✦ LIBER ✦

Production of A B cell lymphoblastoid line from long-term human bone marrow suspension culture

✍ Scribed by L. P. Gerasimova; T. E. Manakova; R. S. Samoilova; G. A. Udalov

Publisher: Springer US
Year: 1987
Tongue: English
Weight: 282 KB
Volume: 104
Category: Article
ISSN: 0007-4888
DOI: 10.1007/bf00836014

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Characterization of reticulofibroblastoi

Characterization of reticulofibroblastoid colonies (CFU-RF) derived from bone marrow and long-term marrow culture monolayers

✍ B. Lim; C. A. Izaguirre; M. T. Aye; L. Huebsch; J. Drouin; C. Richardson; M. D. 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 1021 KB

The maintenance of hemopoietic precursors in long-term liquid bone marrow cultures (LTBMC) is associated with the presence of an adherent stromal layer composed of heterogeneous cell populations. We have used a culture assay to promote the growth of one of its cellular components and characterize it

Self-renewal of factor-dependent hemopoi

Self-renewal of factor-dependent hemopoietic progenitor cell-lines derived from long-term bone marrow cultures demonstrates significant mouse strain genotypic variation

✍ Greenberger, Joel S. 📂 Article 📅 1980 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 681 KB

## Abstract Long‐term bone marrow cultures established from C57Ks/J mice have been shown to spontaneously release endogenous ecotropic RNA type‐C virus (retrovirus). C57Ks/J marrow cultures produced granulocyte‐macrophage progenitor cells (GM‐CFUc) and immature and mature granulocytes for over 45 w

A non-contact suspension culture approac

A non-contact suspension culture approach to the culture of osteogenic cells derived from a CD49elow subpopulation of human bone marrow-derived cells

✍ Dolores Baksh; Peter W. Zandstra; John E. Davies 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 490 KB 👁 1 views

We demonstrate that adult human bone marrow (BM) contains a population of mesenchymal stromal cells (MSCs) that can be expanded in non-adherent, cytokine-dependent, suspension culture conditions for at least 42 days. The cells generated during suspension culture lacked detectable levels of gene expr