The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
In vivo immunological function of mast cells derived from embryonic stem cells: An approach for the rapid analysis of even embryonic lethal mutations in adult mice in vivo
Abstract
An important goal of tissue engineering is to achieve reconstitution of specific functionally active cell types by transplantation of differentiated cell populations derived from normal or genetically altered embryonic stem cells in vitro . We find that mast cells derived in vitro from wild-type or genetically manipulated embryonic stem cells can survive and orchestrate immunologically specific IgE-dependent reactions after transplantation into mast cell-deficient Kit W / Kit W-v mice. These findings define a unique approach for analyzing the effects of mutations of any genes that are expressed in mast cells, including embryonic lethal mutations, in vitro or in vivo .
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Moreover, Tsai et al. showed that one also can generate such mast cells from embryonic stem cells, permitting the analysis in vivo of mast cells which lack products which, if absent in the germ line, would result in embryonic or perinatal lethality [64].”
From Mast cells and IgE in defense against lethality of venoms: Possible “benefit” of allergy (2020) · cites this paper as [64]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
THE HIGH-AFFINITY I g E RECEPTOR (FcεRI): From Physiology to Pathology
Kinet, J.-P. (1999) · Annual Review of Immunology · doi:10.1146/annurev.immunol.17.1.931 · Cited by 968
Research works printed but not linked: 34
- E J Robertson Terotocarcinomas and Embryonic Stem Cells: A Practical Approach. (IRL, Oxford, 1987).
- 10.1126/science.282.5391.1061 · DOI
- 10.1038/5512 · DOI
- 10.1172/JCI118454 · DOI
- 10.1172/JCI118769 · DOI
- 10.1006/exnr.1997.6674 · DOI
- 10.1038/70986 · DOI
- 10.1126/science.285.5428.754 · DOI
- 10.1073/pnas.89.19.9171 · DOI
- 10.1073/pnas.94.19.10295 · DOI
- S J Galli, K M Zsebo, E N Geissler Adv Immunol 55, 1–96 (1994).
- 10.1182/blood.V52.2.447.447 · DOI · Paper page
- 10.1056/NEJM199301283280408 · DOI
- 10.1016/0167-5699(93)90167-J · DOI
- B K Wershil, Y A Mekori, T Murakami, S J Galli J Immunol. 139, 2605–2614 (1987). · DOI
- 10.1038/372794a0 · DOI
- 10.1038/372798a0 · DOI
- 10.1073/pnas.94.7.3004 · DOI
- 10.1073/pnas.95.12.6881 · DOI
- Y Kawakami, S E Hartman, P M Holland, J A Cooper, T Kawakami J Immunol 161, 1795–1802 (1998). · DOI
- 10.1073/pnas.94.12.6358 · DOI
- 10.1182/blood.V89.8.2654 · DOI
- 10.1073/pnas.88.14.6382 · DOI
- M Tsai, M Miyamoto, S-Y Tam, Z-S Wang, S J Galli Am J Pathol 146, 335–343 (1995).
- 10.1084/jem.185.4.663 · DOI
- 10.1002/eji.1830191211 · DOI
- 10.1111/j.1365-2222.1973.tb01321.x · DOI
- 10.1242/dev.111.2.259 · DOI
- 10.1128/mcb.13.1.473-486.1993 · DOI
- 10.1038/32190 · DOI
- 10.1084/jem.174.1.125 · DOI
- 10.1023/A:1020574820797 · DOI
- 10.1126/science.271.5250.818 · DOI · Paper page
- 10.1016/S0065-2660(08)60549-0 · DOI · Paper page
Cited by
Sorted by citations
Visualizing structure and transitions in high-dimensional biological data
Moon, K. R., van Dijk, D., Wang, Z., Gigante, S., Burkhardt, D. B., Chen, W. S., Yim, K., Elzen, A. V. D., Hirn, M. J., Coifman, R. R., et al. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0336-3 · Cited by 1,065
Yu, C., Cantor, A. B., Yang, H., Browne, C., Wells, R. A., Fujiwara, Y., & Orkin, S. H. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020656 · Cited by 600
“To assess mast cell production in dblGATA mice, we cultured wt or hemizygous dblGATA bone marrow cells in medium containing stem cell factor and IL-3 to obtain mast cells (17).”
MethodMast cells and IgE in defense against venoms: Possible “good side” of allergy?
Galli, S. J., Starkl, P., Marichal, T., & Tsai, M. (2016) · Allergology International · doi:10.1016/j.alit.2015.09.002 · Cited by 73
Self-citationMast cells and IgE in defense against lethality of venoms: Possible “benefit” of allergy
Galli, S. J., Metz, M., Starkl, P., Marichal, T., & Tsai, M. (2020) · Allergo Journal International · doi:10.1007/s40629-020-00118-6 · Cited by 57
Self-citation
Metadata
- Authors
- Tsai, M., Wedemeyer, J., Ganiatsas, S., Tam, S.-Y., Zon, L. I., & Galli, S. J.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2000-07-25
- Volume
- 97
- Issue
- 16
- Pages
- 9186-9190
- ISSN
- 0027-8424
- 1091-6490
- Cited by
- 70
- References
- 1
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
