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C Bosman

Showing results (161-170 of 187) with videos related to

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Journal of Translational Autoimmunity|August 4, 2020
CD38-targeted therapy with daratumumab reduces autoantibody levels in multiple myeloma patientsKristine A Frerichs, Christie P M Verkleij, Patricia W C Bosman, et al.
International Journal of Molecular Sciences|December 11, 2022
The Impact of Nanobody Density on the Targeting Efficiency of PEGylated LiposomesBárbara S Mesquita, Marcel H A M Fens, Alessia Di Maggio, et al.
Annals of Neurology|October 24, 1997
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiencyC Dionisi-Vici, W Ruitenbeek, G Fariello, et al.
Haematologica|February 1, 1980
Treatment of non Hodgkin's lymphoma with "PROVECIP" (procarbazine, vinblastine, cyclophosphamide and prednisone)F Mandelli, C Biagini, C D Baroni, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|August 17, 2016
Long-term antidepressant use: a qualitative study on perspectives of patients and GPs in primary careRenske C Bosman, Klaas M Huijbregts, Peter Fm Verhaak, et al.
British Heart Journal|February 1, 1993
Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 familiesE Zachara, A L Caforio, G P Carboni, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|May 19, 2025
Lipopeptide-mediated delivery of CRISPR/Cas9 ribonucleoprotein complexes for gene editing and correctionMert Öktem, Thai Hoang Nguyen, Esmeralda D C Bosman, et al.
Cardiology in the Young|July 1, 1999
Tachycardias in children originating in the right ventricular outflow tract: lack of clinical features predicting the presence and severity of the histopathological substrateF Drago, A Mazza, M G Gagliardi, et al.
Neurology|July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structuresA Teti, S Migliaccio, A Taranta, et al.
Pageof 19

Showing results (161-170 of 187) with videos related to

Sort By:
Pageof 19
Journal of Translational Autoimmunity|August 4, 2020
CD38-targeted therapy with daratumumab reduces autoantibody levels in multiple myeloma patientsKristine A Frerichs, Christie P M Verkleij, Patricia W C Bosman, et al.
International Journal of Molecular Sciences|December 11, 2022
The Impact of Nanobody Density on the Targeting Efficiency of PEGylated LiposomesBárbara S Mesquita, Marcel H A M Fens, Alessia Di Maggio, et al.
Annals of Neurology|October 24, 1997
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiencyC Dionisi-Vici, W Ruitenbeek, G Fariello, et al.
Haematologica|February 1, 1980
Treatment of non Hodgkin's lymphoma with "PROVECIP" (procarbazine, vinblastine, cyclophosphamide and prednisone)F Mandelli, C Biagini, C D Baroni, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|August 17, 2016
Long-term antidepressant use: a qualitative study on perspectives of patients and GPs in primary careRenske C Bosman, Klaas M Huijbregts, Peter Fm Verhaak, et al.
British Heart Journal|February 1, 1993
Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 familiesE Zachara, A L Caforio, G P Carboni, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|May 19, 2025
Lipopeptide-mediated delivery of CRISPR/Cas9 ribonucleoprotein complexes for gene editing and correctionMert Öktem, Thai Hoang Nguyen, Esmeralda D C Bosman, et al.
Cardiology in the Young|July 1, 1999
Tachycardias in children originating in the right ventricular outflow tract: lack of clinical features predicting the presence and severity of the histopathological substrateF Drago, A Mazza, M G Gagliardi, et al.
Neurology|July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structuresA Teti, S Migliaccio, A Taranta, et al.
Pageof 19