Muriel Trask Davisson

Muriel Trask Davisson's AcademicInfluence.com Rankings

Biology

#11948

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#15389

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Neuroscience

#1977

World Rank

#2033

Historical Rank

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Biology

Muriel Trask Davisson's Degrees

PhD Neuroscience University of California, Berkeley
Bachelors Biology Stanford University

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Muriel Trask Davisson'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

A mouse model for Down syndrome exhibits learning and behaviour deficits (1995) (875)
Retinal degeneration mutants in the mouse (2002) (740)
Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice (1997) (724)
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice. (1998) (544)
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration (2006) (537)
The Mouse in biomedical research (2007) (459)
Segmental trisomy of murine chromosome 16: a new model system for studying Down syndrome. (1990) (342)
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4. (2001) (329)
Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene (2007) (322)
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. (1993) (319)
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice (1999) (297)
Segmental trisomy as a mouse model for Down syndrome. (1993) (291)
Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency. (1989) (278)
Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage. (1994) (273)
VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P2 in yeast and mouse (2008) (227)
Report of the committee on comparative mapping. (1982) (227)
Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions. (2003) (207)
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA). (2005) (205)
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse. (2000) (205)
The nob2 mouse, a null mutation in Cacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses (2006) (204)
Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures (1990) (199)
Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome (2008) (165)
Motor dysfunction in a mouse model for Down syndrome (1999) (164)
Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease) (1993) (158)
Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome (2002) (157)
Know thy mouse. (2006) (157)
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn (2011) (144)
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes. (1999) (142)
A standardized nomenclature for endogenous mouse mammary tumor viruses (1987) (139)
MOUSE MODEL OF SUBRETINAL NEOVASCULARIZATION WITH CHOROIDAL ANASTOMOSIS (2003) (138)
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities. (1989) (130)
The Mouse Genome Database (MGD): expanding genetic and genomic resources for the laboratory mouse (2000) (126)
Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype (1997) (116)
A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death. (1994) (116)
Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcripts. (1994) (114)
‘Wasted’, a new mutant of the mouse with abnormalities characteristic of ataxia telangiectasia (1982) (107)
Revised nomenclature for strain 129 mice (1999) (106)
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens. (2000) (105)
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals. (2000) (100)
Recombination suppression by heterozygous Robertsonian chromosomes in the mouse. (1993) (98)
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly. (1998) (98)
Ts65Dn – localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome (2001) (93)
Autosomal aneuploidy in mice: Generation and developmental consequences (1986) (88)
Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome. (2003) (87)
Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse. (2006) (83)
Behavioral, cognitive and biochemical responses to different environmental conditions in male Ts65Dn mice, a model of Down syndrome (2005) (82)
A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice. (2002) (81)
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration (1996) (76)
Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins. (1992) (74)
An improved method for preparing G-banded chromosomes from mouse peripheral blood. (1987) (73)
A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis (2003) (73)
The sequence of human chromosome 21 and implications for research into Down syndrome (2000) (72)
Sandy: a new mouse model for platelet storage pool deficiency. (1991) (72)
Report of the committee on comparative mapping. (1980) (70)
Mouse models of ocular diseases (2005) (67)
The Mouse Genome Database (MGD): genetic and genomic information about the laboratory mouse. The Mouse Genome Database Group (1999) (66)
X-linked genetic homologies between mouse and man. (1987) (65)
Report of the comparative committee for human, mouse and other rodents (1991) (64)
Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b rd1 (2010) (63)
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract. (2000) (63)
Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac. (1995) (62)
Identification and genetic mapping of a new polycystic kidney disease on mouse chromosome 8. (1997) (59)
Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis. (2002) (59)
Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice (2006) (59)
The Mouse Genome Database (MGD). A comprehensive public resource of genetic, phenotypic and genomic data. The Mouse Genome Informatics Group (1997) (58)
The effects of piracetam on cognitive performance in a mouse model of Down's syndrome (2002) (58)
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice (2004) (56)
Transgenic and knockout databases Behavioral profiles of mouse mutants (2001) (51)
Synaptonemal complex analysis of mouse chromosomal rearrangements (2004) (51)
Cytogenetic analysis of pseudolinkage of ldh Loci in the teleost genus salvelinus. (1973) (50)
Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis. (1997) (50)
Mouse models of Down syndrome (2005) (49)
A mouse model for Meckel syndrome type 3. (2009) (48)
The locus map of the mouse. (1990) (47)
FIMRe: Federation of International Mouse Resources: Global Networking of Resource Centers (2006) (47)
The mouse polycystic kidney disease mutation (cpk) is located on proximal chromosome 12. (1991) (46)
A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11. (1989) (46)
Rules and guidelines for nomenclature of mouse genes. International Committee on Standardized Genetic Nomenclature for Mice. (1994) (45)
A method for preparing chromosomes from peripheral blood in the mouse. (1975) (45)
A Survey of Neurological Mutant Mice. pp 99–109 (1988) (42)
Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease. (2013) (42)
Genetic and physical maps of the stargazer locus on mouse chromosome 15. (1997) (42)
Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice. (1990) (41)
Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse (2011) (41)
Neuromuscular degeneration (nmd): a mutation on mouse Chromosome 19 that causes motor neuron degeneration (1995) (40)
A-to-I pre-mRNA editing of the serotonin 2C receptor: comparisons among inbred mouse strains. (2006) (40)
Linkage map of the mouse. (1986) (40)
Operant Conditioning in the Ts65Dn Mouse: Learning (2004) (39)
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiency. (1994) (38)
The mouse mutation severe combined immune deficiency (scid) is on chromosome 16 (2006) (38)
Report of the comparative subcommittee for human and mouse homologies. (1990) (38)
Report of the committee on comparative mapping. (1979) (37)
Comparative genome organization of vertebrates. The First International Workshop on Comparative Genome Organization. (1996) (37)
A pericentric inversion in the mouse. (1981) (37)
Rules and guidelines for mouse gene nomenclature: a condensed version. International Committee on Standardized Genetic Nomenclature for Mice. (1997) (35)
A survey of neurological mutant mice. II. Lipid composition of myelinated tissue in possible myelin mutants. (1988) (35)
Prp (proline-rich protein) genes linked to markers Es-12 (esterase-12), Ea-10 (erythrocyte alloantigen), and loci on distal mouse chromosome 6. (1989) (34)
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse. (1999) (33)
Loss of correlations among proteins in brains of the Ts65Dn mouse model of down syndrome. (2012) (33)
The Mouse Genome Database (MGD): a community resource. Status and enhancements. The Mouse Genome Informatics Group (1998) (32)
Evolutionary breakpoints on human chromosome 21. (2001) (32)
The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization. (2000) (32)
Comparative map for mice and humans (2004) (31)
Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse. (1996) (31)
Otitis media in a mouse model for Down syndrome (2009) (31)
Status of the linkage map of the mouse. (1978) (31)
A new allelic series for the underwhite gene on mouse chromosome 15. (1998) (29)
Forebrain overgrowth (fog): a new mutation in the mouse affecting neural tube development. (1997) (28)
The fatty liver dystrophy (fld) mutation (1989) (28)
Building protein interaction maps for Down's syndrome. (2004) (28)
Linkage map of the mouse (Mus musculus). (1980) (28)
Evolution of mammalian carbonic anhydrase loci by tandem duplication: Close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouse (1976) (28)
Mapping of nucleoside phosphorylase (Np-1) and esterase 10 (Es-10) on mouse chromosome 14 (1977) (28)
The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentials. (2010) (27)
Decreased retinal ganglion cell number and misdirected axon growth associated with fissure defects in Bst/+ mutant mice. (1997) (27)
Editing of the serotonin 2C receptor pre-mRNA: Effects of the Morris Water Maze. (2007) (26)
The Jackson Laboratory Mouse Mutant Resource (1990) (26)
Nucleolus organizer regions (1981) (26)
Congenital progressive hydronephrosis in mice: a new recessive mutation. (1988) (26)
Comparative map for mice and humans (2004) (25)
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5. (2003) (25)
Rules and guidelines for genetic nomenclature in mice: excerpted version (1997) (25)
Chromosomal localization of a new mouse lens opacity gene (lop18) (1996) (25)
Genetic and age related models of neurodegeneration in mice: dystrophic axons. (1992) (24)
Biology and Diseases of Mice (2002) (24)
Gonadotropes in a novel rat pituitary tumor cell line, RC-4B/C. Establishment and partial characterization of the cell line (1990) (23)
A survey of neurological mutant mice. I. Lipid composition of myelinated tissue in known myelin mutants. (1988) (23)
The mouse congenital polycystic kidney (cpk) locus maps within 1.3 cM of the chromosome 12 marker D12Nyu2. (1994) (22)
Informatics for mouse genetics and genome mapping. (1998) (22)
Chromosomal banding patterns of two paracentric inversions in mice. (1973) (22)
New mutation causing sterility in the mouse. (1988) (22)
Abstracts for the committee on the genetic constitution of chromosome 1 (1991) (21)
The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15. (1990) (21)
Locus map of the mouse (Mus musculus). (1987) (20)
Comparative Genome Organization of Vertebrates (2009) (20)
Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
Strains, Stocks and Mutant Mice (2012) (19)
The mouse mutation ulnaless on chromosome 2. (1990) (19)
Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
Balding: a new mutation on mouse chromosome 18 causing hair loss and immunological defects. (1994) (19)
Mouse chromosome fragility. (1986) (19)
Chromosomal inversion discovered in C3H/HeJ mice. (2006) (18)
Age exacerbates abnormal protein expression in a mouse model of Down syndrome (2017) (17)
Standard G-banded karyotype. (1981) (17)
Structure and chromosomal location of the mouse medium-chain acyl-CoA dehydrogenase-encoding gene and its promoter. (1996) (16)
Mapping the Bst mutation on mouse Chromosome 16: a model for human optic atrophy (1995) (16)
Genetic localization of Hao-1, blind-sterile (bs), and Emv-13 on mouse chromosome 2. (1992) (15)
The Mouse Gene Map. (1998) (15)
Genes on chromosome 3 of the mouse. (1976) (15)
Synaptonemal complex analysis of mouse chromosomal rearrangements (2004) (15)
Karyotypes of the Teleost Family Esocidae (1972) (15)
Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse (1994) (14)
Mouse chromosome classification by radial basis function network with fast orthogonal search (1998) (14)
A Spontaneous Mutation in Contactin 1 in the Mouse (2011) (13)
A report on the International Nomenclature Workshop held May 1997 at the Jackson Laboratory, Bar Harbor, Maine, U.S.A. (1997) (13)
Centric Fusion and Trisomy for the LDH-B Locus in Brook Trout, Salvelinus fontinalis (1972) (13)
Position of Igl-1, md, and Bst loci on chromosome 16 of the mouse (2004) (12)
Discovery genetics: serendipity in basic research. (2005) (12)
Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region. (1998) (12)
Cerebellar deficient folia (cdf): A new mutation on mouse Chromosome 6 (1997) (11)
Impact of trisomy on fertility and meiosis in male mice. (2007) (11)
RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase gene. (1995) (11)
Report of the committee on comparative mapping. (1988) (11)
Screening mutant mice for inborn errors of metabolism. (1988) (11)
The Jackson Laboratory Induced Mutant Resource. (1994) (11)
Mitotic Chromosome Preparations from Mouse Cells for Karyotyping (2000) (11)
Mouse Models of RP (2007) (10)
Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
C-band polymorphisms in exotic inbred strains of mice: a method for mapping centromeric ends of chromosomes. (1991) (10)
Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
A multipoint genetic linkage map of mouse chromosome 18. (1992) (10)
Identification and genetic mapping of the murine gene and 20 related sequences encoding chromosomal protein HMG-17 (2004) (9)
Love at First Site (2003) (9)
Abstracts for the committee on comparative gene mapping (1991) (9)
Genetic mapping of the murine gene and 14 related sequences encoding chromosomal protein HMG-14 (2004) (9)
Susceptibility to vinblastine-induced aneuploidy and preferential chromosome segregation during meiosis I in Robertsonian heterozygous mice. (1995) (8)
A new dominant neurological mutant induced in the mouse by ethylene oxide. (1990) (8)
A Point Mutation in the Cnga3 Gene Causes Cone Photoreceptor Function Loss (cpfl5) in Mice (2006) (8)
Locus map of the mouse (Mus musculus/domesticus). (1990) (8)
Genetic nomenclature guide. Mouse. (1995) (8)
Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
Centromeric heterochromatin variants. (1996) (7)
Chromosome aberrations associated with induced mutations: effect on mapping new mutations. (1990) (7)
Availability and characterization of transgenic and knockout mice with behavioral manifestations: where to look and what to search for (2001) (7)
Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
Rough fur (ruf). (1990) (7)
A Point Mutation in the Rpe65 Gene Causes Retinal Degeneration (rd12) in Mice (2002) (7)
Linkage of the Igl-1 structural and regulatory genes to Akv-2 on chromosome 16 (2004) (7)
Identification of a missense mutation in the α A-crystallin gene of the lop 18 mouse (7)
Comparative Study of Cultured Limbal Epithelial Cells on a 3T3 Feeder Layer or in Defined Medium (2003) (7)
Genetic mapping of a new homeobox gene to mouse chromosome 7. (1992) (6)
Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
Heterogeneity of B-lymphoid tumors in E mu-myc transgenic mice. (1996) (6)
Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
Standardized Genetic Nomenclature for Mice (1962) (6)
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene (2001) (6)
CHAPTER 3 – Strains, Stocks, and Mutant Mice (2004) (6)
Harlequin (Hw) produces progressive cerebellar cortical atrophy. (1990) (6)
Dorsal dark stripe (dds). (1990) (5)
Trembly-like (Tyl) - a new X-linked mutation in the mouse. (1990) (5)
In collaboration: the Jackson Laboratory Craniofacial Resource. (2003) (5)
Abstracts for the committee on the genetic constitution of chromosome 17 (1991) (5)
Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7 (2002) (5)
Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
A New Mouse Model of Retinal Degeneration (rd11) (2002) (5)
Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3) (1991) (5)
Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
A New Mouse Model of Retinal Degeneration (rd15) With Retinal Outer Plexiform Dystrophy (2005) (5)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Genetic mapping of variable length rDNA segments to centromeric regions of mouse Chromosomes 11, 12, 15, 16, and 18 (2004) (5)
Strategies for managing an ever increasing mutant mouse repository (2006) (5)
CHAPTER 2 – Historical Foundations (2004) (5)
Report on the committee on comparative mapping. (1987) (5)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
A mouse model for retinitis punctata albescens; a new pathologic finding for retinal white dots (1996) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17 (1999) (4)
Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
Dollars and sense: time and cost factors critical to establishing genetically engineered mouse colonies. (1999) (4)
Genetic and phenotypic definition of laboratory mice and rats. What constitutes an acceptable genetic-phenotypic definition. (1999) (4)
Mouse Chromosome 18 (2004) (4)
Report of the committee on comparative mapping. (1978) (4)
Abstracts for the committee on the genetic constitution of chromosome 6 (1991) (4)
Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
Abstracts for the committee on the genetic constitution of chromosome 2 (1991) (4)
Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
Mouse chromosome 18 (2009) (3)
Differences in the metabolism of the aromatic amino acid hydroxylase cofactor, tetrahydrobiopterin, in mutant mice with neurological and immunological defects (1986) (3)
A New Mouse Model of Retinal Degeneration (RD14) Associated With Neurological Defects (2005) (3)
Abstracts for the committee on the genetic constitution of chromosome 12 (1991) (3)
Location of the 9257 and ataxia mutations on mouse Chromosome 18 (1996) (3)
A New Mouse Model of Retinal Degeneration (rd17) (2007) (3)
A Survey of Neurological Mutant Mice. pp 110–122 (1988) (3)
Mouse Genetics & Transgenics: A Practical Approach (1998) (3)
A new mouse mutation causing male sterility and histoincompatibility (1996) (3)
Dense incisors (din): a new mouse mutation on chromosome 16 affecting tooth eruption and body size. (1996) (3)
Abstracts for the committee on the genetic constitution of chromosome 15 (1991) (3)
Abstracts for the committee on chromosomal changes in neoplasia (1991) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Position of the Igl-1 and Bst loci on chromosome 16 of the mouse. (1986) (3)
Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
The stumbler mutation maps to proximal mouse Chromosome 2 (1994) (3)
Abstracts for the committee on the genetic constitution of chromosome 11 (1991) (2)
Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
Abstracts for the committee on the genetic constitution of chromosome 22 (1991) (2)
Selective Loss Of ERG b–Wave Caused By An Autosomal Recessive Mutation In Mice. (2004) (2)
Report of the committee on comparative mapping. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (2)
The Mouse Genome Database and The Gene Expression Database: Genotype to Phenotype (2002) (2)
Analysing mouse chromosomal rearrangements with G-banded chromosomes. (2000) (2)
Index to Volume III (1930) (2)
A New Mouse Model of Retinal Degeneration (rd13) (2005) (2)
Report and abstracts of the ninth international workshop on the molecular biology of human chromosome 21 and Down syndrome. Bar Harbor, Maine, USA. 23-26 September 2000. (2001) (2)
Abstracts for the committee on the genetic constitution of chromosome 16 (1991) (2)
Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
The mouse urate oxidase gene, Uox, maps to distal Chromosome 3 (1997) (1)
Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis. (2015) (1)
Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
Grey intense: a new mouse mutation affecting pigmentation (2000) (1)
Shimmy (shmy), a new mutation on chromosome 14 of the mouse (1994) (1)
A new mouse microphthalmia and cataract condition caused by a transgene integration (1997) (1)
Neuromuscular ataxia: a new spontaneous mutation in the mouse (2000) (1)
Map of "biochemical loci" in the mouse. (1988) (1)
Mouse chromosome 18 (2004) (1)
Abstracts for the committee on the genetic constitution of chromosome 13 (1991) (1)
Contents Vol. 55, 1990 (1990) (1)
Mouse chromosome 18 (2004) (1)
Abstracts for the committee on the genetic constitution of chromosome 10 (1991) (1)
A Gene Responsible for Light-induced Visual Impairment (lvi) in Mice (2003) (1)
Abstracts for the committee on the genetic constitution of the Y chromosome (1991) (1)
A New Mouse Model of a Retinal Detachment With Secondary Angle Closure Glaucoma (2008) (1)
Report of the ninth international workshop on the molecular biology of human chromosome 21 and Down syndrome (2001) (1)
Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
New W allele W73J. (1990) (1)
Corrigendum: Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice (2006) (1)
The mouse genome database: a resource for today and tomorrow. (2000) (1)
Abstracts for the committee on the genetic constitution of chromosome 4 (1991) (1)
Encyclopedia of the mouse genome VII. Mouse chromosome 18. (1998) (1)
Erratum to: Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn (2011) (1)
Abstracts for the committee on the genetic constitution of chromosome 9 (1991) (1)
The use of comparative mapping to identify loci involved in human carcinogenesis. (1990) (1)
Abstracts for the committee on the genetic constitution of chromosome 7 (2004) (1)
A New Mouse Model of Cone Photoreceptor Function Loss (cpfl6) Associated With the Targeted Hcn1 Gene Mutation (2006) (1)
Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10. (2004) (1)
CHAPTER 21 – Databases, Internet Resources, and Genetic Nomenclature (2002) (0)
Resolution of the staggerer (sg) mutation from the neural cell adhesion molecule locus (Ncam) on mouse Chromosome 9 (2004) (0)
Contents, Vol. 32, 1982 (1982) (0)
Mouse chromosome 18 (2009) (0)
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 18. (1993) (0)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 2 of 3) (2004) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
Contents, Vol. 37, 1984 (1984) (0)
Subject index Vol. 46, 1987 (1987) (0)
Abstracts dscribing resources, technological and other developments (1991) (0)
Nuts and Bolts of Chromosomes (1989) (0)
Index to Volume IV (1964) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Giemsa Banding, Mouse Chromosomes (2001) (0)
Book Review Index Vol. 12, 1973 (1973) (0)
THE FATE OF UNPAIRED CHROMATIN DURING MALE MEIOSIS IN MICE (2007) (0)
Index to Volume I (1907) (0)
Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
Encyclopedia of the mouse genome V. Mouse chromosome 18. (1996) (0)
Index by Keyword (1989) (0)
Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
Referees for volume 29 (1991) (0)
Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
Abstracts for the committee on the genetic constitution of chromosome 19 (1991) (0)
Subject Index Vol. 25, 1979 (1979) (0)
Subject Index Vol. 57, 1991 (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 5 (1991) (0)
Referees for volume 29 (2004) (0)
Abstracts for the comparative subcommittee on human and mouse homologies (1991) (0)
Neuromuscu lar degenerat ion ( nmd ) : a mutat ion on mouse (2004) (0)
Expanded conserved linkage group between human 16p13 and the Scid region of the mouse chromosome 16 (1994) (0)
Nomenclature of Genetics, Mouse (2001) (0)
Embryonic Stem Cells from a Mouse Down Syndrome Model Have Impaired Proliferation and Increased Oxidative Stress. (2011) (0)
Chapter 9 – Cytogenetics (2007) (0)
Catalog of mapped human gene markers. (1980) (0)
Mouse models and genetic approaches to understanding retinal disorders (1996) (0)
Chapter 7 – Gene Mapping (2007) (0)
Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
Abstracts for the committee on clinical disorders and chromosomal deletion syndromes (1991) (0)
Effect of the mouse scid mutation on meiotic recombination (1996) (0)
Subject Index Vol. 32, 1982 (1982) (0)
Abstracts for the committee on linkage and gene order (1991) (0)
A Note on Standardized Genetic Nomenclature for Mice (1997) (0)
Index to Volume II (1903) (0)
Abstracts for the committee on the genetic constitution of chromosome 20 (1991) (0)
Abstractsfor the informatics committee (1991) (0)
Centromeric heterochromatin (C-band) variants. (1981) (0)
Abstracts for the committee on the genetic constitution of chromosome 18 (1991) (0)
Index of GDB source ID numbers (1991) (0)
P1-083 The Alzheimer’s disease mouse model resource (2006) (0)
Abstractsfor the DNA committee (1991) (0)
Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
Abstracts for the committee on the genetic constitution of chromosome 21 (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 8 (1991) (0)
Characterization of a Mouse with /O-Glucuronidase Deficiency (1989) (0)
Contributors for Volume III (2007) (0)
Subject Index Vol. 93, 2001 (2001) (0)
Centralized mouse repositories (2012) (0)
Cumulative Index (2007) (0)
A New Mouse Model Of A Late Onset Retinal Degeneration (2008) (0)
Report of the Committee on Comparative Mapping. (1984) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Index by Abstract Number (1989) (0)
COMPARATIVE PHYSICAL, RECOMBINATIONAL AND BIOLOGICAL MAPPING OF MOUSE CHR16 AND HUMAN CHR21 (HSA21) (1995) (0)
Subject Index Vol. 22, 1978 (1978) (0)
Juvenile bare: a new hair loss mutation on chromosome 7 of the mouse. (1998) (0)
The benefits of strain donation. (2006) (0)
Abstract 5267: Mouse models of cancer at The Jackson Laboratory Repository (2012) (0)
P2-065 Mouse models of alzheimer's disease in the induced mutant resource (2004) (0)
Chromosomal Localization of a New Mouse Lens Opacity Gene (lop18): Volume36,Number 1 (1996), pages 171–173 (1997) (0)
Repositories of mouse mutations and inbred, congenic, and recombinant inbred strains. (2000) (0)
Abstracts for the committee on the genetic constitution of chromosome 14 (1991) (0)
Contents Vol. 93, 2001 (2001) (0)
Subject Index Vol. 58, 1991 (1991) (0)
Abstracts for the committee on the mitochondrial genome (1991) (0)

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