Browsing Universitätsbibliographie by Author "Klimiankou, Maksim"

Now showing items 1-11 of 11

Cooperating, congenital neutropenia-associatedCsf3randRunx1mutations activate pro-inflammatory signaling and inhibit myeloid differentiation of mouse HSPCs

Ritter, Malte; Klimiankou, Maksim; Klimenkova, Olga; Schambach, Axel; Hoffmann, Dirk; Schmidt, Amy; Kanz, Lothar; Link, Daniel C.; Welte, Karl; Skokowa, Julia (2020)
CRISPR/Cas9-mediated ELANE knockout enables neutrophilic maturation of primary hematopoietic stem and progenitor cells and induced pluripotent stem cells o severe congenital neutropenia patients

Nasri, Masoud; Ritter, Malte; Mir, Perihan; Dannenmann, Benjamin; Aghaallaei, Narges; Amend, Diana; Makaryan, Vahagn; Xu, Yun; Fletcher, Breanna; Bernhard, Regine; Steiert, Ingeborg; Haehnel, Karin; Berger, Juergen; Koch, Iris; Sailer, Brigitte; Hipp, Katharina; Zeidler, Cornelia; Klimiankou, Maksim; Bajoghli, Baubak; Dale, David C.; Welte, Karl; Skokowa, Julia (2020)
ELANE mutant-specific activation of different UPR pathways in congenital neutropenia

Nustede, Rainer; Klimiankou, Maksim; Klimenkova, Olga; Kuznetsova, Inna; Zeidler, Cornelia; Welte, Karl; Skokowa, Julia (2016)
Fluorescent labeling of CRISPR/Cas9 RNP for gene knockout in HSPCs and iPSCs reveals an essential role for GADD45b in stress response

Nasri, Masoud; Mir, Perihan; Dannenmann, Benjamin; Amend, Diana; Skroblyn, Tessa; Xu, Yun; Schulze-Osthoff, Klaus; Klimiankou, Maksim; Welte, Karl; Skokowa, Julia (2019)
HAX1-related congenital neutropenia: Long-term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry (SCNIR)

Pogozhykh, Denys; Karapinar, Deniz Yilmaz; Klimiankou, Maksim; Gerschmann, Natali; Ebetsberger-Dachs, Georg; Palmblad, Jan; Carlsson, Goran; Masmas, Tania; Kinsey, Sally; Bartels, Marije; Mellor-Heineke, Sabine; Welte, Karl; Skokowa, Julia; Zeidler, Cornelia (2023)
Human iPSC-based model of severe congenital neutropenia reveals elevated UPR and DNA damage in CD34(+) cells preceding leukemic transformation

Dannenmann, Benjamin; Zahabi, Azadeh; Mir, Perihan; Oswald, Benedikt; Bernhard, Regine; Klimiankou, Maksim; Morishima, Tatsuya; Schulze-Osthoff, Klaus; Zeidler, Cornelia; Kanz, Lothar; Lachmann, Nico; Moritz, Thomas; Welte, Karl; Skokowa, Julia (2019)
iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropenia

Dannenmann, Benjamin; Klimiankou, Maksim; Oswald, Benedikt; Solovyeva, Anna; Mardan, Jehan; Nasri, Masoud; Ritter, Malte; Zahabi, Azadeh; Arreba-Tutusaus, Patricia; Mir, Perihan; Stein, Frederic; Kandabarau, Siarhei; Lachmann, Nico; Moritz, Thomas; Morishima, Tatsuya; Konantz, Martina; Lengerke, Claudia; Ripperger, Tim; Steinemann, Doris; Erlacher, Miriam; Niemeyer, Charlotte M.; Zeidler, Cornelia; Welte, Karl; Skokowa, Julia (2021)
LMO2 activation by deacetylation is indispensable for hematopoiesis and T-ALL leukemogenesis

Morishima, Tatsuya; Krahl, Ann-Christin; Nasri, Masoud; Xu, Yun; Aghaallaei, Narges; Findik, Betuel; Klimiankou, Maksim; Ritter, Malte; Hartmann, Marcus D.; Gloeckner, Christian Johannes; Stefanczyk, Sylwia; Lindner, Christian; Oswald, Benedikt; Bernhard, Regine; Haehnel, Karin; Hermanutz-Klein, Ursula; Ebinger, Martin; Handgretinger, Rupert; Casadei, Nicolas; Welte, Karl; Andre, Maya; Mueller, Patrick; Bajoghli, Baubak; Skokowa, Julia (2019)
New insights into the pathomechanism of cyclic neutropenia

Mir, Perihan; Klimiankou, Maksim; Findik, Betuel; Haehnel, Karin; Mellor-Heineke, Sabine; Zeidler, Cornelia; Skokowa, Julia; Welte, Karl (2020)
Role of CSF3R mutations in the pathomechanism of congenital neutropenia and secondary acute myeloid leukemia

Klimiankou, Maksim; Mellor-Heineke, Sabine; Zeidler, Cornelia; Welte, Karl; Skokowa, Julia (2016)
Ultra-Sensitive CSF3R Deep Sequencing in Patients With Severe Congenital Neutropenia

Klimiankou, Maksim; Uenalan, Murat; Kandabarau, Siarhei; Nustede, Rainer; Steiert, Ingeborg; Mellor-Heineke, Sabine; Zeidler, Cornelia; Skokowa, Julia; Welte, Karl (2019)

Now showing items 1-11 of 11

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