Protocol for editing fibroblasts with in vitro transcribed Cas9 mRNA and profile off-target editing by optimized GUIDE-seq

por Li, Zhuokun, Reint, Ganna, Haapaniemi, Emma Maria
Publicado 2023

Reply to “CRISPR screens are feasible in TP53 wild‐type cells”

por Haapaniemi, Emma, Botla, Sandeep, Persson, Jenna, Schmierer, Bernhard, Taipale, Jussi
Publicado 2019

Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease

por Keskitalo, Salla, Haapaniemi, Emma M., Glumoff, Virpi, Liu, Xiaonan, Lehtinen, Ville, Fogarty, Christopher, Rajala, Hanna, Chiang, Samuel C., Mustjoki, Satu, Kovanen, Panu, Lohi, Jouko, Bryceson, Yenan T., Seppänen, Mikko, Kere, Juha, Heiskanen, Kaarina, Varjosalo, Markku
Publicado 2019

Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

por Keskitalo, Salla, Haapaniemi, Emma, Einarsdottir, Elisabet, Rajamäki, Kristiina, Heikkilä, Hannele, Ilander, Mette, Pöyhönen, Minna, Morgunova, Ekaterina, Hokynar, Kati, Lagström, Sonja, Kivirikko, Sirpa, Mustjoki, Satu, Eklund, Kari, Saarela, Janna, Kere, Juha, Seppänen, Mikko R. J., Ranki, Annamari, Hannula-Jouppi, Katariina, Varjosalo, Markku
Publicado 2019

Rapid genome editing by CRISPR-Cas9-POLD3 fusion

por Reint, Ganna, Li, Zhuokun, Labun, Kornel, Keskitalo, Salla, Soppa, Inkeri, Mamia, Katariina, Tolo, Eero, Szymanska, Monika, Meza-Zepeda, Leonardo A, Lorenz, Susanne, Cieslar-Pobuda, Artur, Hu, Xian, Bordin, Diana L, Staerk, Judith, Valen, Eivind, Schmierer, Bernhard, Varjosalo, Markku, Taipale, Jussi, Haapaniemi, Emma
Publicado 2021

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease

por Flanagan, Sarah E., Haapaniemi, Emma, Russell, Mark A., Caswell, Richard, Allen, Hana Lango, De Franco, Elisa, McDonald, Timothy J., Rajala, Hanna, Ramelius, Anita, Barton, John, Heiskanen, Kaarina, Heiskanen-Kosma, Tarja, Kajosaari, Merja, Murphy, Nuala P., Milenkovic, Tatjana, Seppänen, Mikko, Lernmark, Åke, Mustjoki, Satu, Otonkoski, Timo, Kere, Juha, Morgan, Noel G., Ellard, Sian, Hattersley, Andrew T.
Publicado 2014