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Results 1 to 25 of 8602

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Evolutionary dynamics of extranuclear genesTAKAHATA, N; SLATKIN, M.Genetical research. 1983, Vol 42, Num 3, pp 257-265, issn 0016-6723Article

Occurrence of a rare allele at the Est-6 locus in natural populations of Drosophila melanogasterCAMBISSA, V; NIGRO, L; DANIELI, G. A et al.Bollettino di Zoologia. 1982, Vol 49, Num 3-4, pp 229-233, issn 0373-4137Article

Most rare missense alleles are deleterious in humans : Implications for complex disease and association studiesKRYUKOV, Gregory V; PENNACCHIO, Len A; SUNYAEV, Shamil R et al.American journal of human genetics. 2007, Vol 80, Num 4, pp 727-739, issn 0002-9297, 13 p.Article

Estimating the proportion of neutral mutantsWATTERSON, G. A.Genetical research. 1987, Vol 50, Num 2, pp 155-163, issn 0016-6723Article

On the allelic spectrum of human diseaseREICH, David E; LANDER, Eric S.Trends in genetics (Regular ed.). 2001, Vol 17, Num 9, pp 502-510, issn 0168-9525Article

Standardized SSR allele naming and binning among projectsDEEMER, Dennis L; DANA NELSON, C.BioTechniques. 2010, Vol 49, Num 5, pp 835-836, issn 0736-6205, 2 p.Article

Counting alleles reveals a connection between chromosome 18q loss and vascular invasionWEI ZHOU; GALIZIA, Gennaro; GOODMAN, Steven N et al.Nature biotechnology. 2001, Vol 19, Num 1, pp 78-81, issn 1087-0156Article

A STUDY OF GENETIC LINKAGE RELATIVE TO SUCCESS IN BACKCROSS BREEDING PROGRAMS.FUJIMAKI H; COMSTOCK R.1977; JAP. J. BREEDG; JAP.; DA. 1977; VOL. 27; NO 2; PP. 105-115; ABS. JAP.; BIBL. 12 REF.Article

Silent point mutation in DsRed resulting in enhanced relative fluorescence intensityKLASEN, Maik; WABL, Matthias.BioTechniques. 2004, Vol 36, Num 2, pp 236-238, issn 0736-6205, 2 p.Article

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrumDAVIS, Erica E; QI ZHANG; MUZNY, Donna M et al.Nature genetics. 2011, Vol 43, Num 3, pp 189-196, issn 1061-4036, 8 p.Article

On the survival probability of a slightly advantageous mutant gene in a multitype population: a multidimensional branching process modelESHEL, I.Journal of mathematical biology (Print). 1984, Vol 19, Num 2, pp 201-209, issn 0303-6812Article

High level of gene silencing in the tetraploid goldfishWOODS, T. D; BUTH, D. G.Biochemical systematics and ecology. 1984, Vol 12, Num 4, pp 415-421, issn 0305-1978Article

Allelic imbalance metre (Allim), a new tool for measuring allele-specific gene expression with RNA-seq dataVINAY PANDEY, Ram; FRANSSEN, Susanne U; FUTSCHIK, Andreas et al.Molecular ecology resources (Print). 2013, Vol 13, Num 4, pp 740-745, issn 1755-098X, 6 p.Article

FREQUENCY SPECTRA OF NEUTRAL AND DELETERIOUS ALLELES IN A FINITE POPULATIONEWENS WJ; LI WH.1980; J. MATH. BIOL.; ISSN 0303-6812; DEU; DA. 1980; VOL. 10; NO 2; PP. 155-166; BIBL. 9 REF.Article

Molecular haplotype determination using allele-specific PCR and Pyrosequencing technologyPETTERSSON, Monica; BYLUND, Mattias; ALDERBORN, Anders et al.Genomics (San Diego, Calif.). 2003, Vol 82, Num 3, pp 390-396, issn 0888-7543, 7 p.Article

Identity of different mutations for deleterious genesROBERTSON, A; HILL, W. G; KAZAZIAN, H. H. JR et al.Nature (London). 1983, Vol 301, Num 5896, pp 176-177, issn 0028-0836Article

F2 screen variations and associated statisticsSTODOLA, T. J; ANDOW, D. A.Journal of economic entomology. 2004, Vol 97, Num 5, pp 1756-1764, issn 0022-0493, 9 p.Article

Glyoxalase I null allele in a new family: identification by abnormal segregation pattern and quantitative assaySPARKES, R. S; SPARKES, M. C; CRIST, M et al.Human genetics. 1983, Vol 64, Num 2, pp 146-147, issn 0340-6717Article

Different impacts of alleles αLEPRA and αLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in transDELAUNAY, J; NOUYRIGAT, V; PROUST, A et al.British journal of haematology. 2004, Vol 127, Num 1, pp 118-122, issn 0007-1048, 5 p.Article

Genome-wide allele-specific analysis: insights into regulatory variationPASTINEN, Tomi.Nature reviews. Genetics (Print). 2010, Vol 11, Num 8, pp 533-538, issn 1471-0056, 6 p.Article

ADZE : a rarefaction approach for counting alleles private to combinations of populationsSZPIECH, Zachary A; JAKOBSSON, Mattias; ROSENBERG, Noah A et al.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 21, pp 2498-2504, issn 1367-4803, 7 p.Article

Haemodynamic characterization of young normotensive men carrying the 825T-allele of the G-protein β3 subunitSCHÄFERS, Rafael F; NÜRNBERGER, Lens; RÜTZ, Angelika et al.Pharmacogenetics (London). 2001, Vol 11, Num 6, pp 461-470, issn 0960-314XArticle

Effets de la consanguinité sur la réorganisation et le fonctionnement des allèles-S d'auto-incompatibilité = Effects of consanguinity on self-incompatibility allele-S reorganization and functionKHEYR-POUR, A.«Incompatibilité pollinique et amélioration des plantes». 1984, pp 51-58Conference Paper

Identification of a novel Kmod-1 allele encoded by 977C>T (Pro326Leu)POLIN, Helene; GASZNER, Waltraud; SUESSNER, Susanne et al.Transfusion (Philadelphia, PA). 2014, Vol 54, Num 8, pp 2130-2131, issn 0041-1132, 2 p.Article

Allelic spectrum of the natural variation in CRPCRAWFORD, Dana C; QIAN YI; SMITH, Joshua D et al.Human genetics. 2006, Vol 119, Num 5, pp 496-504, issn 0340-6717, 9 p.Article

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