Chromosome 12
Effects of human chromosome 12 on interactions between Tat and TAR of human immunodeficiency virus type 1.
... Since the loop is required for high levels of Tat trans activation in the presence of human chromosome 12 Table 1, and since we could not develop a direct binding assay between Tat and t[r] ...
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Development of plasma cell myeloma in a B cell chronic lymphocytic leukemia patient with chromosome 12 trisomy
... The Chromosome 12 is considered as a marker of poor prognosis in B-CLL patients [16], but it was never correlated with myeloma ...a chromosome 12- negative clone of B-CLL, or also from a ...
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TAR loop-dependent human immunodeficiency virus trans activation requires factors encoded on human chromosome 12.
... In nonhuman cell lines or hybrid cells without chromosome 12 that supported trans activation, the cellular mechanism was independent of the HIV-1 TAR loop and the response to mutations i[r] ...
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A linkage map of mouse chromosome 12: localization of Igh and effects of sex and interference on recombination.
... Data from backcross experiments and from the analysis of RI strains have been used to construct a detailed linear linkage map that spans most of the genetic le[r] ...
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Mapping QTL Derived from Solanum pimpinellifolium L3707 for Bacterial Spot Disease Resistance and Fruit Morphology in Tomato.
... on chromosome 3, encoding the r (yellow flesh) mutant phenotype confers yellow flesh color in ripe tomato (Fray and Grierson, ...on chromosome 6 increases β-carotene in the tomato fruit that gives the ...
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Genetic pathway to recurrent chromosome translocations in murine lymphoma involves V(D)J recombinase
... Chromosome translocations involving antigen receptor loci are a genetic hallmark of non-Hodgkin’s lymphomas in humans. Most commonly, these translocations result in juxtaposition of the immunoglobulin heavy-chain ...
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Gene deletions correlate with the development of alloantibodies in von Willebrand disease
... deletions within the vWF gene. Both patients had severe vWD (type III) and were the only patients among those studied that had inhibitory alloantibodies to vWF. The extent of deletion was similar in both patients, ...
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Characterization of the MODY3 phenotype Early onset diabetes caused by an insulin secretion defect
... the 12 patients not inher- iting the MODY3-chromosome (NIDDM ...MODY3 chromosome ( MODY3 carri- ers ; n 5 18) with nondiabetic family members not inheriting this copy of chromosome 12 ( ...
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Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy
... For chromosome 3 individual wcp with a chromosome 3-specific library (Vysis Abbott Molecular, ...and 12 (Vysis). The derivative chromosome 12 was also studied by MCB applying the probe ...
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Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay
... between chromosome 7 and chromosome ...to chromosome 12 before being translocated jointly with a segment of chromosome 12 to chromosome ...the Chromosome Analysis ...
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Association mapping of resistance to rice blast in upland field conditions
... on chromosome 1, colocalized with a cluster of four NBS-LRR including the two cloned resistance genes Pi37 and ...on chromosome 12 and is associated with partial resistance to ...on chromosome ...
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Non-coding genomic regions possessing enhancer and silencer potential are associated with healthy aging and exceptional survival
... We have completed a genome-wide linkage scan for healthy aging using data collected from a family study, followed by fine-mapping by association in a separate population, the first such attempt reported. The family ...
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<p>Epidermolytic hyperkeratosis: clinical update</p>
... On chromosome 17, the small, acidic type I keratins are encoded (keratins 9 to 19), while on chromosome 12, the more basic and large type II keratins are encoded (keratins 1 to ...of ...
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<p>Entire ABL1 Gene Deletion Without BCR/ABL1 Rearrangement in a Female Patient with B-Cell Precursor Acute Lymphoblastic Leukemia</p>
... of chromosome 9, EVT6 gene on the short arm of chromosome 12 and DLEU2 gene on the long arm of chromosome 13; the increase in the copies of RET, PTEN, NT5C2 and SMC3 on the long arm of ...
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Localization of the human gene allowing infection by gibbon ape leukemia virus to human chromosome region 2q11-q14 and to the homologous region on mouse chromosome 2.
... The receptor genes which have been mapped include CD4 and Rec-1, which map to human chromosome 12 and mouse chromosome 5, respectively 6, 11, 12, 19, the RD114 receptor on human chromoso[r] ...
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Chromosome variations and diversity of Epidendrum ibaguense Lindl. (Orchidaceae) on the Tepequém's Tepuy, Roraima, Brazil.
... in chromosome number in genus Epidendrum, this study aimed 1) to determine the chromosome numbers, and 2) to test for an association between chromosome number and flower color variation in natural ...
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Fission Yeast Mutants That Alleviate Transcriptional Silencing in Centromeric Flanking Repeats and Disrupt Chromosome Segregation
... 11, 12, and 13 specifically affect silencing at centromeres and mainly within the flanking inverted repeat ...regions. Chromosome loss phenotypes and sensitivity to TBZ: Mutants such as swi6, clr4, and ...
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Chromosome-Specific Painting in Cucumis Species Using Bulked Oligonucleotides
... develop chromosome-specific painting probes in ...and chromosome-specific FISH ...to 12 million ...homeologous chromosome pair- ing in early meiotic ...the chromosome pairing behavior ...
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SigWin detector: a Grid enabled workflow for discovering enriched windows of genomic features related to DNA sequences
... The RIDGEOGRAMS shown in Figures 4 and 5 only take the ordering of the genes into account, and not their actual physical position in the chromosome. However, from a biological perspective it is likely that the ...
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Characterization of AFLP Sequences From Regions of Maize B Chromosome Defined by 12 B-10L Translocations
... 3 p3561 CK, PE, DH1, DH2, DH3, DH4 pachytene chromosome (Figure 7C) and no signal was 4 p3749 No detectable signal detected in root-tip spreads (data not shown). Yet, its 5 p3849 CK, PE, DH1, DH2, DH3, DH4, DE ...
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