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C Jacobsen

Showing results (271-280 of 327) with videos related to

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Ugeskrift for Laeger|October 22, 1984
[Screening for serum alpha-fetoprotein for the detection of congenital malformations in the 16-18th weeks of pregnancy. Results of 24,023 pregnancy screenings]B N Pedersen, P V Bagger, J Bang, et al.
The American Journal of Pathology|October 9, 1999
Megalin knockout mice as an animal model of low molecular weight proteinuriaJ R Leheste, B Rolinski, H Vorum, et al.
The Journal of Biological Chemistry|September 13, 2000
Evidence for the role of megalin in renal uptake of transthyretinM M Sousa, A G Norden, C Jacobsen, et al.
Medical Physics|June 17, 2017
Accuracy of deformable image registration on magnetic resonance images in digital and physical phantomsRachel B Ger, Jinzhong Yang, Yao Ding, et al.
Prehospital Emergency Care|October 16, 2019
Disparity in Receipt and Utilization of Telecommunicator CPR InstructionAmanda Amen, Patrick Karabon, Cherie Bartram, et al.
The Western Journal of Emergency Medicine|November 18, 2020
CODE BLUE-19: Proposal to Mitigate COVID-19 Transmission in the Emergency Department for Out-of-hospital Cardiac ArrestDavid Nguyen, Nima Sarani, Kenneth D Marshall, et al.
Cold Spring Harbor Molecular Case Studies|July 12, 2017
Compound heterozygous <i>SLC19A3</i> mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia diseaseWhitney Whitford, Isobel Hawkins, Emma Glamuzina, et al.
Genes|February 27, 2026
Foundations of an Ovine Model of Fragile X SyndromeVictoria Hawkins, Skye R Rudiger, Clive J McLaughlan, et al.
Brachytherapy|August 23, 2023
Feasibility of quantitative diffusion-weighted imaging during intra-procedural MRI-guided brachytherapy of locally advanced cervical and vaginal cancersMegan C Jacobsen, Bastien Rigaud, Samantha J Simiele, et al.
JIMD Reports|November 22, 2017
Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q<sub>10</sub> Deficiency in a Female Sib-PairJessie C Jacobsen, Whitney Whitford, Brendan Swan, et al.
Pageof 33

Showing results (271-280 of 327) with videos related to

Sort By:
Pageof 33
Ugeskrift for Laeger|October 22, 1984
[Screening for serum alpha-fetoprotein for the detection of congenital malformations in the 16-18th weeks of pregnancy. Results of 24,023 pregnancy screenings]B N Pedersen, P V Bagger, J Bang, et al.
The American Journal of Pathology|October 9, 1999
Megalin knockout mice as an animal model of low molecular weight proteinuriaJ R Leheste, B Rolinski, H Vorum, et al.
The Journal of Biological Chemistry|September 13, 2000
Evidence for the role of megalin in renal uptake of transthyretinM M Sousa, A G Norden, C Jacobsen, et al.
Medical Physics|June 17, 2017
Accuracy of deformable image registration on magnetic resonance images in digital and physical phantomsRachel B Ger, Jinzhong Yang, Yao Ding, et al.
Prehospital Emergency Care|October 16, 2019
Disparity in Receipt and Utilization of Telecommunicator CPR InstructionAmanda Amen, Patrick Karabon, Cherie Bartram, et al.
The Western Journal of Emergency Medicine|November 18, 2020
CODE BLUE-19: Proposal to Mitigate COVID-19 Transmission in the Emergency Department for Out-of-hospital Cardiac ArrestDavid Nguyen, Nima Sarani, Kenneth D Marshall, et al.
Cold Spring Harbor Molecular Case Studies|July 12, 2017
Compound heterozygous <i>SLC19A3</i> mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia diseaseWhitney Whitford, Isobel Hawkins, Emma Glamuzina, et al.
Genes|February 27, 2026
Foundations of an Ovine Model of Fragile X SyndromeVictoria Hawkins, Skye R Rudiger, Clive J McLaughlan, et al.
Brachytherapy|August 23, 2023
Feasibility of quantitative diffusion-weighted imaging during intra-procedural MRI-guided brachytherapy of locally advanced cervical and vaginal cancersMegan C Jacobsen, Bastien Rigaud, Samantha J Simiele, et al.
JIMD Reports|November 22, 2017
Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q<sub>10</sub> Deficiency in a Female Sib-PairJessie C Jacobsen, Whitney Whitford, Brendan Swan, et al.
Pageof 33