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K Hoertnagel

Showing results (1-10 of 6) with videos related to

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Nucleic Acids Research|December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseasesC Scharfe, P Zaccaria, K Hoertnagel, et al.
Nucleic Acids Research|December 11, 1999
MITOP, the mitochondrial proteome database: 2000 updateC Scharfe, P Zaccaria, K Hoertnagel, et al.
Annals of Neurology|August 12, 1999
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiencyV Tiranti, M Jaksch, S Hofmann, et al.
The Journal of Experimental Medicine|October 18, 2000
Burkitt lymphoma in the mouseA L Kovalchuk, C F Qi, T A Torrey, et al.
American Journal of Human Genetics|December 5, 1998
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiencyV Tiranti, K Hoertnagel, R Carrozzo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 23, 2017
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugsC von Stülpnagel, M Ensslen, R S Møller, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Nucleic Acids Research|December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseasesC Scharfe, P Zaccaria, K Hoertnagel, et al.
Nucleic Acids Research|December 11, 1999
MITOP, the mitochondrial proteome database: 2000 updateC Scharfe, P Zaccaria, K Hoertnagel, et al.
Annals of Neurology|August 12, 1999
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiencyV Tiranti, M Jaksch, S Hofmann, et al.
The Journal of Experimental Medicine|October 18, 2000
Burkitt lymphoma in the mouseA L Kovalchuk, C F Qi, T A Torrey, et al.
American Journal of Human Genetics|December 5, 1998
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiencyV Tiranti, K Hoertnagel, R Carrozzo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 23, 2017
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugsC von Stülpnagel, M Ensslen, R S Møller, et al.
Pageof 1