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Showing results (51-60 of 59) with videos related to

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American Journal of Medical Genetics|January 9, 2001
Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndromeA Zankl, M C Addor, A C Gaide, et al.
Vaccine|November 9, 2004
A recombinant rubella virus E1 glycoprotein as a rubella vaccine candidateG Perrenoud, F Messerli, A-C Thierry, et al.
Maturitas|January 4, 2001
Postmenopause hormone treatment in women with NIDDM or impaired glucose tolerance: the MEDIA randomized clinical trialC Cornu, C Mercier, P Ffrench, et al.
Nature Reviews. Drug Discovery|January 6, 2019
Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseasesAntonio Cuadrado, Ana I Rojo, Geoffrey Wells, et al.
Medecine Tropicale Et Sante Internationale|June 10, 2022
[JDS Guyane 2021 - 4<sup>th</sup> day dedicated to the scientific works of caregivers in French Guiana - Cayenne - June 25, 2021]A Lucarelli, A Fremery, A Argoubi, et al.
BMC Cancer|October 17, 2015
Efficacy of trabectedin in malignant solitary fibrous tumors: a retrospective analysis from the French Sarcoma GroupJ Khalifa, M Ouali, L Chaltiel, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 15, 2012
Sarcoma: concordance between initial diagnosis and centralized expert review in a population-based study within three European regionsI Ray-Coquard, M C Montesco, J M Coindre, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Human Molecular Genetics|November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophyS Biswas, F L Munier, J Yardley, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
American Journal of Medical Genetics|January 9, 2001
Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndromeA Zankl, M C Addor, A C Gaide, et al.
Vaccine|November 9, 2004
A recombinant rubella virus E1 glycoprotein as a rubella vaccine candidateG Perrenoud, F Messerli, A-C Thierry, et al.
Maturitas|January 4, 2001
Postmenopause hormone treatment in women with NIDDM or impaired glucose tolerance: the MEDIA randomized clinical trialC Cornu, C Mercier, P Ffrench, et al.
Nature Reviews. Drug Discovery|January 6, 2019
Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseasesAntonio Cuadrado, Ana I Rojo, Geoffrey Wells, et al.
Medecine Tropicale Et Sante Internationale|June 10, 2022
[JDS Guyane 2021 - 4<sup>th</sup> day dedicated to the scientific works of caregivers in French Guiana - Cayenne - June 25, 2021]A Lucarelli, A Fremery, A Argoubi, et al.
BMC Cancer|October 17, 2015
Efficacy of trabectedin in malignant solitary fibrous tumors: a retrospective analysis from the French Sarcoma GroupJ Khalifa, M Ouali, L Chaltiel, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 15, 2012
Sarcoma: concordance between initial diagnosis and centralized expert review in a population-based study within three European regionsI Ray-Coquard, M C Montesco, J M Coindre, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Human Molecular Genetics|November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophyS Biswas, F L Munier, J Yardley, et al.
Pageof 6