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Showing results (561-570 of 779) with videos related to

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Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|April 14, 2005
The Nutritional and Inflammatory Evaluation in Dialysis patients (NIED) study: overview of the NIED study and the role of dietitiansSara Colman, Rochelle Bross, Debbie Benner, et al.
Clinical and Translational Science|June 23, 2015
Strategies to Build Trust and Recruit African American and Latino Community Residents for Health Research: A Cohort StudyIbrahima C Sankaré, Rachelle Bross, Arleen F Brown, et al.
Journal of Clinical and Translational Science|January 30, 2023
A community-partnered approach for diversity in COVID-19 vaccine clinical trialsYelba Castellon-Lopez, Raphael Landovitz, Ejiro Ntekume, et al.
Physical Chemistry Chemical Physics : PCCP|October 20, 2022
Damage in InGaN/GaN bilayers upon Xe and Pb swift heavy ion irradiationPrzemysław Jóźwik, José P S Cardoso, Diogo F Carvalho, et al.
European Journal of Heart Failure|June 27, 2018
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelopeRasha A Al-Saaidi, Torsten B Rasmussen, Rune I D Birkler, et al.
American Journal of Human Genetics|May 12, 2001
Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiencyB S Andresen, S F Dobrowolski, L O'Reilly, et al.
Molecular Genetics and Metabolism|May 1, 2012
MCAD deficiency in DenmarkBrage Storstein Andresen, Allan Meldgaard Lund, David Michael Hougaard, et al.
Clinical Genetics|November 10, 2012
Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanismsT B Rasmussen, J Hansen, P H Nissen, et al.
Human Molecular Genetics|April 1, 1996
Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD geneB S Andresen, P Bross, C Vianey-Saban, et al.
Journal of Human Genetics|October 31, 2006
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potentialPeter Bross, Zhijie Li, Jakob Hansen, et al.
Pageof 78

Showing results (561-570 of 779) with videos related to

Sort By:
Pageof 78
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation|April 14, 2005
The Nutritional and Inflammatory Evaluation in Dialysis patients (NIED) study: overview of the NIED study and the role of dietitiansSara Colman, Rochelle Bross, Debbie Benner, et al.
Clinical and Translational Science|June 23, 2015
Strategies to Build Trust and Recruit African American and Latino Community Residents for Health Research: A Cohort StudyIbrahima C Sankaré, Rachelle Bross, Arleen F Brown, et al.
Journal of Clinical and Translational Science|January 30, 2023
A community-partnered approach for diversity in COVID-19 vaccine clinical trialsYelba Castellon-Lopez, Raphael Landovitz, Ejiro Ntekume, et al.
Physical Chemistry Chemical Physics : PCCP|October 20, 2022
Damage in InGaN/GaN bilayers upon Xe and Pb swift heavy ion irradiationPrzemysław Jóźwik, José P S Cardoso, Diogo F Carvalho, et al.
European Journal of Heart Failure|June 27, 2018
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelopeRasha A Al-Saaidi, Torsten B Rasmussen, Rune I D Birkler, et al.
American Journal of Human Genetics|May 12, 2001
Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiencyB S Andresen, S F Dobrowolski, L O'Reilly, et al.
Molecular Genetics and Metabolism|May 1, 2012
MCAD deficiency in DenmarkBrage Storstein Andresen, Allan Meldgaard Lund, David Michael Hougaard, et al.
Clinical Genetics|November 10, 2012
Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanismsT B Rasmussen, J Hansen, P H Nissen, et al.
Human Molecular Genetics|April 1, 1996
Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD geneB S Andresen, P Bross, C Vianey-Saban, et al.
Journal of Human Genetics|October 31, 2006
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potentialPeter Bross, Zhijie Li, Jakob Hansen, et al.
Pageof 78