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Biochemistry
|
November 23, 2000
Biochemical and biological characterization of neutrophil chemotactic protein, a novel rabbit CXC chemokine from alveolar macrophages
A 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 neuroblastoma
Katleen 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 editing
Jeffrey 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 rhinitis
Janet 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 value
Koen 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 women
Vicky 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 gene
Karen 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 study
D 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 sclerosis
Rebecca 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 disability
Sarah Vergult, Annelies Dheedene, Alfred Meurs, et al.
Page
of 58
Search research articles
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Showing results (221-230 of 571) with videos related to
Sort By:
Page
of 58
Biochemistry
|
November 23, 2000
Biochemical and biological characterization of neutrophil chemotactic protein, a novel rabbit CXC chemokine from alveolar macrophages
A 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 neuroblastoma
Katleen 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 editing
Jeffrey 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 rhinitis
Janet 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 value
Koen 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 women
Vicky 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 gene
Karen 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 study
D 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 sclerosis
Rebecca 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 disability
Sarah Vergult, Annelies Dheedene, Alfred Meurs, et al.
Page
of 58