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Results 1 to 25 of 489

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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

Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in CatarrhiniFRANCESCA CARDONE, Maria; LOMIENTO, Mariana; GRAZIA TETI, Maria et al.Genomics (San Diego, Calif.). 2007, Vol 90, Num 1, pp 35-43, issn 0888-7543, 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

Direct evidence for susceptibility genes for type 2 diabetes on mouse chromosomes 11 and 14BABAYA, N; FUJISAWA, T; IKEGAMI, H et al.Diabetologia (Berlin). 2010, Vol 53, Num 7, pp 1362-1371, issn 0012-186X, 10 p.Article

mgl-1, a mouse homologue of the drosophila tumor-suppressor gene l(2)gl, maps to chromosome 11KUWABARA, K; TAKAHASHI, Y; TOMOTSUNE, D et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 2, pp 337-338, issn 0888-7543Article

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

An interstitial telomere array near Hba on mouse Chr 11 is a candidate for the homolog of the telomere at human 16pELLIOTT, R. W; PAZIK, J.Genomics (San Diego, Calif.). 1995, Vol 27, Num 1, pp 217-218, issn 0888-7543Article

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

Analysis of chromosome-11 aberrations in pulmonary and gastrointestinal carcinoids: an array comparative genomic hybridization-based studyPETZMANN, Susanna; ULLMANN, Reinhard; HALBWEDL, Iris et al.Virchows Archiv. 2004, Vol 445, Num 2, pp 151-159, issn 0945-6317, 9 p.Article

Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastomaCHUGHTAI, Shaheen A; GENUS, Tracey; ROMANI, Pramila et al.European journal of cancer (1990). 2006, Vol 42, Num 12, pp 1826-1834, issn 0959-8049, 9 p.Article

Allelic phasing of a mouse chromosome 11 deficiency influences p53 tumorigenicityBIGGS, Patrick J; VOGEL, Hannes; SAGE, Marijke et al.Oncogene (Basingstoke). 2003, Vol 22, Num 21, pp 3288-3296, issn 0950-9232, 9 p.Article

Somatic deletion of the normal β-globin gene leading to thalassaemia intermedia in heterozygous β-thalassaemic patientsGALANELLO, Renzo; PERSEU, Lucia; PERRA, Chiara et al.British journal of haematology. 2004, Vol 127, Num 5, pp 604-606, issn 0007-1048, 3 p.Article

THY1 is a candidate tumour suppressor gene with decreased expression in metastatic nasopharyngeal carcinomaHONG LOK LUNG; DHINOTH KUMAR BANGARUSAMY; YAN FANG et al.Oncogene (Basingstoke). 2005, Vol 24, Num 43, pp 6525-6532, issn 0950-9232, 8 p.Article

Beckwith-Wiedemann syndromeWEKSBERG, Rosanna; SHUMAN, Cheryl; BECKWITH, J. Bruce et al.European journal of human genetics. 2010, Vol 18, Num 1, pp 8-14, issn 1018-4813, 7 p.Article

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