Pages that link to "Q69809070"

The following pages link to A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination (Q69809070):

Displayed 50 items.

• Human signal recognition particle (SRP) Alu-associated protein also binds Alu interspersed repeat sequence RNAs. Characterization of human SRP9 (Q24315915) ‎ (← links)
• Structural organization of glycophorin A and B genes: glycophorin B gene evolved by homologous recombination at Alu repeat sequences (Q24339514) ‎ (← links)
• Unique sequence organization and erythroid cell-specific nuclear factor-binding of mammalian theta 1 globin promoters (Q24635562) ‎ (← links)
• Alu mobile elements: from junk DNA to genomic gems (Q28661722) ‎ (← links)
• Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era (Q28776504) ‎ (← links)
• DNA methylation in health and disease (Q30659938) ‎ (← links)
• DNA methylation, methyltransferases, and cancer (Q30993657) ‎ (← links)
• Newly arisen DNA repeats in primate phylogeny (Q31160570) ‎ (← links)
• Construction of a human chromosome 4 YAC pool and analysis of artificial chromosome stability (Q33227826) ‎ (← links)
• X/Y translocations resulting from recombination between homologous sequences on Xp and Yq. (Q33412558) ‎ (← links)
• Long-range restriction map of the terminal part of the short arm of the human X chromosome (Q33579172) ‎ (← links)
• Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man (Q33593235) ‎ (← links)
• Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region (Q33594192) ‎ (← links)
• Chromosomal localisation of a pseudoautosomal growth gene(s) (Q33594421) ‎ (← links)
• Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females (Q33847127) ‎ (← links)
• Localization of preferential sites of rearrangement within the BCR gene in Philadelphia chromosome-positive acute lymphoblastic leukemia (Q33867942) ‎ (← links)
• An interspersed repeated sequence specific for human subtelomeric regions (Q33917989) ‎ (← links)
• Allelic and ectopic recombination between Ty elements in yeast. (Q33954284) ‎ (← links)
• Targeted breakage of a human chromosome mediated by cloned human telomeric DNA (Q34231869) ‎ (← links)
• Junctions between genes in the haptoglobin gene cluster of primates (Q34295830) ‎ (← links)
• DNA methylation affects meiotic trans-sensing, not meiotic silencing, in Neurospora (Q34569317) ‎ (← links)
• Is zinc-finger Y the sex-determining gene? (Q35197427) ‎ (← links)
• A high frequency of length polymorphisms in repeated sequences adjacent to Alu sequences (Q35197825) ‎ (← links)
• Suppression of crossing-over by DNA methylation in Ascobolus (Q35198972) ‎ (← links)
• The preference for GT-rich DNA by the yeast Rad51 protein defines a set of universal pairing sequences (Q35199876) ‎ (← links)
• Partial gene duplication as a cause of human disease (Q35221528) ‎ (← links)
• Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH) (Q35246204) ‎ (← links)
• Molecular cytogenetic analysis of telomere rearrangements (Q35540299) ‎ (← links)
• Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis (Q35793506) ‎ (← links)
• A recurrent translocation is mediated by homologous recombination between HERV-H elements (Q35799446) ‎ (← links)
• Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map. (Q36062906) ‎ (← links)
• A genetically determined insertion/deletion related polymorphism in human T cell receptor beta chain (TCRB) includes functional variable gene segments (Q36363844) ‎ (← links)
• Identification of a precursor genomic segment that provided a sequence unique to glycophorin B and E genes (Q36456810) ‎ (← links)
• Gene conversion as a secondary mechanism of short interspersed element (SINE) evolution (Q36566264) ‎ (← links)
• Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene (Q36694090) ‎ (← links)
• Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation (Q37386470) ‎ (← links)
• Human somatic mutation assays as biomarkers of carcinogenesis (Q37528645) ‎ (← links)
• Complex recombination events at the hypermutable minisatellite CEB1 (D2S90). (Q37634399) ‎ (← links)
• A sterile male with 45,X0 and a Y;22 translocation (Q37775853) ‎ (← links)
• Isolation of an Alu repetitive DNA binding protein and effect of CpG methylation on binding to its recognition sequence (Q38338865) ‎ (← links)
• Human Structural Variation: Mechanisms of Chromosome Rearrangements (Q38553771) ‎ (← links)
• Requirements for ectopic homologous recombination in mammalian somatic cells (Q40020577) ‎ (← links)
• Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemia (Q40305071) ‎ (← links)
• One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi. (Q40392697) ‎ (← links)
• The mammalian genome shaping activity of reverse transcriptase (Q40396339) ‎ (← links)
• Sequence conservation in Alu evolution. (Q40448415) ‎ (← links)
• Nucleotide sequence of both reciprocal translocation junction regions in a patient with Ph positive acute lymphoblastic leukaemia, with a breakpoint within the first intron of the BCR gene (Q40520345) ‎ (← links)
• Recombinational resolution in primate cells of two homologous human DNA segments with a gradient of sequence divergence (Q40557573) ‎ (← links)
• Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients (Q40569057) ‎ (← links)
• Mechanisms of tandem duplication in the Duchenne muscular dystrophy gene include both homologous and nonhomologous intrachromosomal recombination (Q41082050) ‎ (← links)