K-ras oncogene mutation in pterygium

Por Ozturk, B T, Yıldırım, M S, Zamani, A, Bozkurt, B
Publicado no Eye (Lond) (2017)

(99m)Tc-MDP bone SPECT in evaluation of the knee in asymptomatic soccer players

Por Yildirim, M, Gursoy, R, Varoglu, E, Oztasyonar, Y, Cogalgil, S
Publicado em 2004

trans-Bis(2-benzoyl­benzoato-κO (1))bis­(ethanol-κO)bis­(1H-imidazole-κN (3))nickel(II)

Por Heren, Zerrin, Paşaoğlu, Hümeyra, Yıldırım, M. Hakkı, Hıra, Derya
Publicado em 2009

Parasitic Appendicitis From Past to Present in Turkey

Por Engin, O, Calik, S, Calik, B, Yildirim, M, Coskun, G
Publicado em 2010

Whole body calcification in a hemodialysis patient

Por Yildirim, M., Acikgoz, S. B., Solak, B., Sipahi, S., Solak, Y.
Publicado no Indian J Nephrol (2016)

[N-(2-Hydroxy­ethyl)ethyl­enediamine]oxalatocopper(II)

Por Paşaoğlu, Hümeyra, Kaştaş, Gökhan, Yeşilel, Okan Z., Yıldırım, M. Hakkı
Publicado em 2009

Bis­(benzimidazole-κN (3))bis(2-benzoyl­benzoato-κO)copper(II)

Por Yıldırım, M. Hakkı, Heren, Zerrin, Paşaoğlu, Hümeyra, Hıra, Derya, Büyükgüngör, Orhan
Publicado em 2009

Enamel Formation Genes Are Associated with High Caries Experience in Turkish Children

Por Patir, A., Seymen, F., Yildirim, M., Deeley, K., Cooper, M.E., Marazita, M.L., Vieira, A.R.
Publicado em 2008

A Rare Cause of Secondary Amyloidosis: Common Variable Immunodeficiency Disease

Por Kadiroğlu, Ali Kemal, Yıldırım, Yaşar, Yılmaz, Zülfükar, Kayabaşı, Hasan, Avcı, Yahya, Yıldırım, M. Serdar, Yılmaz, M. Emin
Publicado em 2012

What works in school-based energy balance behaviour interventions and what does not? A systematic review of mediating mechanisms

Por van Stralen, M M, Yildirim, M, Velde, SJ te, Brug, J, van Mechelen, W, Chinapaw, M J M
Publicado em 2011

STIM1 and SLC24A4 Are Critical for Enamel Maturation

Por Wang, S., Choi, M., Richardson, A.S., Reid, B.M., Seymen, F., Yildirim, M., Tuna, E., Gençay, K., Simmer, J.P., Hu, J.C.
Publicado em 2014

What is your diagnosis?

Por Uçan, Bekir, Şahin, Mustafa, Özbek, Mustafa, Arslan, Müyesser Sayki, Çakal, Erman, Uçan, Berna, Ant, Ömer, Şirvan, Levent, Yıldırım, M. Utku, Dilli, Alper, Delibaşı, Tuncay
Publicado no J Turk Ger Gynecol Assoc (2016)

Novel KLK4 and MMP20 Mutations Discovered by Whole-exome Sequencing

Por Wang, S.-K., Hu, Y., Simmer, J.P., Seymen, F., Estrella, N.M.R.P., Pal, S., Reid, B.M., Yildirim, M., Bayram, M., Bartlett, J.D., Hu, J.C.-C.
Publicado em 2013

LAMB3 Mutations Causing Autosomal-dominant Amelogenesis Imperfecta

Por Kim, J.W., Seymen, F., Lee, K.E., Ko, J., Yildirim, M., Tuna, E.B., Gencay, K., Shin, T.J., Kyun, H.K., Simmer, J.P., Hu, J.C.-C.
Publicado em 2013

Novel WDR72 Mutation and Cytoplasmic Localization

Por Lee, S.-K., Seymen, F., Lee, K.-E., Kang, H.-Y., Yildirim, M., Bahar Tuna, E., Gencay, K., Hwang, Y.-H., Nam, K.H., De La Garza, R.J., Hu, J.C.-C., Simmer, J.P., Kim, J.-W.
Publicado em 2010

Whole Exome Sequencing Identifies Three Novel Mutations in ANTXR1 in Families with GAPO Syndrome

Por Bayram, Yavuz, Pehlivan, Davut, Karaca, Ender, Gambin, Tomasz, Jhangiani, Shalini N., Erdin, Serkan, Gonzaga-Jauregui, Claudia, Wiszniewski, Wojciech, Muzny, Donna, Elcioglu, Nursel H., Yildirim, M. Selman, Bozkurt, Banu, Zamani, Ayse Gul, Boerwinkle, Eric, Gibbs, Richard A., Lupski, James R.
Publicado no Am J Med Genet A (2014)

Fine-Mapping of 5q12.1–13.3 Unveils New Genetic Contributors to Caries

Por Shimizu, T., Deeley, K., Briseño-Ruiz, J., Faraco, I.M., Poletta, F.A., Brancher, J.A., Pecharki, G.D., Küchler, E.C., Tannure, P.N., Lips, A., Vieira, T.C.S., Patir, A., Yildirim, M., Mereb, J.C., Resick, J.M., Brandon, C.A., Cooper, M.E., Seymen, F., Costa, M.C., Granjeiro, J.M., Trevilatto, P.C., Orioli, I.M., Castilla, E.E., Marazita, M.L., Vieira, A.R.
Publicado em 2013