Publications Search Advanced Filters Type - Any -Journal Article Year - Any -2022202120202019201820172016201520142013201220112010200920082007200620052004200320022001200019991998199719961995199419931992199119901989198819871986198519841982198119801979197819771976 AuthorTitleTypeYear DescendingAscending 1198 Publications 1976 1.Wieschaus E, Gehring W. Clonal analysis of primordial disc cells in the early embryo of Drosophila melanogaster. Dev Biol. 1976;50(2):249–63. 1.Gehring WJ, Wieschaus E, Holliger M. The use of ’normal’ and ’transformed’ gynandromorphs in mapping the primordial germ cells and the gonadal mesoderm in Drosophila. J Embryol Exp Morphol. 1976;35(3):607–16. 1977 1.Marsh JL, Wieschaus E. Germ-line dependence of the maroon-like maternal effect in Drosophila. Dev Biol. 1977;60(2):396–403. 1.Marsh JL, van Deusen EB, Wieschaus E, Gehring WJ. Germ line dependence of the deep orange maternal effect in Drosophila. Dev Biol. 1977;56(1):195–9. 1978 1.Wieschaus E. Cell lineage relationships in the Drosophila embryo. Results Probl Cell Differ. 1978;9:97–118. 1.Marsh JL, Wieschaus E. Is sex determination in germ line and soma controlled by separate genetic mechanisms?. Nature. 1978;272(5650):249–51. 1979 1.Wieschaus E, Szabad J. The development and function of the female germ line in Drosophila melanogaster: a cell lineage study. Dev Biol. 1979;68(1):29–46. 1.Szabad J, Schupbach T, Wieschaus E. Cell lineage and development in the larval epidermis of Drosophila melanogaster. Dev Biol. 1979;73(2):256–71. 1980 1.Nusslein-Volhard C, Wieschaus E. Mutations affecting segment number and polarity in Drosophila. Nature. 1980;287(5785):795–801. 1.Wieschaus E. A combined genetic and mosaic approach to the study of oogenesis in Drosophila. Basic Life Sci. 1980;16:85–94. 1981 1.Wieschaus E, Audit C, Masson M. A clonal analysis of the roles of somatic cells and germ line during oogenesis in Drosophila. Dev Biol. 1981;88(1):92–103. 1982 1.Wieschaus E, Nöthiger R. The role of the transformer genes in the development of genitalia and analia of Drosophila melanogaster. Dev Biol. 1982;90(2):320–34. 1984 1.Wieschaus E, Nusslein-Volhard C, Kluding H. Krüppel, a gene whose activity is required early in the zygotic genome for normal embryonic segmentation. Dev Biol. 1984;104(1):172–86. 1985 1.Gergen JP, Wieschaus EF. The localized requirements for a gene affecting segmentation in Drosophila: analysis of larvae mosaic for runt. Dev Biol. 1985;109(2):321–35. 1.Mohler J, Wieschaus EF. Bicaudal mutations of Drosophila melanogaster: alteration of blastoderm cell fate. Cold Spring Harb Symp Quant Biol. 1985;50:105–11. 1.Zusman SB, Wieschaus EF. Requirements for zygotic gene activity during gastrulation in Drosophila melanogaster. Dev Biol. 1985;111(2):359–71. 1986 1.Gergen JP, Wieschaus E. Dosage requirements for runt in the segmentation of Drosophila embryos. Cell. 1986;45(2):289–99. 1.Schupbach T, Wieschaus E. Germline autonomy of maternal-effect mutations altering the embryonic body pattern of Drosophila. Dev Biol. 1986;113(2):443–8. 1.Mohler J, Wieschaus EF. Dominant maternal-effect mutations of Drosophila melanogaster causing the production of double-abdomen embryos. Genetics. 1986;112(4):803–22. 1987 1.Zusman SB, Wieschaus E. A cell marker system and mosaic patterns during early embryonic development in Drosophila melanogaster. Genetics. 1987;115(4):725–36. 1.Wieschaus E, Riggleman R. Autonomous requirements for the segment polarity gene armadillo during Drosophila embryogenesis. Cell. 1987;49(2):177–84. 1988 1.Zusman SB, Sweeton D, Wieschaus EF. short gastrulation, a mutation causing delays in stage-specific cell shape changes during gastrulation in Drosophila melanogaster. Dev Biol. 1988;129(2):417–27. 1.Yoo-Warren H, , Ingram RS, Tilghman SM. Two regulatory domains flank the mouse H19 gene. Mol Cell Biol. 1988;8(11):4707–15. 1., Brannan CI, Tilghman SM. The structure and expression of a novel gene activated in early mouse embryogenesis. EMBO J. 1988;7(3):673–81. 1.Godbout R, Tilghman SM. Configuration of the alpha-fetoprotein regulatory domain during development. Genes Dev. 1988;2(8):949–56. 1.Coulter DE, Wieschaus E. Gene activities and segmental patterning in Drosophila: analysis of odd-skipped and pair-rule double mutants. Genes Dev. 1988;2(12B):1812–23. 1.Wieschaus E, Sweeton D. Requirements for X-linked zygotic gene activity during cellularization of early Drosophila embryos. Development. 1988;104(3):483–93. 1.Merrill PT, Sweeton D, Wieschaus E. Requirements for autosomal gene activity during precellular stages of Drosophila melanogaster. Development. 1988;104(3):495–509. 1.Godbout R, Ingram RS, Tilghman SM. Fine-structure mapping of the three mouse alpha-fetoprotein gene enhancers. Mol Cell Biol. 1988;8(3):1169–78. 1989 1.Camper SA, Tilghman SM. Postnatal repression of the alpha-fetoprotein gene is enhancer independent. Genes Dev. 1989;3(4):537–46. 1.Riggleman B, Wieschaus E, Schedl P. Molecular analysis of the armadillo locus: uniformly distributed transcripts and a protein with novel internal repeats are associated with a Drosophila segment polarity gene. Genes Dev. 1989;3(1):96–113. 1.Schupbach T, Wieschaus E. Female sterile mutations on the second chromosome of Drosophila melanogaster. I. Maternal effect mutations. Genetics. 1989;121(1):101–17. 1.Feuerman MH, Godbout R, Ingram RS, Tilghman SM. Tissue-specific transcription of the mouse alpha-fetoprotein gene promoter is dependent on HNF-1. Mol Cell Biol. 1989;9(10):4204–12. 1990 1.Spear BT, Tilghman SM. Role of alpha-fetoprotein regulatory elements in transcriptional activation in transient heterokaryons. Mol Cell Biol. 1990;10(10):5047–54. 1.Simpson L, Wieschaus E. Zygotic activity of the nullo locus is required to stabilize the actin-myosin network during cellularization in Drosophila. Development. 1990;110(3):851–63. 1.Peifer M, Wieschaus E. Mutations in the Drosophila gene extradenticle affect the way specific homeo domain proteins regulate segmental identity. Genes Dev. 1990;4(7):1209–23. 1.Coulter DE, Swaykus EA, Beran-Koehn MA, Goldberg D, Wieschaus E, Schedl P. Molecular analysis of odd-skipped, a zinc finger encoding segmentation gene with a novel pair-rule expression pattern. EMBO J. 1990;9(11):3795–804. 1.Tyner AL, Godbout R, Compton RS, Tilghman SM. The ontogeny of alpha-fetoprotein gene expression in the mouse gastrointestinal tract. J Cell Biol. 1990;110(4):915–27. 1.Peifer M, Wieschaus E. The segment polarity gene armadillo encodes a functionally modular protein that is the Drosophila homolog of human plakoglobin. Cell. 1990;63(6):1167–76. 1.Brannan CI, Dees EC, Ingram RS, Tilghman SM. The product of the H19 gene may function as an RNA. Mol Cell Biol. 1990;10(1):28–36. 1.Riggleman B, Schedl P, Wieschaus E. Spatial expression of the Drosophila segment polarity gene armadillo is posttranscriptionally regulated by wingless. Cell. 1990;63(3):549–60. 1.Vacher J, Tilghman SM. Dominant negative regulation of the mouse alpha-fetoprotein gene in adult liver. Science. 1990;250(4988):1732–5. 1991 1.Bartolomei MS, Zemel S, Tilghman SM. Parental imprinting of the mouse H19 gene. Nature. 1991;351(6322):153–5. 1.Brunkow ME, Tilghman SM. Ectopic expression of the H19 gene in mice causes prenatal lethality. Genes Dev. 1991;5(6):1092–101. 1.Parks S, Wieschaus E. The Drosophila gastrulation gene concertina encodes a G alpha-like protein. Cell. 1991;64(2):447–58. 1.Schupbach T, Wieschaus E. Female sterile mutations on the second chromosome of Drosophila melanogaster. II. Mutations blocking oogenesis or altering egg morphology. Genetics. 1991;129(4):1119–36. 1.Tilghman SM. Parental imprinting in the mouse. Harvey Lect. 1991;87:69–84. 1.Peifer M, Rauskolb C, Williams M, Riggleman B, Wieschaus E. The segment polarity gene armadillo interacts with the wingless signaling pathway in both embryonic and adult pattern formation. Development. 1991;111(4):1029–43. 1.Sweeton D, Parks S, Costa M, Wieschaus E. Gastrulation in Drosophila: the formation of the ventral furrow and posterior midgut invaginations. Development. 1991;112(3):775–89. 1.Burke DT, Rossi JM, Leung J, Koos DS, Tilghman SM. A mouse genomic library of yeast artificial chromosome clones. Mamm Genome. 1991;1(1):65. Pagination Current page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7 Page 8 Page 9 … Next page Next › Last page Last »