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M Elizabeth Ross

Showing results (41-50 of 75) with videos related to

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Cell Research|July 27, 2019
Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variantsZhongzhong Chen, Yunping Lei, Yufang Zheng, et al.
Human Molecular Genetics|June 19, 2013
LRP6 exerts non-canonical effects on Wnt signaling during neural tube closureJason D Gray, Stanislav Kholmanskikh, Bozena S Castaldo, et al.
Biological Psychiatry|November 19, 2017
Mature Hippocampal Neurons Require LIS1 for Synaptic Integrity: Implications for CognitionAnamaria Sudarov, Xin-Jun Zhang, Leighton Braunstein, et al.
Genes & Development|June 15, 2018
PARD3 dysfunction in conjunction with dynamic HIPPO signaling drives cortical enlargement with massive heterotopiaWenying Angela Liu, She Chen, Zhizhong Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifidaPaul Wolujewicz, Vanessa Aguiar-Pulido, Alice AbdelAleem, et al.
Human Molecular Genetics|October 20, 2006
Parallel changes in metabolite and expression profiles in crooked-tail mutant and folate-reduced wild-type miceSheila Ernest, Michelle Carter, Haifeng Shao, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocationMaha Zaki, Marwa Shehab, Alice Abd El-Aleem, et al.
EMBO Reports|April 10, 2024
Foxp1 suppresses cortical angiogenesis and attenuates HIF-1alpha signaling to promote neural progenitor cell maintenanceJessie E Buth, Catherine E Dyevich, Alexandra Rubin, et al.
Stem Cell Reports|June 27, 2025
Transparency and ongoing communication with participants in brain organoid research: Consensus of an interdisciplinary working groupBetty Cohn, Megan Doerr, Pamela Feliciano, et al.
Neuromuscular Disorders : NMD|May 24, 2020
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients' cohort from Qatar. A population specific founder variantAlice Abdel Aleem, Mahmoud F Elsaid, Nader Chalhoub, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Cell Research|July 27, 2019
Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variantsZhongzhong Chen, Yunping Lei, Yufang Zheng, et al.
Human Molecular Genetics|June 19, 2013
LRP6 exerts non-canonical effects on Wnt signaling during neural tube closureJason D Gray, Stanislav Kholmanskikh, Bozena S Castaldo, et al.
Biological Psychiatry|November 19, 2017
Mature Hippocampal Neurons Require LIS1 for Synaptic Integrity: Implications for CognitionAnamaria Sudarov, Xin-Jun Zhang, Leighton Braunstein, et al.
Genes & Development|June 15, 2018
PARD3 dysfunction in conjunction with dynamic HIPPO signaling drives cortical enlargement with massive heterotopiaWenying Angela Liu, She Chen, Zhizhong Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifidaPaul Wolujewicz, Vanessa Aguiar-Pulido, Alice AbdelAleem, et al.
Human Molecular Genetics|October 20, 2006
Parallel changes in metabolite and expression profiles in crooked-tail mutant and folate-reduced wild-type miceSheila Ernest, Michelle Carter, Haifeng Shao, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocationMaha Zaki, Marwa Shehab, Alice Abd El-Aleem, et al.
EMBO Reports|April 10, 2024
Foxp1 suppresses cortical angiogenesis and attenuates HIF-1alpha signaling to promote neural progenitor cell maintenanceJessie E Buth, Catherine E Dyevich, Alexandra Rubin, et al.
Stem Cell Reports|June 27, 2025
Transparency and ongoing communication with participants in brain organoid research: Consensus of an interdisciplinary working groupBetty Cohn, Megan Doerr, Pamela Feliciano, et al.
Neuromuscular Disorders : NMD|May 24, 2020
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients' cohort from Qatar. A population specific founder variantAlice Abdel Aleem, Mahmoud F Elsaid, Nader Chalhoub, et al.
Pageof 8