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11 results
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The structure and expression of the human neuroligin-3 gene.
Philibert RA, Winfield SL, Sandhu HK, Martin BM, Ginns EI. Philibert RA, et al. Among authors: winfield sl. Gene. 2000 Apr 4;246(1-2):303-10. doi: 10.1016/s0378-1119(00)00049-4. Gene. 2000. PMID: 10767552
The genomic structure and developmental expression patterns of the human OPA-containing gene (HOPA).
Philibert RA, Winfield SL, Damschroder-Williams P, Tengstrom C, Martin BM, Ginns EI. Philibert RA, et al. Among authors: winfield sl. Hum Genet. 1999 Jul-Aug;105(1-2):174-8. doi: 10.1007/s004399900084. Hum Genet. 1999. PMID: 10480376
Structure and organization of the human thrombospondin 3 gene (THBS3).
Adolph KW, Long GL, Winfield S, Ginns EI, Bornstein P. Adolph KW, et al. Genomics. 1995 May 20;27(2):329-36. doi: 10.1006/geno.1995.1050. Genomics. 1995. PMID: 7558000
Structure and organization of the human metaxin gene (MTX) and pseudogene.
Long GL, Winfield S, Adolph KW, Ginns EI, Bornstein P. Long GL, et al. Genomics. 1996 Apr 15;33(2):177-84. doi: 10.1006/geno.1996.0181. Genomics. 1996. PMID: 8660965
Isolation and characterization of the human tyrosine hydroxylase gene: identification of 5' alternative splice sites responsible for multiple mRNAs.
O'Malley KL, Anhalt MJ, Martin BM, Kelsoe JR, Winfield SL, Ginns EI. O'Malley KL, et al. Among authors: winfield sl. Biochemistry. 1987 Nov 3;26(22):6910-4. doi: 10.1021/bi00396a007. Biochemistry. 1987. PMID: 2892528
Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease.
Lau EK, Tayebi N, Ingraham LJ, Winfield SL, Koprivica V, Stone DL, Zimran A, Ginns EI, Sidransky E. Lau EK, et al. Among authors: winfield sl. Hum Genet. 1999 Apr;104(4):293-300. doi: 10.1007/s004390050957. Hum Genet. 1999. PMID: 10369158
Metaxin, a gene contiguous to both thrombospondin 3 and glucocerebrosidase, is required for embryonic development in the mouse: implications for Gaucher disease.
Bornstein P, McKinney CE, LaMarca ME, Winfield S, Shingu T, Devarayalu S, Vos HL, Ginns EI. Bornstein P, et al. Proc Natl Acad Sci U S A. 1995 May 9;92(10):4547-51. doi: 10.1073/pnas.92.10.4547. Proc Natl Acad Sci U S A. 1995. PMID: 7753840 Free PMC article.
Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher disease.
Winfield SL, Tayebi N, Martin BM, Ginns EI, Sidransky E. Winfield SL, et al. Genome Res. 1997 Oct;7(10):1020-6. doi: 10.1101/gr.7.10.1020. Genome Res. 1997. PMID: 9331372 Free PMC article.
Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene.
Tybulewicz VL, Tremblay ML, LaMarca ME, Willemsen R, Stubblefield BK, Winfield S, Zablocka B, Sidransky E, Martin BM, Huang SP, et al. Tybulewicz VL, et al. Nature. 1992 Jun 4;357(6377):407-10. doi: 10.1038/357407a0. Nature. 1992. PMID: 1594045
Association of an X-chromosome dodecamer insertional variant allele with mental retardation.
Philibert RA, King BH, Winfield S, Cook EH, Lee YH, Stubblefield B, Damschroder-Williams P, Dea C, Palotie A, Tengstrom C, Martin BM, Ginns EI. Philibert RA, et al. Mol Psychiatry. 1998 Jul;3(4):303-9. doi: 10.1038/sj.mp.4000442. Mol Psychiatry. 1998. PMID: 9702738
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