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Showing results (221-230 of 571) with videos related to

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Biochemistry|November 23, 2000
Biochemical and biological characterization of neutrophil chemotactic protein, a novel rabbit CXC chemokine from alveolar macrophagesA Wuyts, E Schutyser, P Menten, et al.
Cancer Letters|June 17, 2008
Low-cost dedicated mini-arrays for high-throughput analysis of DNA copy-number alterations in neuroblastomaKatleen De Preter, Björn Menten, Sara De Brouwer, et al.
Stem Cell Research|February 1, 2023
Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editingJeffrey Aalders, Laurens Léger, Anthony Demolder, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|February 27, 2003
Randomized controlled trial evaluating the clinical benefit of montelukast for treating spring seasonal allergic rhinitisJanet van Adelsberg, George Philip, Craig F LaForce, et al.
European Journal of Nuclear Medicine and Molecular Imaging|August 17, 2004
Direct comparison of 18F-FDG and 11C-methionine PET in suspected recurrence of glioma: sensitivity, inter-observer variability and prognostic valueKoen Van Laere, Sarah Ceyssens, Frank Van Calenbergh, et al.
Research in Microbiology|November 19, 2015
A DNA tool for early detection of vaginal dysbiosis in African womenVicky Jespers, Tania Crucitti, Janneke van de Wijgert, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN geneKaren Buysse, Sarah Vergult, Silke Mussche, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|August 1, 1994
Accelerated radiotherapy in glioblastoma multiforme: a dose searching prospective studyD G González, J Menten, D A Bosch, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 16, 2024
Retinal small vessel pathology is associated with disease burden in multiple sclerosisRebecca Wicklein, Linus Kreitner, Anna Wild, et al.
European Journal of Human Genetics : EJHG|July 31, 2014
Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disabilitySarah Vergult, Annelies Dheedene, Alfred Meurs, et al.
Pageof 58

Showing results (221-230 of 571) with videos related to

Sort By:
Pageof 58
Biochemistry|November 23, 2000
Biochemical and biological characterization of neutrophil chemotactic protein, a novel rabbit CXC chemokine from alveolar macrophagesA Wuyts, E Schutyser, P Menten, et al.
Cancer Letters|June 17, 2008
Low-cost dedicated mini-arrays for high-throughput analysis of DNA copy-number alterations in neuroblastomaKatleen De Preter, Björn Menten, Sara De Brouwer, et al.
Stem Cell Research|February 1, 2023
Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editingJeffrey Aalders, Laurens Léger, Anthony Demolder, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|February 27, 2003
Randomized controlled trial evaluating the clinical benefit of montelukast for treating spring seasonal allergic rhinitisJanet van Adelsberg, George Philip, Craig F LaForce, et al.
European Journal of Nuclear Medicine and Molecular Imaging|August 17, 2004
Direct comparison of 18F-FDG and 11C-methionine PET in suspected recurrence of glioma: sensitivity, inter-observer variability and prognostic valueKoen Van Laere, Sarah Ceyssens, Frank Van Calenbergh, et al.
Research in Microbiology|November 19, 2015
A DNA tool for early detection of vaginal dysbiosis in African womenVicky Jespers, Tania Crucitti, Janneke van de Wijgert, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN geneKaren Buysse, Sarah Vergult, Silke Mussche, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|August 1, 1994
Accelerated radiotherapy in glioblastoma multiforme: a dose searching prospective studyD G González, J Menten, D A Bosch, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 16, 2024
Retinal small vessel pathology is associated with disease burden in multiple sclerosisRebecca Wicklein, Linus Kreitner, Anna Wild, et al.
European Journal of Human Genetics : EJHG|July 31, 2014
Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disabilitySarah Vergult, Annelies Dheedene, Alfred Meurs, et al.
Pageof 58