Výsledky vyhledávání - S J Currier

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  1. 1
    SCID newborn screening: What we’ve learned

    SCID newborn screening: What we’ve learned Autor Robert J. Currier, Jennifer M. Puck

    Vydáno 2021
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  2. 2
    Characterization of the azidopine and vinblastine binding site of P-glycoprotein.

    Characterization of the azidopine and vinblastine binding site of P-glycoprotein. Autor Edward Bruggemann, Stephen J. Currier, Michael M. Gottesman, Ira Pastan

    Vydáno 1992
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  3. 3
    Birth prevalence of disorders detectable through newborn screening by race/ethnicity

    Birth prevalence of disorders detectable through newborn screening by race/ethnicity Autor Lisa Feuchtbaum, Jennifer Carter, Sunaina Dowray, Robert J. Currier, Fred Lorey

    Vydáno 2012
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  4. 4
    Identification of residues in the first cytoplasmic loop of P-glycoprotein involved in the function of chimeric human MDR1-MDR2 transporters.

    Identification of residues in the first cytoplasmic loop of P-glycoprotein involved in the function of chimeric human MDR1-MDR2 transporters. Autor Stephen J. Currier, Susan E. Kane, Mark C. Willingham, Carol Cardarelli, Ira Pastan, Michael M. Gottesman

    Vydáno 1992
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  5. 5
    Reference intervals for lymphocyte subsets in preterm and term neonates without immune defects

    Reference intervals for lymphocyte subsets in preterm and term neonates without immune defects Autor George S. Amatuni, Stanley Sciortino, Robert J. Currier, Stanley J. Naides, Joseph A. Church, Jennifer M. Puck

    Vydáno 2019
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  6. 6
    Postanalytical tools improve performance of newborn screening by tandem mass spectrometry

    Postanalytical tools improve performance of newborn screening by tandem mass spectrometry Autor Patricia Hall, Gregg Marquardt, David McHugh, Robert J. Currier, Hao Tang, Stephanie D. Stoway, Piero Rinaldo

    Vydáno 2014
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  7. 7
    Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities

    Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities Autor Mary E. Norton, Rebecca J. Baer, Ronald J. Wapner, Miriam Kuppermann, Laura L. Jelliffe‐Pawlowski, Robert J. Currier

    Vydáno 2015
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  8. 8
    Transepithelial Transport of Drugs by the Multidrug Transporter in Cultured Madin-Darby Canine Kidney Cell Epithelia

    Transepithelial Transport of Drugs by the Multidrug Transporter in Cultured Madin-Darby Canine Kidney Cell Epithelia Autor Masaru Horio, Khew‐Voon Chin, Stephen J. Currier, Sarah Goldenberg, Cheyenne Williams, Ira Pastan, Michael M. Gottesman, Jerome S. Handler

    Vydáno 1989
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  9. 9
    Activity of the multidrug transporter results in alkalinization of the cytosol: measurement of cytosolic pH by microinjection of a pH-sensitive dye.

    Activity of the multidrug transporter results in alkalinization of the cytosol: measurement of cytosolic pH by microinjection of a pH-sensitive dye. Autor F Thiébaut, Stephen J. Currier, J Michael Whitaker, R P Haugland, Michael M. Gottesman, Ira Pastan, Mark C. Willingham

    Vydáno 1990
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  10. 10
    Modulation of the expression of a multidrug resistance gene (mdr-1/P-glycoprotein) by differentiating agents

    Modulation of the expression of a multidrug resistance gene (mdr-1/P-glycoprotein) by differentiating agents Autor Lyn A. Mickley, Susan E. Bates, Nancy Richert, S J Currier, Sachiko Tanaka, Francine M. Foss, N Rosen, Antonio Tito Fojo

    Vydáno 1989
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  11. 11
    Association of early-preterm birth with abnormal levels of routinely collected first- and second-trimester biomarkers

    Association of early-preterm birth with abnormal levels of routinely collected first- and second-trimester biomarkers Autor Laura L. Jelliffe‐Pawlowski, Gary M. Shaw, Robert J. Currier, David K. Stevenson, Rebecca J. Baer, Hugh OʼBrodovich, Jeffrey B. Gould

    Vydáno 2013
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  12. 12
    Newborn Screening for Cystic Fibrosis in California

    Newborn Screening for Cystic Fibrosis in California Autor Martin Kharrazi, Juan Yang, Tracey Bishop, S. Lessing, Suzanne Young, Simon Graham, Michelle Pearl, H. Chow, Timothy Ho, Robert J. Currier, L. Gaffney, Lisa Feuchtbaum

    Vydáno 2015
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  13. 13
    Maternal characteristics and mid‐pregnancy serum biomarkers as risk factors for subtypes of preterm birth

    Maternal characteristics and mid‐pregnancy serum biomarkers as risk factors for subtypes of preterm birth Autor LL Jelliffe‐Pawlowski, RJ Baer, YJ Blumenfeld, Kelli K. Ryckman, HM O'Brodovich, JB Gould, Maurice L. Druzin, YY El‐Sayed, DJ Lyell, DK Stevenson, Gary M. Shaw, Robert J. Currier

    Vydáno 2015
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  14. 14
    Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: Results of the first 2 years

    Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: Results of the first 2 years Autor Antonia Kwan, Joseph A. Church, Morton J. Cowan, Rajni Agarwal, Neena Kapoor, Donald B. Kohn, David B. Lewis, Sean McGhee, Theodore B. Moore, E. Richard Stiehm, Matthew H. Porteus, Constantino P. Aznar, Robert J. Currier, Fred Lorey, Jennifer M. Puck

    Vydáno 2013
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  15. 15
    Recurrence of Preterm Birth and Early Term Birth

    Recurrence of Preterm Birth and Early Term Birth Autor Juan Yang, Rebecca J. Baer, Vincenzo Berghella, Christina Chambers, Paul J. Chung, Tumaini R. Coker, Robert J. Currier, Maurice L. Druzin, Miriam Kuppermann, Louis J. Muglia, Mary E. Norton, Larry Rand, Kelli K. Ryckman, Gary M. Shaw, David K. Stevenson, Laura L. Jelliffe‐Pawlowski

    Vydáno 2016
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  16. 16
    Newborn Screening for Severe Combined Immunodeficiency and T-cell Lymphopenia in California, 2010–2017

    Newborn Screening for Severe Combined Immunodeficiency and T-cell Lymphopenia in California, 2010–2017 Autor George S. Amatuni, Robert J. Currier, Joseph A. Church, Tracey Bishop, Elena Grimbacher, Alan A. Nguyen, Rajni Agarwal‐Hashmi, Constantino P. Aznar, Manish J. Butte, Morton J. Cowan, Morna J. Dorsey, Christopher C. Dvorak, Neena Kapoor, Donald B. Kohn, M. Louise Markert, Theodore B. Moore, Stanley J. Naides, Stanley Sciortino, Lisa Feuchtbaum, Rasoul A. Koupaei, Jennifer M. Puck

    Vydáno 2019
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  17. 17
    The role of exome sequencing in newborn screening for inborn errors of metabolism

    The role of exome sequencing in newborn screening for inborn errors of metabolism Autor Aashish N. Adhikari, Renata C. Gallagher, Yaqiong Wang, Robert J. Currier, George S. Amatuni, Laia Bassaganyas, Flavia Chen, Kunal Kundu, Mark Kvale, Sean D. Mooney, Robert L. Nussbaum, Savanna S. Randi, Jeremy R. Sanford, Joseph T.C. Shieh, Rajgopal Srinivasan, Uma Sunderam, Hao Tang, Dedeepya Vaka, Yangyun Zou, Barbara A. Koenig, Pui‐Yan Kwok, Neil Risch, Jennifer M. Puck, Steven E. Brenner

    Vydáno 2020
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  18. 18
    Lentiviral Gene Therapy for Artemis-Deficient SCID

    Lentiviral Gene Therapy for Artemis-Deficient SCID Autor Morton J. Cowan, Jason Yu, Janelle Facchino, Carol Fraser‐Browne, Ukina Sanford, Misako Kawahara, Jasmeen Dara, Janel Long-Boyle, Jess Oh, Wendy Chan, Shivali Chag, Lori Broderick, Deepak Chellapandian, Hélène Decaluwe, Catherine Golski, Diana Hu, Caroline Y. Kuo, Holly Miller, Aleksandra Petrović, Robert J. Currier, Joan F. Hilton, Divya Punwani, Christopher C. Dvorak, Harry L. Malech, R. Scott McIvor, Jennifer M. Puck

    Vydáno 2022
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  19. 19
    Newborn Sequencing in Genomic Medicine and Public Health

    Newborn Sequencing in Genomic Medicine and Public Health Autor Jonathan S. Berg, Pankaj B. Agrawal, Donald B. Bailey, Alan H. Beggs, Steven E. Brenner, Amy Brower, Julie A. Cakici, Ozge Ceyhan‐Birsoy, Kee Chan, Flavia Chen, Robert J. Currier, Dmitry Dukhovny, Robert C. Green, Julie Harris-Wai, Ingrid A. Holm, Brenda Iglesias, Galen Joseph, Stephen F. Kingsmore, Barbara A. Koenig, Pui‐Yan Kwok, John D. Lantos, Steven J. Leeder, Megan A. Lewis, Amy L. McGuire, Laura V. Milko, Sean D. Mooney, Richard B. Parad, Stacey Pereira, Joshua E. Petrikin, Bradford C. Powell, Cynthia M. Powell, Jennifer M. Puck, Heidi L. Rehm, Neil Risch, Myra I. Roche, Joseph T.C. Shieh, Narayanan Veeraraghavan, Michael S. Watson, Laurel K. Willig, Timothy W. Yu, Tiina K. Urv, Anastasia L. Wise

    Vydáno 2017
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  20. 20
    Newborn Screening for Severe Combined Immunodeficiency in 11 Screening Programs in the United States

    Newborn Screening for Severe Combined Immunodeficiency in 11 Screening Programs in the United States Autor Antonia Kwan, Roshini S. Abraham, Robert J. Currier, Amy Brower, Karen Andruszewski, Jordan K. Abbott, Mei Baker, Mark Ballow, Louis Bartoshesky, Francisco A. Bonilla, Charles D. Brokopp, Edward G. Brooks, Michele Caggana, Jocelyn Celestin, Joseph A. Church, Anne Marie Comeau, James A. Connelly, Morton J. Cowan, Charlotte Cunningham‐Rundles, Trivikram Dasu, Nina Dave, M. Teresa de la Morena, Ulrich Duffner, Chin-To Fong, Lisa R. Forbes, Debra Freedenberg, Erwin W. Gelfand, Jaime E. Hale, I. Celine Hanson, Beverly N. Hay, Diana Hu, Anthony J. Infante, Daisy Johnson, Neena Kapoor, Denise M. Kay, Donald B. Kohn, Rachel Lee, Heather K. Lehman, Zhili Lin, Fred Lorey, Aly Abdel‐Mageed, Adrienne Manning, Sean McGhee, Theodore B. Moore, Stanley J. Naides, Luigi D. Notarangelo, Jordan S. Orange, Sung‐Yun Pai, Matthew H. Porteus, Ray Rodríguez, Neil Romberg, John M. Routes, Mary Ruehle, Arye Rubenstein, Carlos A. Saavedra‐Matiz, G. E. M. Scott, Patricia M. Scott, Elizabeth Secord, Christine M. Seroogy, William T. Shearer, Subhadra Siegel, Stacy K. Silvers, E. Richard Stiehm, Robert W. Sugerman, John L. Sullivan, Susan Tanksley, Millard L. Tierce, James Verbsky, Beth Vogel, Roz Walker, Kelly Walkovich, Jolán E. Walter, Richard L. Wasserman, Michael S. Watson, Geoffrey A. Weinberg, Leonard B. Weiner, Heather Wood, Anne Yates, Jennifer M. Puck

    Vydáno 2014
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