Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity

Por Koç, Altuğ, Onur, S. Ödül, Ergün, Mehmet Ali, Perçin, E. Ferda
Publicado em 2009

Effects of microalgae chlorella species crude extracts on intestinal adaptation in experimental short bowel syndrome

Por Kerem, Mustafa, Salman, Bulent, Pasaoglu, Hatice, Bedirli, Abdulkadir, Alper, Murat, Katircioglu, Hikmet, Atici, Tahir, Perçin, E Ferda, Ofluoglu, Ebru
Publicado em 2008

Blood-Derived Human iPS Cells Generate Optic Vesicle–Like Structures with the Capacity to Form Retinal Laminae and Develop Synapses

Por Phillips, M. Joseph, Wallace, Kyle A., Dickerson, Sarah J., Miller, Michael J., Verhoeven, Amelia D., Martin, Jessica M., Wright, Lynda S., Shen, Wei, Capowski, Elizabeth E., Percin, E. Ferda, Perez, Enio T., Zhong, Xiufeng, Canto-Soler, Maria V., Gamm, David M.
Publicado em 2012

Modeling human retinal development with patient-specific iPS cells reveals multiple roles for VSX2

Por Phillips, M. Joseph, Perez, Enio T., Martin, Jessica M., Reshel, Samantha T., Wallace, Kyle A., Capowski, Elizabeth E., Singh, Ruchira, Wright, Lynda S., Clark, Eric M., Barney, Patrick M., Stewart, Ron, Dickerson, Sarah J., Miller, Michael J., Percin, E. Ferda, Thomson, James A., Gamm, David M.
Publicado em 2014

RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome

Por Bögershausen, Nina, Tsai, I-Chun, Pohl, Esther, Kiper, Pelin Özlem Simsek, Beleggia, Filippo, Percin, E. Ferda, Keupp, Katharina, Matchan, Angela, Milz, Esther, Alanay, Yasemin, Kayserili, Hülya, Liu, Yicheng, Banka, Siddharth, Kranz, Andrea, Zenker, Martin, Wieczorek, Dagmar, Elcioglu, Nursel, Prontera, Paolo, Lyonnet, Stanislas, Meitinger, Thomas, Stewart, A. Francis, Donnai, Dian, Strom, Tim M., Boduroglu, Koray, Yigit, Gökhan, Li, Yun, Katsanis, Nicholas, Wollnik, Bernd
Publicado no J Clin Invest (2015)

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

Por Reynolds, John J, Bicknell, Louise S, Carroll, Paula, Higgs, Martin R, Shaheen, Ranad, Murray, Jennie E, Papadopoulos, Dimitrios K, Leitch, Andrea, Murina, Olga, Tarnauskaitė, Žygimantė, Wessel, Sarah R, Zlatanou, Anastasia, Vernet, Audrey, von Kriegsheim, Alex, Mottram, Rachel MA, Logan, Clare V, Bye, Hannah, Li, Yun, Brean, Alexander, Maddirevula, Sateesh, Challis, Rachel C, Skouloudaki, Kassiani, Almoisheer, Agaadir, Alsaif, Hessa S, Amar, Ariella, Prescott, Natalie J, Bober, Michael B, Duker, Angela, Faqeih, Eissa, Seidahmed, Mohammed Zain, Al Tala, Saeed, Alswaid, Abdulrahman, Ahmed, Saleem, Al-Aama, Jumana Yousuf, Altmüller, Janine, Al Balwi, Mohammed, Brady, Angela F, Chessa, Luciana, Cox, Helen, Fischetto, Rita, Heller, Raoul, Henderson, Bertram D, Hobson, Emma, Nürnberg, Peter, Percin, E Ferda, Peron, Angela, Spaccini, Luigina, Quigley, Alan J, Thakur, Seema, Wise, Carol A, Yoon, Grace, Alnemer, Maha, Tomancak, Pavel, Yigit, Gökhan, Taylor, A Malcolm R, Reijns, Martin AM, Simpson, Michael A, Cortez, David, Alkuraya, Fowzan S, Mathew, Christopher G, Jackson, Andrew P, Stewart, Grant S
Publicado no Nat Genet (2017)