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Noncomplementation Phenomena and Their Bearing on Nondisjunctional Effects

Data up to Jan 2025

Published1985
Citations52
References37

Total Citations Per Year

Abstract

References (37)

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1984 • 1,529 citations

Genetic variants and strains of the laboratory mouse

1990 • 1,519 citations

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

1984 • 1,402 citations

Differential activity of maternally and paternally derived chromosome regions in mice

1985 • 708 citations

Role of paternal and maternal genomes in mouse development

1984 • 704 citations

TRISOMY IN MAN

1984 • 652 citations

Lengths of chromosomal segments conserved since divergence of man and mouse.

1984 • 599 citations

The T-locus of the mouse

1975 • 567 citations

X-RAY-INDUCED MUTATIONS IN MICE

1951 • 486 citations

Radiation-Induced Chromosome Damage in Man

1984 • 387 citations

Human triploidy: relationship between parental origin of the additional haploid complement and development of partial hydatidiform mole

1982 • 371 citations

Development of Gynogenetic Eggs in the Mouse: Implications for Parthenogenetic Embryos

1983 • 303 citations

Mutation Induction in Mice

1974 • 228 citations

Normal postimplantation development of mouse parthenogenetic embryos to the forelimb bud stage

1977 • 224 citations

Systematic approach to the study of trisomy in the mouse. II

1975 • 210 citations

Radiation-induced chromosome damage in man

1983 • 188 citations

HAIRPIN-TAIL: A CASE OF POST-REDUCTIONAL GENE ACTION IN THE MOUSE EGG?

1974 • 163 citations

Complementation studies with mouse translocations

1978 • 113 citations

Dominant cataract mutations and specific-locus mutations in mice induced by radiation or ethylnitrosourea

1982 • 111 citations

Biology of the house mouse.

1981 • 110 citations

Parental origin of autosomal trisomies

1984 • 103 citations

Parental source of chromosome imprinting and its relevance for X chromosome inactivation

1984 • 92 citations

Further observations on the hairpin-tail (Thp) mutation in the mouse

1974 • 88 citations

Chromosome maps of man and mouse

1981 • 87 citations

Maternal Thp lethality in the mouse is a nuclear, not cytoplasmic, defect

1984 • 79 citations

CHARACTERIZATION OF A RECOMBINANT MOUSE t HAPLOTYPE THAT EXPRESSES A DOMINANT LETHAL MATERNAL EFFECT

1984 • 76 citations

Meiotic disjunction in mouse translocations and the determination of centromere position

1971 • 75 citations

Radiation-induced mutations at mouse hemoglobin loci.

1976 • 75 citations

AN ANALYSIS OF TRANSLOCATIONS IN THE MOUSE

1946 • 71 citations

Factors affecting the observed number of young resulting from adjacent-2 disjunction in mice carrying a translocation

1977 • 53 citations

Parthenogenesis, homozygosity, and cloning in mammals

1982 • 51 citations

Genetic analysis of induced deletions and of spontaneous nondisjuction involving chromosome 2 of the mouse

1960 • 45 citations

Chromosome maps of man and mouse II

1984 • 39 citations

THE T6 TRANSLOCATION IN THE MOUSE: ITS USE IN TRISOMY MAPPING, CENTROMERE LOCALIZATION, AND CYTOLOGICAL IDENTIFICATION OF LINKAGE GROUP III

1972 • 34 citations

A genetic method for measuring non-disjunction in mice with Robertsonian translocations

1975 • 24 citations

The use of Robertsonian translocations in the mouse for studies on non-disjunction

1982 • 12 citations

Genetic tests for autosomal non-disjunction and chromosome loss in mice

1984 • 12 citations

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