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Kornberg

Showing results (951-960 of 1,008) with videos related to

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American Journal of Human Genetics|May 3, 2001
Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin geneB Ilkovski, S T Cooper, K Nowak, et al.
Journal of Medicinal Chemistry|June 23, 2006
3-arylimino-2-indolones are potent and selective galanin GAL3 receptor antagonistsMichael J Konkel, Bharat Lagu, Lakmal W Boteju, et al.
Biorxiv : the Preprint Server for Biology|September 11, 2023
PKC modulator bryostatin-1 therapeutically targets CNS innate immunity to attenuate neuroinflammation and promote remyelinationPayam Gharibani, Efrat Abramson, Shruthi Shanmukha, et al.
The Journal of Physical Chemistry. A|January 17, 2024
Combining Force Fields and Neural Networks for an Accurate Representation of Bonded InteractionsGanesh Kamath, Alexey Illarionov, Serzhan Sakipov, et al.
Clinical Breast Cancer|October 9, 2012
Phase II study of gemcitabine and bevacizumab as first-line treatment in taxane-pretreated, HER2-negative, locally recurrent or metastatic breast cancerRachel Borson, Graydon Harker, James Reeves, et al.
European Urology Oncology|August 15, 2019
Genomic Risk Predicts Molecular Imaging-detected Metastatic Nodal Disease in Prostate CancerMelody J Xu, Zachary Kornberg, Adam J Gadzinski, et al.
Acta Neuropathologica|September 6, 2021
Complement component 3 from astrocytes mediates retinal ganglion cell loss during neuroinflammationMarjan Gharagozloo, Matthew D Smith, Jing Jin, et al.
Nature Methods|March 22, 2022
DaXi-high-resolution, large imaging volume and multi-view single-objective light-sheet microscopyBin Yang, Merlin Lange, Alfred Millett-Sikking, et al.
Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.
Brain : a Journal of Neurology|August 21, 2016
Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasiaJijun Wan, Janos Steffen, Michael Yourshaw, et al.
Pageof 101

Showing results (951-960 of 1,008) with videos related to

Sort By:
Pageof 101
American Journal of Human Genetics|May 3, 2001
Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin geneB Ilkovski, S T Cooper, K Nowak, et al.
Journal of Medicinal Chemistry|June 23, 2006
3-arylimino-2-indolones are potent and selective galanin GAL3 receptor antagonistsMichael J Konkel, Bharat Lagu, Lakmal W Boteju, et al.
Biorxiv : the Preprint Server for Biology|September 11, 2023
PKC modulator bryostatin-1 therapeutically targets CNS innate immunity to attenuate neuroinflammation and promote remyelinationPayam Gharibani, Efrat Abramson, Shruthi Shanmukha, et al.
The Journal of Physical Chemistry. A|January 17, 2024
Combining Force Fields and Neural Networks for an Accurate Representation of Bonded InteractionsGanesh Kamath, Alexey Illarionov, Serzhan Sakipov, et al.
Clinical Breast Cancer|October 9, 2012
Phase II study of gemcitabine and bevacizumab as first-line treatment in taxane-pretreated, HER2-negative, locally recurrent or metastatic breast cancerRachel Borson, Graydon Harker, James Reeves, et al.
European Urology Oncology|August 15, 2019
Genomic Risk Predicts Molecular Imaging-detected Metastatic Nodal Disease in Prostate CancerMelody J Xu, Zachary Kornberg, Adam J Gadzinski, et al.
Acta Neuropathologica|September 6, 2021
Complement component 3 from astrocytes mediates retinal ganglion cell loss during neuroinflammationMarjan Gharagozloo, Matthew D Smith, Jing Jin, et al.
Nature Methods|March 22, 2022
DaXi-high-resolution, large imaging volume and multi-view single-objective light-sheet microscopyBin Yang, Merlin Lange, Alfred Millett-Sikking, et al.
Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.
Brain : a Journal of Neurology|August 21, 2016
Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasiaJijun Wan, Janos Steffen, Michael Yourshaw, et al.
Pageof 101