kw.\*:("Variante")
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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
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
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
Rare and common variants: twenty argumentsGIBSON, Greg.Nature reviews. Genetics (Print). 2012, Vol 13, Num 2, pp 135-145, issn 1471-0056, 11 p.Article
A common variant of HMGA2 is associated with adult and childhood height in the general populationWEEDON, Michael N; LETTRE, Guillaume; ZEGGINI, Eleftheria et al.Nature genetics. 2007, Vol 39, Num 10, pp 1245-1250, issn 1061-4036, 6 p.Article
AHSG gene variant is associated with leanness among Swedish menLAVEBRATT, Catharina; WAHLQVIST, Sofia; NORDFORS, Louise et al.Human genetics. 2005, Vol 117, Num 1, pp 54-60, issn 0340-6717, 7 p.Article
HB Las Palmas or α2β249 (CD8) Ser→Phe, a midly unstable hemoglobin variantMALCORRA-AZPIAZU, J. J; BALDA-AGUIRRE, M. I; DIAZ-CHICO, J. C et al.Hemoglobin. 1988, Vol 12, Num 2, pp 163-170, issn 0363-0269Article