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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1994 | 2 |
1996 | 1 |
2008 | 1 |
2024 | 0 |
PubMed (cited) for id: 601001
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The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.
J Am Acad Dermatol. 2008 Jun;58(6):931-50. doi: 10.1016/j.jaad.2008.02.004. Epub 2008 Apr 18.
J Am Acad Dermatol. 2008.
PMID: 18374450
Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplex.
Jonkman MF, Heeres K, Pas HH, van Luyn MJ, Elema JD, Corden LD, Smith FJ, McLean WH, Ramaekers FC, Burton M, Scheffer H.
Jonkman MF, et al.
J Invest Dermatol. 1996 Nov;107(5):764-9. doi: 10.1111/1523-1747.ep12365805.
J Invest Dermatol. 1996.
PMID: 8875963
Free article.
Item in Clipboard
A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex.
Hovnanian A, Pollack E, Hilal L, Rochat A, Prost C, Barrandon Y, Goossens M.
Hovnanian A, et al.
Nat Genet. 1993 Apr;3(4):327-32. doi: 10.1038/ng0493-327.
Nat Genet. 1993.
PMID: 7526933
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A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein.
Chan Y, Anton-Lamprecht I, Yu QC, Jäckel A, Zabel B, Ernst JP, Fuchs E.
Chan Y, et al.
Genes Dev. 1994 Nov 1;8(21):2574-87. doi: 10.1101/gad.8.21.2574.
Genes Dev. 1994.
PMID: 7525408
Free article.
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A functional "knockout" of human keratin 14.
Rugg EL, McLean WH, Lane EB, Pitera R, McMillan JR, Dopping-Hepenstal PJ, Navsaria HA, Leigh IM, Eady RA.
Rugg EL, et al.
Genes Dev. 1994 Nov 1;8(21):2563-73. doi: 10.1101/gad.8.21.2563.
Genes Dev. 1994.
PMID: 7525407
Free article.
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