Generation of transgene-free iPSC lines from three patients with Friedreich’s ataxia (FRDA) carrying GAA triplet expansions in the first intron of FXN gene
Kelekçi, Simge, Uğurlu-Çimen, Deniz, Demir, Ata Berk, Özçimen, Burcu, Burak Yıldız, Abdullah, Batuhan Karakuş, Mehmet, Börklü Yücel, Esra, Önder, Tamer T.
Published in Stem cell research (01.07.2021)
Published in Stem cell research (01.07.2021)
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Perspectives on current models of Friedreich’s ataxia
Kelekçi, Simge, Yıldız, Abdullah Burak, Sevinç, Kenan, Çimen, Deniz Uğurlu, Önder, Tamer
Published in Frontiers in cell and developmental biology (11.08.2022)
Published in Frontiers in cell and developmental biology (11.08.2022)
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AF10 (MLLT10) prevents somatic cell reprogramming through regulation of DOT1L-mediated H3K79 methylation
Uğurlu-Çimen, Deniz, Odluyurt, Deniz, Sevinç, Kenan, Özkan-Küçük, Nazlı Ezgi, Özçimen, Burcu, Demirtaş, Deniz, Enüstün, Eray, Aztekin, Can, Philpott, Martin, Oppermann, Udo, Özlü, Nurhan, Önder, Tamer T
Published in Epigenetics & chromatin (02.07.2021)
Published in Epigenetics & chromatin (02.07.2021)
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Exposure of antral follicles to medroxyprogesterone acetate during stimulation does not cause molecular perturbations in gonadotropin-responsiveness and steroidogenic function of granulosa cells in progestin-primed cycles
Oktem, Ozgur, Esmaeilian, Yashar, İltumur, Ece, Yusufoglu, Sevgi, Çimen, Deniz Uğurlu, Incir, Said, Yakin, Kayhan, Ata, Baris, Urman, Bulent
Published in Human reproduction (Oxford) (01.10.2024)
Published in Human reproduction (Oxford) (01.10.2024)
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Patients with gynecological malignancies are similar to other IVF patients without cancer for clinical and molecular reproductive parameters and DNA damage response pattern
Esmaeilian, Yashar, Yusufoglu, Sevgi, İltumur, Ece, Cimen, Deniz Ugurlu, Vatansever, Dogan, Taskiran, Cagatay, Turan, Volkan, Yakin, Kayhan, İncir, Said, Urman, Bulent, Oktem, Ozgur
Published in Scientific reports (13.06.2024)
Published in Scientific reports (13.06.2024)
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Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy
Wong, Hui Hui, Seet, Sze Hwee, Maier, Michael, Gurel, Ayse, Traspas, Ricardo Moreno, Lee, Cheryl, Zhang, Shan, Talim, Beril, Loh, Abigail Y.T., Chia, Crystal Y., Teoh, Tze Shin, Sng, Danielle, Rensvold, Jarred, Unal, Sule, Shishkova, Evgenia, Cepni, Ece, Nathan, Fatima M., Sirota, Fernanda L., Liang, Chao, Yarali, Nese, Simsek-Kiper, Pelin O., Mitani, Tadahiro, Ceylaner, Serdar, Arman-Bilir, Ozlem, Mbarek, Hamdi, Gumruk, Fatma, Efthymiou, Stephanie, Uğurlu Çi̇men, Deniz, Georgiadou, Danai, Sotiropoulou, Kortessa, Houlden, Henry, Paul, Franziska, Pehlivan, Davut, Lainé, Candice, Chai, Guoliang, Ali, Nur Ain, Choo, Siew Chin, Keng, Soh Sok, Boisson, Bertrand, Yılmaz, Elanur, Xue, Shifeng, Coon, Joshua J., Ly, Thanh Thao Nguyen, Gilani, Naser, Hasbini, Dana, Kayserili, Hulya, Zaki, Maha S., Isfort, Robert J., Ordonez, Natalia, Tripolszki, Kornelia, Bauer, Peter, Rezaei, Nima, Seyedpour, Simin, Khotaei, Ghamar Taj, Bascom, Charles C., Maroofian, Reza, Chaabouni, Myriam, Alsubhi, Afaf, Eyaid, Wafaa, Işıkay, Sedat, Gleeson, Joseph G., Lupski, James R., Casanova, Jean-Laurent, Pagliarini, David J., Akarsu, Nurten A., Maurer-Stroh, Sebastian, Cetinkaya, Arda, Bertoli-Avella, Aida, Mathuru, Ajay S., Ho, Lena, Bard, Frederic A., Reversade, Bruno
Published in American journal of human genetics (01.07.2021)
Published in American journal of human genetics (01.07.2021)
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Journal Article
AF10 (MLLT10) prevents somatic cell reprogramming through regulation of DOT1L-mediated H3K79 methylation
Uğurlu-Çimen, Deniz, Odluyurt, Deniz, Sevinç, Kenan, Nazlı Ezgi Özkan-Küçük, Özçimen, Burcu, Demirtaş, Deniz, Enüstün, Eray, Aztekin, Can, Philpott, Martin, Oppermann, Udo, Özlü, Nurhan, Önder, Tamer T
Published in bioRxiv (09.02.2021)
Published in bioRxiv (09.02.2021)
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Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy
Wong, Hui Hui, Seet, Sze Hwee, Maier, Michael, Gurel, Ayse, Traspas, Ricardo Moreno, Lee, Cheryl, Zhang, Shan, Talim, Beril, Loh, Abigail Y.T., Chia, Crystal Y., Teoh, Tze Shin, Sng, Danielle, Rensvold, Jarred, Unal, Sule, Shishkova, Evgenia, Cepni, Ece, Nathan, Fatima M., Sirota, Fernanda L., Liang, Chao, Yarali, Nese, Simsek-Kiper, Pelin O., Mitani, Tadahiro, Ceylaner, Serdar, Arman-Bilir, Ozlem, Mbarek, Hamdi, Gumruk, Fatma, Efthymiou, Stephanie, Çïmen, Deniz Uğurlu, Georgiadou, Danai, Sotiropoulou, Kortessa, Houlden, Henry, Paul, Franziska, Pehlivan, Davut, Lainé, Candice, Chai, Guoliang, Ali, Nur Ain, Choo, Siew Chin, Keng, Soh Sok, Boisson, Bertrand, Yılmaz, Elanur, Xue, Shifeng, Coon, Joshua J., Nguyen Ly, Thanh Thao, Gilani, Naser, Hasbini, Dana, Kayserili, Hulya, Zaki, Maha S., Isfort, Robert J., Ordonez, Natalia, Tripolszki, Kornelia, Bauer, Peter, Rezaei, Nima, Seyedpour, Simin, Khotaei, Ghamar Taj, Bascom, Charles C., Maroofian, Reza, Chaabouni, Myriam, Alsubhi, Afaf, Eyaid, Wafaa, Işıkay, Sedat, Gleeson, Joseph G., Lupski, James R., Casanova, Jean-Laurent, Pagliarini, David J., Akarsu, Nurten A., Maurer-Stroh, Sebastian, Cetinkaya, Arda, Bertoli-Avella, Aida, Mathuru, Ajay S., Ho, Lena, Bard, Frederic A., Reversade, Bruno
Published in American journal of human genetics (01.07.2021)
Published in American journal of human genetics (01.07.2021)
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