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M DURAND

Showing results (921-930 of 977) with videos related to

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Molecular Syndromology|December 23, 2011
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyE Schaefer, A Zaloszyc, J Lauer, et al.
Cell|November 1, 2011
Lineage regulators direct BMP and Wnt pathways to cell-specific programs during differentiation and regenerationEirini Trompouki, Teresa V Bowman, Lee N Lawton, et al.
Lancet Regional Health. Americas|August 21, 2023
Living kidney donors with HIV: experience and outcomes from a case series by the HOPE in Action ConsortiumChristine M Durand, Nina Martinez, Karl Neumann, et al.
Clinical Transplantation|September 12, 2020
Evolving Impact of COVID-19 on Transplant Center Practices and Policies in the United StatesBrian J Boyarsky, Jessica M Ruck, Teresa Po-Yu Chiang, et al.
Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.
Transplantation|November 9, 2020
Incidence and Outcomes of COVID-19 in Kidney and Liver Transplant Recipients With HIV: Report From the National HOPE in Action ConsortiumSapna A Mehta, Meenakshi M Rana, Jennifer D Motter, et al.
Annals of Intensive Care|August 5, 2018
Characteristics and outcome of patients with newly diagnosed advanced or metastatic lung cancer admitted to intensive care units (ICUs)C Barth, M Soares, A C Toffart, et al.
Journal of Internal Medicine|October 27, 2020
Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56A Legrand, C Pujol, C M Durand, et al.
Nature Communications|April 23, 2016
The Gonium pectorale genome demonstrates co-option of cell cycle regulation during the evolution of multicellularityErik R Hanschen, Tara N Marriage, Patrick J Ferris, et al.
Human Mutation|October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Pageof 98

Showing results (921-930 of 977) with videos related to

Sort By:
Pageof 98
Molecular Syndromology|December 23, 2011
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyE Schaefer, A Zaloszyc, J Lauer, et al.
Cell|November 1, 2011
Lineage regulators direct BMP and Wnt pathways to cell-specific programs during differentiation and regenerationEirini Trompouki, Teresa V Bowman, Lee N Lawton, et al.
Lancet Regional Health. Americas|August 21, 2023
Living kidney donors with HIV: experience and outcomes from a case series by the HOPE in Action ConsortiumChristine M Durand, Nina Martinez, Karl Neumann, et al.
Clinical Transplantation|September 12, 2020
Evolving Impact of COVID-19 on Transplant Center Practices and Policies in the United StatesBrian J Boyarsky, Jessica M Ruck, Teresa Po-Yu Chiang, et al.
Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.
Transplantation|November 9, 2020
Incidence and Outcomes of COVID-19 in Kidney and Liver Transplant Recipients With HIV: Report From the National HOPE in Action ConsortiumSapna A Mehta, Meenakshi M Rana, Jennifer D Motter, et al.
Annals of Intensive Care|August 5, 2018
Characteristics and outcome of patients with newly diagnosed advanced or metastatic lung cancer admitted to intensive care units (ICUs)C Barth, M Soares, A C Toffart, et al.
Journal of Internal Medicine|October 27, 2020
Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56A Legrand, C Pujol, C M Durand, et al.
Nature Communications|April 23, 2016
The Gonium pectorale genome demonstrates co-option of cell cycle regulation during the evolution of multicellularityErik R Hanschen, Tara N Marriage, Patrick J Ferris, et al.
Human Mutation|October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Pageof 98