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  1. AU="López Panadés, Maria"
  2. AU="Tormo, Hélène"
  3. AU="Gardham, Alice"
  4. AU="Chisa Inoue"
  5. AU=Savcenko Michal AU=Savcenko Michal
  6. AU=Dinda Biswanath AU=Dinda Biswanath
  7. AU="Heikinheimo Annamari"
  8. AU="Currie, Geoffrey"
  9. AU="Konno, Adriana Y C"
  10. AU="Nashmi, Raad"
  11. AU="Doligkeit, Daniel"
  12. AU="Caparello, Basilio"
  13. AU="Fricke, T T"
  14. AU="Mummery, C J"
  15. AU="Krantz, Emily"
  16. AU="Bedoya-Arias, Juan E"
  17. AU="Zhou, Heyang"
  18. AU=Latson Larry A
  19. AU=Alhuzimi Eman
  20. AU="Wuerzberger-Davis, Shelly M"
  21. AU="Clippinger, Amy J"
  22. AU="M. S. Islam"
  23. AU="Borrego-Jiménez, Jaime"
  24. AU="Kaoru Dohi"
  25. AU="Tornai, Gábor J"
  26. AU="D'Avella, Christopher"
  27. AU="Lim, Boon L."
  28. AU="Heselden, Marie"
  29. AU=Dias?Polak David
  30. AU="Shahid Umar"
  31. AU="Abu-Shmais, Alexandria A"
  32. AU="Takenaka, Haruka"
  33. AU="Bramley, Andrea"
  34. AU="Sang Hong Lee"

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  1. Artikel ; Online: Histological and Cytological Techniques to Study Perinatal Mouse Ovaries and Oocytes.

    Nikou, Nikoleta / López Panadés, Maria / Roig, Ignasi

    Methods in molecular biology (Clifton, N.J.)

    2024  Band 2770, Seite(n) 151–170

    Abstract: The regulation of female fertility in mammals depends on critical processes during oocyte development and maturation. Therefore, it is crucial to use specific approaches when studying mammalian female fertility to preserve ovary and oocyte structures ... ...

    Abstract The regulation of female fertility in mammals depends on critical processes during oocyte development and maturation. Therefore, it is crucial to use specific approaches when studying mammalian female fertility to preserve ovary and oocyte structures effectively. The methods of collecting and culturing ovaries and oocytes play an essential role in the study of mammalian follicle development and oocyte quality. This chapter presents a collection of protocols that focus on various methods for studying mammalian ovaries and oocytes, providing researchers with a variety of approaches to choose from.
    Mesh-Begriff(e) Animals ; Pregnancy ; Mice ; Female ; Ovary ; Ovarian Follicle ; Oocytes/physiology ; Oogenesis ; Cytological Techniques ; Mammals
    Sprache Englisch
    Erscheinungsdatum 2024-02-14
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-0716-3698-5_12
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: p53 Controls Meiotic Prophase Progression and Crossover Formation.

    Marcet-Ortega, Marina / Maldonado-Linares, Andros / López-Panadés, Maria / Roig, Ignasi

    International journal of molecular sciences

    2022  Band 23, Heft 17

    Abstract: Meiosis initiates with the formation of double strand breaks (DSBs) throughout the genome. To avoid genomic instability, these DSBs need to be correctly repaired by homologous recombination. Surveillance mechanisms involving the DNA damage response (DDR) ...

    Abstract Meiosis initiates with the formation of double strand breaks (DSBs) throughout the genome. To avoid genomic instability, these DSBs need to be correctly repaired by homologous recombination. Surveillance mechanisms involving the DNA damage response (DDR) pathway ATM-CHK2-p53 can detect the persistence of unrepaired DBSs and activate the recombination-dependent arrest at the pachytene stage. However, a complete understanding of p53 functions under normal physiological conditions remains lacking. Here, we report a detailed analysis of the p53 role during meiotic prophase in mice spermatocytes. We show that the absence of p53 regulates prophase progression by slowing down the pachytene stage when the recombination-dependent arrest occurs. Furthermore, our results show that p53 is necessary for proper crossover (CO) formation and localization. Our study contributes to a deeper understanding of p53 roles during the meiotic prophase.
    Mesh-Begriff(e) Animals ; Cell Cycle Proteins/metabolism ; DNA Breaks, Double-Stranded ; Male ; Meiosis ; Mice ; Prophase ; Spermatocytes/metabolism ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/metabolism
    Chemische Substanzen Cell Cycle Proteins ; Trp53 protein, mouse ; Tumor Suppressor Protein p53
    Sprache Englisch
    Erscheinungsdatum 2022-08-29
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms23179818
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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