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Caleb Webber

Showing results (31-40 of 76) with videos related to

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Genome Research|March 21, 2015
Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cellsJennifer Y Tan, Tamara Sirey, Frantisek Honti, et al.
Nature Communications|August 23, 2020
A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disordersDevika Agarwal, Cynthia Sandor, Viola Volpato, et al.
Disease Models & Mechanisms|October 18, 2022
Lipopolysaccharide distinctively alters human microglia transcriptomes to resemble microglia from Alzheimer's disease mouse modelsJimena Monzón-Sandoval, Elena Burlacu, Devika Agarwal, et al.
Plos Computational Biology|April 28, 2010
Accurate distinction of pathogenic from benign CNVs in mental retardationJayne Y Hehir-Kwa, Nienke Wieskamp, Caleb Webber, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2013
Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophreniaAnna Hoerder-Suabedissen, Franziska M Oeschger, Michelle L Krishnan, et al.
Human Molecular Genetics|January 19, 2017
Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's diseaseCynthia Sandor, Paul Robertson, Charmaine Lang, et al.
Plos Genetics|March 18, 2015
Gene networks underlying convergent and pleiotropic phenotypes in a large and systematically-phenotyped cohort with heterogeneous developmental disordersTallulah Andrews, Stephen Meader, Anneke Vulto-van Silfhout, et al.
Alzheimer'S Research & Therapy|November 17, 2020
TREM2 Alzheimer's variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophagesHazel Hall-Roberts, Devika Agarwal, Juliane Obst, et al.
Neurobiology of Disease|May 16, 2019
RNA sequencing reveals MMP2 and TGFB1 downregulation in LRRK2 G2019S Parkinson's iPSC-derived astrocytesHeather D E Booth, Frank Wessely, Natalie Connor-Robson, et al.
Plos Genetics|June 12, 2013
Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autismHyun Ji Noh, Chris P Ponting, Hannah C Boulding, et al.
Pageof 8

Showing results (31-40 of 76) with videos related to

Sort By:
Pageof 8
Genome Research|March 21, 2015
Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cellsJennifer Y Tan, Tamara Sirey, Frantisek Honti, et al.
Nature Communications|August 23, 2020
A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disordersDevika Agarwal, Cynthia Sandor, Viola Volpato, et al.
Disease Models & Mechanisms|October 18, 2022
Lipopolysaccharide distinctively alters human microglia transcriptomes to resemble microglia from Alzheimer's disease mouse modelsJimena Monzón-Sandoval, Elena Burlacu, Devika Agarwal, et al.
Plos Computational Biology|April 28, 2010
Accurate distinction of pathogenic from benign CNVs in mental retardationJayne Y Hehir-Kwa, Nienke Wieskamp, Caleb Webber, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2013
Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophreniaAnna Hoerder-Suabedissen, Franziska M Oeschger, Michelle L Krishnan, et al.
Human Molecular Genetics|January 19, 2017
Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's diseaseCynthia Sandor, Paul Robertson, Charmaine Lang, et al.
Plos Genetics|March 18, 2015
Gene networks underlying convergent and pleiotropic phenotypes in a large and systematically-phenotyped cohort with heterogeneous developmental disordersTallulah Andrews, Stephen Meader, Anneke Vulto-van Silfhout, et al.
Alzheimer'S Research & Therapy|November 17, 2020
TREM2 Alzheimer's variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophagesHazel Hall-Roberts, Devika Agarwal, Juliane Obst, et al.
Neurobiology of Disease|May 16, 2019
RNA sequencing reveals MMP2 and TGFB1 downregulation in LRRK2 G2019S Parkinson's iPSC-derived astrocytesHeather D E Booth, Frank Wessely, Natalie Connor-Robson, et al.
Plos Genetics|June 12, 2013
Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autismHyun Ji Noh, Chris P Ponting, Hannah C Boulding, et al.
Pageof 8