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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1999 | 3 |
2010 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
PubMed (cited) for id: 613630
5 results
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Page 1
Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome.
Am J Hum Genet. 2012 Jan 13;90(1):76-85. doi: 10.1016/j.ajhg.2011.11.014. Epub 2011 Dec 22.
Am J Hum Genet. 2012.
PMID: 22197489
Free PMC article.
Mutant CHUK and severe fetal encasement malformation.
Lahtela J, Nousiainen HO, Stefanovic V, Tallila J, Viskari H, Karikoski R, Gentile M, Saloranta C, Varilo T, Salonen R, Kestilä M.
Lahtela J, et al.
N Engl J Med. 2010 Oct 21;363(17):1631-7. doi: 10.1056/NEJMoa0911698.
N Engl J Med. 2010.
PMID: 20961246
Free article.
Item in Clipboard
IKK1-deficient mice exhibit abnormal development of skin and skeleton.
Li Q, Lu Q, Hwang JY, Büscher D, Lee KF, Izpisua-Belmonte JC, Verma IM.
Li Q, et al.
Genes Dev. 1999 May 15;13(10):1322-8. doi: 10.1101/gad.13.10.1322.
Genes Dev. 1999.
PMID: 10346820
Free PMC article.
Item in Clipboard
Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase.
Hu Y, Baud V, Delhase M, Zhang P, Deerinck T, Ellisman M, Johnson R, Karin M.
Hu Y, et al.
Science. 1999 Apr 9;284(5412):316-20. doi: 10.1126/science.284.5412.316.
Science. 1999.
PMID: 10195896
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Limb and skin abnormalities in mice lacking IKKalpha.
Takeda K, Takeuchi O, Tsujimura T, Itami S, Adachi O, Kawai T, Sanjo H, Yoshikawa K, Terada N, Akira S.
Takeda K, et al.
Science. 1999 Apr 9;284(5412):313-6. doi: 10.1126/science.284.5412.313.
Science. 1999.
PMID: 10195895
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