The Dynamics of Fast- and Slow- Cycling Stem Cells in Liver Homeostasis and Injury von Cao, W, Smits, R, Tuysuz, N, Chen, K, Bolkestein, M, van der Laan, L.J.W, ten Berge, D, Sprengers, D, Metselaar, H.J, Kwekkeboom, J, Peppelenbosch, M, Pan, Q

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PS129 - The Dynamics of Fast- and Slow- Cycling Stem Cells in Liver Homeostasis and Injury von Cao, W., Smits, R., Tuysuz, N., Chen, K., Bolkestein, M., van der Laan, L.J.W., ten Berge, D., Sprengers, D., Metselaar, H.J., Kwekkeboom, J., Peppelenbosch, M., Pan, Q.

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Soil geochemical prospection for gold deposit in the Arzular area (NE Turkey) von Yaylali-Abanuz, Guelten, Tueysuez, Necati, Akaryali, Enver

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Lipid-mediated Wnt protein stabilization enables serum-free culture of human organ stem cells von Tuysuz, N., Bloois, L. van, Brink, S. van den, Begthel, H., Verstegen, M.M.A., Cruz, L.J., Hui, L.J., Laan, L.J.W. van der, Jonge, J. de, Vries, R., Braakman, E., Mastrobattista, E., Cornelissen, J.J., Clevers, H., Berge, D. ten

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Distribution and origin of detrital gold in Kazikkaya (Kagizman-Kars) placers von TUYSUZ, N

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Endogenous WNT signals mediate BMP-induced and spontaneous differentiation of epiblast stem cells and human embryonic stem cells von Kurek, D., Neagu, A., Tastemel, M., Tuysuz, N., Lehmann, J., Werken, H.J.G. van de, Philipsen, S., Linden, R. van der, Maas, A., IJcken, W.F.J. van, Drukker, M., Berge, D. ten

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Geochemistry and Evolution of the Volcanism in the Eastern Pontides, NE-Turkey von Korkmaz, S.

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Ortakale (Sarikamis-Kars) kromit zuhurlarinin özellikleri ve kökeni von TUYSUZ, N

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Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity von Bachmann-Gagescu, R, Dempsey, J C, Phelps, I G, O'Roak, B J, Knutzen, D M, Rue, T C, Ishak, G E, Isabella, C R, Gorden, N, Adkins, J, Boyle, E A, de Lacy, N, O'Day, D, Alswaid, A, Ramadevi A, Radha, Lingappa, L, Lourenço, C, Martorell, L, Garcia-Cazorla, À, Ozyürek, H, Haliloğlu, G, Tuysuz, B, Topçu, M, Chance, P, Parisi, M A, Glass, I A, Shendure, J, Doherty, D

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The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance von Pehlivan, Davut, Bayram, Yavuz, Gunes, Nilay, Coban Akdemir, Zeynep, Shukla, Anju, Bierhals, Tatjana, Tabakci, Burcu, Sahin, Yavuz, Gezdirici, Alper, Fatih, Jawid M., Gulec, Elif Yilmaz, Yesil, Gozde, Punetha, Jaya, Ocak, Zeynep, Grochowski, Christopher M., Karaca, Ender, Albayrak, Hatice Mutlu, Radhakrishnan, Periyasamy, Erdem, Haktan Bagis, Sahin, Ibrahim, Yildirim, Timur, Bayhan, Ilhan A., Bursali, Aysegul, Elmas, Muhsin, Yuksel, Zafer, Ozdemir, Ozturk, Silan, Fatma, Yildiz, Onur, Yesilbas, Osman, Isikay, Sedat, Balta, Burhan, Gu, Shen, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Boerwinkle, Eric, Gibbs, Richard A., Tsiakas, Konstantinos, Hempel, Maja, Girisha, Katta Mohan, Gul, Davut, Posey, Jennifer E., Elcioglu, Nursel H., Tuysuz, Beyhan, Lupski, James R.

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Ust kretase yasli Saraf Tepe (Trabzon) bazanitinin jeokimyasal özellikleri ve jeotektonik anlami von KORKMAZ, S, BURHAN SADIKLAR, M, VAN, A, TUYSUZ, N, ERCAN, T

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Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans von Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, Czarnecki, Peter G., Lehman, Anna M., Trnka, Peter, Nitschké, Patrick, Bole-Feysot, Christine, Schueler, Markus, Knebelmann, Bertrand, Burtey, Stéphane, Szabó, Attila J., Tory, Kálmán, Leo, Paul J., Gardiner, Brooke, McKenzie, Fiona A., Zankl, Andreas, Brown, Matthew A., Hartley, Jane L., Maher, Eamonn R., Li, Chunmei, Leroux, Michel R., Scambler, Peter J., Zhan, Shing H., Jones, Steven J., Kayserili, Hülya, Tuysuz, Beyhan, Moorani, Khemchand N., Constantinescu, Alexandru, Krantz, Ian D., Kaplan, Bernard S., Shah, Jagesh V., Hurd, Toby W., Doherty, Dan, Katsanis, Nicholas, Duncan, Emma L., Otto, Edgar A., Beales, Philip L., Mitchison, Hannah M., Saunier, Sophie, Hildebrandt, Friedhelm

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Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin von Bayram, Yavuz, Karaca, Ender, Coban Akdemir, Zeynep, Yilmaz, Elif Ozdamar, Tayfun, Gulsen Akay, Aydin, Hatip, Torun, Deniz, Bozdogan, Sevcan Tug, Gezdirici, Alper, Isikay, Sedat, Atik, Mehmed M, Gambin, Tomasz, Harel, Tamar, El-Hattab, Ayman W, Charng, Wu-Lin, Pehlivan, Davut, Jhangiani, Shalini N, Muzny, Donna M, Karaman, Ali, Celik, Tamer, Yuregir, Ozge Ozalp, Yildirim, Timur, Bayhan, Ilhan A, Boerwinkle, Eric, Gibbs, Richard A, Elcioglu, Nursel, Tuysuz, Beyhan, Lupski, James R

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Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy von Chatron, Nicolas, Becker, Felicitas, Morsy, Heba, Schmidts, Miriam, Hardies, Katia, Tuysuz, Beyhan, Roselli, Sandra, Najafi, Maryam, Alkaya, Dilek Uludag, Ashrafzadeh, Farah, Nabil, Amira, Omar, Tarek, Maroofian, Reza, Karimiani, Ehsan Ghayoor, Hussien, Haytham, Kok, Fernando, Ramos, Luiza, Gunes, Nilay, Bilguvar, Kaya, Labalme, Audrey, Alix, Eudeline, Sanlaville, Damien, de Bellescize, Julitta, Poulat, Anne-Lise, Moslemi, Ali-Reza, Lerche, Holger, May, Patrick, Lesca, Gaetan, Weckhuysen, Sarah, Tajsharghi, Homa

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The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis von Bakircioglu, Mehmet, Carvalho, Ofélia P., Khurshid, Maryam, Cox, James J., Tuysuz, Beyhan, Barak, Tanyeri, Yilmaz, Saliha, Caglayan, Okay, Dincer, Alp, Nicholas, Adeline K., Quarrell, Oliver, Springell, Kelly, Karbani, Gulshan, Malik, Saghira, Gannon, Caroline, Sheridan, Eamonn, Crosier, Moira, Lisgo, Steve N., Lindsay, Susan, Bilguvar, Kaya, Gergely, Fanni, Gunel, Murat, Woods, C. Geoffrey

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CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration von Schaffer, Ashleigh E., Eggens, Veerle R.C., Caglayan, Ahmet Okay, Reuter, Miriam S., Scott, Eric, Coufal, Nicole G., Silhavy, Jennifer L., Xue, Yuanchao, Kayserili, Hulya, Yasuno, Katsuhito, Rosti, Rasim Ozgur, Abdellateef, Mostafa, Caglar, Caner, Kasher, Paul R., Cazemier, J. Leonie, Weterman, Marian A., Cantagrel, Vincent, Cai, Na, Zweier, Christiane, Altunoglu, Umut, Satkin, N. Bilge, Aktar, Fesih, Tuysuz, Beyhan, Yalcinkaya, Cengiz, Caksen, Huseyin, Bilguvar, Kaya, Fu, Xiang-Dong, Trotta, Christopher R., Gabriel, Stacey, Reis, André, Gunel, Murat, Baas, Frank, Gleeson, Joseph G.

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Two novel mutations in XYLT2 cause spondyloocular syndrome von Taylan, Fulya, Yavaş Abalı, Zehra, Jäntti, Nina, Güneş, Nilay, Darendeliler, Feyza, Baş, Firdevs, Poyrazoğlu, Şükran, Tamçelik, Nevbahar, Tüysüz, Beyhan, Mäkitie, Outi

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Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival von Hucthagowder, Vishwanathan, Morava, Eva, Kornak, Uwe, Lefeber, Dirk J., Fischer, Björn, Dimopoulou, Aikaterini, Aldinger, Annika, Choi, Jiwon, Davis, Elaine C., Abuelo, Dianne N., Adamowicz, Maciej, Al-Aama, Jumana, Basel-Vanagaite, Lina, Fernandez, Bridget, Greally, Marie T., Gillessen-Kaesbach, Gabriele, Kayserili, Hulya, Lemyre, Emmanuelle, Tekin, Mustafa, Türkmen, Seval, Tuysuz, Beyhan, Yüksel-Konuk, Berrin, Mundlos, Stefan, Van Maldergem, Lionel, Wevers, Ron A., Urban, Zsolt

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Langerhans Cell Histiocytosis: Single Center Experience of 25 Years von Tuysuz, G, Yildiz, I, Ozdemir, N, Adaletli, I, Kurugoglu, S, Apak, H, Dervisoglu, S, Bozkurt, S, Celkan, T

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Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 cases von Ranza, E., Huber, C., Levin, N., Baujat, G., Bole‐Feysot, C., Nitschke, P., Masson, C., Alanay, Y., Al‐Gazali, L., Bitoun, P., Boute, O., Campeau, P., Coubes, C., McEntagart, M., Elcioglu, N., Faivre, L., Gezdirici, A., Johnson, D., Mihci, E., Nur, B.G., Perrin, L., Quelin, C., Terhal, P., Tuysuz, B., Cormier‐Daire, V.

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