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The role of aminoacyl-tRNA synthetases in genetic diseases.
Antonellis A, Green ED. Antonellis A, et al. Among authors: green ed. Annu Rev Genomics Hum Genet. 2008;9:87-107. doi: 10.1146/annurev.genom.9.081307.164204. Annu Rev Genomics Hum Genet. 2008. PMID: 18767960 Review.
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.
Everett LA, Belyantseva IA, Noben-Trauth K, Cantos R, Chen A, Thakkar SI, Hoogstraten-Miller SL, Kachar B, Wu DK, Green ED. Everett LA, et al. Among authors: green ed. Hum Mol Genet. 2001 Jan 15;10(2):153-61. doi: 10.1093/hmg/10.2.153. Hum Mol Genet. 2001. PMID: 11152663
Mitotic checkpoint locus MAD1L1 maps to human chromosome 7p22 and mouse chromosome 5.
Jin DY, Kozak CA, Pangilinan F, Spencer F, Green ED, Jeang KT. Jin DY, et al. Among authors: green ed. Genomics. 1999 Feb 1;55(3):363-4. doi: 10.1006/geno.1998.5654. Genomics. 1999. PMID: 10049595 No abstract available.
Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31.
Zenklusen JC, Conti CJ, Green ED. Zenklusen JC, et al. Among authors: green ed. Nat Genet. 2001 Apr;27(4):392-8. doi: 10.1038/86891. Nat Genet. 2001. PMID: 11279520
A family of mammalian anion transporters and their involvement in human genetic diseases.
Everett LA, Green ED. Everett LA, et al. Among authors: green ed. Hum Mol Genet. 1999;8(10):1883-91. doi: 10.1093/hmg/8.10.1883. Hum Mol Genet. 1999. PMID: 10469841 Review.
The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical map.
Ellsworth RE, Ionasescu V, Searby C, Sheffield VC, Braden VV, Kucaba TA, McPherson JD, Marra MA, Green ED. Ellsworth RE, et al. Among authors: green ed. Genome Res. 1999 Jun;9(6):568-74. Genome Res. 1999. PMID: 10400924 Free PMC article.
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).
Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED. Everett LA, et al. Among authors: green ed. Nat Genet. 1997 Dec;17(4):411-22. doi: 10.1038/ng1297-411. Nat Genet. 1997. PMID: 9398842
Adaptive evolution of foundation kinetochore proteins in primates.
Schueler MG, Swanson W, Thomas PJ; NISC Comparative Sequencing Program, Green ED. Schueler MG, et al. Among authors: green ed. Mol Biol Evol. 2010 Jul;27(7):1585-97. doi: 10.1093/molbev/msq043. Epub 2010 Feb 8. Mol Biol Evol. 2010. PMID: 20142441 Free PMC article.
Effort required to finish shotgun-generated genome sequences differs significantly among vertebrates.
Blakesley RW, Hansen NF, Gupta J, McDowell JC, Maskeri B, Barnabas BB, Brooks SY, Coleman H, Haghighi P, Ho SL, Schandler K, Stantripop S, Vogt JL, Thomas PJ; NISC Comparative Sequencing Program, Bouffard GG, Green ED. Blakesley RW, et al. Among authors: green ed. BMC Genomics. 2010 Jan 11;11:21. doi: 10.1186/1471-2164-11-21. BMC Genomics. 2010. PMID: 20064230 Free PMC article.
Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome.
Antonellis A, Bennett WR, Menheniott TR, Prasad AB, Lee-Lin SQ; NISC Comparative Sequencing Program, Green ED, Paisley D, Kelsh RN, Pavan WJ, Ward A. Antonellis A, et al. Among authors: green ed. Hum Mol Genet. 2006 Jan 15;15(2):259-71. doi: 10.1093/hmg/ddi442. Epub 2005 Dec 5. Hum Mol Genet. 2006. PMID: 16330480
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