Homology requirements for unequal crossing over in humans.
about
A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous diseaseIdentification of class-mu glutathione transferase genes GSTM1-GSTM5 on human chromosome 1p13PRBI gene variants coding for length and null polymorphisms among human salivary Ps, PmF, PmS, and Pe proline-rich proteins (PRPs)Molecular basis for secretor type alpha(1,2)-fucosyltransferase gene deficiency in a Japanese population: a fusion gene generated by unequal crossover responsible for the enzyme deficiencyRare germinal unequal crossing-over leading to recombinant gene formation and gene duplication in Arabidopsis thalianaOrigin and ascendancy of a chimeric fusion gene: the beta/delta-globin gene of paenungulate mammalsBovine Carboxylesterases: Evidence for Two CES1 and Five Families of CES Genes on Chromosome 18Synaptonemal complexes from DNase-treated rat pachytene chromosomes contain (GT)n and LINE/SINE sequences.Reciprocal and nonreciprocal recombination at the glucocerebrosidase gene region: implications for complexity in Gaucher disease.Population genetics of tandem repeats in centromeric heterochromatin: unequal crossing over and chromosomal divergence at the Responder locus of Drosophila melanogaster.The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patientsGenetic variation at the tomato Cf-4/Cf-9 locus induced by EMS mutagenesis and intralocus recombinationProcesses of copy-number change in human DNA: the dynamics of {alpha}-globin gene deletion.Genome destabilization by homologous recombination in the germ linePRB2/1 fusion gene: a product of unequal and homologous crossing-over between proline-rich protein (PRP) genes PRB1 and PRB2.Alu-specific microhomology-mediated deletion of the final exon of SPAST in three unrelated subjects with hereditary spastic paraplegia.Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin.New genes originated via multiple recombinational pathways in the beta-globin gene family of rodentsUnequal homologous recombination of human DNA on a yeast artificial chromosome.Integration of a vector containing a repetitive LINE-1 element in the human genome.Somatic generation of hybrid antibody H chain genes in transgenic mice via interchromosomal gene conversion.The extent, mechanism, and consequences of genetic variation, for recombination rateDifferential evolution of antiretroviral restriction factors in pteropid bats as revealed by APOBEC3 gene complexity.
P2860
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P2860
Homology requirements for unequal crossing over in humans.
description
1991 nî lūn-bûn
@nan
1991 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
name
Homology requirements for unequal crossing over in humans.
@ast
Homology requirements for unequal crossing over in humans.
@en
type
label
Homology requirements for unequal crossing over in humans.
@ast
Homology requirements for unequal crossing over in humans.
@en
prefLabel
Homology requirements for unequal crossing over in humans.
@ast
Homology requirements for unequal crossing over in humans.
@en
P2093
P2860
P1433
P1476
Homology requirements for unequal crossing over in humans.
@en
P2093
A B Metzenberg
T H Huisman
P2860
P304
P407
P577
1991-05-01T00:00:00Z