Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality

Thiel C, Lübke T, Matthijs G, von Figura K, Körner C (2006)
Molecular and Cellular Biology 26(15): 5615-5620.

Journal Article | Published | English

No fulltext has been uploaded

Author
; ; ; ;
Publishing Year
ISSN
PUB-ID

Cite this

Thiel C, Lübke T, Matthijs G, von Figura K, Körner C. Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality. Molecular and Cellular Biology. 2006;26(15):5615-5620.
Thiel, C., Lübke, T., Matthijs, G., von Figura, K., & Körner, C. (2006). Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality. Molecular and Cellular Biology, 26(15), 5615-5620.
Thiel, C., Lübke, T., Matthijs, G., von Figura, K., and Körner, C. (2006). Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality. Molecular and Cellular Biology 26, 5615-5620.
Thiel, C., et al., 2006. Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality. Molecular and Cellular Biology, 26(15), p 5615-5620.
C. Thiel, et al., “Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality”, Molecular and Cellular Biology, vol. 26, 2006, pp. 5615-5620.
Thiel, C., Lübke, T., Matthijs, G., von Figura, K., Körner, C.: Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality. Molecular and Cellular Biology. 26, 5615-5620 (2006).
Thiel, Christian, Lübke, Torben, Matthijs, Gert, von Figura, Kurt, and Körner, Christian. “Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality”. Molecular and Cellular Biology 26.15 (2006): 5615-5620.
This data publication is cited in the following publications:
This publication cites the following data publications:

26 Citations in Europe PMC

Data provided by Europe PubMed Central.

Proteomic analysis of platelet N-glycoproteins in PMM2-CDG patients.
de la Morena-Barrio ME, Di Michele M, Lozano ML, Rivera J, Perez-Duenas B, Altisent C, Sevivas T, Vicente V, Jaeken J, Freson K, Corral J., Thromb. Res. 133(3), 2014
PMID: 24388574

30 References

Data provided by Europe PubMed Central.


AUTHOR UNKNOWN, 2000
Increased recurrence risk in congenital disorders of glycosylation type Ia (CDG-Ia) due to a transmission ratio distortion.
Schollen E, Kjaergaard S, Martinsson T, Vuillaumier-Barrot S, Dunoe M, Keldermans L, Seta N, Matthijs G., J. Med. Genet. 41(11), 2004
PMID: 15520415
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder.
Wu X, Steet RA, Bohorov O, Bakker J, Newell J, Krieger M, Spaapen L, Kornfeld S, Freeze HH., Nat. Med. 10(5), 2004
PMID: 15107842

Export

0 Marked Publications

Open Data PUB

Web of Science

View record in Web of Science®

Sources

PMID: 16847317
PubMed | Europe PMC

Search this title in

Google Scholar