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Emily Huber

Showing results (1-10 of 12) with videos related to

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Kentucky Nurse|May 2, 2015
Ellen Hudson: a transformational leaderEmily Huber
Genome Medicine|October 18, 2021
Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletionMatthew Jensen, Anastasia Tyryshkina, Lucilla Pizzo, et al.
Acta Neuropathologica Communications|May 3, 2025
Systemic IGF-1 administration prevents traumatic brain injury induced gut permeability, dysmorphia, dysbiosis, and the increased number of immature dentate granule cellsLavanya Venkatasamy, Jaclyn Iannucci, Aleksandr Pereverzev, et al.
Plos Genetics|February 14, 2020
NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis modelsMayanglambam Dhruba Singh, Matthew Jensen, Micaela Lasser, et al.
Breast Cancer Research and Treatment|February 21, 2026
Investigating initial patterns of progression on first-line treatment in patients with de novo metastatic breast cancerEmily Huber, Gaorav P Gupta, Ryan Morse, et al.
Nature Communications|July 1, 2018
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogasterJanani Iyer, Mayanglambam Dhruba Singh, Matthew Jensen, et al.
Plos Genetics|April 5, 2021
Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevisLucilla Pizzo, Micaela Lasser, Tanzeen Yusuff, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
American Journal of Human Genetics|November 18, 2023
Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variantsLucilla Pizzo, Matthew Jensen, Andrew Polyak, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Kentucky Nurse|May 2, 2015
Ellen Hudson: a transformational leaderEmily Huber
Genome Medicine|October 18, 2021
Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletionMatthew Jensen, Anastasia Tyryshkina, Lucilla Pizzo, et al.
Acta Neuropathologica Communications|May 3, 2025
Systemic IGF-1 administration prevents traumatic brain injury induced gut permeability, dysmorphia, dysbiosis, and the increased number of immature dentate granule cellsLavanya Venkatasamy, Jaclyn Iannucci, Aleksandr Pereverzev, et al.
Plos Genetics|February 14, 2020
NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis modelsMayanglambam Dhruba Singh, Matthew Jensen, Micaela Lasser, et al.
Breast Cancer Research and Treatment|February 21, 2026
Investigating initial patterns of progression on first-line treatment in patients with de novo metastatic breast cancerEmily Huber, Gaorav P Gupta, Ryan Morse, et al.
Nature Communications|July 1, 2018
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogasterJanani Iyer, Mayanglambam Dhruba Singh, Matthew Jensen, et al.
Plos Genetics|April 5, 2021
Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevisLucilla Pizzo, Micaela Lasser, Tanzeen Yusuff, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
American Journal of Human Genetics|November 18, 2023
Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variantsCorrine Smolen, Matthew Jensen, Lisa Dyer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variantsLucilla Pizzo, Matthew Jensen, Andrew Polyak, et al.
Pageof 2