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Results: 4

1.

Infantile systemic hyalinosis: a case report with a novel mutation.

Al Sinani S, Al Murshedy F, Abdwani R.

Oman Med J. 2013 Jan;28(1):53-5. doi: 10.5001/omj.2013.12.

PMID:
23386947
[PubMed]
Free PMC Article
2.

Human genetic variation altering anthrax toxin sensitivity.

Martchenko M, Candille SI, Tang H, Cohen SN.

Proc Natl Acad Sci U S A. 2012 Feb 21;109(8):2972-7. doi: 10.1073/pnas.1121006109. Epub 2012 Feb 6.

PMID:
22315420
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

The dark sides of capillary morphogenesis gene 2.

Deuquet J, Lausch E, Superti-Furga A, van der Goot FG.

EMBO J. 2012 Jan 4;31(1):3-13. doi: 10.1038/emboj.2011.442. Epub 2011 Dec 6. Review.

PMID:
22215446
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Hyaline fibromatosis syndrome inducing mutations in the ectodomain of anthrax toxin receptor 2 can be rescued by proteasome inhibitors.

Deuquet J, Lausch E, Guex N, Abrami L, Salvi S, Lakkaraju A, Ramirez MC, Martignetti JA, Rokicki D, Bonafe L, Superti-Furga A, van der Goot FG.

EMBO Mol Med. 2011 Apr;3(4):208-21. doi: 10.1002/emmm.201100124. Epub 2011 Feb 15.

PMID:
21328543
[PubMed - indexed for MEDLINE]
Free PMC Article
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