Mary Frances Lyon

Mary Frances Lyon's AcademicInfluence.com Rankings

Mary Frances Lyon

Biology

#2483

World Rank

#3929

Historical Rank

Genetics

#160

World Rank

#199

Historical Rank

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Biology

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Mary Frances Lyon's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Gene Action in the X-chromosome of the Mouse (Mus musculus L.) (1961) (3678)
Sex chromatin and gene action in the mammalian X-chromosome. (1962) (981)
Genetic variants and strains of the laboratory mouse (1989) (690)
X‐CHROMOSOME INACTIVATION AND DEVELOPMENTAL PATTERNS IN MAMMALS (1972) (594)
X-linked Gene for Testicular Feminization in the Mouse (1970) (551)
X-Chromosome inactivation: a repeat hypothesis (1998) (431)
Small eyes (Sey): a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouse. (1986) (398)
X-chromosome inactivation (1999) (248)
The Mouse Pink-Eyed Dilution Gene: Association with Human Prader-Willi and Angelman Syndromes (1992) (220)
Age related reactivation of an X-linked gene (1987) (218)
Chromosome maps of man and mouse. IV (1989) (207)
Mouse chromosome atlas. (1990) (204)
Transmission ratio distortion in mouse t-haplotypes is due to multiple distorter genes acting on a responder locus (1984) (202)
The scurfy mouse mutant has previously unrecognized hematological abnormalities and resembles Wiskott-Aldrich syndrome. (1990) (198)
An 85-kb tandem triplication in the slow Wallerian degeneration (Wlds) mouse. (1998) (197)
Eighth International Workshop on Human Gene Mapping (1984) (195)
Transmission ratio distortion in mice. (2003) (164)
Chromosomal and Subchromosomal Inactivation (1968) (163)
Male sterility of the mouse t-complex is due to homozygosity of the distorter genes (1986) (154)
Chromosome maps of man and mouse, III. (1987) (148)
A MOUSE TRANSLOCATION SUPPRESSING SEX-LINKED VARIEGATION. (1964) (144)
Review Lecture: Mechanisms and evolutionary origins of variable X-chromosome activity in mammals (1974) (138)
Biological Sciences: X Chromosome Inactivation studied by Injection of a Single Cell into the Mouse Blastocyst (1971) (135)
Genetic variants and strains of the laboratory mouse. Volume 2. (1996) (134)
Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification. (2004) (127)
Clonal analysis of X-chromosome inactivation and the origin of the germ line in the mouse embryo. (1985) (124)
The Gy mutation: another cause of X-linked hypophosphatemia in mouse. (1986) (124)
Autosomal translocations causing male sterility and viable aneuploidy in the mouse. (1966) (119)
A gene affecting Wallerian nerve degeneration maps distally on mouse chromosome 4. (1993) (119)
Some milestones in the history of X-chromosome inactivation. (1992) (113)
X‐Linked testicular feminization in the mouse as a non‐inducible regulatory mutation of the Jacob‐Monod type (1970) (111)
Possible mechanisms of X chromosome inactivation. (1971) (110)
LINE-1 elements and X chromosome inactivation: a function for "junk" DNA? (2000) (109)
A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract. (1998) (109)
Gene and chromosome mutation after large fractionated or unfractionated radiation doses to mouse spermatogonia. (1969) (107)
Molecular probes define different regions of the mouse t complex (1985) (103)
A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice. (1998) (97)
A new allele sash (Wsh) at the W-locus and a spontaneous recessive lethal in mice. (1982) (97)
Reproductive lifespan in irradiated and unirradiated chromosomally XO mice. (1973) (96)
Direct evidence of the capacity of the XY germ cell in the mouse to become an oocyte (1977) (95)
Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse. (1992) (95)
The overall rates of dominant and recessive lethal and visible mutation induced by spermatogonial X-irradiation of mice (1964) (94)
Parental source of chromosome imprinting and its relevance for X chromosome inactivation. (1984) (86)
The Lyon and the LINE hypothesis. (2003) (84)
Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death. (2000) (84)
Chromosome maps of man and mouse. (1981) (84)
Induction of congenital anomalies in offspring of female mice exposed to varying doses of X-rays. (1982) (83)
Evolution of X-chromosome inactivation in mammals (1974) (82)
An inherited kidney disease of mice resembling human nephronophthisis. (1971) (80)
Mutation rates at a new set of specific loci in the mouse. (1966) (80)
Evidence that preaxial polydactyly in the Doublefoot mutant is due to ectopic Indian Hedgehog signaling. (1998) (79)
Epigenetic inheritance in mammals. (1993) (79)
Identification of a mutation in the MP19 gene, Lim2, in the cataractous mouse mutant To3. (1997) (79)
Attempts to test the inactive-X theory of dosage compensation in mammals (1963) (78)
Information on the nature of t -haplotypes from the interaction of mutant haplotypes in male fertility and segregation ratio (1977) (78)
t-Haplotypes of the mouse may involve a change in intercalary DNA (1979) (77)
Chromosome maps of man and mouse (1981) (76)
X-chromosome inactivation in extra-embryonic membranes of diploid parthenogenetic mouse embryos demonstrated by differential staining (1980) (74)
The t complex polypeptide 1 (TCP-1) is associated with the cytoplasmic aspect of Golgi membranes (1989) (74)
Hereditary absence of otoliths in the house mouse (1951) (71)
Normal spermatozoa from androgen-resistant germ cells of chimaeric mice and the role of androgen in spermatogenesis (1975) (70)
Investigations of the nature of t-alleles in the mouse (1964) (68)
Reduced reproductive performance in androgen-resistant Tfm/Tfm female mice (1980) (67)
Investigations of the nature of t-alleles in the mouse (1964) (64)
The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome (1987) (62)
Long-term storage of mouse embryos at —196 °C: the effect of background radiation (1977) (61)
The sex chromosome in the house mouse (1947) (60)
A mouse translocation giving a metacentric marker chromosome. (1967) (60)
Factors affecting the observed number of young resulting from adjacent-2 disjunction in mice carrying a translocation. (1977) (59)
Further studies on the effect of radiation during the storage of frozen 8-cell mouse embryos at −196°C (1984) (58)
Mutagenic effects of repeated small radiation doses to mouse spermatogonia. I. Specific-locus mutation rates. (1972) (58)
X-chromosome inactivation as a system of gene dosage compensation to regulate gene expression. (1989) (58)
Dose-rate and mutation frequency after irradiation of mouse spermatogonia. (1972) (58)
Expression of H–Y (male) antigen in phenotypically female Tfm/Y mice (1975) (57)
HEREDITARY HAIR LOSS IN THE TUFTED MUTANT OF THE HOUSE MOUSE (1956) (56)
Crossing-over in mice heterozygous for t-alleles (1959) (55)
Genetic activity of sex chromosomes in somatic cells of mammals. (1970) (54)
Genetic Hazard of Ionizing Radiations (1958) (54)
Tenth International Workshop on Human Gene Mapping (1988) (53)
Dose-response curves for radiation-induced gene mutations in mouse oocytes and their interpretation. (1979) (52)
DNA Replication and Genetic Expression in Female Mice with Morphologically Distinguishable X Chromosomes (1965) (52)
Analysis of male sterile mutations in the mouse using haploid stage expressed cDNA probes. (1984) (51)
The induction by X-rays of chromosome aberrations in male Guinea-pigs, rabbits and golden hamsters. III. Dose-response relationship after single doses of X-rays to spermatogonia. (1975) (51)
A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding. (2003) (51)
Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths. (1998) (50)
Imprinting and X-chromosome inactivation. (1999) (49)
The Genetic Basis of Transmission-Ratio Distortion and Male Sterility Due to the t Complex (1991) (48)
Induction of congenital malformations in the offspring of male mice treated with X-rays at pre-meiotic and post-meiotic stages. (1984) (48)
Do LINEs Have a Role in X-Chromosome Inactivation? (2006) (48)
Derivation of mutant t-haplotypes of the mouse by presumed duplication or deletion. (1977) (47)
Standardized Nomenclature for Inbred Strains of Mice Second Listing Prepared by The Committee on Standardized Genetic Nomenclature for Mice (1960) (46)
Sensitivity of various germ-cell stages to environmental mutagens. (1981) (45)
Lens opacity: a new gene for congenital cataract on chromosome 10 of the mouse. (1981) (44)
Isolation and characterisation of a testis-expressed developmentally regulated gene from the distal inversion of the mouse t-complex. (1991) (44)
Twirler: a mutant affecting the inner ear of the house mouse. (1958) (44)
Pinpointing the centre (1996) (43)
Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses. (1987) (41)
The submaxillary salivary glands as test organs for response to androgen in mice with testicular feminization. (1973) (41)
Mapping of six dominant cataract genes in the mouse. (1994) (40)
Induction of congenital malformation in mice by parental irradiation: transmission to later generations. (1988) (40)
Some evidence concerning the “Mutational load” in inbred strains of mice (1959) (40)
Re-establishment of breeding stocks of mutant and inbred strains of mice from embryos stored at –196 °C for prolonged periods (1977) (39)
Induction of translocations in mouse spermatogonia by X-ray doses divided into many small fractions. (1970) (39)
X chromosome inactivation in diploid parthenogenetic mouse embryos (1978) (38)
An investigation into the possible genetic hazards of ultrasound. (1974) (38)
A REVISION OF THE STANDARDIZED GENETIC NOMENCLATURE FOR MICE. (1963) (38)
Investigations of the nature of t-alleles in the mouse (1964) (37)
Failure of mercaptoethylamine to protect against the mutagenic effects of radiation. II. Experiments with mice. (1953) (37)
Deletion of mouse t-complex distorter-1 produces an effect like that of the t-form of the distorter. (1992) (36)
Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. (1969) (36)
The genetic sensitivity to x-rays of mouse foetal gonads. (1960) (36)
The t- complex and the genetical control of development. (1981) (36)
Evidence from Tfm/0 that Androgen is Inessential for Reproduction in Female Mice (1974) (35)
Dose-response data for X-ray induced translocations in spermatogonia of Rhesus monkeys. (1976) (35)
Dose-response curve for x-ray-induced translocations in mouse spermatogonia. I. Single doses. (1970) (35)
The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes. (1988) (35)
The induction of chromosome aberrations in mouse dictyate oocytes by X-rays and chemical mutagens. (1977) (33)
A presumed deletion covering the W and Ph loci of the mouse. (1984) (33)
The positions of the centromeres in linkage groups II and IX of the mouse. (1968) (32)
X-ray induced dominant lethal mutations in mature and immature oocytes of guinea-pigs and golden hamsters. (1975) (31)
Sonic hedgehog is not required for polarising activity in the Doublefoot mutant mouse limb bud. (1998) (31)
X-chromosome inactivation spreads itself: effects in autosomes. (1998) (31)
Biology of mammalian germ cell mutagenesis (1990) (31)
Two new cataract loci, Ccw and To3, and further mapping of the Npp and Opj cataracts in the mouse. (1996) (30)
A further mutation of the mottled type in the house mouse. (1960) (30)
Lack of evidence that inactivation of the mouse X-chromosome is incomplete. (1966) (29)
The Development of the Otoliths of the Mouse (1955) (29)
Unusual molecular characteristics of a repeat sequence island within a Giemsa-positive band on the mouse X chromosome. (1990) (28)
Occurrences and linkage relations of the mutant "extra-toes" in the mouse. (1967) (27)
Maternal histidine metabolism and its effect on foetal development in the mouse (1977) (27)
Induction of mutations in mice by chronic gamma irradiation; interim report. (1956) (27)
Species comparisons concerning radiation-induced dominant lethals and chromosome aberrations. (1971) (26)
Doublefoot: a new mouse mutant affecting development of limbs and head. (1996) (26)
The Developmental Origin of Hereditary Absence of Otoliths in Mice (1955) (26)
A comparative study of the coats of chimaeric mice and those of heterozygotes for X-linked genes. (1972) (25)
Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop). (2000) (25)
Specific locus mutation rates after repeated small radiation doses to mouse oocytes. (1975) (25)
A personal history of the mouse genome. (2002) (24)
A genetic method for measuring non-disjunction in mice with Robertsonian translocations. (1975) (24)
X-ray-induced dominant lethal mutations in male guinea-pigs, hamsters and rabbits. (1970) (24)
ATAXIA — A NEW RECESSIVE MUTANT OF THE HOUSE MOUSE (1955) (24)
Do the H-2 and T-Loci of the Mouse have a Function in the Haploid Phase of Sperm ? (1972) (24)
Mapping of four mouse genes encoding eye lens-specific structural, gap junction, and integral membrane proteins: Cryba1 (crystallin beta A3/A1), Crybb2 (crystallin beta B2), Gja8 (MP70), and Lim2 (MP19). (1995) (24)
Distorter genes of the mouse t-complex impair male fertility when heterozygous. (1987) (24)
X-chromosome inactivation in mammals. (1966) (24)
Failure of Mercaptoethylamine to Protectagainst the Mutagenic Effects of RadiationI: Experiments with Drosophila (1953) (23)
The quest for the X-inactivation centre. (1991) (23)
An attempt to estimate the induction by x-rays of recessive lethal and visible mutations in mice. (1961) (23)
Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes. (1990) (22)
LYONISATION OF THE X CHROMOSOME. (1963) (22)
Distribution of crossing-over in mouse chromosomes. (1976) (21)
Evidence for a defective seminiferous tubule barrier in testes of Tfm and Sxr mice. (1983) (21)
Dose-response curve for the yield of translocations in mouse spermatogonia after repeated small radiation doses. (1970) (21)
Differences in or near the responder region of complete and partial mouse t-haplotypes. (1987) (21)
X chromosomes and dosage compensation (1986) (20)
Localization of the Hprt locus by in situ hybridization and distribution of loci on the mouse X-chromosome. (1987) (20)
Long-term storage of frozen mouse embryos under increased background irradiation. (1977) (19)
A recessive allele of the mouse agouti locus showing lethality with yellow, Ay. (1985) (19)
Mutagenic effects of repeated small radiation doses to mouse spermatogonia. II. Translocation yield at various dose intervals. (1972) (19)
Foam-cell Reticulosis of Mice: An Inherited Condition Resembling Gaucher's and Niemann-Pick Diseases (1965) (19)
The X Inactivation Centre and X Chromosome Imprinting (1994) (18)
Extent of the mouse t complex and its inversions shown by in situ hybridization (2004) (17)
Long-term storage of eight-cell mouse embryos at −196°C (1986) (17)
Mouse globin gene nomenclature. (1988) (17)
Cytological study of Searle's X-autosome translocation in Mus musculus (1965) (17)
Discrimination between the effects of X-ray irradiation of the mouse oocyte and uterus on the induction of dominant lethals and congenital anomalies. (1985) (16)
Centennial of Wilhelm Waldeyer’s introduction of the term “chromosome” (1988) (16)
Induction of congenital malformations in the offspring of mutagen treated mice. (1986) (16)
Use of an inversion to test for induced X-linked lethals in mice. (1982) (16)
A NEW DOMINANT T-ALLELE IN THE HOUSE MOUSE (1959) (16)
Complementation reactions of a lethal mouse t-haplotype believed to include a deletion. (1979) (16)
Linkage relations and some pleiotropic effects of the dreher mutant of the house mouse (1961) (16)
Search for differences among t haplotypes in distorter and responder genes. (1990) (16)
Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1. (1994) (16)
Further studies on the effect of radiation during the storage of frozen 8-cell mouse embryos at -196 degrees C. (1984) (16)
GENETIC FACTORS ON THE X CHROMOSOME (1961) (16)
The induction by X-rays of chromosome aberrations in male Guinea-pigs and golden hamsters. IV. Dose response for spermatogonia treated with fractionated doses. (1975) (16)
A UK-centric history of studies on the mouse t-complex. (2000) (16)
Gene-tagged chromosome translocations in eleven stocks of mice (2008) (15)
Induction of sterility in male mice by chronic gamma irradiation. (1954) (15)
X Chromosome Inactivation: No longer ‘all-or-none’ (2005) (15)
Mouse chromosome 17 (2004) (14)
Morphogenesis of Doublefoot (Dbf), a mouse mutant with polydactyly and craniofacial defects (1998) (14)
Evolution of the X chromosome (1990) (13)
X-chromosome inactivation. Pinpointing the centre. (1996) (13)
Effect of X-rays on the mutation of t-alleles in the mouse (1960) (13)
Order of loci on the X-chromosome of the mouse. (1966) (13)
Investigating inborn errors of phenylalanine metabolism by efficient mutagenesis of the mouse germ line. (1990) (13)
A test for mutagenicity of caffeine in mice (1962) (13)
Elucidating mouse transmission ratio distortion (2005) (12)
Hereditary effects of radiation: some evidence from animal experiments (1987) (12)
Lack of inactivation of a mouse X-linked gene physically separated from the inactivation centre. (1986) (12)
A true hermaphrodite mouse presumed to be an XO-XY mosaic. (1969) (12)
Reproductive capacity and dominant lethal mutations in female guinea-pigs and Djungarian hamsters following X-rays or chemical mutagens. (1979) (11)
Genetic differences between two substrains of the inbred 101 mouse strain. (1984) (11)
Narrowing the critical regions for mouse t complex transmission ratio distortion factors by use of deletions. (2000) (11)
Molecular genetics of X-chromosome inactivation (1996) (11)
The induction by X-rays of chromosome aberrations in male guinea-pigs, golden hamsters and rabbits. II. Properties of translocations induced in post-meiotic stages. (1975) (11)
Chromosome maps of man and mouse II (1984) (10)
Discrimination between the effects of X-ray irradiation of the mouse oocyte and uterus on the induction of dominant lethals and congenital anomalies. II. Localised irradiation experiments. (1985) (10)
Endogenous retroviral insertion in Cryge in the mouse No3 cataract mutant. (2007) (10)
Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolution. (1988) (10)
Genetic differences between substrains of the inbred mouse strain 101 and designation of a new strain 102. (1985) (10)
Genetic analysis of the organic cation transporter genes Orct2/Slc22a2 and Orct3/Slc22a3 reduces the critical region for the t haplotype mutant tw73 to 200 kb (2001) (10)
Symposium No. 6: Gene and chromosome inactivation. Introduction by the Chairman. (1974) (10)
The mutagenic effect of triethylenemelamine (tem) on germ cells of male golden hamsters and guinea pigs. (1975) (9)
The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the tw18 or th20 deletions. (1995) (8)
Controlling the X chromosome (1993) (8)
THE ARRANGEMENT OF H‐2 CLASS I GENES IN MOUSE t HAPLOTYPES (1985) (8)
Location of the t complex on mouse chromosome 17 by in situ hybridization with Tcp-1 (2004) (8)
Zigzag, a genetic defect of the horizontal canals in the mouse. (1960) (8)
A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35. (2001) (8)
Isolation and characterization of a cDNA clone corresponding to the mouse t-complex gene Tcp-1x. (1991) (7)
L. C. Dunn and mouse genetic mapping. (1990) (7)
The mutagenic effect of repeated small radiation doses to mouse spermatogonia. 3. Does repeated irradiation reduce translocation yield from a large radiation dose? (1973) (7)
Problems in Extrapolation of Animal Data to Humans (1983) (7)
Evolution of mammalian sex chromosomes. (1994) (7)
The activity of the sex chromosomes in mammals. (1970) (7)
Experimental work on induced mutations. (1988) (7)
Long-term storage of mouse embryos at--196 degrees C: the effect of background radiation. (1977) (7)
X Chromosome Inactivation and Imprinting (1996) (6)
Human genitics: Measuring mutation in man (1985) (6)
Long-term storage of eight-cell mouse embryos at - 196 degrees C. (1986) (6)
An additional type of male sterility and inherited urinary obstruction in mice with the t-haplotype th7. (1996) (6)
Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome (2018) (6)
The major brain isoform of Kif1b lacks the putative mitochondria-binding domain (1999) (6)
The long-range mapping of mammalian chromosomes. (1988) (6)
Further genetic studies of eleven translocations in the mouse (1956) (5)
Absence of otoliths in the mouse: An effect of the pallid mutant (1953) (5)
An answer to a complex problem: cloning the mouse t-complex responder (2000) (5)
Identification of a mutation in the MP 19 gene , Lim 2 , in the cataractous mouse mutant To 3 (1997) (5)
H-2 typing of mutants of thet6 haplotype in the mouse (1978) (4)
Nomenclature for homoeobox-containing genes (1987) (4)
Sex chromosome activity in germ cells. (1974) (4)
Mosaic mutants induced by ethylnitrosourea in late germ cells of mice. (1990) (4)
Role of X and Y chromosomes in mammalian sex determination and differentiation. (1974) (3)
Mouse Chromosome 17 (2004) (3)
Failure of mercaptoethylamine to protect against the mutagenic effects of radiation. I. Experiments with Drosophila. (1953) (3)
X-inactivation: controlling the X chromosome. (1993) (2)
Stage of action of the litter-size effect on absence of otoliths in mice (2004) (2)
Genetic basis of male sterility and segregation distortion due to t-haplotypes in the mouse. Abstr. (1982) (2)
FORM-CELL RETICULOSIS OF MICE: AN INHERITED CONDITION RESEMBLING GAUCHER'S AND NIERMANN-PICK DISEASES. (1965) (2)
A search for strain differences in response of mice to mutagenesis by thio-TEPA. (1991) (2)
How X-chromosome inactivation was discovered (2007) (2)
STANDARDIZED GENETIC NOMENCLATURE FOR MICE: PAST, PRESENT, AND FUTURE (1978) (2)
The history of X-chromosome inactivation and relation of recent findings to understanding of human X-linked conditions. (1995) (2)
James Neel and the doubling dose concept. (2003) (2)
Mutagenicity of Selected Chemicals in In Vivo Cytogenetic Assays (1981) (2)
High-resolution mapping of the genes Kcnb3 and Ly63 on distal mouse Chromosome 4 (1996) (2)
The gene triplet Rw W Ph controls murine haematopoiesis (1985) (2)
X-LINKED FACTOR IN ACQUIRED IMMUNODEFICIENCY SYNDROME? (1983) (2)
Regulation of testicular postmeiotic genes. (1990) (2)
Manipulation of the mouse genome by homologous recombination. (1990) (1)
Problems of extrapolation from experimental data to human mutagenesis. (1983) (1)
Use of heritable mutations in the analysis of meiosis. (1990) (1)
X-chromosome Inactivation and Disease (2006) (1)
THE MOLECULAR MAPPING OF THE MOUSE X-CHROMOSOME (1986) (1)
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 17. (1993) (1)
Mouse chromosome 17 (2004) (1)
The nature of t-alleles in the mouse. Abstr. (1961) (1)
Isolation and characterisation of a testis-expressed developmental ly regulated gene from the distal inversion of the mouse f-complex (2005) (1)
7 – X-Chromosome Inactivation (1994) (1)
Partial Sex Linkage in the Mouse (1954) (1)
Quantification of germ-cell risk associated with the induction of heritable translocations. (1990) (0)
Isolation and characterization of a cDNA clone corresponding to the mouse ^-complex gene Tcp-lx (2008) (0)
Genetic nomenclature and nomenclatorial rules in the mouse (1977) (0)
Construction ofa detailed molecular map ofthemouse X chromosome bymicroclonmg andinterspecific crosses (1987) (0)
A Historical Perspective on Ideas on X-Chromosome Inactivation (2007) (0)
Bruce Cattanach: Mutagenesis and where it can lead you (1998) (0)
Genetics. Evolution of the X chromosome. (1990) (0)
Further mapping data on extra-toes-spotting, Xs. (1990) (0)
A true hermaphrodite mouse presumed to be an XO/XY mosaic. (1969) (0)
The Prevention and avoidance of genetic disease : proceedings of a Royal Society discussion meeting held on 29 and 30 april 1987 (1988) (0)
Correction and Clarification: Unusual Molecular Characteristics of a Repeat Sequence Island within a Giemsa-Positive Band on the Mouse X Chromosome (1990) (0)
Effect of imprinting on analysis of genetic mutations. (1990) (0)
Genetic mapping of the doublefoot (Dbf) mutation (1997) (0)
Nuf mice with an activating calcium sensing receptor mutation, Leu723Gln, have hypercalciuria and diabetes insipidus (2009) (0)
From the editor’s desk (2015) (0)
Flaked maize as a source of tapeworm infestation in mice. (1960) (0)
Controlling the X chromosome Inactivation of the mammalian X chromosome begins at the X-inactivation centre. The gene Xist has a unique expression pattern, suggesting that it may be a functional part of the centre. (1993) (0)
Nuf mice with an activating calcium sensing receptor mutation, Leu723Gln, have a metabolic acidosis and impaired urinary acidification (2010) (0)
Vertebrate Sex Chromosomes. Edited by N. TAKAGI. S. Karger AG. 2003. 352 pages. ISBN 3 8055 7637 4. Price $138.25 (hardback). (2004) (0)
Sex Determination (1967) (0)
Mutant mice and their use in research. (1963) (0)
Present concepts concerning x-chromosome inactivation in mammals. Abstr. (1967) (0)
Margaret C. Green (1995) (0)
Relative problems of assessing the genetic hazards of radiation and chemicals (1979) (0)

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