chromosome 11
X-RAY-INDUCED DEFICIENCIES OF CHROMOSOME 11 IN THE TOMATO
... Preparations revealed terminal deficiencies with the achromatic region and most of the chromatic zone of the short arm of chromosome 11 missing for three individuals, and a n inter[r] ...
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Viral Load and a Locus on Chromosome 11 Affect the Late Clinical Disease Caused by Theiler’s Virus
... nonaffected and affected mice were compared as a function of genotype (Fig. 5). Clinical signs were associated with a high level of persistent infection regardless of the genotype. How- ever, when one compares mice with ...
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A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human.
... We have generated a multilocus linkage map of mouse chromosome 11. Thus, we are quite confident of detecting most, if not all, double recombinants. A total of 69 singl[r] ...
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Embryonic Lethality and Tumorigenesis Caused by Segmental Aneuploidy on Mouse Chromosome 11
... human chromosome 17 that can be rapidly generated using this approach, the corresponds to this region of mouse chromosome 11 is breakpoints are randomly distributed and, therefore, unusually high ( ...
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Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
... Multiple biochemical pathways and several genes are related to the pathogenesis of PCOS; however, the etiology of PCOS is multifactorial, and finding a single gene responsible for the syndrome is unlikely. We ...
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Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations
... of chromosome 11 allele loss occurring in non-MEN1 somatotrophinomas, indicate that a recessive oncogene on 11q13 is specifically involved in the monoclonal development of ...
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A Genetic Mechanism Implicates Chromosome 11 in Schizophrenia and Bipolar Diseases
... mouse chromosome 7 with the biased human chromosome 11 segregation proposal of the SSIS model, synteny between the mouse and human chromosomes was searched within the GenBank ...mouse ...
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The Paternal Gene of the DDK Syndrome Maps to the Schlafen Gene Cluster on Mouse Chromosome 11
... The DDK syndrome is an early embryonic lethal phenotype observed in crosses between females of the DDK inbred mouse strain and many non-DDK males. Lethality results from an incompatibility between a maternal DDK factor ...
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The wooly mutation (wly) on mouse chromosome 11 is associated with a genetic defect in Fam83g
... mouse Chromosome (Chr) 11, it was immediately tested for genetic complementation in crosses with the waved 2 (wa2) mutant [2], but since no affected progeny were produced, these recessive variants must be ...
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Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)
... Dependent on the size of the 11q deletion, which usually lies between 7 and 20 Mb [8,9], the clinical features may vary also. Previous cytogenetic studies in JBS patients characterized the crucial band for the 11q ...
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CONSERVED LINKAGE WITHIN A 4-cM REGION OF MOUSE CHROMOSOME 9 AND HUMAN CHROMOSOME 11
... MEISLER, 1982 Linkage of the structural gene for uroporphyrinogen I synthase to markers on mouse chromosome 9 in a cross between feral and inbred mice.. Localization of th[r] ...
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The polar-lethal Ovum mutant gene maps to the distal portion of mouse chromosome 11.
... Here we report our genetic analysis of the behavior of the interstrain, polar, embryonic-lethal phenotype known as the “DDK syndrome.” We have mapped the interstrain, pol[r] ...
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The Hox-2 homeo box gene complex on mouse chromosome 11 is closely linked to Re.
... I n this paper we have bridged part of the resolution gap between the DNA sequence and the chromosome by identifying RFLP alleles for the Hox-2 locus and using them to e[r] ...
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Roles of microRNA-99 family in human glioma
... to chromosome 11, has been found to be a diagnostic and/or prognostic marker for human cancer due to its dysregulation and aberrant expres- sion in the tumorigenesis and tumor progression of several types ...
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Sint1, a Common Integration Site in SL3-3-Induced T-Cell Lymphomas, Harbors a Putative Proto-Oncogene with Homology to the Septin Gene Family
... mouse chromosome 11 linked to Grin2c, Hfh4, and ...mouse chromosome 11 shares a region of homology with human chromosome 17q25 (summarized in ...
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Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review
... After considering all the collected clinical information, we drew the conclusion that it is not possible to define a distinctive phenotype of the 11q partial monosomy due to the heterogeneity in size and position of the ...
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Original Article Chromosome aberrations and spermatogenic disorders in mice with Robertsonian translocation (11; 13)
... mosome 11 and some genes located on human chromosome 17 are associated with male fer- ...human chromosome 17q21.33 with a location on mouse chromosome 11, was previously shown to be ...
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Prostate-specific membrane antigen: evidence for the existence of a second related human gene
... Chromosome sublocalisation PCR analysis of a number of cell lines containing fragments of human chromosome 11 was next performed.. The human component of these various cell lines is illu[r] ...
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A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross.
... COPELAND, 1988 Localization of Evi-2 to chromosome 11: linkage to other proto-oncogene and growth factor loci using interspecific backcross mice.. COPELAND, 1989 A compreh[r] ...
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Genome Wide Association Analysis of Avian Resistance to Campylobacter jejuni Colonization Identifies Risk Locus Spanning the CDH13 Gene
... suppressor that localizes to adherens junctions on the basolateral membrane of epithelial cells. Despite its typical location below tight junctions, it interacts with several bacteria, facilitating internalization and ...
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