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Results 1 to 25 of 25185

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Swainsonine and Endophyte Relationships in Astragalus mollissimus and Astragalus lentiginosusCOOK, Daniel; GARDNER, Dale R; GRUM, Daniel et al.Journal of agricultural and food chemistry (Print). 2011, Vol 59, Num 4, pp 1281-1287, issn 0021-8561, 7 p.Article

Common variants at 12ql4 and 12q24 are associated with hippocampal volumeBIS, Joshua C; DECARLI, Charles; SCHUUR, Maaike et al.Nature genetics. 2012, Vol 44, Num 5, pp 545-551, issn 1061-4036, 7 p.Article

YGFP: a spectral variant or GFPHANSEN, Flemming G; ATLUNG, Tove.BioTechniques. 2011, Vol 50, Num 6, pp 411-412, issn 0736-6205, 2 p.Article

Diamonds in the Rough: Rare Variants Scratch the SurfacePODOLAK, Erin.BioTechniques. 2010, Vol 49, Num 4, issn 0736-6205, 697-701 [3 p.]Article

Differential confounding of rare and common variants in spatially structured populationsMATHIESON, Iain; MCVEAN, Gil.Nature genetics. 2012, Vol 44, Num 3, pp 243-246, issn 1061-4036, 4 p.Article

Common and rare variants in multifactorial susceptibility to common diseasesBODMER, Walter; BONILLA, Carolina.Nature genetics. 2008, Vol 40, Num 6, pp 695-701, issn 1061-4036, 7 p.Article

Variants in MTNR1B influence fasting glucose levelsPROKOPENKO, Inga; LANGENBERG, Claudia; POTTER, Simon C et al.Nature genetics. 2009, Vol 41, Num 1, pp 77-81, issn 1061-4036, 5 p.Article

Common variants in the GDF5-UQCC region are associated with variation in human heightSANNA, Serena; JACKSON, Anne U; CHINES, Peter S et al.Nature genetics. 2008, Vol 40, Num 2, pp 198-203, issn 1061-4036, 6 p.Article

Common variants near TERC are associated with mean telomere lengthCODD, Veryan; MANGINO, Massimo; GUANGJU ZHAI et al.Nature genetics. 2010, Vol 42, Num 3, pp 197-199, issn 1061-4036, 3 p.Article

H3.3/H2A.Z double variant-containing nucleosomes mark 'nucleosome-free regions' of active promoters and other regulatory regionsCHUNYUAN JIN; CHONGZHI ZANG; GANG WEI et al.Nature genetics. 2009, Vol 41, Num 8, pp 941-945, issn 1061-4036, 5 p.Article

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarizationARKING, Dan E; PFEUFER, Arne; JALILZADEH, Shapour et al.Nature genetics. 2006, Vol 38, Num 6, pp 644-651, issn 1061-4036, 8 p.Article

Some notes about Hb Q-India and Hb Q-IranAKSOY, M; GURGEY, A; ALTAY, C et al.Hemoglobin. 1986, Vol 10, Num 2, pp 215-219, issn 0363-0269Article

G-6-PD Walter Reed: possible insight into structural NADP in G-6-PDBEUTLER, E; HARTMAN, K; GELBART, T et al.American journal of hematology. 1986, Vol 23, Num 1, pp 25-30, issn 0361-8609Article

Common variants in TMPRSS6 are associated with iron status and erythrocyte volumeBENYAMIN, Beben; FERREIRA, Manuel A. R; FRAZER, Ian H et al.Nature genetics. 2009, Vol 41, Num 11, pp 1173-1175, issn 1061-4036, 3 p.Article

Les variantes dans la technique du Curl LiftFOURNIER, Pierre.La Revue de chirurgie esthétique de langue française. 2004, Vol 28, Num 117, pp 35-37, issn 0336-7525, 3 p.Article

Variants of Uncertain Significance in BRCA1 and BRCA2 assessment of in silico analysis and a proposal for communication in genetic counsellingMOGHADASI, Setareh; HOFLAND, Nandy; WOUTS, Joyce N et al.Journal of medical genetics. 2013, Vol 50, Num 2, pp 74-79, issn 0022-2593, 6 p.Article

MLXIPL variant in individuals with low and high triglyceridemia in white population in Central EuropeVRABLIK, Michal; CESKA, Richard; ADAMKOVA, Vera et al.Human genetics. 2008, Vol 124, Num 5, pp 553-555, issn 0340-6717, 3 p.Article

Metabolic and cardiovascular traits : an abundance of recently identified common genetic variantsMOHLKE, Karen L; BOEHNKE, Michael; ABECASIS, Goncalo R et al.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R102-R108, NS2Article

Detecting changes in the relative expression of KRAS2 splice variants using polymerase coloniesBUTZ, James A; ROBERTS, Kim G; EDWARDS, Jeremy S et al.Biotechnology progress. 2004, Vol 20, Num 6, pp 1836-1839, issn 8756-7938, 4 p.Article

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleHEWITT, Alex W; SHARMA, Shiwani; BURDON, Kathryn P et al.Human molecular genetics (Print). 2008, Vol 17, Num 5, pp 710-716, issn 0964-6906, 7 p.Article

Many sequence variants affecting diversity of adult human heightGUDBJARTSSON, Daniel F; WALTERS, G. Bragi; HELGADOTTIR, Anna et al.Nature genetics. 2008, Vol 40, Num 5, pp 609-615, issn 1061-4036, 7 p.Article

Pharmacological properties of the naturally occurring Ala457Pro variant of the human norepinephrine transporterPACZKOWSKI, Filip A; BÖNISCH, Heinz; BRYAN-LLUKA, Lesley J et al.Pharmacogenetics (London). 2002, Vol 12, Num 2, pp 165-173, issn 0960-314XArticle

Hemoglobin La Desirade αA2β2129(H7)Ala→Val: a new unstable hemoglobinMERAULT, G; KECLARD, L; GARIN, J et al.Hemoglobin. 1986, Vol 10, Num 6, pp 593-605, issn 0363-0269Article

De novo assembly and genotyping of variants using colored de Bruijn graphsIQBAL, Zamin; CACCAMO, Mario; TURNER, Isaac et al.Nature genetics. 2012, Vol 44, Num 2, pp 226-232, issn 1061-4036, 7 p.Article

Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variantsPAGENSTECHER, Constanze; WEHNER, Maria; MANGOLD, Elisabeth et al.Human genetics. 2006, Vol 119, Num 1-2, pp 9-22, issn 0340-6717, 14 p.Article

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