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22q11.2 Low Copy Repeats Expanded in the Human Lineage.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.706641
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- Publication type:
- Article
Human centromere repositioning activates transcription and opens chromatin fibre structure.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33426-2
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- Publication type:
- Article
t(5;6;12) associated with resistance to imatinib mesylate in chronic myeloid leukemia.
- Published in:
- 2009
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- Publication type:
- journal article
Localization of a new highly repeated DNA sequence of Lemurcatta (Lemuridae, Strepsirhini).
- Published in:
- Genome, 2002, v. 45, n. 5, p. 973, doi. 10.1139/g02-048
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- Publication type:
- Article
A Novel Type of c-myc Translocation in a T Lymphoma Cell Linea.
- Published in:
- Annals of the New York Academy of Sciences, 1987, v. 511, n. 1, p. 338, doi. 10.1111/j.1749-6632.1987.tb36262.x
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- Publication type:
- Article
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer.
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. 14, p. 9131, doi. 10.1093/nar/gku590
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- Publication type:
- Article
Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report.
- Published in:
- 2012
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- Publication type:
- journal article
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.
- Published in:
- Nature Genetics, 2001, v. 27, n. 2, p. 159, doi. 10.1038/84781
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- Publication type:
- Article
Non random distribution of genomic features inbreakpoint regions involved in chronic myeloidleukemia cases with variant t(9;22) or additionalchromosomal rearrangements.
- Published in:
- Molecular Cancer, 2010, v. 9, p. 120, doi. 10.1186/1476-4598-9-120
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- Publication type:
- Article
Refinement of macaque synteny arrangement with respect to the official rheMac2 macaque sequence assembly.
- Published in:
- Chromosome Research, 2008, v. 16, n. 7, p. 977, doi. 10.1007/s10577-008-1255-1
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- Publication type:
- Article
Epigenetic origin of evolutionary novel centromeres.
- Published in:
- Scientific Reports, 2017, p. 41980, doi. 10.1038/srep41980
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- Publication type:
- Article
De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0039180
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- Publication type:
- Article
The nm23 gene maps to human chromosome band 17q22 and shows a restriction fragment length polymorphism with bg/II.
- Published in:
- Genes, Chromosomes & Cancer, 1992, v. 4, n. 1, p. 84, doi. 10.1002/gcc.2870040113
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- Publication type:
- Article
Direct duplication 12p11.21–p13.31 mediated by segmental duplications: a new recurrent rearrangement?
- Published in:
- Human Genetics, 2005, v. 118, n. 2, p. 207, doi. 10.1007/s00439-005-0008-x
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- Publication type:
- Article
Reciprocal translocations: a trap for cytogenetists?
- Published in:
- Human Genetics, 2005, v. 117, n. 6, p. 571, doi. 10.1007/s00439-005-1324-x
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- Publication type:
- Article
AcroM fluorescent in situ hybridization analyses of marker chromosomes.
- Published in:
- Human Genetics, 2001, v. 109, n. 2, p. 152, doi. 10.1007/s004390100571
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- Publication type:
- Article
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).
- Published in:
- Human Genetics, 2001, v. 108, n. 3, p. 199, doi. 10.1007/s004390100459
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- Publication type:
- Article
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 797, doi. 10.1038/sj.ejhg.5201203
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- Publication type:
- Article
Inverted duplications: how many of them are mosaic?
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- European Journal of Human Genetics, 2004, v. 12, n. 9, p. 713, doi. 10.1038/sj.ejhg.5201240
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- Publication type:
- Article
Saturating density of STSs (1/6 kb) in a 1.1 Mb region on 3q28-q29: a valuable resource for cloning of disease genes.
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- European Journal of Human Genetics, 2001, v. 9, n. 4, p. 307, doi. 10.1038/sj.ejhg.5200630
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- Publication type:
- Article
The Rest Repression of the Neurosecretory Phenotype Is Negatively Modulated by BHC80, a Protein of the BRAF/HDAC Complex.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 19, p. 6296, doi. 10.1523/JNEUROSCI.5943-08.2009
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- Publication type:
- Article
DDXIIL: a novel transcript family emerging from human subtelomeric regions.
- Published in:
- BMC Genomics, 2009, v. 10, p. 250, doi. 10.1186/1471-2164-10-250
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- Publication type:
- Article
Organization and Evolution of Primate Centromeric DNA from Whole-Genome Shotgun Sequence Data.
- Published in:
- PLoS Computational Biology, 2007, v. 3, n. 9, p. 1807, doi. 10.1371/journal.pcbi.0030181
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- Publication type:
- Article
Centromere Remodeling in Hoolock leuconedys (Hylobatidae) by a New Transposable Element Unique to the Gibbons.
- Published in:
- Genome Biology & Evolution, 2012, v. 4, n. 9, p. 648, doi. 10.1093/gbe/evs048
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- Publication type:
- Article
Centromere Remodeling in Hoolock leuconedys (Hylobatidae) by a New Transposable Element Unique to the Gibbons.
- Published in:
- Genome Biology & Evolution, 2012, v. 4, n. 7, p. 648, doi. 10.1093/gbe/evs048
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- Publication type:
- Article
The double deceit generated by an insertion mechanism in chronic myeloid leukemia with t(9;9;22).
- Published in:
- 2008
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- Publication type:
- Letter
Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia.
- Published in:
- 2006
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- Publication type:
- Letter
Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case.
- Published in:
- 2001
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- Publication type:
- journal article
Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case.
- Published in:
- 2001
- By:
- Publication type:
- Erratum
Evolutionary History of Chromosome 20.
- Published in:
- Molecular Biology & Evolution, 2005, v. 22, n. 2, p. 360
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- Publication type:
- Article
Chromosome 6 Phylogeny in Primates and Centromere Repositioning.
- Published in:
- Molecular Biology & Evolution, 2003, v. 20, n. 9, p. 1506, doi. 10.1093/molbev/msg165
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- Publication type:
- Article
A genome-wide comparison of recent chimpanzee and human segmental duplications.
- Published in:
- Nature, 2005, v. 437, n. 7055, p. 88, doi. 10.1038/nature04000
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- Publication type:
- Article
The structure and evolution of centromeric transition regions within the human genome.
- Published in:
- Nature, 2004, v. 430, n. 7002, p. 857, doi. 10.1038/nature02806
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- Publication type:
- Article
Positive selection of a gene family during the emergence of humans and African apes.
- Published in:
- Nature, 2001, v. 413, n. 6855, p. 514, doi. 10.1038/35097067
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- Publication type:
- Article
Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1->qter in prenatal diagnosis: a case report.
- Published in:
- Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13039-014-0069-4
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- Publication type:
- Article
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.
- Published in:
- Genes, Chromosomes & Cancer, 2015, v. 54, n. 3, p. 156, doi. 10.1002/gcc.22228
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- Publication type:
- Article
Translocation–excision–deletion–amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1This text presents research results of the Belgian program of Interuniversity Poles of attraction initiated by the Belgian State, Prime Minister's Office, Science Policy Programming (IUAP).
- Published in:
- Genes, Chromosomes & Cancer, 2006, v. 45, n. 2, p. 107, doi. 10.1002/gcc.20272
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- Publication type:
- Article
Insertions generating the 5′RUNX1/3′CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 41, n. 1, p. 86, doi. 10.1002/gcc.20061
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- Publication type:
- Article
Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma.
- Published in:
- Genes, Chromosomes & Cancer, 2003, v. 37, n. 3, p. 261, doi. 10.1002/gcc.10211
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- Publication type:
- Article
Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases.
- Published in:
- Genes, Chromosomes & Cancer, 2003, v. 36, n. 4, p. 353, doi. 10.1002/gcc.10183
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- Publication type:
- Article
Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients.
- Published in:
- Genes, Chromosomes & Cancer, 2002, v. 35, n. 3, p. 271, doi. 10.1002/gcc.10116
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- Publication type:
- Article
Episomal amplification of MYCN in a case of medulloblastoma.
- Published in:
- Virchows Archiv: European Journal of Pathology, 2008, v. 452, n. 5, p. 491
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- Publication type:
- Article
Gibbon genome and the fast karyotype evolution of small apes.
- Published in:
- Nature, 2014, v. 513, n. 7517, p. 195, doi. 10.1038/nature13679
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- Publication type:
- Article
The Hidden Genomic and Transcriptomic Plasticity of Giant Marker Chromosomes in Cancer.
- Published in:
- Genetics, 2018, v. 208, n. 3, p. 951, doi. 10.1534/genetics.117.300552
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- Publication type:
- Article
MIRN199B downregulation in chronic myeloid leukaemia is associated with deletions on der(9).
- Published in:
- 2009
- By:
- Publication type:
- Letter
Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16·3;q32) chromosomal translocation.
- Published in:
- 2004
- By:
- Publication type:
- Letter
Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph<sup>+</sup> adult acute lymphoblastic leukaemia.
- Published in:
- British Journal of Haematology, 2002, v. 119, n. 2, p. 488, doi. 10.1046/j.1365-2141.2002.03846.x
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- Publication type:
- Article
Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2.
- Published in:
- Human Mutation, 2007, v. 28, n. 5, p. 459, doi. 10.1002/humu.20465
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- Publication type:
- Article
Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 21, p. 2572, doi. 10.1093/hmg/ddm209
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- Publication type:
- Article
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 14, p. 1479, doi. 10.1093/hmg/ddh164
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- Publication type:
- Article