Pages that link to "Q42012580"
Jump to navigation
Jump to search
The following pages link to Recombination at the human alpha-globin gene cluster: sequence features and topological constraints (Q42012580):
Displayed 50 items.
- Homology-mediated recombination between type I collagen gene exons results in an internal tandem duplication and lethal osteogenesis imperfecta (Q24321763) (← links)
- Structural organization of glycophorin A and B genes: glycophorin B gene evolved by homologous recombination at Alu repeat sequences (Q24339514) (← links)
- A composite transposon 3' to the cow fetal globin gene binds a sequence specific factor (Q24630905) (← links)
- Unique sequence organization and erythroid cell-specific nuclear factor-binding of mammalian theta 1 globin promoters (Q24635562) (← links)
- Chromosome translocation based on illegitimate recombination in human tumors (Q24678527) (← links)
- Homeostatic control of uridine and the role of uridine phosphorylase: a biological and clinical update (Q28207314) (← links)
- Homology of a 130-kb region enclosing the alpha-globin gene cluster, the alpha-locus controlling region, and two non-globin genes in human and mouse (Q28259968) (← links)
- Structure and expression of the human theta 1 globin gene (Q28298075) (← links)
- The relationship between chromosome structure and function at a human telomeric region (Q28304976) (← links)
- Alu mobile elements: from junk DNA to genomic gems (Q28661722) (← links)
- Molecular pathology of single gene disorders (Q30499074) (← links)
- Alpha thalassaemia: a potential source of error in DNA linkage studies for adult polycystic kidney disease (Q33592685) (← links)
- Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man (Q33593235) (← links)
- Chromosomes, 11Q and cancer: a review (Q33643315) (← links)
- Intramolecular recombination of chloroplast genome mediated by short direct-repeat sequences in wheat species (Q33671219) (← links)
- The mechanisms involved in formation of deletions and duplications of 15q11-q13. (Q33680198) (← links)
- DNA-directed mutations. Leading and lagging strand specificity (Q33692307) (← links)
- Roles of retrotransposons in benign and malignant hematologic disease (Q33697456) (← links)
- Filler DNA is associated with spontaneous deletions in maize (Q33888422) (← links)
- Inactivation of human alpha-globin gene expression by a de novo deletion located upstream of the alpha-globin gene cluster (Q33919342) (← links)
- Recombination resulting in unusual features in the polyomavirus genome isolated from a murine tumor cell line. (Q33924800) (← links)
- Analysis of the human alpha globin upstream regulatory element (HS-40) in transgenic mice (Q33938795) (← links)
- Identification of a conserved erythroid specific domain of histone acetylation across the alpha-globin gene cluster (Q33947031) (← links)
- Allelic and ectopic recombination between Ty elements in yeast. (Q33954284) (← links)
- Unequal exchange and meiotic instability of disease-resistance genes in the Rp1 region of maize. (Q33960331) (← links)
- A new α0-thalassemia deletion found in a Dutch family (--AW) (Q34129490) (← links)
- Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndrome (Q34145305) (← links)
- Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene (Q34286847) (← links)
- Junctions between genes in the haptoglobin gene cluster of primates (Q34295830) (← links)
- Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. (Q34314269) (← links)
- Molecular studies of deletions at the human steroid sulfatase locus (Q34316988) (← links)
- De novo generation of simple sequence during gene amplification (Q34603892) (← links)
- Processes of copy-number change in human DNA: the dynamics of {alpha}-globin gene deletion. (Q34694670) (← links)
- Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene. (Q34727386) (← links)
- DICER1 deficit induces Alu RNA toxicity in age-related macular degeneration (Q34796058) (← links)
- The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors (Q34804028) (← links)
- The control of expression of the alpha-globin gene cluster (Q35038968) (← links)
- Detection of α-thalassemia-1 Southeast Asian and Thai type deletions and β-thalassemia 3.5-kb deletion by single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting analysis (Q35085497) (← links)
- Mutagen-induced recombination in mammalian cells in vitro (Q35148350) (← links)
- A high frequency of length polymorphisms in repeated sequences adjacent to Alu sequences (Q35197825) (← links)
- Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation (Q35198016) (← links)
- Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex (Q35198385) (← links)
- Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3. (Q35198409) (← 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)
- Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene (Q35221861) (← links)
- Globin genes are useful markers to identify genetic similarities between Fijians and Pacific Islanders from Polynesia and Melanesia (Q35245975) (← links)
- Genotypic influence of α-deletions on the phenotype of Indian sickle cell anemia patients (Q35524762) (← links)
- Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements (Q35587356) (← links)
- Human retinoblastoma gene: long-range mapping and analysis of its deletion in a breast cancer cell line (Q36038523) (← links)