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Bohr

Showing results (881-890 of 1,348) with videos related to

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Molecular Genetics and Metabolism Reports|March 4, 2016
Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutationsKirstine Ravn, Bitten Schönewolf-Greulich, Rikke M Hansen, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|August 7, 2017
Inhalable siRNA-loaded nano-embedded microparticles engineered using microfluidics and spray dryingMonica Agnoletti, Adam Bohr, Kaushik Thanki, et al.
The Journal of Investigative Dermatology|December 23, 2020
Skin Abnormalities in Disorders with DNA Repair Defects, Premature Aging, and Mitochondrial DysfunctionMansoor Hussain, Sudarshan Krishnamurthy, Jaimin Patel, et al.
Nature Communications|December 7, 2016
WRN regulates pathway choice between classical and alternative non-homologous end joiningRaghavendra A Shamanna, Huiming Lu, Jessica K de Freitas, et al.
Nucleic Acids Research|December 30, 2022
Werner syndrome protein works as a dimer for unwinding and replication fork regressionSoochul Shin, Kwangbeom Hyun, Jinwoo Lee, et al.
DNA Repair|April 16, 2013
Functional deficit associated with a missense Werner syndrome mutationTakashi Tadokoro, Ivana Rybanska-Spaeder, Tomasz Kulikowicz, et al.
Journal of Medicinal Chemistry|May 19, 2012
Structure-activity relationship study of selective excitatory amino acid transporter subtype 1 (EAAT1) inhibitor 2-amino-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (UCPH-101) and absolute configurational assignment using infrared and vibrational circular dichroism spectroscopy in combination with ab initio Hartree-Fock calculationsTri H V Huynh, Irene Shim, Henrik Bohr, et al.
Oncogene|December 8, 2009
Depletion of WRN protein causes RACK1 to activate several protein kinase C isoformsL Massip, C Garand, A Labbé, et al.
The Journal of Infection|July 1, 1983
Eight hundred and seventy-five cases of bacterial meningitis. Part I of a three-part series: clinical data, prognosis, and the role of specialised hospital departmentsV Bohr, B Hansen, O Jessen, et al.
Mechanisms of Ageing and Development|May 9, 2003
The pattern of chromosome-specific variations in telomere length in humans is determined by inherited, telomere-near factors and is maintained throughout lifeJesper Graakjaer, Claus Bischoff, Lars Korsholm, et al.
Pageof 135

Showing results (881-890 of 1,348) with videos related to

Sort By:
Pageof 135
Molecular Genetics and Metabolism Reports|March 4, 2016
Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutationsKirstine Ravn, Bitten Schönewolf-Greulich, Rikke M Hansen, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|August 7, 2017
Inhalable siRNA-loaded nano-embedded microparticles engineered using microfluidics and spray dryingMonica Agnoletti, Adam Bohr, Kaushik Thanki, et al.
The Journal of Investigative Dermatology|December 23, 2020
Skin Abnormalities in Disorders with DNA Repair Defects, Premature Aging, and Mitochondrial DysfunctionMansoor Hussain, Sudarshan Krishnamurthy, Jaimin Patel, et al.
Nature Communications|December 7, 2016
WRN regulates pathway choice between classical and alternative non-homologous end joiningRaghavendra A Shamanna, Huiming Lu, Jessica K de Freitas, et al.
Nucleic Acids Research|December 30, 2022
Werner syndrome protein works as a dimer for unwinding and replication fork regressionSoochul Shin, Kwangbeom Hyun, Jinwoo Lee, et al.
DNA Repair|April 16, 2013
Functional deficit associated with a missense Werner syndrome mutationTakashi Tadokoro, Ivana Rybanska-Spaeder, Tomasz Kulikowicz, et al.
Journal of Medicinal Chemistry|May 19, 2012
Structure-activity relationship study of selective excitatory amino acid transporter subtype 1 (EAAT1) inhibitor 2-amino-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (UCPH-101) and absolute configurational assignment using infrared and vibrational circular dichroism spectroscopy in combination with ab initio Hartree-Fock calculationsTri H V Huynh, Irene Shim, Henrik Bohr, et al.
Oncogene|December 8, 2009
Depletion of WRN protein causes RACK1 to activate several protein kinase C isoformsL Massip, C Garand, A Labbé, et al.
The Journal of Infection|July 1, 1983
Eight hundred and seventy-five cases of bacterial meningitis. Part I of a three-part series: clinical data, prognosis, and the role of specialised hospital departmentsV Bohr, B Hansen, O Jessen, et al.
Mechanisms of Ageing and Development|May 9, 2003
The pattern of chromosome-specific variations in telomere length in humans is determined by inherited, telomere-near factors and is maintained throughout lifeJesper Graakjaer, Claus Bischoff, Lars Korsholm, et al.
Pageof 135