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Results 1 to 25 of 329

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Tomato fruit weight 11.3 maps close to fasciated on the bottom of chromosome 11ZEJUN HUANG; VAN DER KNAAP, Esther.Theoretical and applied genetics. 2011, Vol 123, Num 3, pp 465-474, issn 0040-5752, 10 p.Article

A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14SILANDER, Kaisa; SCOTT, Laura J; NARISU, Narisu et al.Diabetes (New York, NY). 2004, Vol 53, Num 3, pp 821-829, issn 0012-1797, 9 p.Article

Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndromeWENG ONN LUI; JINDONG CHEN; GLÄSKER, Sven et al.Oncogene (Basingstoke). 2002, Vol 21, Num 7, pp 1117-1122, issn 0950-9232Article

Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)] : Further evidence for phenotypic heterogeneityGIAMPIETRO, Philip F; BABU, Deepti; ZABEL, Carrie A et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 4, pp 385-387, issn 1552-4825, 3 p.Article

Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancerTAKAI, Daiya; GONZALES, Felicidad A; TSAI, Yvonne C et al.Human molecular genetics (Print). 2001, Vol 10, Num 23, pp 2619-2626, issn 0964-6906Article

The GABAA receptor α6 subunit gene (Gabra6) is tightly linked to the α12 subunit cluster on mouse chromosome 11GARRETT, K. M; HAQUE, D; BERRY, D et al.Molecular brain research. 1997, Vol 45, Num 1, pp 133-137, issn 0169-328XArticle

Allelotype of ampulla of Vater cancer: highly frequent involvement of chromosome 11MOORE, Patrick S; MISSIAGLIA, Edoardo; BEGHELLI, Stefania et al.Journal of cancer research and clinical oncology. 2004, Vol 130, Num 6, pp 339-345, issn 0171-5216, 7 p.Article

Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian familyPILUSO, Giulio; CARELLA, Massimo; D'AVANZO, Michele et al.Human genetics. 2003, Vol 112, Num 2, pp 124-130, issn 0340-6717, 7 p.Article

Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3→q21LI, L; MOORE, P; NGO, C et al.Cytogenetic and genome research. 2002, Vol 97, Num 3-4, pp 158-162, issn 1424-8581, 5 p.Article

Long AT-rich palindromes and the constitutional t(11;22) breakpointKURAHASHI, Hiroki; EMANUEL, Beverly S.Human molecular genetics (Print). 2001, Vol 10, Num 23, pp 2605-2617, issn 0964-6906Article

Functional genetic analysis of mouse chromosome 11KILE, Benjamin T; HENTGES, Kathryn E; BRADLEY, Allan et al.Nature (London). 2003, Vol 425, Num 6953, pp 81-86, issn 0028-0836, 6 p.Article

An integrated gene and SSLP BAC map framework of mouse chromosome 11KLYSIK, J; CAI, W.-W; CHUN YANG et al.Genomics (San Diego, Calif.). 1999, Vol 62, Num 1, pp 123-128, issn 0888-7543Article

Assignment of mouse inwardly rectifying potassium channel Kcnj16 to the distal region of mouse chromosome 11MOURI, T; KITTAKA, N; HORIO, Y et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 1, pp 181-182, issn 0888-7543Article

Identification of clinically relevant genes on chromosome 11 in a functional model of ovarian cancer tumor suppressionSTRONACH, Euan A; SELLAR, Grant C; GABRA, Hani et al.Cancer research (Baltimore). 2003, Vol 63, Num 24, pp 8648-8655, issn 0008-5472, 8 p.Article

Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre-and postnatal growth retardationSHIURA, Hirosuke; NAKAMURA, Kenji; HIKICHI, Takafusa et al.Human molecular genetics (Print). 2009, Vol 18, Num 8, pp 1424-1438, issn 0964-6906, 15 p.Article

GpaXIltar originating from Solanum tarijense is a major resistance locus to Globodera pallida and is localised on chromosome 11 of potatoTAN, M. Y. Adillah; PARK, Tae-Ho; ALLES, René et al.Theoretical and applied genetics. 2009, Vol 119, Num 8, pp 1477-1487, issn 0040-5752, 11 p.Article

Origine cellulaire des tumeurs d'Ewing : Un coin de voile est levé = Mesenchymal stem cell is the target of transformation in Ewing tumorTIRODE, Franck; LAUD-DUVAL, Karine; DELATTRE, Olivier et al.MS. Médecine sciences. 2008, Vol 24, Num 3, pp 248-250, issn 0767-0974, 3 p.Article

A genetic association study of chromosome 11 q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophreniaCHOUDHURY, Khalid; MCQUILLIN, Andrew; CROMBIE, Caroline et al.American journal of human genetics. 2007, Vol 80, Num 4, pp 664-672, issn 0002-9297, 9 p.Article

Additional Cyclin D1 gene copies associated with chromosome 11 aberrations in cutaneous malignant melanomaJOCHENUTIKAL; UDART, Martin; LEITER, Ulrike et al.International journal of oncology. 2005, Vol 26, Num 3, pp 597-605, issn 1019-6439, 9 p.Article

Two new mouse chromosome 11 balancersKLYSIK, Jan; DINH, Chris; BRADLEY, Allan et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 2, pp 303-310, issn 0888-7543, 8 p.Article

Localization of the gene causing autosomal dominant osteopetrosis type I to chromosome 11q12-13VAN HUL, Els; GRAM, Jeppe; BOLLERSLEV, Jens et al.Journal of bone and mineral research (Print). 2002, Vol 17, Num 6, pp 1111-1117, issn 0884-0431Article

Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesisPHILLIPS, Helen M; RENFORTH, Glenn L; SALMON, Tony et al.Genomics (San Diego, Calif.). 2002, Vol 79, Num 4, pp 475-478, issn 0888-7543Article

Quantitative trait loci that harbor genes regulating muscle size in (MRL/MPJ x SJL/J) F2 miceMASINDE, Godfred L; XINMIN LI; WEIKUAN GU et al.Functional & integrative genomics (Print). 2002, Vol 2, Num 3, pp 120-125, issn 1438-793X, 6 p.Article

Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorderVAUGHAN, Carl J; CASEY, Mairead; BASSON, Craig T et al.Circulation (New York, N.Y.). 2001, Vol 103, Num 20, pp 2469-2475, issn 0009-7322Article

Novel methylation targets in de novo acute myeloid leukemia with prevalence of chromosome 11 lociRUSH, Laura J; ZUNYAN DAI; KOLITZ, Jonathan E et al.Blood. 2001, Vol 97, Num 10, pp 3226-3233, issn 0006-4971Article

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