| In silico predictions of Escherichia coli metabolic capabilities are consistent with experimental data. |
J.S. Edwards; R.U. Ibarra; B.Ø. Palsson |
2001 |
| Metabolic modeling of microbial strains in silico. |
M.W. Covert; C.H. Schilling; I. Famili; J.S. Edwards; I.I. Goryanin; E. Selkov; B.Ø. Palsson |
2001 |
| Dynamic simulation of the human red blood cell metabolic network. |
N. Jamshidi; J.S. Edwards; T. Fahland; G.M. Church; B.Ø. Palsson |
2001 |
| In situ labeling of adherent cells with PKH26. |
G.M. Lee; S. Fong; K. Francis; D.J. Oh; B.Ø. Palsson |
2000 |
| Theory for the systemic definition of metabolic pathways and their use in interpreting metabolic function from a pathway-oriented perspective. |
C.H. Schilling; D. Letscher; B.Ø. Palsson |
2000 |
| 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 |
| Extension of osmolality-induced podia is observed from fluorescently labeled hematopoietic cell lines in hyperosmotic medium. |
D.J. Oh; A.R. Martinez; G.M. Lee; K. Francis; B.Ø. Palsson |
2000 |
| Intercellular adhesion can be visualized using fluorescently labeled fibrosarcoma HT1080 cells cocultured with hematopoietic cell lines or CD34(+) enriched human mobilized peripheral blood cells. |
D.J. Oh; A.R. Martinez; G.M. Lee; K. Francis; B.Ø. Palsson |
2000 |
| Metabolic flux balance analysis and the in silico analysis of Escherichia coli K-12 gene deletions. |
J.S. Edwards; B.Ø. Palsson |
2000 |
| Multiple steady states in kinetic models of red cell metabolism. |
J.S. Edwards; B.Ø. Palsson |
2000 |
| Robustness analysis of the Escherichia coli metabolic network. |
J.S. Edwards; B.Ø. Palsson |
2000 |
| Combining pathway analysis with flux balance analysis for the comprehensive study of metabolic systems. |
C.H. Schilling; J.S. Edwards; D. Letscher; 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 |
| 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 |
| What lies beyond bioinformatics? |
B.Ø. Palsson |
1997 |