Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

21 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.
Arnell H, Hjälmås K, Jägervall M, Läckgren G, Stenberg A, Bengtsson B, Wassén C, Emahazion T, Annerén G, Pettersson U, Sundvall M, Dahl N. Arnell H, et al. J Med Genet. 1997 May;34(5):360-5. doi: 10.1136/jmg.34.5.360. J Med Genet. 1997. PMID: 9152831 Free PMC article.
apolipoprotein-E dependent role for the FAS receptor in early onset Alzheimer's disease: finding of a positive association for a polymorphism in the TNFRSF6 gene.
Feuk L, Prince JA, Breen G, Emahazion T, Carothers A, St Clair D, Brookes AJ. Feuk L, et al. Hum Genet. 2000 Oct;107(4):391-6. doi: 10.1007/s004390000383. Hum Genet. 2000. PMID: 11129341
Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis.
Zhang Z, Duvefelt K, Svensson F, Masterman T, Jonasdottir G, Salter H, Emahazion T, Hellgren D, Falk G, Olsson T, Hillert J, Anvret M. Zhang Z, et al. Genes Immun. 2005 Mar;6(2):145-52. doi: 10.1038/sj.gene.6364171. Genes Immun. 2005. PMID: 15674389
Multiple sclerosis (MS) is a T-cell-mediated disease of the central nervous system, characterized by damage to myelin and axons, resulting in progressive neurological disability. ...LAG3 inhibits activated T cells, while IL7R is necessary for the maturation of T
Multiple sclerosis (MS) is a T-cell-mediated disease of the central nervous system, characterized by damage to myelin and axons, resu …
Genetic linkage analysis of collagen-induced arthritis in the mouse.
Jirholt J, Cook A, Emahazion T, Sundvall M, Jansson L, Nordquist N, Pettersson U, Holmdahl R. Jirholt J, et al. Eur J Immunol. 1998 Oct;28(10):3321-8. doi: 10.1002/(SICI)1521-4141(199810)28:10<3321::AID-IMMU3321>3.0.CO;2-M. Eur J Immunol. 1998. PMID: 9808201
SNP association studies in Alzheimer's disease highlight problems for complex disease analysis.
Emahazion T, Feuk L, Jobs M, Sawyer SL, Fredman D, St Clair D, Prince JA, Brookes AJ. Emahazion T, et al. Trends Genet. 2001 Jul;17(7):407-13. doi: 10.1016/s0168-9525(01)02342-3. Trends Genet. 2001. PMID: 11418222 Review.
Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation.
Prince JA, Feuk L, Howell WM, Jobs M, Emahazion T, Blennow K, Brookes AJ. Prince JA, et al. Genome Res. 2001 Jan;11(1):152-62. doi: 10.1101/gr.150201. Genome Res. 2001. PMID: 11156624 Free PMC article.
Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism.
Stranneheim H, Engvall M, Naess K, Lesko N, Larsson P, Dahlberg M, Andeer R, Wredenberg A, Freyer C, Barbaro M, Bruhn H, Emahazion T, Magnusson M, Wibom R, Zetterström RH, Wirta V, von Döbeln U, Wedell A. Stranneheim H, et al. Among authors: emahazion t. BMC Genomics. 2014 Dec 11;15(1):1090. doi: 10.1186/1471-2164-15-1090. BMC Genomics. 2014. PMID: 25495354 Free PMC article.
21 results
Jump to page
Feedback