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M Duran

Showing results (621-630 of 646) with videos related to

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Nature Genetics|June 16, 1999
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndromeS M Houten, W Kuis, M Duran, et al.
The Journal of Trauma and Acute Care Surgery|April 24, 2013
Examining prehospital intubation for penetrating trauma in a swine hemorrhagic shock modelSharven Taghavi, Senthil N Jayarajan, Swapnil Khoche, et al.
Stroke|June 1, 1996
Evaluation of the presence of premature atherosclerosis in adults with heterozygosity for cystathionine-beta-synthase deficiencyH W de Valk, M K van Eeden, J D Banga, et al.
The American Psychologist|January 23, 2018
Community-based participatory research (CBPR): Towards equitable involvement of community in psychology researchSusan E Collins, Seema L Clifasefi, Joey Stanton, et al.
Nature|August 28, 2024
Spatially clustered type I interferon responses at injury borderzonesV K Ninh, D M Calcagno, J D Yu, et al.
Developmental Cell|March 18, 2022
Excess neuropeptides in lung signal through endothelial cells to impair gas exchangeJinhao Xu, Le Xu, Pengfei Sui, et al.
Journal of Inherited Metabolic Disease|January 5, 2007
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)S Kölker, E Christensen, J V Leonard, et al.
American Journal of Medical Genetics|June 27, 1997
The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromesA M Zwamborn-Hanssen, J B Bijlsma, E F Hennekam, et al.
Nature Communications|December 9, 2023
The DNA glycosylase NEIL2 is protective during SARS-CoV-2 infectionNisha Tapryal, Anirban Chakraborty, Kaushik Saha, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 14, 2019
Structural, functional, and behavioral insights of dopamine dysfunction revealed by a deletion in <i>SLC6A3</i>Nicholas G Campbell, Aparna Shekar, Jenny I Aguilar, et al.
Pageof 65

Showing results (621-630 of 646) with videos related to

Sort By:
Pageof 65
Nature Genetics|June 16, 1999
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndromeS M Houten, W Kuis, M Duran, et al.
The Journal of Trauma and Acute Care Surgery|April 24, 2013
Examining prehospital intubation for penetrating trauma in a swine hemorrhagic shock modelSharven Taghavi, Senthil N Jayarajan, Swapnil Khoche, et al.
Stroke|June 1, 1996
Evaluation of the presence of premature atherosclerosis in adults with heterozygosity for cystathionine-beta-synthase deficiencyH W de Valk, M K van Eeden, J D Banga, et al.
The American Psychologist|January 23, 2018
Community-based participatory research (CBPR): Towards equitable involvement of community in psychology researchSusan E Collins, Seema L Clifasefi, Joey Stanton, et al.
Nature|August 28, 2024
Spatially clustered type I interferon responses at injury borderzonesV K Ninh, D M Calcagno, J D Yu, et al.
Developmental Cell|March 18, 2022
Excess neuropeptides in lung signal through endothelial cells to impair gas exchangeJinhao Xu, Le Xu, Pengfei Sui, et al.
Journal of Inherited Metabolic Disease|January 5, 2007
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)S Kölker, E Christensen, J V Leonard, et al.
American Journal of Medical Genetics|June 27, 1997
The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromesA M Zwamborn-Hanssen, J B Bijlsma, E F Hennekam, et al.
Nature Communications|December 9, 2023
The DNA glycosylase NEIL2 is protective during SARS-CoV-2 infectionNisha Tapryal, Anirban Chakraborty, Kaushik Saha, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 14, 2019
Structural, functional, and behavioral insights of dopamine dysfunction revealed by a deletion in <i>SLC6A3</i>Nicholas G Campbell, Aparna Shekar, Jenny I Aguilar, et al.
Pageof 65