Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster
about
Saturating the region of the polycystic kidney disease gene with NotI linking clones.Multipoint mapping of adult onset polycystic kidney disease (PKD1) on chromosome 16.Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism.Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish populationThe non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.High resolution gene mapping of the human alpha globin locusPhenotypic variation of tuberous sclerosis in a single extended kindredLocalisation of a mutation producing autosomal dominant polycystic kidney disease without renal failure.Localisation of human alpha globin to 16p13.3----pter.Genetic linkage map of 46 DNA markers on human chromosome 16.Inactivation of human alpha-globin gene expression by a de novo deletion located upstream of the alpha-globin gene clusterTwo highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomesIntrinsic polymorphism of variable number tandem repeat loci in the human genome.Structure and expression of the rat neuropeptide Y geneCharacterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysisHigh-resolution analysis of a hypervariable region in the human apolipoprotein B geneIdentification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.Clinical 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.Genetic analysis of eight loci tightly linked to neurofibromatosis 1Assessment of clonality in gastrointestinal cancer by DNA fingerprinting.Long-term follow-up of recipients of combined human leukocyte antigen-matched bone marrow and kidney transplantation for multiple myeloma with end-stage renal disease.A VNTR immediately adjacent to the human pseudoautosomal telomere.ABR, an active BCR-related geneA large deletion encompassing the entire alpha-like globin gene cluster in a family of northern European extractionClonal allele loss in gastrointestinal cancers.Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic HybridizationGenetic differences at four DNA typing loci in Finnish, Italian, and mixed Caucasian populationsComparative analysis of the alpha-like globin clusters in mouse, rat, and human chromosomes indicates a mechanism underlying breaks in conserved syntenyCpG methylation modifies the genetic stability of cloned repeat sequences.Alkaline transfer of small restriction fragments from polyacrylamide gelsSimple human DNA-repeats associated with genomic hypervariability, flanking the genomic retroposons and similar to retroviral sites.De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).DNA tertiary structures formed in vitro by misaligned hybridization of multiple tandem repeat sequences.A clinically homogeneous group of families with facioscapulohumeral (Landouzy-Déjérine) muscular dystrophy: linkage analysis of six autosomesMolecular analysis of a polymorphic domain of alpha satellite from the human X chromosome.Contrasting effects of alpha and beta globin regulatory elements on chromatin structure may be related to their different chromosomal environments.
P2860
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P2860
Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年学术文章
@wuu
1986年学术文章
@zh-cn
1986年学术文章
@zh-hans
1986年学术文章
@zh-my
1986年学术文章
@zh-sg
1986年學術文章
@yue
1986年學術文章
@zh
1986年學術文章
@zh-hant
name
Molecular characterisation of ...... uman alpha-globin gene cluster
@ast
Molecular characterisation of ...... uman alpha-globin gene cluster
@en
type
label
Molecular characterisation of ...... uman alpha-globin gene cluster
@ast
Molecular characterisation of ...... uman alpha-globin gene cluster
@en
prefLabel
Molecular characterisation of ...... uman alpha-globin gene cluster
@ast
Molecular characterisation of ...... uman alpha-globin gene cluster
@en
P2093
P2860
P1433
P1476
Molecular characterisation of ...... uman alpha-globin gene cluster
@en
P2093
Nicholls RD
Weatherall DJ
P2860
P304
P356
10.1002/J.1460-2075.1986.TB04437.X
P407
P577
1986-08-01T00:00:00Z