Recombination at the human alpha-globin gene cluster: sequence features and topological constraints.
about
Structural organization of glycophorin A and B genes: glycophorin B gene evolved by homologous recombination at Alu repeat sequencesA composite transposon 3' to the cow fetal globin gene binds a sequence specific factorUnique sequence organization and erythroid cell-specific nuclear factor-binding of mammalian theta 1 globin promotersChromosome translocation based on illegitimate recombination in human tumorsThe relationship between chromosome structure and function at a human telomeric regionAlu mobile elements: from junk DNA to genomic gemsMolecular pathology of single gene disorders.Alpha thalassaemia: a potential source of error in DNA linkage studies for adult polycystic kidney diseaseAsymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in manChromosomes, 11Q and cancer: a review.Intramolecular recombination of chloroplast genome mediated by short direct-repeat sequences in wheat speciesThe mechanisms involved in formation of deletions and duplications of 15q11-q13.DNA-directed mutations. Leading and lagging strand specificity.Roles of retrotransposons in benign and malignant hematologic disease.Filler DNA is associated with spontaneous deletions in maize.Inactivation of human alpha-globin gene expression by a de novo deletion located upstream of the alpha-globin gene clusterRecombination resulting in unusual features in the polyomavirus genome isolated from a murine tumor cell line.Analysis of the human alpha globin upstream regulatory element (HS-40) in transgenic miceIdentification of a conserved erythroid specific domain of histone acetylation across the alpha-globin gene cluster.Allelic and ectopic recombination between Ty elements in yeast.Unequal exchange and meiotic instability of disease-resistance genes in the Rp1 region of maize.Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndromeShort, direct repeats at the breakpoints of deletions of the retinoblastoma gene.Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.Molecular studies of deletions at the human steroid sulfatase locus.De novo generation of simple sequence during gene amplification.Processes of copy-number change in human DNA: the dynamics of {alpha}-globin gene deletion.Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.DICER1 deficit induces Alu RNA toxicity in age-related macular degenerationThe role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors.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.A high frequency of length polymorphisms in repeated sequences adjacent to Alu sequencesDuplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlationClinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complexClinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.The preference for GT-rich DNA by the yeast Rad51 protein defines a set of universal pairing sequencesGlobin genes are useful markers to identify genetic similarities between Fijians and Pacific Islanders from Polynesia and MelanesiaGenotypic influence of α-deletions on the phenotype of Indian sickle cell anemia patients.Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements.Human retinoblastoma gene: long-range mapping and analysis of its deletion in a breast cancer cell line
P2860
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P2860
Recombination at the human alpha-globin gene cluster: sequence features and topological constraints.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh
1987年學術文章
@zh-hant
name
Recombination at the human alp ...... s and topological constraints.
@en
Recombination at the human alp ...... s and topological constraints.
@nl
type
label
Recombination at the human alp ...... s and topological constraints.
@en
Recombination at the human alp ...... s and topological constraints.
@nl
prefLabel
Recombination at the human alp ...... s and topological constraints.
@en
Recombination at the human alp ...... s and topological constraints.
@nl
P2093
P1433
P1476
Recombination at the human alp ...... s and topological constraints.
@en
P2093
Fischel-Ghodsian N
Nicholls RD
P304
P356
10.1016/0092-8674(87)90289-3
P407
P577
1987-05-01T00:00:00Z