Hasil Pencarian - Gorjana Robevska

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  1. 1
    Analysis of the androgen receptor (AR) gene in a cohort of Indonesian undermasculinized 46, XY DSD patients

    Analysis of the androgen receptor (AR) gene in a cohort of Indonesian undermasculinized 46, XY DSD patients oleh Nurin Aisyiyah Listyasari, Achmad Zulfa Juniarto, Gorjana Robevska, Katie L. Ayers, Andrew H. Sinclair, Sultana M. H. Faradz

    Diterbitkan 2021-02-01
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  2. 2
    Clinical lesson learned from genetic analysis in patients prior to surgical repair of hypospadias

    Clinical lesson learned from genetic analysis in patients prior to surgical repair of hypospadias oleh Nurin A. Listyasari, Gorjana Robevska, Katie L. Ayers, Tiong Yang Tan, Andrew H. Sinclair, Sultana M.H. Faradz

    Diterbitkan 2022-04-01
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  3. 3
    Genetic Analysis Reveals Complete Androgen Insensitivity Syndrome in Female Children Surgically Treated for Inguinal Hernia

    Genetic Analysis Reveals Complete Androgen Insensitivity Syndrome in Female Children Surgically Treated for Inguinal Hernia oleh Nurin A. Listyasari, Gorjana Robevska, Ardy Santosa, Aurore Bouty, AZ Juniarto, Jocelyn van den Bergen, Katie L. Ayers, Andrew H. Sinclair, Sultana MH Faradz

    Diterbitkan 2021-02-01
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  4. 4
    Generation of heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout human iPSC lines

    Generation of heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout human iPSC lines oleh Svenja Pachernegg, Gorjana Robevska, Lucas G. A. Ferreira, Jocelyn A. van den Bergen, Katerina Vlahos, Sara E. Howden, Andrew H. Sinclair, Katie L. Ayers

    Diterbitkan 2024-09-01
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  5. 5
    Generation of a homozygous (MCRIi031-A-3) WT1 knockout human iPSC line

    Generation of a homozygous (MCRIi031-A-3) WT1 knockout human iPSC line oleh Svenja Pachernegg, Gorjana Robevska, Lucas G.A. Ferreira, Jocelyn A. van den Bergen, Katerina Vlahos, Sara E. Howden, Andrew H. Sinclair, Katie L. Ayers

    Diterbitkan 2024-09-01
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  6. 6
    A citizen science model for implementing statewide educational DNA barcoding.

    A citizen science model for implementing statewide educational DNA barcoding. oleh Anthony Chiovitti, Frazer Thorpe, Christopher Gorman, Jennifer L Cuxson, Gorjana Robevska, Christopher Szwed, Jacinta C Duncan, Hannah K Vanyai, Joseph Cross, Kirby R Siemering, Joanna Sumner

    Diterbitkan 2019-01-01
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  7. 7
    COUP-TFII regulates early bipotential gonad signaling and commitment to ovarian progenitors

    COUP-TFII regulates early bipotential gonad signaling and commitment to ovarian progenitors oleh Lucas G. A. Ferreira, Marina M. L. Kizys, Gabriel A. C. Gama, Svenja Pachernegg, Gorjana Robevska, Andrew H. Sinclair, Katie L. Ayers, Magnus R. Dias-da-Silva

    Diterbitkan 2024-01-01
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  8. 8
    Generation of heterozygous (MCRIi030-A-1) and homozygous (MCRIi030-A-2) NR2F2/COUP-TFII knockout human iPSC lines

    Generation of heterozygous (MCRIi030-A-1) and homozygous (MCRIi030-A-2) NR2F2/COUP-TFII knockout human iPSC lines oleh Lucas G.A. Ferreira, Mauricio C. Cabral-da-Silva, Svenja Pachernegg, Jocelyn A. van den Bergen, Gorjana Robevska, Katerina Vlahos, Sara E. Howden, Elizabeth S. Ng, Magnus R. Dias-da-Silva, Andrew H. Sinclair, Katie L. Ayers

    Diterbitkan 2024-04-01
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  9. 9
    Author Correction: Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9

    Author Correction: Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9 oleh Brittany Croft, Thomas Ohnesorg, Jacqueline Hewitt, Josephine Bowles, Alexander Quinn, Jacqueline Tan, Vincent Corbin, Emanuele Pelosi, Jocelyn van den Bergen, Rajini Sreenivasan, Ingrid Knarston, Gorjana Robevska, Dung Chi Vu, John Hutson, Vincent Harley, Katie Ayers, Peter Koopman, Andrew Sinclair

    Diterbitkan 2019-07-01
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  10. 10
    Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9

    Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9 oleh Brittany Croft, Thomas Ohnesorg, Jacqueline Hewitt, Josephine Bowles, Alexander Quinn, Jacqueline Tan, Vincent Corbin, Emanuele Pelosi, Jocelyn van den Bergen, Rajini Sreenivasan, Ingrid Knarston, Gorjana Robevska, Dung Chi Vu, John Hutson, Vincent Harley, Katie Ayers, Peter Koopman, Andrew Sinclair

    Diterbitkan 2018-12-01
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  11. 11
    The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice.

    The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice. oleh Stefan Bagheri-Fam, Huijun Chen, Sean Wilson, Katie Ayers, James Hughes, Frederique Sloan-Bena, Pierre Calvel, Gorjana Robevska, Beatriz Puisac, Kamila Kusz-Zamelczyk, Stefania Gimelli, Anna Spik, Jadwiga Jaruzelska, Alina Warenik-Szymankiewicz, Sultana Faradz, Serge Nef, Juan Pié, Paul Thomas, Andrew Sinclair, Dagmar Wilhelm

    Diterbitkan 2020-01-01
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  12. 12
    Analysis of variants in GATA4 and FOG2/ZFPM2 demonstrates benign contribution to 46,XY disorders of sex development

    Analysis of variants in GATA4 and FOG2/ZFPM2 demonstrates benign contribution to 46,XY disorders of sex development oleh Jocelyn A. van denBergen, Gorjana Robevska, Stefanie Eggers, Stefan Riedl, Sonia R. Grover, Philip B. Bergman, Chris Kimber, Ashish Jiwane, Sophy Khan, Csilla Krausz, Jamal Raza, Irum Atta, Susan R. Davis, Makato Ono, Vincent Harley, Sultana M. H. Faradz, Andrew H. Sinclair, Katie L. Ayers

    Diterbitkan 2020-03-01
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  13. 13
    Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects

    Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects oleh Katie L. Ayers, Stefanie Eggers, Ben N. Rollo, Katherine R. Smith, Nadia M. Davidson, Nicole A. Siddall, Liang Zhao, Josephine Bowles, Karin Weiss, Ginevra Zanni, Lydie Burglen, Shay Ben-Shachar, Jenny Rosensaft, Annick Raas-Rothschild, Anne Jørgensen, Ralf B. Schittenhelm, Cheng Huang, Gorjana Robevska, Jocelyn van den Bergen, Franca Casagranda, Justyna Cyza, Svenja Pachernegg, David K. Wright, Melanie Bahlo, Alicia Oshlack, Terrence J. O’Brien, Patrick Kwan, Peter Koopman, Gary R. Hime, Nadine Girard, Chen Hoffmann, Yuval Shilon, Amnon Zung, Enrico Bertini, Mathieu Milh, Bochra Ben Rhouma, Neila Belguith, Anu Bashamboo, Kenneth McElreavey, Ehud Banne, Naomi Weintrob, Bruria BenZeev, Andrew H. Sinclair

    Diterbitkan 2023-06-01
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  14. 14
    Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects

    Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects oleh Katie L. Ayers, Stefanie Eggers, Ben N. Rollo, Katherine R. Smith, Nadia M. Davidson, Nicole A. Siddall, Liang Zhao, Josephine Bowles, Karin Weiss, Ginevra Zanni, Lydie Burglen, Shay Ben-Shachar, Jenny Rosensaft, Annick Raas-Rothschild, Anne Jørgensen, Ralf B. Schittenhelm, Cheng Huang, Gorjana Robevska, Jocelyn van den Bergen, Franca Casagranda, Justyna Cyza, Svenja Pachernegg, David K. Wright, Melanie Bahlo, Alicia Oshlack, Terrence J. O’Brien, Patrick Kwan, Peter Koopman, Gary R. Hime, Nadine Girard, Chen Hoffmann, Yuval Shilon, Amnon Zung, Enrico Bertini, Mathieu Milh, Bochra Ben Rhouma, Neila Belguith, Anu Bashamboo, Kenneth McElreavey, Ehud Banne, Naomi Weintrob, Bruria BenZeev, Andrew H. Sinclair

    Diterbitkan 2023-06-01
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