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H Dahl

Showing results (221-230 of 233) with videos related to

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Frontiers in Physiology|September 22, 2022
Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failureJacob Peter Hartmann, Rasmus H Dahl, Stine Nymand, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|March 20, 2015
Two cases of acute severe flaccid myelitis associated with enterovirus D68 infection in children, Norway, autumn 2014H C Pfeiffer, K Bragstad, M K Skram, et al.
Pediatric Transplantation|July 12, 2016
Heart transplantation after Fontan: Results from a surgical Fontan cohortKavitha N Pundi, Krishna Pundi, David J Driscoll, et al.
Journal of the American College of Cardiology|October 10, 2015
40-Year Follow-Up After the Fontan Operation: Long-Term Outcomes of 1,052 PatientsKavitha N Pundi, Jonathan N Johnson, Joseph A Dearani, et al.
Nature Biotechnology|October 22, 2013
Engineering dynamic pathway regulation using stress-response promotersRobert H Dahl, Fuzhong Zhang, Jorge Alonso-Gutierrez, et al.
Human Genetics|June 1, 2000
High frequency hearing loss correlated with mutations in the GJB2 geneS A Wilcox, K Saunders, A H Osborn, et al.
Journal of Medical Genetics|January 3, 2001
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing lossM J Houseman, L A Ellis, A Pagnamenta, et al.
The Medical Journal of Australia|October 6, 2001
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafnessH H Dahl, K Saunders, T M Kelly, et al.
The Journal of Physiology|February 13, 2024
Severe hypoxaemic hypercapnia compounds cerebral oxidative-nitrosative stress during extreme apnoea: Implications for cerebral bioenergetic functionDamian M Bailey, Anthony R Bain, Ryan L Hoiland, et al.
Human Mutation|October 9, 2007
An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing lossMichel Guipponi, Min-Yen Toh, Justin Tan, et al.
Pageof 24

Showing results (221-230 of 233) with videos related to

Sort By:
Pageof 24
Frontiers in Physiology|September 22, 2022
Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failureJacob Peter Hartmann, Rasmus H Dahl, Stine Nymand, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|March 20, 2015
Two cases of acute severe flaccid myelitis associated with enterovirus D68 infection in children, Norway, autumn 2014H C Pfeiffer, K Bragstad, M K Skram, et al.
Pediatric Transplantation|July 12, 2016
Heart transplantation after Fontan: Results from a surgical Fontan cohortKavitha N Pundi, Krishna Pundi, David J Driscoll, et al.
Journal of the American College of Cardiology|October 10, 2015
40-Year Follow-Up After the Fontan Operation: Long-Term Outcomes of 1,052 PatientsKavitha N Pundi, Jonathan N Johnson, Joseph A Dearani, et al.
Nature Biotechnology|October 22, 2013
Engineering dynamic pathway regulation using stress-response promotersRobert H Dahl, Fuzhong Zhang, Jorge Alonso-Gutierrez, et al.
Human Genetics|June 1, 2000
High frequency hearing loss correlated with mutations in the GJB2 geneS A Wilcox, K Saunders, A H Osborn, et al.
Journal of Medical Genetics|January 3, 2001
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing lossM J Houseman, L A Ellis, A Pagnamenta, et al.
The Medical Journal of Australia|October 6, 2001
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafnessH H Dahl, K Saunders, T M Kelly, et al.
The Journal of Physiology|February 13, 2024
Severe hypoxaemic hypercapnia compounds cerebral oxidative-nitrosative stress during extreme apnoea: Implications for cerebral bioenergetic functionDamian M Bailey, Anthony R Bain, Ryan L Hoiland, et al.
Human Mutation|October 9, 2007
An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing lossMichel Guipponi, Min-Yen Toh, Justin Tan, et al.
Pageof 24