檢索結果 - Perçin, E. Ferda

Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity 由 Koç, Altuğ, Onur, S. Ödül, Ergün, Mehmet Ali, Perçin, E. Ferda

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Effects of microalgae chlorella species crude extracts on intestinal adaptation in experimental short bowel syndrome 由 Kerem, Mustafa, Salman, Bulent, Pasaoglu, Hatice, Bedirli, Abdulkadir, Alper, Murat, Katircioglu, Hikmet, Atici, Tahir, Perçin, E Ferda, Ofluoglu, Ebru

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

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

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HACE1 deficiency leads to structural and functional neurodevelopmental defects 由 Nagy, Vanja, Hollstein, Ronja, Pai, Tsung-Pin, Herde, Michel K., Buphamalai, Pisanu, Moeseneder, Paul, Lenartowicz, Ewelina, Kavirayani, Anoop, Korenke, Georg Christoph, Kozieradzki, Ivona, Nitsch, Roberto, Cicvaric, Ana, Monje Quiroga, Francisco J., Deardorff, Matthew A., Bedoukian, Emma C., Li, Yun, Yigit, Gökhan, Menche, Jörg, Perçin, E. Ferda, Wollnik, Bernd, Henneberger, Christian, Kaiser, Frank J., Penninger, Josef M.

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RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome 由 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

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Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism 由 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

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