檢索結果 - Dimitra Dafou

  • Showing 1 - 12 results of 12
Refine Results
  1. 1
    Senescent Fibroblasts Promote Neoplastic Transformation of Partially Transformed Ovarian Epithelial Cells in a Three-dimensional Model of Early Stage Ovarian Cancer

    Senescent Fibroblasts Promote Neoplastic Transformation of Partially Transformed Ovarian Epithelial Cells in a Three-dimensional Model of Early Stage Ovarian Cancer 由 Kate Lawrenson, Barbara Grün, Elizabeth Benjamin, Ian Jacobs, Dimitra Dafou, Simon A. Gayther

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  2. 2
    Profiling Microglia through Single-Cell RNA Sequencing over the Course of Development, Aging, and Disease

    Profiling Microglia through Single-Cell RNA Sequencing over the Course of Development, Aging, and Disease 由 Spyros Pettas, Korina Karagianni, Ειrini Kanata, Athanasia Chatziefstathiou, Nikoletta Christoudia, Konstantinos Xanthopoulos, Theodoros Sklaviadis, Dimitra Dafou

    出版 2022
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  3. 3
    Mutations in the γ-Secretase Genes NCSTN , PSENEN , and PSEN1 Underlie Rare Forms of Hidradenitis Suppurativa (Acne Inversa)

    Mutations in the γ-Secretase Genes NCSTN , PSENEN , and PSEN1 Underlie Rare Forms of Hidradenitis Suppurativa (Acne Inversa) 由 Andrew Pink, Michael A. Simpson, Nemesha Desai, Dimitra Dafou, Alison Hills, Peter Mortimer, Catherine Smith, Richard C. Trembath, Juliet N. Barker

    出版 2012
    獲取全文 獲取全文
    Carta
    加到收藏夾
    Saved in:
  4. 4
    HPV16 E6 Oncogene Contributes to Cancer Immune Evasion by Regulating PD-L1 Expression through a miR-143/HIF-1a Pathway

    HPV16 E6 Oncogene Contributes to Cancer Immune Evasion by Regulating PD-L1 Expression through a miR-143/HIF-1a Pathway 由 Georgios Konstantopoulos, Danai Leventakou, Despoina-Rozi Saltiel, Efthalia Zervoudi, Eirini Logotheti, Spyros Pettas, Korina Karagianni, Angeliki Daiou, Konstantinos E. Hatzistergos, Dimitra Dafou, Minas Arsenakis, Amanda Psyrri, Christine Kottaridi

    出版 2024
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  5. 5
    De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome

    De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome 由 Wendy D. Jones, Dimitra Dafou, Meriel McEntagart, Wesley J. Woollard, Frances Elmslie, Muriel Holder‐Espinasse, Melita Irving, Anand Saggar, Sarah Smithson, Richard C. Trembath, Charu Deshpande, Michael A. Simpson

    出版 2012
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  6. 6
    A physicochemical model for rationalizing SARS-CoV-2 concentration in sewage. Case study: The city of Thessaloniki in Greece

    A physicochemical model for rationalizing SARS-CoV-2 concentration in sewage. Case study: The city of Thessaloniki in Greece 由 Maria Petala, Dimitra Dafou, Margaritis Kostoglou, Thodoris D. Karapantsios, Ειrini Kanata, A. Chatziefstathiou, Foteini Sakaveli, K. Kotoulas, Minas Arsenakis, Emmanuel Roilides, Theodoros Sklaviadis, Symeon Metallidis, Anna Papa, Efstratios Stylianidis, Athanasios N. Papadopoulos, Nikolaos Papaioannou

    出版 2020
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  7. 7
    3D In Vitro Model of a Functional Epidermal Permeability Barrier from Human Embryonic Stem Cells and Induced Pluripotent Stem Cells

    3D In Vitro Model of a Functional Epidermal Permeability Barrier from Human Embryonic Stem Cells and Induced Pluripotent Stem Cells 由 Anastasia Petrova, Anna Celli, Laureen Jacquet, Dimitra Dafou, Debra Crumrine, Melanie Hupe, Matthew Arno, Carl Hobbs, Aleksandra Čvoro, Panagiotis Karagiannis, Liani Devito, Richard Sun, Lillian Adame, Robert Vaughan, John A. McGrath, Theodora M. Mauro, Duško Ilić

    出版 2014
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  8. 8
    De Novo Mutations of the Gene Encoding the Histone Acetyltransferase KAT6B Cause Genitopatellar Syndrome

    De Novo Mutations of the Gene Encoding the Histone Acetyltransferase KAT6B Cause Genitopatellar Syndrome 由 Michael A. Simpson, Charu Deshpande, Dimitra Dafou, Lisenka E.L.M. Vissers, Wesley J. Woollard, Susan Holder, Gabriele Gillessen‐Kaesbach, Ronny Derks, Susan M. White, Ruthy Cohen‐Snuijf, Sarina G. Kant, Lies H. Hoefsloot, William Reardon, Han G. Brunner, Ernie M.H.F. Bongers, Richard C. Trembath

    出版 2012
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  9. 9
    Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

    Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) 由 Pia Østergaard, Michael A. Simpson, Fiona Connell, Colin G. Steward, Glen Brice, Wesley J. Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt, Victoria A. Murday, Shirley Hodgson, Russell Keenan, Daniela T. Pilz, Inés Martínez‐Corral, Taija Mäkinen, Peter Mortimer, Steve Jeffery, Richard C. Trembath, Sahar Mansour

    出版 2011
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  10. 10
    Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

    Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome 由 Gabriela Petrof, Arti Nanda, Jake Davey Howden, Takuya Takeichi, James R. McMillan, Sophia Aristodemou, Linda Ozoemena, Lu Liu, Andrew P. South, Céline Pourreyron, Dimitra Dafou, Laura E. Proudfoot, Hejab Al‐Ajmi, Masashi Akiyama, W.H. Irwin McLean, Michael A. Simpson, Maddy Parsons, John A. McGrath

    出版 2014
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  11. 11
    Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

    Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies 由 Laura Southgate, Rajiv D. Machado, Katie Snape, Martin Primeau, Dimitra Dafou, Deborah Ruddy, Peter Branney, Malcolm E Fisher, Grace J. Lee, Michael A. Simpson, Yi He, Teisha Y. Bradshaw, Bettina Blaumeiser, W S Winship, William Reardon, Eamonn R. Maher, David Fitzpatrick, Wim Wuyts, Martin Zenker, Nathalie Lamarche‐Vane, Richard C. Trembath

    出版 2011
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  12. 12
    Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer

    Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer 由 Maria Notaridou, Lydia Quaye, Dimitra Dafou, Chris Jones, Honglin Song, Estrid Høgdall, Susanne K. Kjær, Lise L. Christensen, Claus Høgdall, Jan Blaakær, Valerie McGuire, Anna H. Wu, David J. Van Den Berg, Malcolm C. Pike, Aleksandra Gentry‐Maharaj, Eva Wozniak, Tanya Sher, Ian Jacobs, Jonathan P. Tyrer, Joellen M. Schildkraut, Patricia G. Moorman, Edwin S. Iversen, Anna Jakubowska, Krzysztof Mędrek, Jan Lubiński, Roberta B. Ness, Kirsten B. Moysich, Galina Lurie, Lynne R. Wilkens, Michael E. Carney, Shan Wang‐Gohrke, Jennifer A. Doherty, Mary Anne Rossing, Matthias W. Beckmann, Falk C. Thiel, Arif B. Ekici, Xiaohong Chen, Jonathan Beesley, Jacek Gronwald, Peter A. Fasching, Jenny Chang‐Claude, Marc T. Goodman, Georgia Chenevix‐Trench, Andrew Berchuck, Celeste Leigh Pearce, Alice S. Whittemore, Usha Menon, Paul D.P. Pharoah, Simon A. Gayther, Susan J. Ramus

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: