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Assignment1 of ankyrin repeat, family A (RFXANK-like) 2 (ANKRA2) to human chromosome 5q12→q13 by radiation hybrid mapping and somatic cell hybrid PCRRADER, K; BOYER, A. D; FARQUHAR, M. G et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 3-4, pp 164-165, issn 0301-0171Article

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

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

Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosomeSZAMALEK, Justyna M; GOIDTS, Violaine; CHUZHANOVA, Nadia et al.Human genetics. 2005, Vol 117, Num 2-3, pp 168-176, issn 0340-6717, 9 p.Article

The gene for human glutaredoxin (GLRX) is localized to human chromosome 5q14PADILLA, C. A; BAJALICA, S; LAGERCRANTZ, J et al.Genomics (San Diego, Calif.). 1996, Vol 32, Num 3, pp 455-457, issn 0888-7543Article

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

Biological and prognostic significance of chromosome 5q deletions in myeloid malignanciesGIAGOUNIDIS, Aristoteles A. N; GERMING, Ulrich; AUL, Carlo et al.Clinical cancer research. 2006, Vol 12, Num 1, pp 5-10, issn 1078-0432, 6 p.Article

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

RING CHROMOSOME 5 IN TWO MALFORMED BOYS WITH CRI DU CHAT SYNDROMESUERINCK E; NOEL B; RETHORE MO et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 3; PP. 125-129; BIBL. 5 REF.Article

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

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemiaJAJU, R. J; HAAS, O. A; MORRIS, S. W et al.Blood. 1999, Vol 94, Num 2, pp 773-780, issn 0006-4971Article

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

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

RIL, a LIM gene on 5q31, is silenced by methylation in cancer and sensitizes cancer cells to apoptosisBOUMBER, Yanis A; KONDO, Yutaka; XUQI CHEN et al.Cancer research (Baltimore). 2007, Vol 67, Num 5, pp 1997-2005, issn 0008-5472, 9 p.Article

Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletionLIST, Alan; DEWALD, Gordon; REEDER, Craig et al.The New England journal of medicine. 2006, Vol 355, Num 14, pp 1456-1465, issn 0028-4793, 10 p.Article

Cloning, expression, and mapping of PDCD9, the human homolog of Gallus gallus pro-apoptotic protein p52CARIM, L; SUMOY, L; NADAL, M et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 85-88, issn 0301-0171Article

Protease-activated receptor genes are clustered on 5q13GUYONNET DUPERAT, V; JACQUELIN, B; BOISSEAU, P et al.Blood. 1998, Vol 92, Num 1, pp 25-31, issn 0006-4971Article

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