Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Larissa Doll"'
Autor:
Natalia Borbaran Bravo, Larissa Doll, Ekaterina Deordieva, Sandro Bräuning, Benjamin Dannenmann, Mohammad Elgamacy, Viktoria Zakharova, Claudia Lengerke, Cornelia Zeidler, Karl Welte, Anna Shcherbina, Julia Skokowa, Maksim Klimiankou
Publikováno v:
HemaSphere, Vol 7, p e9362349 (2023)
Externí odkaz:
https://doaj.org/article/b8cb225264be43d690962a810725cb2d
Autor:
Larissa Doll, Narges Aghaallaei, Claudia Lengerke, Cornelia Zeidler, Karl Welte, Julia Skokowa, Baubak Bajoghli
Publikováno v:
HemaSphere, Vol 7, p e69758f3 (2023)
Externí odkaz:
https://doaj.org/article/0998c5acdfa0430593af8d5ae2f26bd2
Publikováno v:
Haematologica, Vol 106, Iss 5 (2020)
Severe congenital neutropenia (CN) is a rare heterogeneous group of diseases, characterized by a granulocytic maturation arrest. Autosomal recessive mutations in the HAX1 gene are frequently detected in affected individuals. However, the precise role
Externí odkaz:
https://doaj.org/article/df6abd2cbb374869b7db564f38bcbe21
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 17, p 4179 (2019)
Over the past two decades, studies have demonstrated that several features of T-cell and thymic development are conserved from teleosts to mammals. In particular, works using zebrafish (Danio rerio) and medaka (Oryzias latipes) have shed light on the
Externí odkaz:
https://doaj.org/article/1cea50276d9443ce98bde6829a0982c4
Autor:
Hisayoshi, Hashimoto, Derya, Güngör, Naomi, Krickeberg, Johanna, Schmitt, Larissa, Doll, Marina, Schmidt, Sabine, Schleicher, Elvira, Criado-Moronati, Karin, Schilbach
Publikováno v:
Leukemia research. 117
Cancer testis antigen PRAME is over-expressed in a variety of malignant cells but is not or minimally expressed in normal non-germ line cells. Adoptive transfer of PRAME-specific T cells is thus under investigation in clinical trials as an innovative
Publikováno v:
Haematologica
Severe congenital neutropenia is a rare heterogeneous group of diseases, characterized by an arrest of granulocyte maturation. Autosomal recessive mutations in the HAX1 gene are frequently detected in affected individuals. However, the precise role o
Publikováno v:
Bioconjugate Chemistry. 31:990-1011
Bioorthogonal chemistry has mainly been developed for proteins and carbohydrates. The chemistry of nucleic acids is different, and bioorthogonal labeling strategies that were successfully applied for proteins and carbohydrates cannot be simply transf
Autor:
Hisayoshi Hashimoto, Derya Güngör, Naomi Krickeberg, Johanna Schmitt, Larissa Doll, Marina Schmidt, Sabine Schleicher, Elvira Criado-Moronati, Karin Schilbach
Publikováno v:
Leukemia Research. 117:106842
Publikováno v:
ChemBioChem, 22 (15), 2561-2567
Chembiochem
Chembiochem
For monitoring the intracellular pathway of small interfering RNA (siRNA), both strands were labelled at internal positions by two ATTO dyes as an interstrand Förster resonance energy transfer pair. siRNA double strands show red emission and a short
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a98bac4b3bb9cf163a718afb3a07adad
Publikováno v:
Blood. 136:14-14
Severe congenital neutropenia (CN) is a bone marrow failure characterized by an impaired neutrophil development. This disease can be caused by different germline mutations, which one of them is Jagunal homolog 1 (JAGN1). CN patients are prone to deve