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Loci at chromosomes 13, 19 and 20 influence age at natural menopauseSTOLK, Lisette; GUANGJU ZHAI; SORANZO, Nicole et al.Nature genetics. 2009, Vol 41, Num 6, pp 645-647, issn 1061-4036, 3 p.Article

Transgene expression after rep-mediated site-specific integration into chromosome 19PHILPOTT, Nicola J; GOMOS, Janette; FALCK-PEDERSEN, Erik et al.Human gene therapy. 2004, Vol 15, Num 1, pp 47-61, issn 1043-0342, 15 p.Article

Apolipoprotein E regulatory region genotype in schizophreniaSHINKAI, T; OHMORI, O; KOJIMA, H et al.Neuroscience letters. 1998, Vol 256, Num 1, pp 57-60, issn 0304-3940Article

CARTOGRAPHIE DU CHROMOSOME 19 DE LA SOURIS = MAPPING OF MOUSE CHROMOSOME 19Poirier, Christophe; Guenet, Jean-Louis.1997, 214 p.Thesis

Malignant hyperthermia : a large kindred linked to the RYR1 geneWALLACE, A. J; WOOLDRIDGE, W; KINGSTON, H. M et al.Anaesthesia. 1996, Vol 51, Num 1, pp 16-23, issn 0003-2409Article

Assignment of the mouse Vegfb gene to mouse chromosome 19 B by in situ hybridizationGERACE, L; CIRENEI, N; CAPPELLETTI, M et al.Cytogenetics and cell genetics. 2001, Vol 95, Num 3-4, pp 242-243, issn 0301-0171Article

Gene structure and chromosome location of mouse Cd39 coding for an ecto-apyraseSCHOENBORN, M. A; JENKINS, N. A; COPELAND, N. G et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 3-4, pp 287-289, issn 0301-0171Conference Paper

A small regulatory element from chromosome 19 enhances liver-specific gene expressionLI, C; HIRSCH, M; CARTER, P et al.Gene therapy (Basingstoke). 2009, Vol 16, Num 1, pp 43-51, issn 0969-7128, 9 p.Article

Combined effects of apoE-CI-CII cluster and LDL-R gene polymorphisms on chromosome 19 and coronary artery disease riskCHUNHONG WANG; XIN ZHOU; SHUIQING YE et al.International journal of hygiene and environmental health. 2006, Vol 209, Num 3, pp 265-273, issn 1438-4639, 9 p.Article

Idiopathic scoliosis : Identification of candidate regions on chromosome 19p13ALDEN, Kris J; MAROSY, Beth; NZEGWU, Nneka et al.Spine (Philadelphia, PA. 1976). 2006, Vol 31, Num 16, pp 1815-1819, issn 0362-2436, 5 p.Article

Relationship between the efficacy of rivastigmine and apolipoprotein E (ε4) in patients with mild to moderately severe alzheimer diseaseBLESA, Rafael; AGUILAR, Miquel; MASSO, Jose Félix Marti et al.Alzheimer disease and associated disorders. 2006, Vol 20, Num 4, pp 248-254, issn 0893-0341, 7 p.Article

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosisROETTO, Antonella; PAPANIKOLAOU, George; POLITOU, Marianna et al.Nature genetics. 2003, Vol 33, Num 1, pp 21-22, issn 1061-4036, 2 p.Article

Genome-wide scan of swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3WIKLUND, Fredrik; GILLANDERS, Elizabeth M; JONSSON, Björn-Anders et al.The Prostate. 2003, Vol 57, Num 4, pp 290-297, issn 0270-4137, 8 p.Article

DNA amplification associated with double minutes originating from chromosome 19 in mouse hepatocellular carcinomaZIMONJIC, D. B; ZHANG, H; SHAN, Z et al.Cytogenetics and cell genetics. 2001, Vol 93, Num 1-2, pp 114-116, issn 0301-0171Article

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locusJONES, Keith W; EHM, Margaret G; PERICAK-VANCE, Margaret A et al.Genomics (San Diego, Calif.). 2001, Vol 78, Num 3, pp 150-154, issn 0888-7543Article

19p deletion in recurring leiomyosarcoma lesions from the same patientRIVA, P; DALPRA, L; GUALANDRI, V et al.Cancer genetics and cytogenetics. 2000, Vol 119, Num 2, pp 102-108, issn 0165-4608Article

Genomic structure and chromosome location of the mouse RelA p65 gene (Rela)LEMMER, E. R; WELCH, J. L; TSAI, T et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 1-2, pp 129-132, issn 0301-0171Article

Molecular cloning of mouse Lrp7(Lr3) cDNA and chromosomal mapping of orthologous genes in mouse and humanCHEN, D; LATHROP, W; YU DONG et al.Genomics (San Diego, Calif.). 1999, Vol 55, Num 3, pp 314-321, issn 0888-7543Article

Spinocerebellar ataxia type 6 : Evidence for a strong founder effect among German familiesDICHGANS, M; SCHÖLS, L; RIESS, O et al.Neurology. 1999, Vol 52, Num 4, pp 849-851, issn 0028-3878Article

Familial typical migraine : linkage to chromosome 19p13 and evidence for genetic heterogeneityNYHOLT, D. R; LEA, R. A; GOADSBY, P. J et al.Neurology. 1998, Vol 50, Num 5, pp 1428-1432, issn 0028-3878Article

Structure and mapping of the G protein γ3 subunit gene and a divergently transcribed novel gene, Gng3lgDOWNES, G. B; COPELAND, N. G; JENKINS, N. A et al.Genomics (San Diego, Calif.). 1998, Vol 53, Num 2, pp 220-230, issn 0888-7543Article

Comparative mapping of two adjacent regions of MMU19 with their human counterpart on HSA11q13FERNANDES, M; LESPINASSE, F; ROTOMONDO, F et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 3-4, pp 237-246, issn 0301-0171Conference Paper

Genetic mapping of mouse centromere protein (Incenp and Cenpe) genesFOWLER, K. J; SAFFERY, R; KILE, B. T et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 1-2, pp 67-70, issn 0301-0171Conference Paper

Isolation of a new homeobox gene belonging to the Pitx/Rieg family : expression during lens development and mapping to the aphakia region on mouse chromosome 19SEMINA, E. V; REITER, R. S; MURRAY, J. C et al.Human molecular genetics (Print). 1997, Vol 6, Num 12, pp 2109-2116, issn 0964-6906Article

Coexistence of trisomies of chromosomes 12 and 19 in chronic lymphocytic leukemia occurs exclusively in the rare IgG-positive variantIBBOTSON, R; ATHANASIADOU, A; OSCIER, D et al.Leukemia. 2012, Vol 26, Num 1, pp 170-172, issn 0887-6924, 3 p.Article

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