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Cloning and structural analysis of the human c-kit gene.
Oncogene. 1992 Jul;7(7):1259-66.
Oncogene. 1992.
PMID: 1377810
Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.
Liu NP, Dew-Knight S, Jonasson F, Gilbert JR, Klintworth GK, Vance JM.
Liu NP, et al. Among authors: dew knight s.
Mol Vis. 2000 Jun 19;6:95-100.
Mol Vis. 2000.
PMID: 10869098
Free article.
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Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.
Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM.
Baxter RV, et al. Among authors: dew knight s.
Nat Genet. 2002 Jan;30(1):21-2. doi: 10.1038/ng796. Epub 2001 Dec 17.
Nat Genet. 2002.
PMID: 11743579
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Negative regulation of DNA replication by the retinoblastoma protein is mediated by its association with MCM7.
Sterner JM, Dew-Knight S, Musahl C, Kornbluth S, Horowitz JM.
Sterner JM, et al. Among authors: dew knight s.
Mol Cell Biol. 1998 May;18(5):2748-57. doi: 10.1128/MCB.18.5.2748.
Mol Cell Biol. 1998.
PMID: 9566894
Free PMC article.
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Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I gene.
Liu NP, Baldwin J, Jonasson F, Dew-Knight S, Stajich JM, Lennon F, Pericak-Vance MA, Klintworth GK, Vance JM.
Liu NP, et al. Among authors: dew knight s.
Am J Hum Genet. 1998 Sep;63(3):912-7. doi: 10.1086/302001.
Am J Hum Genet. 1998.
PMID: 9718332
Free PMC article.
No abstract available.
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Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.
Liu NP, Dew-Knight S, Rayner M, Jonasson F, Akama TO, Fukuda MN, Bao W, Gilbert JR, Vance JM, Klintworth GK.
Liu NP, et al. Among authors: dew knight s.
Mol Vis. 2000 Dec 13;6:261-4.
Mol Vis. 2000.
PMID: 11139648
Free article.
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