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Results 1 to 25 of 8721

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Isoelectric focusing in agarose gel for detection and identification of hemoglobin variantsBLACK, J.Hemoglobin. 1984, Vol 8, Num 2, pp 117-127, issn 0363-0269Article

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

Immunochemical identification of normal and variant hemoglobins after electrophoretic separation and transfer to nitrocellulose membranesGARVER, F. A; SINGH, H; MOSCOSO, H et al.Hemoglobin. 1984, Vol 8, Num 2, pp 105-115, issn 0363-0269Article

Antithrombin Chicagö: a functionally abnormal molecule with increased heparin affinity causing familial thrombophiliaBAUER, K. A; ASHENHURST, J. B; CHEDIAK, J et al.Blood. 1983, Vol 62, Num 6, pp 1242-1250, issn 0006-4971Article

Hemoglobin Sendagi (β42 PHE→VAL): a new unstable hemoglobin variant having an amino acid substitution at CD1 of the β-chainOGATA, K; ITO, T; OKAZAKI, T et al.Hemoglobin. 1986, Vol 10, Num 5, pp 469-481, issn 0363-0269Article

Hemoglobin Hamilton or α2β211(A8)Val→Ile: a silent β-chain variant detected by Triton X-100 acid-urea polyacrylamide gel electrophoresisWONG, S. C; ALI, M. A. M; LAM, H et al.American journal of hematology. 1984, Vol 16, Num 1, pp 47-52, issn 0361-8609Article

Functional effects of genetic variants in the 11β-hydrnxylase (CYP11B1)geneBARR, Marianne; MACKENZIE, Scott M; WILKINSON, Donna M et al.Clinical endocrinology (Oxford. Print). 2006, Vol 65, Num 6, pp 816-825, issn 0300-0664, 10 p.Article

Fibrinogen Baltimore II: congenital hypodysfibrinogenemia with delayed release of fibrinopeptide B and decreased rate of fibrinogen synthesisEBERT, R. F; BELL, W. R.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1983, Vol 80, Num 23, pp 7318-7322, issn 0273-1134Article

Crossed immunoelectrophoresis in the study of abnormal antithrombins. III: behaviour of at III trentoGIROLAMI, A; RUBETELLI, M; MARAFIOTTI, P et al.British journal of haematology. 1983, Vol 55, Num 3, pp 559-561, issn 0007-1048Article

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

Isolation and characterization of a hereditary abnormal untithrombin III Antithrombin III ToyamäKOIDE, T; TAKAHASHI, K; ODANI, S et al.Thrombosis research. 1983, Vol 31, Num 2, pp 319-328, issn 0049-3848Article

Cases of unstable hemoglobin and methemoglobin produced by de novo mutationSTAMATOYANNOPOULOS, G; NUTE, P. E.Hemoglobin. 1984, Vol 8, Num 1, pp 85-95, issn 0363-0269Article

Brief report of rare human hemoglobin variantsHUISMAN, T. H. J.Hemoglobin. 1983, Vol 7, Num 6, issn 0363-0269, 595Article

Plasma cholinesterase genetic variants phenotyped using a cobas-fara centrifugal analyserBROCK, A.Journal of clinical chemistry and clinical biochemistry. 1988, Vol 26, Num 12, pp 873-875, issn 0340-076XArticle

An abnormal plasma antithrombin with no apparent affinity for heparinCHASSE, J. F; ESNARD, F; GUITTON, J. D et al.Thrombosis research. 1984, Vol 34, Num 4, pp 297-302, issn 0049-3848Article

A variant of von Willebrand's disease characterized by recessive inheritance and missing triplet structure of von Willebrand factor multimersMANNUCCI, P. M; LOMBARDI, R; PARETI, F. I et al.Blood. 1983, Vol 62, Num 5, pp 1000-1005, issn 0006-4971Article

Specific ligand binding on genetic variants of human α1-acid glycoprotein studied by circular dichroism spectroscopyFITOS, Ilona; VISY, Julia; ZSILA, Ferenc et al.Biochemical pharmacology. 2004, Vol 67, Num 4, pp 679-688, issn 0006-2952, 10 p.Article

Rethinking mechanisms of autoimmune pathogenesisPILLAI, Shiv.Journal of autoimmunity (Print). 2013, Vol 45, pp 97-103, issn 0896-8411, 7 p.Article

Assessing and managing risk when sharing aggregate genetic variant dataCRAIG, David W; GOOR, Robert M; ZHENYUAN WANG et al.Nature reviews. Genetics (Print). 2011, Vol 12, Num 10, pp 730-736, issn 1471-0056, 7 p.Article

Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profileKILPELÄINEN, Tuomas O; CAROLA ZILLIKENS, M; STYRKARSDOTTIR, Unnur et al.Nature genetics. 2011, Vol 43, Num 8, pp 753-760, issn 1061-4036, 8 p.Article

Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 DiabetesNEJENTSEV, Sergey; WALKER, Neil; RICHES, David et al.Science (Washington, D.C.). 2009, Vol 324, Num 5925, pp 387-389, issn 0036-8075, 3 p.Article

Ahorro de levadura en la panificación por el método de masas madres esponjas = Yeast saving in the manufacture of bread buns by the sponge sour dough methodALVAREZ, M; GARCIA, I; SILVEIRA, I et al.Alimentaria. 1996, Num 273, pp 81-82, issn 0300-5755Article

A new unstable and low oxygen affinity hemoglobin variant: Hb J-Auckland [β25(B7)Gly→Asp]WILLIAMSON, D; WELLS, R. M. G; ANDERSON, R et al.Hemoglobin. 1987, Vol 11, Num 3, pp 221-230, issn 0363-0269Article

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