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The landscape of receptor-mediated precision cancer combination therapy via a single-cell perspective.
Published in:
Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29154-2
By:
- Ahmadi, Saba;
- Sukprasert, Pattara;
- Vegesna, Rahulsimham;
- Sinha, Sanju;
- Schischlik, Fiorella;
- Artzi, Natalie;
- Khuller, Samir;
- Schäffer, Alejandro A.;
- Ruppin, Eytan
Publication type:
Article
The landscape of receptor-mediated precision cancer combination therapy via a single-cell perspective.
Published in:
Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29154-2
By:
- Ahmadi, Saba;
- Sukprasert, Pattara;
- Vegesna, Rahulsimham;
- Sinha, Sanju;
- Schischlik, Fiorella;
- Artzi, Natalie;
- Khuller, Samir;
- Schäffer, Alejandro A.;
- Ruppin, Eytan
Publication type:
Article
A reversible gene trap collection empowers haploid genetics in human cells.
Published in:
Nature Methods, 2013, v. 10, n. 10, p. 965, doi. 10.1038/nmeth.2609
By:
- Bürckstümmer, Tilmann;
- Banning, Carina;
- Hainzl, Philipp;
- Schobesberger, Richard;
- Kerzendorfer, Claudia;
- Pauler, Florian M;
- Chen, Doris;
- Them, Nicole;
- Schischlik, Fiorella;
- Rebsamen, Manuele;
- Smida, Michal;
- de la Cruz, Ferran Fece;
- Lapao, Ana;
- Liszt, Melissa;
- Eizinger, Benjamin;
- Guenzl, Philipp M;
- Blomen, Vincent A;
- Konopka, Tomasz;
- Gapp, Bianca;
- Parapatics, Katja
Publication type:
Article
PD‐L1 overexpression correlates with JAK2‐V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms.
Published in:
American Journal of Hematology, 2022, v. 97, n. 4, p. 390, doi. 10.1002/ajh.26461
By:
- Milosevic Feenstra, Jelena D.;
- Jäger, Roland;
- Schischlik, Fiorella;
- Ivanov, Daniel;
- Eisenwort, Gregor;
- Rumi, Elisa;
- Schuster, Michael;
- Gisslinger, Bettina;
- Machherndl‐Spandl, Sigrid;
- Bettelheim, Peter;
- Krauth, Maria‐Theresa;
- Keil, Felix;
- Bock, Christoph;
- Cazzola, Mario;
- Gisslinger, Heinz;
- Kralovics, Robert;
- Valent, Peter
Publication type:
Article
Myelomonocytic Skewing In Vitro Discriminates Subgroups of Patients with Myelofibrosis with A Different Phenotype, A Different Mutational Profile and Different Prognosis.
Published in:
Cancers, 2020, v. 12, n. 8, p. 2291, doi. 10.3390/cancers12082291
By:
- Geissler, Klaus;
- Gisslinger, Bettina;
- Jäger, Eva;
- Jäger, Roland;
- Schiefer, Ana-Iris;
- Bogner, Edith;
- Fuchs, Elisabeth;
- Schischlik, Fiorella;
- Alpar, Donat;
- Simonitsch-Klupp, Ingrid;
- Kralovics, Robert;
- Gisslinger, Heinz
Publication type:
Article
Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia.
Published in:
Nature Communications, 2017, v. 8, n. 11, p. 1, doi. 10.1038/s41467-017-01439-x
By:
- Moder, Martin;
- Velimezi, Georgia;
- Owusu, Michel;
- Mazouzi, Abdelghani;
- Wiedner, Marc;
- Ferreira da Silva, Joana;
- Robinson-Garcia, Lydia;
- Schischlik, Fiorella;
- Slavkovsky, Rastislav;
- Kralovics, Robert;
- Schuster, Michael;
- Bock, Christoph;
- Ideker, Trey;
- Jackson, Stephen P.;
- Menche, Jörg;
- Loizou, Joanna I.
Publication type:
Article

Found: 6

The landscape of receptor-mediated precision cancer combination therapy via a single-cell perspective.

The landscape of receptor-mediated precision cancer combination therapy via a single-cell perspective.

A reversible gene trap collection empowers haploid genetics in human cells.

PD‐L1 overexpression correlates with JAK2‐V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms.

Myelomonocytic Skewing In Vitro Discriminates Subgroups of Patients with Myelofibrosis with A Different Phenotype, A Different Mutational Profile and Different Prognosis.

Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia.