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Katrin Koehler

Showing results (21-30 of 46) with videos related to

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European Journal of Pediatrics|October 9, 2010
Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathyMiroslav Dumić, Nina Barišić, Nataša Rojnić-Putarek, et al.
Molecular Biology of the Cell|August 4, 2017
ALADIN is required for the production of fertile mouse oocytesSara Carvalhal, Michelle Stevense, Katrin Koehler, et al.
Plos One|April 14, 2015
Role of ALADIN in human adrenocortical cells for oxidative stress response and steroidogenesisRamona Jühlen, Jan Idkowiak, Angela E Taylor, et al.
European Journal of Pediatrics|June 14, 2008
Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndromeAlma Toromanovic, Husref Tahirovic, Tatjana Milenkovic, et al.
European Journal of Pediatrics|April 28, 2012
Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndromeMiroslav Dumic, Nina Barišic, Vesna Kusec, et al.
Frontiers in Endocrinology|March 28, 2024
Fertility and sexual activity in patients with Triple A syndromeKatja K Dumic, Claudine Heinrichs, Katrin Koehler, et al.
Cancers|March 28, 2026
Pan-Cancer Targeted Sequencing Reveals Genomic Heterogeneity and Prognostic Subgroups in Urothelial Bladder CancerDimitar Ugrinovski, Skender Saidi, Viktor Stankov, et al.
Molecular Biology of the Cell|August 7, 2015
The nucleoporin ALADIN regulates Aurora A localization to ensure robust mitotic spindle formationSara Carvalhal, Susana Abreu Ribeiro, Miguel Arocena, et al.
Hormone Research|October 28, 2008
Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and managementAndrea Salmaggi, Lucia Zirilli, Chiara Pantaleoni, et al.
Molecular Endocrinology (Baltimore, Md.)|October 27, 2009
Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanismHelen L Storr, Barbara Kind, David A Parfitt, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
European Journal of Pediatrics|October 9, 2010
Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathyMiroslav Dumić, Nina Barišić, Nataša Rojnić-Putarek, et al.
Molecular Biology of the Cell|August 4, 2017
ALADIN is required for the production of fertile mouse oocytesSara Carvalhal, Michelle Stevense, Katrin Koehler, et al.
Plos One|April 14, 2015
Role of ALADIN in human adrenocortical cells for oxidative stress response and steroidogenesisRamona Jühlen, Jan Idkowiak, Angela E Taylor, et al.
European Journal of Pediatrics|June 14, 2008
Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndromeAlma Toromanovic, Husref Tahirovic, Tatjana Milenkovic, et al.
European Journal of Pediatrics|April 28, 2012
Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndromeMiroslav Dumic, Nina Barišic, Vesna Kusec, et al.
Frontiers in Endocrinology|March 28, 2024
Fertility and sexual activity in patients with Triple A syndromeKatja K Dumic, Claudine Heinrichs, Katrin Koehler, et al.
Cancers|March 28, 2026
Pan-Cancer Targeted Sequencing Reveals Genomic Heterogeneity and Prognostic Subgroups in Urothelial Bladder CancerDimitar Ugrinovski, Skender Saidi, Viktor Stankov, et al.
Molecular Biology of the Cell|August 7, 2015
The nucleoporin ALADIN regulates Aurora A localization to ensure robust mitotic spindle formationSara Carvalhal, Susana Abreu Ribeiro, Miguel Arocena, et al.
Hormone Research|October 28, 2008
Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and managementAndrea Salmaggi, Lucia Zirilli, Chiara Pantaleoni, et al.
Molecular Endocrinology (Baltimore, Md.)|October 27, 2009
Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanismHelen L Storr, Barbara Kind, David A Parfitt, et al.
Pageof 5