Activation of the Estrogen Receptor Contributes to the Progression of Pulmonary Lymphangioleiomyomatosis via Matrix Metalloproteinase-Induced Cell Invasiveness von Glassberg, Marilyn K., Elliot, Sharon J., Fritz, Jason, Catanuto, Paola, Potier, Mylene, Donahue, Roger, Stetler-Stevenson, William, Karl, Michael

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46,XX sex reversal with partial duplication of chromosome arm 22q von Seeherunvong, Tossaporn, Perera, Erasmo M., Bao, Yong, Benke, Paul J., Benigno, Adelaida, Donahue, Roger P., Berkovitz, Gary D.

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Activation of the Estrogen Receptor Contributes to the Progression of Pulmonary Lymphangioleiomyomatosis via Matrix Metalloproteinase-lnduced Cell Invasiveness von GLASSBERG, Marilyn K, ELLIOT, Sharon J, FRITZ, Jason, CATANUTO, Paola, POTIER, Mylene, DONAHUE, Roger, STETLER-STEVENSON, William, KARL, Michael

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Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations von Wallerstein, Robert, Yu, Ming-Tsung, Neu, Richard L., Benn, Peter, Lee Bowen, Catherine, Crandall, Barbara, Disteche, Christine, Donahue, Roger, Harrison, Betty, Hershey, Douglas, Higgins, Rodney R., Jenkins, Lauren S., Jackson-Cook, Colleen, Keitges, Elizabeth, Khodr, Gabriel, Lin, C. C., Luthardt, Frederick W., Meisner, Lorraine, Mengden, Gregory, Patil, Shivanand R., Rodriguez, Maria, Sciorra, Leonard J., Shaffer, Lisa G., Stetten, Gail, Van Dyke, Daniel L., Wang, Hungshu, Williams, Fran, Zaslav, Ann-Leslie, Hsu, Lillian Y. F.

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Cytogenetic Analysis of the First Cleavage Division in Mouse Embryos von Donahue, Roger P.

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Isolation and characterization of conditionally immortalized astrocyte cell lines derived from adult human spinal cord von Whittemore, Scott R., Neary, Joseph T., Kleitman, Naomi, Sanon, Henry R., Benigno, Adelaida, Donahue, Roger P., Norenberg, Michael D.

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Myelodysplastic Syndrome with Atypical Eosinophilia in Association with Ring Chromosome 7: A Case Report von Bakotic, Bradley W, Poniecka, Anna W, Dominguez, Carlos J, Benigno, Adelaida, Donahue, Roger P, Cabello-Inchausti, Beria

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Human Ooeytes: Maturation in Chemically Defined Media von Kennedy, Joseph F., Donahue, Roger P.

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Chromosome Banding Patterns in Preimplantation Mouse Embryos von Nesbitt, Muriel N., Donahue, Roger P.

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Preimplantational Ectogenesis von Karp, Laurence E., Donahue, Roger P.

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Maturation of the mouse oocyte in vitro. I. Sequence and timing of nuclear progression von Donahue, Roger P.

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Detection of Mosaicism in amniotic fluid cultures: A CYT02000 collaborative study von Ing, Paul S., Van Dyke, Daniel L., Caudill, Samuel P., Reidy, John A., Bice, Gillian, Bieber, Frederick R., Buchanan, Phillip D., Carroll, Andrew J., Cheung, Sau W., DeWald, Gordon, Donahue, Roger P., Gardner, H. Allen, Higgins, James, Hsu, Lillian Y.F., Jamehdor, Mehdi, Keitges, Elisabeth A., Laundon, Caroline H., Luthardt, Frederick W., Mascarello, James, May, Kristin M., Meek, Jeanne M., Morton, Cynthia, Patil, Shiva, Peakman, David, Pettenati, Mark J., Rao, Nagesh, Sanger, Warren G., Saxe, Deborah F., Schwartz, Stuart, Sekhon, Gurbax S., Vance, Gail H., Wyandt, Herman E., Yu, Cheng W., Zenger-Hain, Julie, Chen, Andrew T.L.

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Probable Assignment of the Duffy Blood Group Locus to Chromosome 1 in Man von Donahue, Roger P., Bias, Wilma B., Renwick, James H., McKusick, Victor A.

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DNA synthesis in developing two-cell mouse embryos von Luthardt, Frederick W., Donahue, Roger P.

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Human Oocytes: Maturation in Chemically Defined Media von Kennedy, Joseph F., Donahue, Roger P.

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Fertilization of the mouse oocyte: Sequence and timing of nuclear progression to the two-cell stage von Donahue, Roger P.

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Preimplantational Ectogenesis: Science and Speculation Concerning von Karp, Laurence E., Donahue, Roger P.

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Characterization of Phosphoglycerate Kinase from Human Spermatozoa von Chen, Shi-Han, Donahue, Roger P., Ronald Scott, C.

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Myelodysplastic Syndrome with Atypical Eosinophilia in Association with Ring Chromosome 7 von Bakotic, Bradley W, Poniecka, Anna W, Dominguez, Carlos J, Benigno, Adelaida, Donahue, Roger P, Cabello-Inchausti, Beria

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Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3) von Estabrooks, Laurel L., Rao, Kathleen W., Donahue, Roger P., Aylsworth, Arthur S.

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