Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Pathogenic effects of Leu200Pro and Arg387His VRK1 protein variants on phosphorylation targets and H4K16 acetylation in distal hereditary motor neuropathy.
J Mol Med (Berl). 2024 Jun;102(6):801-817. doi: 10.1007/s00109-024-02442-8. Epub 2024 Mar 30.
J Mol Med (Berl). 2024.
PMID: 38554151
Free PMC article.
STAG2: Computational Analysis of Missense Variants Involved in Disease.
Ros-Pardo D, Gómez-Puertas P, Marcos-Alcalde Í.
Ros-Pardo D, et al.
Int J Mol Sci. 2024 Jan 20;25(2):1280. doi: 10.3390/ijms25021280.
Int J Mol Sci. 2024.
PMID: 38279279
Free PMC article.
Item in Clipboard
Structural and functional insights into GSDMB isoforms complex roles in pathogenesis.
Colomo S, Ros-Pardo D, Oltra SS, Gomez-Puertas P, Sarrio D, Moreno-Bueno G.
Colomo S, et al. Among authors: ros pardo d.
Cell Cycle. 2023 Oct;22(20):2346-2359. doi: 10.1080/15384101.2023.2287933. Epub 2023 Dec 15.
Cell Cycle. 2023.
PMID: 38037340
Review.
Item in Clipboard
Distinct GSDMB protein isoforms and protease cleavage processes differentially control pyroptotic cell death and mitochondrial damage in cancer cells.
Oltra SS, Colomo S, Sin L, Pérez-López M, Lázaro S, Molina-Crespo A, Choi KH, Ros-Pardo D, Martínez L, Morales S, González-Paramos C, Orantes A, Soriano M, Hernández A, Lluch A, Rojo F, Albanell J, Gómez-Puertas P, Ko JK, Sarrió D, Moreno-Bueno G.
Oltra SS, et al. Among authors: ros pardo d.
Cell Death Differ. 2023 May;30(5):1366-1381. doi: 10.1038/s41418-023-01143-y. Epub 2023 Mar 11.
Cell Death Differ. 2023.
PMID: 36899106
Free PMC article.
Item in Clipboard
A Novel Intragenic Duplication in the HDAC8 Gene Underlying a Case of Cornelia de Lange Syndrome.
Lucia-Campos C, Valenzuela I, Latorre-Pellicer A, Ros-Pardo D, Gil-Salvador M, Arnedo M, Puisac B, Castells N, Plaja A, Tenes A, Cuscó I, Trujillano L, Ramos FJ, Tizzano EF, Gómez-Puertas P, Pié J.
Lucia-Campos C, et al. Among authors: ros pardo d.
Genes (Basel). 2022 Aug 8;13(8):1413. doi: 10.3390/genes13081413.
Genes (Basel). 2022.
PMID: 36011323
Free PMC article.
Item in Clipboard
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.
Christensen MB, Levy AM, Mohammadi NA, Niceta M, Kaiyrzhanov R, Dentici ML, Al Alam C, Alesi V, Benoit V, Bhatia KP, Bierhals T, Boßelmann CM, Buratti J, Callewaert B, Ceulemans B, Charles P, De Wachter M, Dehghani M, D'haenens E, Doco-Fenzy M, Geßner M, Gobert C, Guliyeva U, Haack TB, Hammer TB, Heinrich T, Hempel M, Herget T, Hoffmann U, Horvath J, Houlden H, Keren B, Kresge C, Kumps C, Lederer D, Lermine A, Magrinelli F, Maroofian R, Vahidi Mehrjardi MY, Moudi M, Müller AJ, Oostra AJ, Pletcher BA, Ros-Pardo D, Samarasekera S, Tartaglia M, Van Schil K, Vogt J, Wassmer E, Winkelmann J, Zaki MS, Zech M, Lerche H, Radio FC, Gomez-Puertas P, Møller RS, Tümer Z.
Christensen MB, et al. Among authors: ros pardo d.
Clin Genet. 2022 Aug;102(2):98-109. doi: 10.1111/cge.14165. Epub 2022 Jun 8.
Clin Genet. 2022.
PMID: 35616059
Free PMC article.
Item in Clipboard
Cite
Cite