Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.
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References (32)
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
1983 • 26,063 citations
Amyloid β Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage Near the Alzheimer Locus
1987 • 1,589 citations
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene
1986 • 1,033 citations
Lengths of chromosomal segments conserved since divergence of man and mouse.
1984 • 599 citations
Report of the committee on methods of linkage analysis and reporting
1985 • 325 citations
The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid β-protein gene
1987 • 271 citations
Confidence limits for estimates of gene linkage based on analysis of recombinant inbred strains
1985 • 230 citations
Genetic analysis of the proximal portion of the mouse t complex: Evidence for a second inversion within t haplotypes
1986 • 193 citations
The ets sequence from the transforming gene of avian erythroblastosis virus, E26, has unique domains on human chromosomes 11 and 21: both loci are transcriptionally active.
1985 • 177 citations
Precise localization of human beta-globin gene complex on chromosome 11.
1979 • 175 citations
Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross
1985 • 175 citations
Trisomie 21 et superoxyde dismutase-1 (IPO-A)
1976 • 175 citations
Human Cu/Zn superoxide dismutase cDNA: isolation of clones synthesising high levels of active or inactive enzyme from an expression library
1985 • 149 citations
Down's syndrome
1974 • 134 citations
Complete structure of the alpha B-crystallin gene: conservation of the exon-intron distribution in the two nonlinked alpha-crystallin genes.
1985 • 130 citations
The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.
1988 • 126 citations
Isolation of polymorphic DNA fragments from human chromosome 4
1987 • 100 citations
Partial trisomy 21
1977 • 99 citations
Genetic basis for a mouse model of down syndrome
1986 • 93 citations
Cloned DNA probes regionally mapped to human Chromosome 21 and their use in determining the origin of nondisjunction
1985 • 93 citations
Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.
1975 • 77 citations
Genetic mapping of <i>Prm-1, Igl-1, Smst, Mtv-6, Sod-1,</i> and <i>Ets-2</i>and localization of the Down syndrome region on mouse chromosome 16
1987 • 62 citations
Glyoxalase I Polymorphism in the Mouse: A New Genetic Marker Linked to H-2
1977 • 56 citations
Deletion and duplication of DNA sequences is associated with the embryonic lethal phenotype of the t9 complementation group of the mouse t complex.
1987 • 56 citations
Genetic Variants and Strains of the Laboratory Mouse
1983 • 46 citations
THE LOCUS ENCODING αA-CRYSTALLIN IS CLOSELY LINKED TO H-2K ON MOUSE CHROMOSOME 17
1985 • 43 citations
The Putative Oncogene Pim-1 in the Mouse: Its Linkage and Variation Among t Haplotypes
1987 • 42 citations
The alpha-globin pseudogene on mouse chromosome 17 is closely linked to H-2.
1984 • 32 citations
Molecular genetics of human chromosome 21.
1987 • 25 citations
Recombination between the t6 complex and linked loci in the house mouse
1985 • 17 citations
Assignment of the mouse alpha A-crystallin structural gene to chromosome 17
1985 • 10 citations
Genetic control of the quantitative variation of erythrocytic glyoxalase-1 (GLO-1) in mice
1982 • 7 citations
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