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Showing results (511-520 of 547) with videos related to

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Neurogenetics|November 19, 2015
De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autismLinshan Shang, Lindsay B Henderson, Megan T Cho, et al.
Neurogenetics|March 23, 2016
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic featuresHallie Steinfeld, Megan T Cho, Kyle Retterer, et al.
Environmental Pollution (Barking, Essex : 1987)|December 1, 2018
Evaluation of random forest regression and multiple linear regression for predicting indoor fine particulate matter concentrations in a highly polluted cityWeiran Yuchi, Enkhjargal Gombojav, Buyantushig Boldbaatar, et al.
Journal for Immunotherapy of Cancer|November 16, 2019
CRISPR-Cas9 disruption of PD-1 enhances activity of universal EGFRvIII CAR T cells in a preclinical model of human glioblastomaBryan D Choi, Xiaoling Yu, Ana P Castano, et al.
Journal of Medical Genetics|October 14, 2022
Heterozygous pathogenic variants involving <i>CBFB</i> cause a new skeletal disorder resembling cleidocranial dysplasiaTessi Beyltjens, Eveline Boudin, Nicole Revencu, et al.
The Lancet. Planetary Health|March 7, 2024
Estimates of global mortality burden associated with short-term exposure to fine particulate matter (PM<sub>2·5</sub>)Wenhua Yu, Rongbin Xu, Tingting Ye, et al.
Clinical Genetics|November 1, 2020
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variantsEva Z Jacobs, Kathleen Brown, Melissa C Byler, et al.
Plos One|October 16, 2010
Iridovirus and microsporidian linked to honey bee colony declineJerry J Bromenshenk, Colin B Henderson, Charles H Wick, et al.
American Journal of Medical Genetics. Part A|April 9, 2023
Biallelic variants in TUBGCP6 result in microcephaly and chorioretinopathy 1: Report of four cases and a literature reviewAmanda Thomas-Wilson, John P Schacht, David Chitayat, et al.
European Journal of Human Genetics : EJHG|February 17, 2021
Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K<sup>+</sup> channelopathiesKaren W Gripp, Sarah F Smithson, Ingrid J Scurr, et al.
Pageof 55

Showing results (511-520 of 547) with videos related to

Sort By:
Pageof 55
Neurogenetics|November 19, 2015
De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autismLinshan Shang, Lindsay B Henderson, Megan T Cho, et al.
Neurogenetics|March 23, 2016
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic featuresHallie Steinfeld, Megan T Cho, Kyle Retterer, et al.
Environmental Pollution (Barking, Essex : 1987)|December 1, 2018
Evaluation of random forest regression and multiple linear regression for predicting indoor fine particulate matter concentrations in a highly polluted cityWeiran Yuchi, Enkhjargal Gombojav, Buyantushig Boldbaatar, et al.
Journal for Immunotherapy of Cancer|November 16, 2019
CRISPR-Cas9 disruption of PD-1 enhances activity of universal EGFRvIII CAR T cells in a preclinical model of human glioblastomaBryan D Choi, Xiaoling Yu, Ana P Castano, et al.
Journal of Medical Genetics|October 14, 2022
Heterozygous pathogenic variants involving <i>CBFB</i> cause a new skeletal disorder resembling cleidocranial dysplasiaTessi Beyltjens, Eveline Boudin, Nicole Revencu, et al.
The Lancet. Planetary Health|March 7, 2024
Estimates of global mortality burden associated with short-term exposure to fine particulate matter (PM<sub>2·5</sub>)Wenhua Yu, Rongbin Xu, Tingting Ye, et al.
Clinical Genetics|November 1, 2020
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variantsEva Z Jacobs, Kathleen Brown, Melissa C Byler, et al.
Plos One|October 16, 2010
Iridovirus and microsporidian linked to honey bee colony declineJerry J Bromenshenk, Colin B Henderson, Charles H Wick, et al.
American Journal of Medical Genetics. Part A|April 9, 2023
Biallelic variants in TUBGCP6 result in microcephaly and chorioretinopathy 1: Report of four cases and a literature reviewAmanda Thomas-Wilson, John P Schacht, David Chitayat, et al.
European Journal of Human Genetics : EJHG|February 17, 2021
Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K<sup>+</sup> channelopathiesKaren W Gripp, Sarah F Smithson, Ingrid J Scurr, et al.
Pageof 55