Assessment of the metabolic capabilities of Haemophilus influenzae Rd through a genome-scale pathway analysis. |
C.H. Schilling; B.Ø. Palsson |
2000 |
The Escherichia coli MG1655 in silico metabolic genotype: its definition, characteristics, and capabilities. |
J.S. Edwards; B.Ø. Palsson |
2000 |
Toward metabolic phenomics: analysis of genomic data using flux balances. |
C.H. Schilling; J.S. Edwards; B.Ø. Palsson |
1999 |
Metabolic pathway analysis: basic concepts and scientific applications in the post-genomic era. |
C.H. Schilling; S. Schuster; B.Ø. Palsson; R. Heinrich |
1999 |
Systems properties of the Haemophilus influenzae Rd metabolic genotype. |
J.S. Edwards; B.Ø. Palsson |
1999 |
Phototoxicity of the fluorescent membrane dyes PKH2 and PKH26 on the human hematopoietic KG1a progenitor cell line. |
D.J. Oh; G.M. Lee; K. Francis; B.Ø. Palsson |
1999 |
Symmetry of initial cell divisions among primitive hematopoietic progenitors is independent of ontogenic age and regulatory molecules. |
S. Huang; P. Law; K. Francis; B.Ø. Palsson; A.D. Ho |
1999 |
Key adhesion molecules are present on long podia extended by hematopoietic cells. |
W. Holloway; A.R. Martinez; D.J. Oh; K. Francis; R. Ramakrishna; B.Ø. Palsson |
1999 |
The underlying pathway structure of biochemical reaction networks. |
C.H. Schilling; B.Ø. Palsson |
1998 |
Two new pseudopod morphologies displayed by the human hematopoietic KG1a progenitor cell line and by primary human CD34(+) cells. |
K. Francis; R. Ramakrishna; W. Holloway; B.Ø. Palsson |
1998 |
Tissue culture surface characteristics influence the expansion of human bone marrow cells. |
M.R. Koller; M.A. Palsson; I. Manchel; R.J. Maher; B.Ø. Palsson |
1998 |
Elemental balancing of biomass and medium composition enhances growth capacity in high-density Chlorella vulgaris cultures. |
R.K. Mandalam; B.Ø. Palsson |
1998 |
How will bioinformatics influence metabolic engineering? |
J.S. Edwards; B.Ø. Palsson |
1998 |
Cell cycle dependence of retroviral transduction: An issue of overlapping time scales. |
S.T. Andreadis; A.O. Fuller; B.Ø. Palsson |
1998 |
What lies beyond bioinformatics? |
B.Ø. Palsson |
1997 |
Importance of parenchymal:stromal cell ratio for the ex vivo reconstitution of human hematopoiesis. |
M.R. Koller; I. Manchel; B.Ø. Palsson |
1997 |
Coupled effects of polybrene and calf serum on the efficiency of retroviral transduction and the stability of retroviral vectors. |
S.T. Andreadis; B.Ø. Palsson |
1997 |
Moloney murine leukemia virus-derived retroviral vectors decay intracellularly with a half-life in the range of 5.5 to 7.5 hours. |
S.T. Andreadis; D.A. Brott; A.O. Fuller; B.Ø. Palsson |
1997 |
Effective intercellular communication distances are determined by the relative time constants for cyto/chemokine secretion and diffusion. |
K. Francis; B.Ø. Palsson |
1997 |
Determination of specific oxygen uptake rates in human hematopoietic cultures and implications for bioreactor design. |
C.A. Peng; B.Ø. Palsson |
1996 |
Cell growth and differentiation on feeder layers is predicted to be influenced by bioreactor geometry. |
C.A. Peng; B.Ø. Palsson |
1996 |
Different measures of human hematopoietic cell culture performance are optimized under vastly different conditions. |
M.R. Koller; I. Manchel; M.A. Palsson; R.J. Maher; B.Ø. Palsson |
1996 |
Membrane adsorption characteristics determine the kinetics of flow-through transductions. |
A.S. Chuck; B.Ø. Palsson |
1996 |
Retroviral infection is limited by Brownian motion. |
A.S. Chuck; M.F. Clarke; B.Ø. Palsson |
1996 |
Kinetics of retrovirus mediated gene transfer: the importance of intracellular half-life of retroviruses. |
S.T. Andreadis; B.Ø. Palsson |
1996 |
flt-3 ligand is more potent than c-kit ligand for the synergistic stimulation of ex vivo hematopoietic cell expansion. |
M.R. Koller; M. Oxender; D.A. Brott; B.Ø. Palsson |
1996 |
Unilineage model of hematopoiesis predicts self-renewal of stem and progenitor cells based on ex vivo growth data. |
C.A. Peng; M.R. Koller; B.Ø. Palsson |
1996 |
Donor-to-donor variability in the expansion potential of human bone marrow cells is reduced by accessory cells but not by soluble growth factors. |
M.R. Koller; I. Manchel; D.A. Brott; D.A. Brott |
1996 |
Flow cytometric analysis of human bone marrow perfusion cultures: erythroid development and relationship with burst-forming units-erythroid. |
C.E. Rogers; M.S. Bradley; B.Ø. Palsson; M.R. Koller |
1996 |
Consistent and high rates of gene transfer can be obtained using flow-through transduction over a wide range of retroviral titers. |
A.S. Chuck; B.Ø. Palsson |
1996 |