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E Ehrlich

Showing results (431-440 of 492) with videos related to

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Neuropharmacology|June 3, 2015
Prenatal stress, regardless of concurrent escitalopram treatment, alters behavior and amygdala gene expression of adolescent female ratsDavid E Ehrlich, Gretchen N Neigh, Chase H Bourke, et al.
Biomedicines|October 27, 2022
Postnatal Conditional Deletion of <i>Bcl11b</i> in Striatal Projection Neurons Mimics the Transcriptional Signature of Huntington's DiseaseSicheng Song, Jordi Creus Muncunill, Carlos Galicia Aguirre, et al.
Cancer Research|May 19, 2025
Adaptation to Volumetric Compression Drives an Apoptosis-Resistant and Invasive Phenotype in Liver CancerXiangyu Gong, Noriyoshi Ogino, M Fátima Leite, et al.
Molecular Psychiatry|October 5, 2018
Integrative approach to sporadic Alzheimer's disease: deficiency of TYROBP in cerebral Aβ amyloidosis mouse normalizes clinical phenotype and complement subnetwork molecular pathology without reducing Aβ burdenJean-Vianney Haure-Mirande, Minghui Wang, Mickael Audrain, et al.
Genes & Development|September 15, 2017
Calcium-dependent O-GlcNAc signaling drives liver autophagy in adaptation to starvationHai-Bin Ruan, Yina Ma, Sara Torres, et al.
Molecular Psychiatry|August 13, 2014
Proneurogenic Group II mGluR antagonist improves learning and reduces anxiety in Alzheimer Aβ oligomer mouseS H Kim, J W Steele, S W Lee, et al.
Molecular Psychiatry|November 23, 2018
Correction: Integrative approach to sporadic Alzheimer's disease: deficiency of TYROBP in cerebral Aβ amyloidosis mouse normalizes clinical phenotype and complement subnetwork molecular pathology without reducing Aβ burdenJean-Vianney Haure-Mirande, Minghui Wang, Mickael Audrain, et al.
American Journal of Human Genetics|October 21, 2021
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelinAloysius Domingo, Rachita Yadav, Shivangi Shah, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 30, 2022
Microglial INPP5D limits plaque formation and glial reactivity in the PSAPP mouse model of Alzheimer's diseaseEmilie L Castranio, Philip Hasel, Jean-Vianney Haure-Mirande, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|May 18, 2004
A novel promoter polymorphism in the gene encoding complement component 5 receptor 1 on chromosome 19q13.3 is not associated with asthma and atopy in three independent populationsK C Barnes, L Caraballo, M Muñoz, et al.
Pageof 50

Showing results (431-440 of 492) with videos related to

Sort By:
Pageof 50
Neuropharmacology|June 3, 2015
Prenatal stress, regardless of concurrent escitalopram treatment, alters behavior and amygdala gene expression of adolescent female ratsDavid E Ehrlich, Gretchen N Neigh, Chase H Bourke, et al.
Biomedicines|October 27, 2022
Postnatal Conditional Deletion of <i>Bcl11b</i> in Striatal Projection Neurons Mimics the Transcriptional Signature of Huntington's DiseaseSicheng Song, Jordi Creus Muncunill, Carlos Galicia Aguirre, et al.
Cancer Research|May 19, 2025
Adaptation to Volumetric Compression Drives an Apoptosis-Resistant and Invasive Phenotype in Liver CancerXiangyu Gong, Noriyoshi Ogino, M Fátima Leite, et al.
Molecular Psychiatry|October 5, 2018
Integrative approach to sporadic Alzheimer's disease: deficiency of TYROBP in cerebral Aβ amyloidosis mouse normalizes clinical phenotype and complement subnetwork molecular pathology without reducing Aβ burdenJean-Vianney Haure-Mirande, Minghui Wang, Mickael Audrain, et al.
Genes & Development|September 15, 2017
Calcium-dependent O-GlcNAc signaling drives liver autophagy in adaptation to starvationHai-Bin Ruan, Yina Ma, Sara Torres, et al.
Molecular Psychiatry|August 13, 2014
Proneurogenic Group II mGluR antagonist improves learning and reduces anxiety in Alzheimer Aβ oligomer mouseS H Kim, J W Steele, S W Lee, et al.
Molecular Psychiatry|November 23, 2018
Correction: Integrative approach to sporadic Alzheimer's disease: deficiency of TYROBP in cerebral Aβ amyloidosis mouse normalizes clinical phenotype and complement subnetwork molecular pathology without reducing Aβ burdenJean-Vianney Haure-Mirande, Minghui Wang, Mickael Audrain, et al.
American Journal of Human Genetics|October 21, 2021
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelinAloysius Domingo, Rachita Yadav, Shivangi Shah, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 30, 2022
Microglial INPP5D limits plaque formation and glial reactivity in the PSAPP mouse model of Alzheimer's diseaseEmilie L Castranio, Philip Hasel, Jean-Vianney Haure-Mirande, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|May 18, 2004
A novel promoter polymorphism in the gene encoding complement component 5 receptor 1 on chromosome 19q13.3 is not associated with asthma and atopy in three independent populationsK C Barnes, L Caraballo, M Muñoz, et al.
Pageof 50