Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Franziska Boiti"'
Autor:
Julia Körholz, Nadja Lucas, Franziska Boiti, Karina Althaus, Oliver Tiebel, Mingyan Fang, Reinhard Berner, Min Ae Lee-Kirsch, Ralf Knöfler
Publikováno v:
TH Open, Vol 04, Iss 04, Pp e413-e416 (2020)
Next-generation sequencing is increasingly applied during the diagnostic work-up of patients with bleeding diathesis and has facilitated the diagnosis of rare bleeding disorders such as inherited platelet function disorders. Mutations in RAS guanyl r
Externí odkaz:
https://doaj.org/article/924c99b7622343c4b6376e00269effbb
Autor:
Anna Floriane Hennig, Uta Rössler, Franziska Boiti, Maja von der Hagen, Manfred Gossen, Uwe Kornak, Harald Stachelscheid
Publikováno v:
Stem Cell Research, Vol 35, Iss , Pp - (2019)
Autosomal recessive osteopetrosis (ARO) is a genetic bone disease that can be caused by mutations in the CLCN7 gene preventing osteoclast-mediated bone resorption. We generated a human induced pluripotent stem cell (hiPSC) line, BIHi002-A, from perip
Externí odkaz:
https://doaj.org/article/e28caa609e2f424abd3611662f060788
Autor:
Uwe Kornak, Harald Stachelscheid, Anna Floriane Hennig, Maja von der Hagen, Uta Rössler, Franziska Boiti, Manfred Gossen
Publikováno v:
Stem Cell Research, Vol 35, Iss, Pp-(2019)
Henning, A.F.; Roessler, U.; Boiti, F.; Hagen, M.von der; Gossen, M.; Kornak, U.; Stachelscheid, H.: Generation of a human induced pluripotent stem cell line (BIHi002-A) from a patient with CLCN7-related infantile malignant autosomal recessive osteopetrosis. In: Stem Cell Research. Vol. 35 (2019) 101367. (DOI: /10.1016/j.scr.2018.101367)
Henning, A.F.; Roessler, U.; Boiti, F.; Hagen, M.von der; Gossen, M.; Kornak, U.; Stachelscheid, H.: Generation of a human induced pluripotent stem cell line (BIHi002-A) from a patient with CLCN7-related infantile malignant autosomal recessive osteopetrosis. In: Stem Cell Research. Vol. 35 (2019) 101367. (DOI: /10.1016/j.scr.2018.101367)
Autosomal recessive osteopetrosis (ARO) is a genetic bone disease that can be caused by mutations in the CLCN7 gene preventing osteoclast-mediated bone resorption. We generated a human induced pluripotent stem cell (hiPSC) line, BIHi002-A, from perip