus protocol for functional connectivity analysis in the rat brainJoanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
Nature Neuroscience|March 27, 2023
A consensus protocol for functional connectivity analysis in the rat brainJoanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
Pageof 31