SIP1 is downregulated in hepatocellular carcinoma by promoter hypermethylation von Acun, Tolga, Oztas, Emin, Yagci, Tamer, Yakicier, Mustafa C

Volltext

Associating IDH and TERT Mutations in Glioma with Diffusion Anisotropy in Normal-Appearing White Matter von Halilibrahimoğlu, H, Polat, K, Keskin, S, Genç, O, Aslan, O, Öztürk-Işık, E, Yakıcıer, C, Danyeli, A E, Pamir, M N, Özduman, K, Dinçer, A, Özcan, A

Volltext

Smad2 and Smad4 gene mutations in hepatocellular carcinoma von YAKICIER, M. C, IRMAK, M. B, ROMANO, A, KEW, M, OZTURK, M

Volltext

PP-088 A PATIENT WITH MYELOPROLIFERATIVE NEOPLASM EXHIBITING HETEROZYGOUS JAK2V617F MUTATION AND TRISOMY 14 ROBERTSONIAN TRANSLOCATION SIMULTANEOUSLY von Gokgoz, Z, Türkgenç, B, Yakicier, C

Volltext

MEFV gene is a probable susceptibility gene for Behçet's disease von Im rzal oglu, N., Dursun, A., Tastan, B., Soysal, Y., Yak c er, M. C.

Volltext

Association of NFKB1 and NFKBIA Polymorphisms in Relation to Susceptibility of Behçet's Disease von Yenmis, G., Oner, T., Cam, C., Koc, A., Kucuk, O. S., Yakicier, M. C., Dizman, D., Kanigur Sultuybek, G.

Volltext

Identification of homozygous deletions at chromosome 16q23 in Aflatoxin B1 exposed hepatocellular carcinoma von CENGIZ YAKICIER, M, LEGOIX, Patricia, VAURY, Christelle, GRESSIN, Laetitia, TUBACHER, Emmanuel, CAPRON, Frederique, BAYER, Jan, DEGOTT, Claude, BALABAUD, Charles, ZUCMAN-ROSSI, Jessica

Volltext

Injectable tissue-engineered cartilage using commercially available fibrin glue von Cakmak, Ozcan, Babakurban, Seda T., Akkuzu, Hatice G., Bilgi, Selcuk, Ovalı, Ercüment, Kongur, Merve, Altintas, Hande, Yilmaz, Bayram, Bilezikçi, Banu, Y. Celik, Zerrin, Yakicier, Mustafa C., Sahin, Feride I.

Volltext

Expression of CK-19 and CEA mRNA in peripheral blood of gastric cancer patients von Kutun, S, Celik, A, Cem Kockar, M, Erkorkmaz, U, Eroğlu, A, Cetin, A, Erkosar, B, Yakicier, C

Volltext

Genetic heterogeneity of hepatocellular carcinoma von Unsal, H, Yakicier, C, Marcais, C, Kew, M, Volkman, M, Zentgraf, H, Isselbacher, K.J, Ozturk, M

Volltext

Mutations and copy number alterations in diffuse gliomas are shaped by different mechanisms von Ozduman, K., Ulgen, E., Karacan, S., Gerlevik, U., Can, O., Bilguvar, K., Akyerli, C.B., Yuksel, S.K., Ersen-Danyeli, A., Tihan, T., Yakicier, C., Sezerman, O.U., Pamir, M.N.

Volltext

A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC34A2 gene von Stokman, Lara, Nossent, Esther J., Grunberg, Katrien, Meijboom, Lilian, Yakicier, Mustafa C., Voorhoeve, Els, Houweling, Arjan C.

Volltext

A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC 34A2 gene von Stokman, Lara, Nossent, Esther J., Grunberg, Katrien, Meijboom, Lilian, Yakicier, Mustafa C., Voorhoeve, Els, Houweling, Arjan C.

Volltext

Reprogramming of Replicative Senescence in Hepatocellular Carcinoma-Derived Cells von Ozturk, Nuri, Erdal, Esra, Mumcuoglu, Mine, Akcali, Kamil C., Yalcin, Ozden, Senturk, Serif, Arslan-Ergul, Ayca, Gur, Bala, Yulug, Isik, Cetin-Atalay, Rengul, Yakicier, Cengiz, Yagci, Tamer, Tez, Mesut, Ozturk, Mehmet

Volltext

A chronic myeloid leukemia‐like syndrome case with del (12) (p12) in a Li‐Fraumeni syndrome family von GURAN, Ş., BEYAN, C., NEVRUZ, O., YAKICIER, C., TUNCA, Y.

Volltext

A novel homozygous nonsense mutation in CAST associated with PLACK syndrome von Temel, Şehime Gülsün, Karakaş, B., Şeker, Ü., Turkgenç, B., Zorlu, Ö., Sarıcaoğlu, H., Oğur, Ç., Kütük, Ö., Kelsell, D. P., Yakıcıer, M. C.

Volltext

Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate von Breckpot, Jeroen, Anderlid, Britt-Marie, Alanay, Yasemin, Blyth, Moira, Brahimi, Afane, Duban-Bedu, Bénédicte, Gozé, Odile, Firth, Helen, Yakicier, Mustafa Cengiz, Hens, Greet, Rayyan, Maissa, Legius, Eric, Vermeesch, Joris Robert, Devriendt, Koen

Volltext

Association of NFKB 1 and NFKBIA Polymorphisms in Relation to Susceptibility of B ehçet's Disease von Yenmis, G., Oner, T., Cam, C., Koc, A., Kucuk, O. S., Yakicier, M. C., Dizman, D., Kanigur Sultuybek, G.

Volltext

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan von Dinçer, Pervin, Balcı, Burcu, Yuva, Yeliz, Talim, Beril, Brockington, Martin, Dinçel, Deniz, Torelli, Silvia, Brown, Sue, Kale, Gülsev, Haliloǧlu, Göknur, Gerçeker, Filiz Özbas, Atalay, Rengül Çetin, Yakıcıer, Cengiz, Longman, Cheryl, Muntoni, Francesco, Topaloǧlu, Haluk

Volltext

An investigation of microRNAs mapping to breast cancer related genomic gain and loss regions von Selcuklu, S.D, Yakicier, M.C, Erson, A.E

Volltext