Latest papers

Microsatellite and mitochondrial haplotype diversity reveals population differentiation in the tiger shrimp (Penaeus monodon) in the Indo-Pacific region.

Beta-globin LCR and intron elements cooperate and direct spatial reorganization for gene therapy.

Position effect variegation and imprinting of transgenes in lymphocytes.

Transcription and chromatin organization of a housekeeping gene cluster containing an integrated beta-globin locus control region.

Long-range communication between the silencers of HMR.

Sequence change in the HS2-LCR and Ggamma-globin gene promoter region of sickle cell anemia patients.

Role of chromatin structure in integration of helper-dependent adenoviral vectors containing the beta-globin locus control region.

Beta-globin regulation and long-range interactions.

5'HS5 of the human beta-globin locus control region is dispensable for the formation of the beta-globin active chromatin hub.

Halibut mitochondrial genomes contain extensive heteroplasmic tandem repeat arrays involved in DNA recombination.

MafK/NF-E2 p18 is required for beta-globin genes activation by mediating the proximity of LCR and active beta-globin genes in MEL cell line.

Rapid morphological and genetic change in Chicago-area Peromyscus.

Cluster specific regulation pattern of upstream regulatory elements in human alpha- and beta-globin gene clusters.

Deletion of the core-H region in mice abolishes the expression of three proximal odorant receptor genes in cis.

A positive role for NLI/Ldb1 in long-range beta-globin locus control region function.

Beta-globin gene cluster polymorphisms are strongly associated with severity of HbE/beta(0)-thalassemia.

Mitochondrial DNA control region population data from Macedonia.

Three divergent mitochondrial genomes from California populations of the copepod Tigriopus californicus.

An intronic locus control region plays an essential role in the establishment of an autonomous hepatic chromatin domain for the human vitamin D-binding protein gene.

Increased gamma-globin gene expression in beta-thalassemia intermedia patients correlates with a mutation in 3'HS1.