Developing genetic reagents to facilitate recovery, analysis, and maintenance of mouse mutations

[1]  A. Bradley,et al.  Engineering a mouse balancer chromosome , 1999, Nature Genetics.

[2]  D. Carpenter,et al.  N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations. , 1999, Genetics.

[3]  Kathryn E. Hentges,et al.  The flat-top gene is required for the expansion and regionalization of the telencephalic primordium. , 1999, Development.

[4]  T. Doetschman,et al.  Interpretation of phenotype in genetically engineered mice. , 1999, Laboratory animal science.

[5]  J. Eppig,et al.  Finding a mouse: the International Mouse Strain Resource (IMSR). , 1999, Trends in genetics : TIG.

[6]  A. Bradley,et al.  Embryonic lethality and tumorigenesis caused by segmental aneuploidy on mouse chromosome 11. , 1998, Genetics.

[7]  W. Pavan,et al.  Linkage disequilibrium mapping reveals suppressed recombination at the Os locus , 1998, Mammalian Genome.

[8]  M. Bucan,et al.  Functional genomics in the mouse: phenotype-based mutagenesis screens. , 1998, Genome research.

[9]  A. Kasarskis,et al.  A phenotype-based screen for embryonic lethal mutations in the mouse. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[10]  I. Jackson,et al.  White-based brown (Tyrp1B-w) is a dominant mutation causing reduced hair pigmentation owing to a chromosomal inversion , 1998, Mammalian Genome.

[11]  M. Justice,et al.  Functional genomics in the post-genome era. , 1998, Mutation research.

[12]  T. Magnuson,et al.  X-ray-induced mutations in mouse embryonic stem cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[13]  N. Copeland,et al.  The itchy locus encodes a novel ubiquitin protein ligase that is disrupted in a18H mice , 1998, Nature Genetics.

[14]  J. Schimenti,et al.  Generation of radiation-induced deletion complexes in the mouse genome using embryonic stem cells. , 1997, Methods.

[15]  M. Justice,et al.  Using targeted large deletions and high-efficiency N-ethyl-N-nitrosourea mutagenesis for functional analyses of the mammalian genome. , 1997, Methods.

[16]  T H Roderick,et al.  A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse. , 1997, Genomics.

[17]  Rudolf Jaenisch,et al.  Chromosomal deletion complexes in mice by radiation of embryonic stem cells , 1997, Nature Genetics.

[18]  S. Tilghman,et al.  Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex. , 1996, Genetics.

[19]  N. Copeland,et al.  Deletion and interallelic complementation analysis of Steel mutant mice. , 1996, Genetics.

[20]  A. Bradley,et al.  Chromosome engineering in mice , 1995, Nature.

[21]  L. B. Russell,et al.  Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse. , 1995, Genetics.

[22]  L. Stubbs,et al.  Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus. , 1995, Genetics.

[23]  M. Handel,et al.  Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[24]  N. Copeland,et al.  DNA rearrangements located over 100 kb 5' of the Steel (Sl)-coding region in Steel-panda and Steel-contrasted mice deregulate Sl expression and cause female sterility by disrupting ovarian follicle development. , 1995, Genes & development.

[25]  I. Jackson,et al.  Molecular genetics of the brown (b)-locus region of mouse chromosome 4. I. Origin and molecular mapping of radiation- and chemical-induced lethal brown deletions. , 1994, Genetics.

[26]  E. Rinchik Molecular genetics of the brown (b)-locus region of mouse chromosome 4. II. Complementation analyses of lethal brown deletions. , 1994, Genetics.

[27]  D. Carpenter,et al.  Deletion mapping of four loci defined by N-ethyl-N-nitrosourea-induced postimplantation-lethal mutations within the pid-Hbb region of mouse chromosome 7. , 1993, Genetics.

[28]  R. Woychik,et al.  Molecular characterization of the mouse agouti locus , 1992, Cell.

[29]  M. Lyon,et al.  Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[30]  T. Roderick,et al.  The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15. , 1990, Genetical research.

[31]  I. Jackson,et al.  Characterization of TRP-1 mRNA levels in dominant and recessive mutations at the mouse brown (b) locus. , 1990, Genetics.

[32]  P. Selby,et al.  A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[33]  M. Jacob A personal communication , 1989 .

[34]  M. Hammer,et al.  Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[35]  M. Lyon,et al.  A presumed deletion covering the W and Ph loci of the mouse. , 1984, Genetical research.

[36]  C. Epstein,et al.  Oligosyndactyly: A lethal mutation in the mouse that results in mitotic arrest very early in development , 1984, Cell.

[37]  F. Serres,et al.  Utilization of Mammalian Specific Locus Studies in Hazard Evaluation and Estimation of Genetic Risk , 1983 .

[38]  L. B. Russell,et al.  Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies. , 1982, Genetics.

[39]  M. Lyon,et al.  Use of an inversion to test for induced X-linked lethals in mice. , 1982, Mutation research.

[40]  D. Bennett The T-locus of the mouse , 1975, Cell.

[41]  D. Johnson Hairpin-tail: a case of post-reductional gene action in the mouse egg. , 1974, Genetics.

[42]  T. Kaufman,et al.  The anatomy and function of a segment of the X chromosome of Drosophila melanogaster. , 1972, Genetics.

[43]  A. Bradley,et al.  A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice. , 1999, Nucleic acids research.

[44]  Karen P. Steel,et al.  The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells , 1995, Nature Genetics.

[45]  S. Tilghman,et al.  Fine structure mapping and deletion analysis of the murine piebald locus. , 1994, Genetics.

[46]  E. P. Evans,et al.  Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse , 1993, Nature Genetics.

[47]  E. Rinchik Chemical mutagenesis and fine-structure functional analysis of the mouse genome. , 1991, Trends in genetics : TIG.

[48]  T. Roderick Using Inversions to Detect and Study Recessive Lethals and Detrimentals in Mice , 1983 .

[49]  A. Malan,et al.  Hairy ears. , 1982, Pediatrics.

[50]  T. Roderick,et al.  A pericentric inversion in the mouse. , 1981, Cytogenetics and cell genetics.

[51]  L. B. Russell Definition of functional units in a small chromosomal segment of the mouse and its use in interpreting the nature of radiation-induced mutations. , 1971, Mutation research.

[52]  W. Russell X-ray-induced mutations in mice. , 1951, Cold Spring Harbor symposia on quantitative biology.