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Topography, Clinical, and Genomic Correlates of 5q Myeloid Malignancies RevisitedJEREZ, Andres; GONDEK, Lukasz P; MCDEVITT, Michael A et al.Journal of clinical oncology. 2012, Vol 30, Num 12, pp 1343-1349, issn 0732-183X, 7 p.Article

The DNA sequence and comparative analysis of human chromosome 5SCHMUTZ, Jeremy; MARTIN, Joel; HELLSTEN, Uffe et al.Nature (London). 2004, Vol 431, Num 7006, pp 268-274, issn 0028-0836, 7 p.Article

Assignment of the ectodermal-neural cortex 1 gene (ENC1) to human chromosome band 5q13 by in situ hybridizationHERNANDEZ, M.-C; ANDRES-BARQUIN, P. J; KUO, W.-L et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 89-90, issn 0301-0171Article

Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locusHENG, H. H. Q; BEI XIE; XIAO-MEI SHI et al.Genomics (San Diego, Calif.). 1993, Vol 18, Num 2, pp 429-431, issn 0888-7543Article

A new RFLP for L1.4 (D5S4) an anonymous genomic clone localised to chromosome 5BAILEY, C. J; RIDER, S. H; BODMER, W. F et al.Nucleic acids research. 1987, Vol 15, Num 16, issn 0305-1048, 6762Article

Submicroscopic deletions in 5q- associated malignanciesCRESCENZI, Barbara; LA STARZA, Roberta; MARTELLI, Massimo Fabrizio et al.Haematologica (Roma). 2004, Vol 89, Num 3, pp 281-285, issn 0390-6078, 5 p.Article

Linkage of circulating eosinophils to markers on chromosome 5qMARTINEZ, F. D; SOLOMON, S; HOLBERG, C. J et al.American journal of respiratory and critical care medicine. 1998, Vol 158, Num 6, pp 1739-1744, issn 1073-449XArticle

Human selenoprotein P gene maps to 5q31HILL, K. E; DASOUKI, M; PHILLIPS, J. A et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 3, pp 550-551, issn 0888-7543Article

Trisomy 5 mosaicism in amniotic fluid with normal outcomeCASAMASSIMA, A. C; WILMOT, P. L; MAHONEY, M. J et al.Clinical genetics. 1989, Vol 35, Num 4, pp 282-284, issn 0009-9163, 3 p.Article

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15SUTHERLAND, G. R; BAKER, E; VADAS, M. A et al.Human genetics. 1988, Vol 79, Num 4, pp 335-337, issn 0340-6717Article

Dysgranulopoiesis is an independent adverse prognostic factor in chronic myeloid disorders with an isolated interstitial deletion of chromosome 5qCHEN, D; HOYER, J. D; KETTERLING, R. P et al.Leukemia. 2009, Vol 23, Num 4, pp 796-800, issn 0887-6924, 5 p.Article

Chromosome mapping of 11 human pobes in the region 5q2→q3 by fluorescence in situ hybridizationRICHARD, F; MULERIS, M; DUTRILLAUX, B et al.Cytogenetics and cell genetics. 1995, Vol 68, Num 3-4, pp 207-210, issn 0301-0171Conference Paper

Assignment of the human α-catenin gene (CTNNA1) to chromosome 5q21-q22MCPHERSON, J. D; MORTON, R. A; EWING, C. M et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 1, pp 188-190, issn 0888-7543Article

Human cyclin B1 gene (CCNB1) assigned to chromosome 5 (q13-qter)MILATOVICH, A; FRANCKE, U.Somatic cell and molecular genetics. 1992, Vol 18, Num 3, pp 303-307, issn 0740-7750Article

Assignment1 of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mappingLEE-KIRSCH, M. A; ENGEL, K; PADITZ, E et al.Cytogenetics and cell genetics. 2001, Vol 92, Num 3-4, issn 0301-0171, p. 358Article

Assignment of the human translation termination factor 1 (ETF1) to 5q31.1 and of the proximal marker D5S1995 by radiation hybrid mappingHANSEN, L. L; JAKOBSEN, C. G; JUSTESEN, J et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 256-257, issn 0301-0171Article

Trinucleotide repeat polymorphism at the D5S556 locusBURLET, P; ABDELHAK, S; PASCAL, F et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, issn 0964-6906, p. 1328Article

Assignment of two human cell cycle genes, CDC25C and CCNB1, to 5q31 and 5q12, respectivelySARTOR, H; EHLERT, F; GRZESCHIK, K.-H et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 3, pp 911-912, issn 0888-7543Article

Supernumerary marker chromosomes 5: Confirmation of a critical region and resultant phenotypeSIZONENKO, Loredana D'Amato; NG, Daniel; OEI, Paul et al.American journal of medical genetics. 2002, Vol 111, Num 1, pp 19-26, issn 0148-7299Article

Lenalidomide for Treatment of Myelodysplastic Syndromes : New Treatment Strategy of the Myelodysplastic SyndromesKOMROKJI, Rami S; LIST, Alan F.Current pharmaceutical design (Print). 2012, Vol 18, Num 22, pp 3198-3203, issn 1381-6128, 6 p.Article

A fine structure physical map of the short arm of chromosomeOVERHAUSER, J; BEAUDET, A. L; WASMUTH, J. J et al.American journal of human genetics. 1986, Vol 39, Num 5, pp 562-572, issn 0002-9297Article

Assignment of ACVR2 and ACVR2B the human activin receptor type II and IIb genes to chromosome bands 2q22.2→q23.3 and 3p22 and the human follistatin gene (FST) to chromosome 5q11.2 by FISHBONDESTAM, J; HORELLI-KUITUNEN, N; HILDEN, K et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 219-220, issn 0301-0171Article

Assignment of the human tumor transforming gene TUTR1 to chromosome band 5q35.1 by fluorescence in situ hybridizationKAKAR, S. S.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 93-95, issn 0301-0171Article

The gene for calcium-modulated cyclophilin ligand (CAMLG) is located on human chromosome 5q23 and a syntenic region of mouse chromosome 13BRAM, R. J; VALENTINE, V; SHAPIRO, D. N et al.Genomics (San Diego, Calif.). 1996, Vol 31, Num 2, pp 257-260, issn 0888-7543Article

Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridizationCOLOSIMO, A; CALABRESE, G; GENNARELLI, M et al.Cytogenetics and cell genetics. 1996, Vol 74, Num 3, pp 187-188, issn 0301-0171Conference Paper

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