LACE1 interacts with p53 and mediates its mitochondrial translocation and apoptosis

Por Cesnekova, Jana, Spacilova, Jana, Hansikova, Hana, Houstek, Josef, Zeman, Jiri, Stiburek, Lukas
Publicado no Oncotarget (2016)

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1

Por Stiburek, Lukas, Vesela, Katerina, Hansikova, Hana, Pecina, Petr, Tesarova, Marketa, Cerna, Leona, Houstek, Josef, Zeman, Jiri
Publicado em 2005

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206

Por Ješina, Pavel, Tesařová, Markéta, Fornůsková, Daniela, Vojtíšková, Alena, Pecina, Petr, Kaplanová, Vilma, Hansíková, Hana, Zeman, Jiří, Houštěk, Josef
Publicado em 2004

Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry

Por Pecina, Petr, Houšťková, Hana, Mráček, Tomáš, Pecinová, Alena, Nůsková, Hana, Tesařová, Markéta, Hansíková, Hana, Janota, Jan, Zeman, Jiří, Houštěk, Josef
Publicado no BBA Clin (2014)

Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders

Por Vondráčková, Alžběta, Veselá, Kateřina, Kratochvílová, Hana, Kučerová Vidrová, Vendula, Vinšová, Kamila, Stránecký, Viktor, Honzík, Tomáš, Hansíková, Hana, Zeman, Jiří, Tesařová, Markéta
Publicado em 2014

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I

Por Guillard, Mailys, Wada, Yoshinao, Hansikova, Hana, Yuasa, Isao, Vesela, Katerina, Ondruskova, Nina, Kadoya, Machiko, Janssen, Alice, Van den Heuvel, Lambertus P. W. J., Morava, Eva, Zeman, Jiri, Wevers, Ron A., Lefeber, Dirk J.
Publicado em 2011

Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F(1)F(o )ATP synt...

Por Čížková, Alena, Stránecký, Viktor, Ivánek, Robert, Hartmannová, Hana, Nosková, Lenka, Piherová, Lenka, Tesařová, Markéta, Hansíková, Hana, Honzík, Tomáš, Zeman, Jiří, Divina, Petr, Potocká, Andrea, Paul, Jan, Sperl, Wolfgang, Mayr, Johannes A, Seneca, Sara, Houštĕk, Josef, Kmoch, Stanislav
Publicado em 2008

Mutation of NgBR, a subunit of cis-prenyltransferase, causes a congenial disorder of glycosylation

Por Park, Eon Joo, Grabińska, Kariona A., Guan, Ziqiang, Stránecký, Viktor, Hartmannová, Hana, Hodaňová, Kateřina, Barešová, Veronika, Sovová, Jana, Jozsef, Levente, Ondrušková, Nina, Hansíková, Hana, Honzík, Tomáš, Zeman, Jiří, Hůlková, Helena, Wen, Rong, Kmoch, Stanislav, Sessa, William C.
Publicado em 2014

Warburg Effect’s Manifestation in Aggressive Pheochromocytomas and Paragangliomas: Insights from a Mouse Cell Model Applied to Human Tumor Tissue

Por Fliedner, Stephanie M. J., Kaludercic, Nina, Jiang, Xiao-Sheng, Hansikova, Hana, Hajkova, Zuzana, Sladkova, Jana, Limpuangthip, Andrea, Backlund, Peter S., Wesley, Robert, Martiniova, Lucia, Jochmanova, Ivana, Lendvai, Nikoletta K., Breza, Jan, Yergey, Alfred L., Paolocci, Nazareno, Tischler, Arthur S., Zeman, Jiri, Porter, Forbes D., Lehnert, Hendrik, Pacak, Karel
Publicado em 2012

Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model

Por Martins, Carla, Hůlková, Helena, Dridi, Larbi, Dormoy-Raclet, Virginie, Grigoryeva, Lubov, Choi, Yoo, Langford-Smith, Alexander, Wilkinson, Fiona L., Ohmi, Kazuhiro, DiCristo, Graziella, Hamel, Edith, Ausseil, Jerôme, Cheillan, David, Moreau, Alain, Svobodová, Eva, Hájková, Zuzana, Tesařová, Markéta, Hansíková, Hana, Bigger, Brian W., Hrebícek, Martin, Pshezhetsky, Alexey V.
Publicado no Brain (2015)

ORAL D-GALACTOSE SUPPLEMENTATION IN PGM1-CDG

Por Wong, Sunnie Yan-Wai, Gadomski, Therese, van Scherpenzeel, Monique, Honzik, Tomas, Hansikova, Hana, Brocke Holmefjord, Katja S., Mork, Marit, Bowling, Francis, Cegielska, Jolanta Sykut, Koch, Dieter, Hertecant, Jozef, Preston, Graeme, Jaeken, Jaak, Peeters, Nicole, Perez, Stefanie, Nguyen, David Do, Crivelly, Kea, Emmerzaal, Tim, Gibson, K. Michael, Raymond, Kimiyo, Bakar, Nurulamin Abu, Foulquier, Francois, Poschet, Gernot, Ackermann, Amanda, He, Miao, Lefeber, Dirk, Thiel, Christian, Kozicz, Tamas, Morava, Eva
Publicado no Genet Med (2017)