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Author/Creator Ondruskova, Nina

1. C17 Increased mitochondrial number, cellular stress and glycogen accumulation in heart of minipig model transgenic for N-terminal part of human mutated huntingtin. (13th September 2016)

Authors:
Rodinova, Marie; Ondruskova, Nina; Dosoudilova, Zaneta; Juhas, Stefan; Juhasova, Jana; Ellederova, Zdenka; Motlik, Jan; Hansikova, Hana
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 87(2016)Supplement 1
Page Start:
A32
Record Type:
Journal Article
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2. Elevated oxysterol and N‐palmitoyl‐O‐phosphocholineserine levels in congenital disorders of glycosylation. Issue 2 (3rd February 2023)

Authors:
Dang Do, An N.; Chang, Irene J.; Jiang, Xutian; Wolfe, Lynne A.; Ng, Bobby G.; Lam, Christina; Schnur, Rhonda E.; Allis, Katrina; Hansikova, Hana; Ondruskova, Nina; O'Connor, Shawn D.; Sanchez‐Valle, Amarilis; Vollo, Arve; Wang, Raymond Y.; Wolfenson, Zoe; Perreault, John; Ory, Daniel S.; Freeze,...
Journal:
Journal of inherited metabolic disease
Issue:
Volume 46:Issue 2(2023)
Page Start:
326
Record Type:
Journal Article
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3. Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation. (5th June 2018)

Authors:
Ashikov, Angel; Abu Bakar, Nurulamin; Wen, Xiao-Yan; Niemeijer, Marco; Rodrigues Pinto Osorio, Glentino; Brand-Arzamendi, Koroboshka; Hasadsri, Linda; Hansikova, Hana; Raymond, Kimiyo; Vicogne, Dorothée; Ondruskova, Nina; Simon, Marleen E H; Pfundt, Rolph; Timal, Sharita; Beumers, Roel; Biot, Chr...
Journal:
Human molecular genetics
Issue:
Volume 27:Number 17(2018:Sep. 01)
Page Start:
3029
Record Type:
Journal Article
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4. Severe phenotype of ATP6AP1‐CDG in two siblings with a novel mutation leading to a differential tissue‐specific ATP6AP1 protein pattern, cellular oxidative stress and hepatic copper accumulation. Issue 4 (7th April 2020)

Authors:
Ondruskova, Nina; Honzik, Tomas; Vondrackova, Alzbeta; Stranecky, Viktor; Tesarova, Marketa; Zeman, Jiri; Hansikova, Hana
Journal:
Journal of inherited metabolic disease
Issue:
Volume 43:Issue 4(2020)
Page Start:
694
Record Type:
Journal Article
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