Latest papers

IG/MYC rearrangements are the main cytogenetic alteration in plasmablastic lymphomas.

Encapsulated papillary oncocytic neoplasms of the thyroid: morphologic, immunohistochemical, and molecular analysis of 18 cases.

[Towards an inventory of oncogenic mutations in cancer].

Long-term survival of a patient with squamous cell carcinoma harboring NUT gene rearrangement.

Degeneration of an intracellular ion channel in the primate lineage by relaxation of selective constraints.

Large-scale tRNA intron transposition in the archaeal order Thermoproteales represents a novel mechanism of intron gain.

BCL2 chromosomal translocation is not a general feature of the interdigitating dendritic cell sarcoma.

Replication termination at eukaryotic chromosomes is mediated by Top2 and occurs at genomic loci containing pausing elements.

A prenatally recognizable malformation syndrome associated with a recurrent post-zygotic chromosome rearrangement der(Y)t(Y;1)(q12:q21).

[Molecular genome organization in ciliates].

Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints.

Homozygosity for constitutional chromosomal rearrangements: a systematic review with reference to origin, ascertainment and phenotype.

Determination of gross chromosomal rearrangement rates.

Primate chromosome evolution: with reference to marker order and neocentromeres.

Complete mitochondrial DNA sequence of the endangered frog Odorrana ishikawae (family Ranidae) and unexpected diversity of mt gene arrangements in ranids

Androgen-induced TOP2B-mediated double-strand breaks and prostate cancer gene rearrangements.

Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism.

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly.

Diffuse large B-cell lymphoma in the spinal epidural space: A study of the Osaka Lymphoma Study Group

Comprehensive Characterization of a Novel Intronic Pseudo-Exon Inserted within an e14/a2 BCR-ABL Rearrangement in a Patient with Chronic Myeloid Leukemia