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K Ravn

Showing results (11-20 of 35) with videos related to

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Clinical Genetics|April 29, 2005
Mutations found within exon 1 of MECP2 in Danish patients with Rett syndromeK Ravn, J B Nielsen, M Schwartz
Angewandte Chemie (International Ed. in English)|November 2, 2021
Regioselective Hydroalkylation of Vinylarenes by Cooperative Cu and Ni CatalysisAnne K Ravn, Martin B Johansen, Troels Skrydstrup
Chempluschem|June 9, 2020
Controlled Release of Reactive Gases: A Tale of Taming Carbon MonoxideAnne K Ravn, Martin B Johansen, Troels Skrydstrup
Molecular Genetics and Metabolism|January 4, 2001
Changes in the carboxyl terminus of the beta subunit of human propionyl-CoA carboxylase affect the oligomer assembly and catalysis: expression and characterization of seven patient-derived mutant forms of PCC in Escherichia coliM Chloupková, K Ravn, M Schwartz, et al.
Journal of Medical Genetics|January 15, 2003
No correlation between phenotype and genotype in boys with a truncating MECP2 mutationK Ravn, J B Nielsen, P Uldall, et al.
Annals of Neurology|October 17, 2001
Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b geneF Wibrand, K Ravn, M Schwartz, et al.
Clinical Genetics|December 21, 2011
Deletion of CUL4B leads to concordant phenotype in a monozygotic twin pairK Ravn, S G Lindquist, K Nielsen, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndromeK Ravn, F Wibrand, F J Hansen, et al.
Clinical Genetics|March 19, 2010
Identification of a novel locus for a USH3 like syndrome combined with congenital cataractS Dad, E Østergaard, T Thykjaer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 8, 2015
Brain derived neurotrophic factor (BDNF) and autism spectrum disorders (ASD) in childhoodV Bryn, B Halvorsen, T Ueland, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Clinical Genetics|April 29, 2005
Mutations found within exon 1 of MECP2 in Danish patients with Rett syndromeK Ravn, J B Nielsen, M Schwartz
Angewandte Chemie (International Ed. in English)|November 2, 2021
Regioselective Hydroalkylation of Vinylarenes by Cooperative Cu and Ni CatalysisAnne K Ravn, Martin B Johansen, Troels Skrydstrup
Chempluschem|June 9, 2020
Controlled Release of Reactive Gases: A Tale of Taming Carbon MonoxideAnne K Ravn, Martin B Johansen, Troels Skrydstrup
Molecular Genetics and Metabolism|January 4, 2001
Changes in the carboxyl terminus of the beta subunit of human propionyl-CoA carboxylase affect the oligomer assembly and catalysis: expression and characterization of seven patient-derived mutant forms of PCC in Escherichia coliM Chloupková, K Ravn, M Schwartz, et al.
Journal of Medical Genetics|January 15, 2003
No correlation between phenotype and genotype in boys with a truncating MECP2 mutationK Ravn, J B Nielsen, P Uldall, et al.
Annals of Neurology|October 17, 2001
Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b geneF Wibrand, K Ravn, M Schwartz, et al.
Clinical Genetics|December 21, 2011
Deletion of CUL4B leads to concordant phenotype in a monozygotic twin pairK Ravn, S G Lindquist, K Nielsen, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndromeK Ravn, F Wibrand, F J Hansen, et al.
Clinical Genetics|March 19, 2010
Identification of a novel locus for a USH3 like syndrome combined with congenital cataractS Dad, E Østergaard, T Thykjaer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 8, 2015
Brain derived neurotrophic factor (BDNF) and autism spectrum disorders (ASD) in childhoodV Bryn, B Halvorsen, T Ueland, et al.
Pageof 4