qmwwallace's polymorphism [24 articles] Export

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	Splicing mutation of the prostacyclin synthase gene in a family associated with hypertension. [My Copy] Biochem Biophys Res Commun, Vol. 297, No. 5. (Oct 2002), pp. 1135-9. by Tomohiro Nakayama, Masayoshi Soma, Yoshiyasu Watanabe, et al.Buaijiaer Hasimu, Mikano Sato, Noriko Aoi, Kotoko Kosuge, Katsuo Kanmatsuse, Shinichiro Kokubun, Jason D. Marrow, John A. Oates posted to 12372404 alleles biosynthesis conformational cytochrome data enzyme exons family female genetic genotype govt health humans hypertension intramolecular introns male models molecular mutation non-us oxidoreductases p-450 pedigree phs polymorphism protein research rna sequence single-stranded splicing support system us combinedbib by qmwwallace on 2007-07-05 14:55:21 as
	Nonsense mutation of prostacyclin synthase gene in a family. [My Copy] Lancet, Vol. 349, No. 9069. (Jun 1997), pp. 1887-8. by T. Nakayama, M. Soma, D. Rahmutula, Y. Izumi, K. Kanmatsuse posted to 9217767 aged alleles biosynthesis cerebral codon conformational cytochrome data enzyme exons family female genetic genotype govt health humans hypertension infarction intramolecular introns isomerases male middle models molecular mutation non-us nonsense oxidoreductases p-450 pedigree phs point polymorphism protein research rna sequence single-stranded splicing support system us combinedbib by qmwwallace on 2007-07-05 14:55:20 as
	Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. [My Copy] Am J Hum Genet, Vol. 74, No. 5. (May 2004), pp. 886-897. by F. A. Middleton, M. T. Pato, K. L. Gentile, et al.C. P. Morley, X. Zhao, A. F. Eisener, A. Brown, T. L. Petryshen, A. N. Kirby, H. Medeiros, C. Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M. J. Soares, C. P. Ferreira, M. Lei, M. H. Azevedo, J. L. Kennedy, M. J. Daly, P. Sklar, C. N. Pato posted to bipolar chromosomes combinedbib comparative disorder family female genetics genome genotype govt haplotypes human humans linkage lod male microsatellite non-us nucleotide pair phs polymorphism repeats research score single study support us by qmwwallace on 2007-07-05 14:55:18 as
	Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23. [My Copy] Hum Mol Genet, Vol. 2, No. 7. (Jul 1993), pp. 969-974. by C. M. Mcconville, P. J. Byrd, H. J. Ambrose, et al.T. Stankovic, Y. Ziv, Bar A. Shira, L. Vanagaite, G. Rotman, Y. Shiloh, G. T. Gillett posted to antigens ataxia base cell cells chromosome chromosomes chronic combinedbib complex cystic data deletion diseases dna factor-alpha failure family female fragment fungal gene genetic genetics genome govt haplotypes histocompatibility hla human humans hybrid kidney length library line linkage ma major male mapping markers molecular multigene mutation necrosis non-us pair pedigree polymorphism pping research restriction satellite sequence serotyping sites support tagged telangiectasia testing tumor by qmwwallace on 2007-07-05 14:55:18 as
	Common deletion polymorphisms in the human genome. [My Copy] Nat Genet, Vol. 38, No. 1. (Jan 2006), pp. 86-92. by Steven A. Mccarroll, Tracy N. Hadnott, George H. Perry, et al.Pardis C. Sabeti, Michael C. Zody, Jeffrey C. Barrett, Stephanie Dallaire, Stacey B. Gabriel, Charles Lee, Mark J. Daly, David M. Altshuler, International H. Consortium posted to chain combinedbib continental databases deletion disequilibrium exons fluorescence genetic genome groups homozygote human humans hybridization in linkage models nucleotide polymerase polymorphism population reaction sequence single situ techniques by qmwwallace on 2007-07-05 14:55:18 as
	The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis. [My Copy] Proc Natl Acad Sci U S A, Vol. 99, No. 4. (Feb 2002), pp. 2228-2233. by N. Maniatis, A. Collins, C. F. Xu, et al.L. C. Mccarthy, D. R. Hewett, W. Tapper, S. Ennis, X. Ke, N. E. Morton posted to chromosome chromosomes combinedbib disequilibrium evolution factors genetic genotype haplotypes human humans linkage mapping models molecular nucleotide pair physical polymorphism single statistical time by qmwwallace on 2007-07-05 14:55:18 as
	Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions [My Copy] Vol. 66, No. 2. (2000), pp. 605-614. by K. L. Lunetta, S. V. Faraone, J. Biederman, N. M. Laird posted to adhd deficit disequilibrium disorder dopamine drd4 gene hyperactivity loci polymorphism quantitative receptor tests traits transmission transmissiondisequilibrium transporter combinedbib by qmwwallace on 2007-07-05 14:55:16 as
	Cost-effective analysis of candidate genes using htSNPs: a staged approach. [My Copy] Genes Immun, Vol. 5, No. 4. (Jun 2004), pp. 301-5. by C. E. Lowe, J. D. Cooper, J. M. Chapman, et al.B. J. Barratt, Twells, E. A. Green, D. A. Savage, C. Guja, Ionescu C. Tîrgovi?te, Tuomilehto E. Wolf, J. Tuomilehto, J. A. Todd, D. G. Clayton posted to adolescent and carrier case-control child combinedbib cytoplasmic diabetes disease disequilibrium dna-binding epistasis female genetic genetics genotype glycoproteins govt haplotypes humans interleukin-13 interleukin-4 linkage male markers mellitus membrane models non-us nuclear nucleotide polymorphism population predisposition preschool proteins receptors research single statistical studies support to trans-activators type by qmwwallace on 2007-07-05 14:55:16 as
	Coverage and power in genomewide association studies. [My Copy] Am J Hum Genet, Vol. 78, No. 5. (May 2006), pp. 884-888. by Eric Jorgenson, John S. Witte posted to chromosome disequilibrium genetics genome heritable human humans linkage mapping models nucleotide polymorphism quantitative single statistical trait variation combinedbib by qmwwallace on 2007-07-05 14:55:11 as
	Haplotype tagging for the identification of common disease genes. [My Copy] Nat Genet, Vol. 29, No. 2. (Oct 2001), pp. 233-7. by G. C. Johnson, L. Esposito, B. J. Barratt, et al.A. N. Smith, J. Heward, G. Di Genova, H. Ueda, H. J. Cordell, I. A. Eaves, F. Dudbridge, R. C. Twells, F. Payne, W. Hughes, S. Nutland, H. Stevens, P. Carr, Tuomilehto E. Wolf, J. Tuomilehto, S. C. Gough, D. G. Clayton, J. A. Todd posted to 11586306 acid base disease disequilibrium dna genetic govt haplotypes homology humans linkage non-us nucleic nucleotide polymorphism predisposition research sequence single support to combinedbib by qmwwallace on 2007-07-05 14:55:11 as
	Common deletions and SNPs are in linkage disequilibrium in the human genome. [My Copy] Nat Genet, Vol. 38, No. 1. (Jan 2006), pp. 82-85. by David A. Hinds, Andrew P. Kloek, Michael Jen, Xiyin Chen, Kelly A. Frazer posted to analysis combinedbib continental deletion disequilibrium frequency gene genetic genetics genome groups human humans linkage microarray nucleotide polymorphism population sequence single variation by qmwwallace on 2007-07-05 14:55:09 as
	Accuracy of haplotype reconstruction from haplotype-tagging single-nucleotide polymorphisms. [My Copy] Am J Hum Genet, Vol. 76, No. 3. (Mar 2005), pp. 438-48. by Julian Forton, Dominic Kwiatkowski, Kirk Rockett, Gaia Luoni, Martin Kimber, Jeremy Hull posted to 15660292 biometry comparative disequilibrium female genetic genomics genotype govt haplotypes humans linkage male markers models non-us nucleotide polymorphism research single study support combinedbib by qmwwallace on 2007-07-05 14:54:56 as
	Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes. [My Copy] Diabetes, Vol. 53, No. 3. (Mar 2004), pp. 870-3. by Christina Eftychi, Joanna M. M. Howson, Bryan J. Barratt, et al.Adrian Vella, Felicity Payne, Deborah J. Smyth, Rebecca C. J. Twells, Neil M. Walker, Helen E. Rance, Eva T. Wolf, Jaakko Tuomilehto, Dag E. Undlien, Kjersti S. Rønningen, Cristian Guja, Constantin I. Tîirgovi?te, David A. Savage, John A. Todd posted to acid adult amino and canada channels child combinedbib cytoplasmic diabetes europe factors female govt humans inwardly male mellitus non-us nuclear nucleotide phosphoproteins polymorphism potassium receptors rectifying research single substitution support transcription type by qmwwallace on 2007-07-05 14:54:52 as
	Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies. [My Copy] Am J Hum Genet, Vol. 75, No. 3. (Sep 2004), pp. 424-435. by Frank Dudbridge, Bobby P. C. Koeleman posted to association chromosome databases disequilibrium genetic genetics genome genotype govt human humans linkage mapping markers models non-us nucleotide polymorphism research single statistical statistics support techniques combinedbib by qmwwallace on 2007-07-05 14:54:51 as
	Genomic MHC haplotyping of mutant cell lines using a novel marker. [My Copy] Eur J Immunogenet, Vol. 20, No. 5. (Oct 1993), pp. 373-380. by Degli M. A. Esposti, J. F. Williamson, G. K. Tay, et al.B. Salmon, G. A. Joseph, A. A. Morley, R. L. Dawkins posted to 2 9098405 antigens cell chromosome chromosomes chronic complex cystic deletion diseases dna factor-alpha failure family female fragment gene genetic genetics genome govt haplotypes histocompatibility hla human humans kidney length line linkage ma major male markers multigene mutation necrosis non-us pair pedigree polymorphism pping research restriction satellite serotyping support testing tumor combinedbib by qmwwallace on 2007-07-05 14:54:46 as
	Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups. [My Copy] Cytogenet Cell Genet, Vol. 50, No. 4. (1989), pp. 181-187. by S. P. Daiger, M. M. Humphries, N. Giesenschlag, et al.E. Sharp, P. Mcwilliam, J. Farrer, D. Bradley, P. Kenna, D. J. Mcconnell, R. S. Sparkes posted to acid adolescent adult aged amino antigens ataxia atrophy autoantibodies base blotting cell cells chains child chromosome chromosomes chronic combinedbib complex cosmids cultured cystic data deletion diseases dna dominant factor-alpha failure family female fragment fungal gene genes genetic genetics genome genomic govt haplotypes heavy histocompatibility hla human humans hybrid immunoglobulin interpretation kidney length library line linkage ma major male mapping markers middle molecular multigene muscular mutation necrosis non-us pair pedigree pigmentosa polymorphism pping recombination region research restriction retinitis satellite sequence serotyping sites southern spinal statistical support tagged telangiectasia testing transformed tumor variable by qmwwallace on 2007-07-05 14:54:44 as
	A high-resolution survey of deletion polymorphism in the human genome. [My Copy] Nat Genet, Vol. 38, No. 1. (Jan 2006), pp. 75-81. by Donald F. Conrad, Daniel T. Andrews, Nigel P. Carter, Matthew E. Hurles, Jonathan K. Pritchard posted to analysis combinedbib cooperation databases deletion extramural genetic genome govt human humans hybridization in international microarray models nih non-us nucleotide of polymorphism reproducibility research results sequence single situ support by qmwwallace on 2007-07-05 14:54:40 as
	Use of unphased multilocus genotype data in indirect association studies. [My Copy] Genet Epidemiol, Vol. 27, No. 4. (Dec 2004), pp. 415-28. by David Clayton, Juliet Chapman, Jason Cooper posted to adolescent case-control child combinedbib diabetes disease disequilibrium dna-binding epistasis female genetic genetics genotype govt haplotypes humans interleukin-13 interleukin-4 linkage male markers mellitus models non-us nucleotide polymorphism population predisposition preschool proteins research single statistical studies support to trans-activators type by qmwwallace on 2007-07-05 14:54:39 as
	Ascertainment bias in studies of human genome-wide polymorphism. [My Copy] Genome Res, Vol. 15, No. 11. (Nov 2005), pp. 1496-1502. by Andrew G. Clark, Melissa J. Hubisz, Carlos D. Bustamante, Scott H. Williamson, Rasmus Nielsen posted to 16251459 algorithms alleles analysis chromatin chromosome comparative cooperation design disease disequilibrium dna drug entropy epoxide expression extramural frequency gene genetic genetics genome govt haplotypes human humans hydrolases ii immunoprecipitation industry international isposition laboratories linkage mapping markers nih non-us nucleotide pharmacogenetics phenotype phs polymerase polymorphism pport pred predisposition regulation research rna selection sequence single study su support to us variation combinedbib by qmwwallace on 2007-07-05 14:54:38 as
	Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power. [My Copy] Hum Hered, Vol. 56, No. 1-3. (2003), pp. 18-31. by Juliet M. Chapman, Jason D. Cooper, John A. Todd, David G. Clayton posted to adolescent analysis and carrier case-control child combinedbib cytoplasmic data diabetes disease disequilibrium dna-binding epistasis female genetic genetics genotype glycoproteins govt haplotypes humans interleukin-13 interleukin-4 interpretation linkage male markers mellitus membrane models multivariate non-us nuclear nucleotide polymorphism population predisposition preschool proteins receptors research single statistical studies support to trans-activators type by qmwwallace on 2007-07-05 14:54:37 as
	The serotonin transporter gene and peer-rated neuroticism. [My Copy] Neuroreport, Vol. 8, No. 5. (Mar 1997), pp. 1301-1304. by D. Ball, L. Hill, B. Freeman, et al.T. C. Eley, J. Strelau, R. Riemann, F. M. Spinath, A. Angleitner, R. Plomin posted to 9175133 adolescent adult aged carrier chi-square disorders distribution frequency gene genetic genotype glycoproteins govt group humans membrane middle nerve neurotic non-us peer polymorphism proteins research serotonin support tissue transport combinedbib by qmwwallace on 2007-07-05 14:54:12 as
	Dopamine markers and general cognitive ability. [My Copy] Neuroreport, Vol. 9, No. 2. (Jan 1998), pp. 347-349. by D. Ball, L. Hill, T. C. Eley, et al.M. J. Chorney, K. Chorney, L. A. Thompson, D. K. Detterman, C. Benbow, D. Lubinski, M. Owen, P. Mcguffin, R. Plomin posted to 9507981 adolescent alleles biological child cognition dna dopamine female genetic genotype heritable humans intelligence male markers polymorphism quantitative tests trait combinedbib by qmwwallace on 2007-07-05 14:54:12 as
	Association studies for quantitative traits in structured populations. [My Copy] Genet Epidemiol, Vol. 22, No. 1. (Jan 2002), pp. 78-93. by Silviu A. Bacanu, Bernie Devlin, Kathryn Roeder posted to 11754475 algorithms alleles analysis bias carlo case-control chains chi-square chromosome comparative computer confidence confounding disease disequilibrium distribution epidemiology factors genetic genetics genome genotype govt heritable heterogeneity human humans intervals linkage mapping markers markov method models monte mutation non-phs phenotype phs poisson polymorphism population predisposition probability quantitative recombination regression research simulation statistical statistics studies study support theoretical to trait us combinedbib by qmwwallace on 2007-07-05 14:54:11 as
	Haplotypic analysis of the TNF locus by association efficiency and entropy. [My Copy] Genome Biol, Vol. 4, No. 4. (2003) by Hans Ackerman, Stanley Usen, Richard Mott, et al.Anna Richardson, Fatoumatta S. Joof, Pauline Katundu, Terrie Taylor, Ryk Ward, Malcolm Molyneux, Margaret Pinder, Dominic P. Kwiatkowski posted to 12702205 adult case-control disease disequilibrium entropy factor-alpha frequency gambia gene genetic govt haplotypes humans linkage malawi necrosis non-us nucleotide polymorphism predisposition recombination research single studies support to tumor combinedbib by qmwwallace on 2007-07-05 14:53:46 as

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qmwwallace's polymorphism [24 articles] Export

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