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Good genes in bad neighbourhoods

Published in: Nature Genetics

Date of publication: March 1, 1996

Language: English

Bibliographic databases:

Cites articles 32

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A foreign beta-globin gene in transgenic mice: integration at abnormal chromosomal positions and expression in inappropriate tissues,A foreign β-globin gene in transgenic mice: Integration at abnormal chromosomal positions and expression in inappropriate tissues
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Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites
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The bithorax complex
May 1, 1989

Three breakpoints of variant t(2;8) translocations in Burkitt's lymphoma cells fall within a region 140 kilobases distal from c-myc
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Position effect variegation in Drosophila: towards a genetics of chromatin assembly
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Activation of the Mlvi-1/mis1/pvt-1 locus in Moloney murine leukemia virus-induced T-cell lymphomas
October 1, 1989

Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites
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Position-effect variegation after 60 years
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Human globin locus activation region (LAR): role in temporal control
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Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin
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Neoplastic development in B-lymphocytes
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Retroviral insertions 90 kilobases proximal to the Evi-1 myeloid transforming gene activate transcription from the normal promoter
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Mosaic expression of a tyrosinase fusion gene in albino mice yields a heritable striped coat color pattern in transgenic homozygotes
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Developmental abnormalities in Steel17H mice result from a splicing defect in the steel factor cytoplasmic tail

,
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Activation of EVI1 gene expression in human acute myelogenous leukemias by translocations spanning 300-400 kilobases on chromosome band 3q26
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Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal
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Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

,
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The mouse segmentation gene kr encodes a novel basic domain-leucine zipper transcription factor
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Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
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Position-dependent variegation of globin transgene expression in mice
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DNA rearrangements located over 100 kb 5' of the Steel (Sl)-coding region in Steel-panda and Steel-contrasted mice deregulate Sl expression and cause female sterility by disrupting ovarian follicle development
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Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype
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Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
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A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene
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Y chromosome short arm-Sxr recombination in XSxr/Y males causes deletion of Rbm and XY female sex reversal
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The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
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The Wsh and Ph mutations affect the c-kit expression profile: c-kit misexpression in embryogenesis impairs melanogenesis in Wsh and Ph mutant mice
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The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins

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