Výsledky vyhledávání - Schultz, Roger A

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  1. 1
    Cryptic chromosome abnormalities in a patient with mixed phenotype acute leukemia

    Cryptic chromosome abnormalities in a patient with mixed phenotype acute leukemia Autor Ning, Yi, Slovak, Marilyn L., Schultz, Roger A., Gojo, Ivana, Baer, Maria R.

    Vydáno 2013
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  2. 2
    Human and mouse homologs of Escherichia coli DinB (DNA polymerase IV), members of the UmuC/DinB superfamily

    Human and mouse homologs of Escherichia coli DinB (DNA polymerase IV), members of the UmuC/DinB superfamily Autor Gerlach, Valerie L., Aravind, L., Gotway, Garrett, Schultz, Roger A., Koonin, Eugene V., Friedberg, Errol C.

    Vydáno 1999
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  3. 3
    MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes

    MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes Autor Bhoj, Elizabeth J, Romeo, Stefano, Baroni, Marco G, Bartov, Guy, Schultz, Roger A, Zinn, Andrew R

    Vydáno 2009
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  4. 4
    Structure of the Highly Conserved HERC2 Gene and of Multiple Partially Duplicated Paralogs in Human

    Structure of the Highly Conserved HERC2 Gene and of Multiple Partially Duplicated Paralogs in Human Autor Ji, Yonggang, Rebert, Nancy A., Joslin, John M., Higgins, Michael J., Schultz, Roger A., Nicholls, Robert D.

    Vydáno 2000
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  5. 5
    The Gene Mutated in Variant Late-Infantile Neuronal Ceroid Lipofuscinosis (CLN6) and in nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein

    The Gene Mutated in Variant Late-Infantile Neuronal Ceroid Lipofuscinosis (CLN6) and in nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein Autor Wheeler, Ruth B., Sharp, Julie D., Schultz, Roger A., Joslin, John M., Williams, Ruth E., Mole, Sara E.

    Vydáno 2002
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  6. 6
    Value of Oligonucleotide-Based Array Comparative Genomic Hybridization for Diagnosis of Acute Promyelocytic Leukemia in a Patient Negative for t(15;17)(q24.1;q21.2)/Promyelocytic Leukemia-Retinoic Acid Receptor, Alpha by Conventional Cytogenetics and Fluorescence In Situ Hybridization

    Value of Oligonucleotide-Based Array Comparative Genomic Hybridization for Diagnosis of Acute Promyelocytic Leukemia in a Patient Negative for t(15;17)(q24.1;q21.2)/Promyelocytic L... Autor Alayed, Khaled, Medeiros, L. Jeffrey, Schultz, Roger A., Cortes, Jorge, Lu, Gary, Bueso-Ramos, Carlos E., Konoplev, Sergej

    Vydáno 2013
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  7. 7
    Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells

    Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells Autor McDaniel, Lisa D. , Tomkins, Darrell J. , Stanbridge, Eric J. , Somerville, Martin J. , Friedberg, Errol C. , Schultz, Roger A. 

    Vydáno 2005
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  8. 8
    Cloning the human and mouse MMS19 genes and functional complementation of a yeast mms19 deletion mutant

    Cloning the human and mouse MMS19 genes and functional complementation of a yeast mms19 deletion mutant Autor Queimado, Lurdes, Rao, Malini, Schultz, Roger A., Koonin, Eugene V., Aravind, L., Nardo, Tiziana, Stefanini, Miria, Friedberg, Errol C.

    Vydáno 2001
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  9. 9
    Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH

    Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH Autor Neill, Nicholas J., Ballif, Blake C., Lamb, Allen N., Parikh, Sumit, Ravnan, J. Britt, Schultz, Roger A., Torchia, Beth S., Rosenfeld, Jill A., Shaffer, Lisa G.

    Vydáno 2011
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  10. 10
    DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13

    DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13 Autor Garcia, Nilda M., Allgood, Jocelyn, Santos, Lane J., Lonergan, D., Batanian, J.R., Henkemeyer, Mark, Bartsch, Oliver, Schultz, Roger A., Zinn, Andrew R., Baker, Linda A.

    Vydáno 2006
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  11. 11
    Loss of Blm enhances basal cell carcinoma and rhabdomyosarcoma tumorigenesis in Ptch1(+/−) mice

    Loss of Blm enhances basal cell carcinoma and rhabdomyosarcoma tumorigenesis in Ptch1(+/−) mice Autor Davari, Parastoo, Hebert, Jennifer L., Albertson, Donna G., Huey, Bing, Roy, Ritu, Mancianti, Maria L., Horvai, Andrew E., McDaniel, Lisa D., Schultz, Roger A., Epstein, Ervin H.

    Vydáno 2010
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  12. 12
    Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis

    Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis Autor Schultz, Roger A, Delioukina, Maria, Gaal, Karl, Bedell, Victoria, Smith, David D, Forman, Stephen J, McDaniel, Lisa D, Ballif, Blake C, Shaffer, Lisa G, Slovak, Marilyn L

    Vydáno 2011
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  13. 13
    A Tlr7 translocation accelerates systemic autoimmunity in murine lupus

    A Tlr7 translocation accelerates systemic autoimmunity in murine lupus Autor Subramanian, Srividya, Tus, Katalin, Li, Quan-Zhen, Wang, Andrew, Tian, Xiang-Hong, Zhou, Jinchun, Liang, Chaoying, Bartov, Guy, McDaniel, Lisa D., Zhou, Xin J., Schultz, Roger A., Wakeland, Edward K.

    Vydáno 2006
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  14. 14
    Upregulation of TRAG3 gene in urothelial carcinoma of the bladder

    Upregulation of TRAG3 gene in urothelial carcinoma of the bladder Autor Karam, Jose A., Huang, Sandra, Fan, Jinhai, Stanfield, Jennifer, Schultz, Roger A., Pong, Rey-Chen, Sun, Xiankai, Mason, Ralph P., Xie, Xian-Jin, Niu, Gang, Chen, Xiaoyuan, Frenkel, Eugene P., Sagalowsky, Arthur I., Hsieh, Jer-Tsong

    Vydáno 2010
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  15. 15
    Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis

    Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis Autor Kolquist, Kathryn A, Schultz, Roger A, Slovak, Marilyn L, McDaniel, Lisa D, Brown, Theresa C, Tubbs, Raymond R, Cook, James R, Theil, Karl S, Cawich, Victoria, Valentin, Caitlin, Minier, Sara, Neill, Nicholas J, Byerly, Steve, Morton, S Annie, Sahoo, Trilochan, Ballif, Blake C, Shaffer, Lisa G

    Vydáno 2011
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  16. 16
    MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways

    MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways Autor Paciorkowski, Alex R., Traylor, Ryan N., Rosenfeld, Jill A., Hoover, Jacqueline M., Harris, Catharine J., Winter, Susan, Lacassie, Yves, Bialer, Martin, Lamb, Allen N., Schultz, Roger A., Berry-Kravis, Elizabeth, Porter, Brenda E., Falk, Marni, Venkat, Anu, Vanzo, Rena J., Cohen, Julie S., Fatemi, Ali, Dobyns, William B., Shaffer, Lisa G., Ballif, Blake C., Marsh, Eric D.

    Vydáno 2013
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  17. 17
    Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features

    Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features Autor Lamb, Allen N., Rosenfeld, Jill A., Neill, Nicholas J., Talkowski, Michael E., Blumenthal, Ian, Girirajan, Santhosh, Keelean-Fuller, Debra, Fan, Zheng, Pouncey, Jill, Stevens, Cathy, Mackay-Loder, Loren, Terespolsky, Deborah, Bader, Patricia, Rosenbaum, Kenneth, Vallee, Stephanie, Moeschler, John B., Ladda, Roger, Sell, Susan, Martin, Judith, Ryan, Shawnia, Jones, Marilyn C., Moran, Rocio, Shealy, Amy, Madan-Khetarpal, Suneeta, McConnell, Juliann, Surti, Urvashi, Delahaye, Andrée, Heron-Longe, Bénédicte, Pipiras, Eva, Benzacken, Brigitte, Passemard, Sandrine, Verloes, Alain, Isidor, Bertrand, Le Caignec, Cedric, Glew, Gwen M., Opheim, Kent E., Eichler, Evan E., Morton, Cynthia C., Gusella, James F., Schultz, Roger A., Ballif, Blake C., Shaffer, Lisa G.

    Vydáno 2012
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