Exploring the influence from whole blood DNA extraction methods on Infinium 450K DNA methylation

por Hjorthaug, Hanne Sagsveen, Gervin, Kristina, Mowinckel, Petter, Munthe-Kaas, Monica Cheng
Publicado 2018

Differential Glial Activation in Early Epileptogenesis—Insights From Cell-Specific Analysis of DNA Methylation and Gene Expression in the Contralateral Hippocampus

por Berger, Toni C., Vigeland, Magnus D., Hjorthaug, Hanne S., Nome, Cecilie G., Taubøll, Erik, Selmer, Kaja K., Heuser, Kjell
Publicado 2020

Neuronal and glial DNA methylation and gene expression changes in early epileptogenesis

por Berger, Toni C., Vigeland, Magnus D., Hjorthaug, Hanne S., Etholm, Lars, Nome, Cecilie G., Taubøll, Erik, Heuser, Kjell, Selmer, Kaja K.
Publicado 2019

Limitations and possibilities of low cell number ChIP-seq

por Gilfillan, Gregor D, Hughes, Timothy, Sheng, Ying, Hjorthaug, Hanne S, Straub, Tobias, Gervin, Kristina, Harris, Jennifer R, Undlien, Dag E, Lyle, Robert
Publicado 2012

Human thymic putative CD8αα precursors exhibit a biased TCR repertoire in single cell AIRR-seq

por Heimli, Marte, Tennebø Flåm, Siri, Sagsveen Hjorthaug, Hanne, Bjørnstad, Pål Marius, Chernigovskaya, Maria, Le, Quy Khang, Tekpli, Xavier, Greiff, Victor, Lie, Benedicte Alexandra
Publicado 2023

Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood

por Gervin, Kristina, Andreassen, Bettina Kulle, Hjorthaug, Hanne Sagsveen, Carlsen, Karin C. Lødrup, Carlsen, Kai-Håkon, Undlien, Dag Erik, Lyle, Robert, Munthe-Kaas, Monica Cheng
Publicado 2016

Multimodal human thymic profiling reveals trajectories and cellular milieu for T agonist selection

por Heimli, Marte, Flåm, Siri Tennebø, Hjorthaug, Hanne Sagsveen, Trinh, Don, Frisk, Michael, Dumont, Karl-Andreas, Ribarska, Teodora, Tekpli, Xavier, Saare, Mario, Lie, Benedicte Alexandra
Publicado 2023

Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study

por Wiedmann, Markus K.H., Steinsvåg, Ingunn V., Dinh, Tovy, Vigeland, Magnus D., Larsson, Pål G., Hjorthaug, Hanne, Sheng, Ying, Mero, Inger-Lise, Selmer, Kaja K.
Publicado 2023

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

por Rydning, Siri L, Koht, Jeanette, Sheng, Ying, Sowa, Piotr, Hjorthaug, Hanne S, Wedding, Iselin M, Erichsen, Anne Kjersti, Hovden, Inger Anette, Backe, Paul H, Tallaksen, Chantal M E, Vigeland, Magnus D, Selmer, Kaja K
Publicado 2019

A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome

por Fjær, Roar, Marciniak, Katarzyna, Sundnes, Olav, Hjorthaug, Hanne, Sheng, Ying, Hammarström, Clara, Sitek, Jan Cezary, Vigeland, Magnus Dehli, Backe, Paul Hoff, Øye, Ane-Marte, Fosse, Johanna Hol, Stav-Noraas, Tor Espen, Uchiyama, Yuri, Matsumoto, Naomichi, Comi, Anne, Pevsner, Jonathan, Haraldsen, Guttorm, Selmer, Kaja Kristine
Publicado 2021