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P Coucke

Showing results (121-130 of 157) with videos related to

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Cancer Research|January 1, 1995
Combined radioimmunotherapy and radiotherapy of human colon carcinoma grafted in nude miceF Buchegger, A Rojas, A B Delaloye, et al.
Human Reproduction (Oxford, England)|June 14, 2022
TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryoP Stamatiadis, G Cosemans, A Boel, et al.
In Vivo (Athens, Greece)|March 1, 1992
Influence of laminin or fibroblasts upon colony formation in the mouse by B16 melanoma cell spheroids: a morphometric analysisP Coucke, L De Leval, P Leyh, et al.
Heart (British Cardiac Society)|June 16, 2006
Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndromeJ De Backer, G J Nollen, D Devos, et al.
Journal of Assisted Reproduction and Genetics|April 1, 2024
Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryosB Bekaert, A Boel, A Rybouchkin, et al.
Annals of the Rheumatic Diseases|August 17, 2004
Radiological sacroiliitis, a hallmark of spondylitis, is linked with CARD15 gene polymorphisms in patients with Crohn's diseaseH Peeters, B Vander Cruyssen, D Laukens, et al.
Clinical Genetics|February 1, 1991
Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patientsJ G Wauters, J Hendrickx, P Coucke, et al.
Genomics|October 1, 1990
Assignment of X-linked hydrocephalus to Xq28 by linkage analysisP J Willems, I Dijkstra, B J Van der Auwera, et al.
Human Reproduction (Oxford, England)|July 3, 2020
Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrestM Tang, M Popovic, P Stamatiadis, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Cytogenetic and array-CGH characterization of a 6q27 deletion in a patient with developmental delay and features of Ehlers-Danlos syndromeA L Mosca, P Callier, A Masurel-Paulet, et al.
Pageof 16

Showing results (121-130 of 157) with videos related to

Sort By:
Pageof 16
Cancer Research|January 1, 1995
Combined radioimmunotherapy and radiotherapy of human colon carcinoma grafted in nude miceF Buchegger, A Rojas, A B Delaloye, et al.
Human Reproduction (Oxford, England)|June 14, 2022
TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryoP Stamatiadis, G Cosemans, A Boel, et al.
In Vivo (Athens, Greece)|March 1, 1992
Influence of laminin or fibroblasts upon colony formation in the mouse by B16 melanoma cell spheroids: a morphometric analysisP Coucke, L De Leval, P Leyh, et al.
Heart (British Cardiac Society)|June 16, 2006
Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndromeJ De Backer, G J Nollen, D Devos, et al.
Journal of Assisted Reproduction and Genetics|April 1, 2024
Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryosB Bekaert, A Boel, A Rybouchkin, et al.
Annals of the Rheumatic Diseases|August 17, 2004
Radiological sacroiliitis, a hallmark of spondylitis, is linked with CARD15 gene polymorphisms in patients with Crohn's diseaseH Peeters, B Vander Cruyssen, D Laukens, et al.
Clinical Genetics|February 1, 1991
Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patientsJ G Wauters, J Hendrickx, P Coucke, et al.
Genomics|October 1, 1990
Assignment of X-linked hydrocephalus to Xq28 by linkage analysisP J Willems, I Dijkstra, B J Van der Auwera, et al.
Human Reproduction (Oxford, England)|July 3, 2020
Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrestM Tang, M Popovic, P Stamatiadis, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Cytogenetic and array-CGH characterization of a 6q27 deletion in a patient with developmental delay and features of Ehlers-Danlos syndromeA L Mosca, P Callier, A Masurel-Paulet, et al.
Pageof 16