Works matching AU Palanduz, Sukru

Results: 52
    1

    ERAP1 Gen İfadesinin Plazma Hücre Diskrazilerinde İncelenmesi.

    Published in:
    Medical Journal of Istanbul Kanuni Sultan Süleyman / İstanbul Kanuni Sultan Süleyman Tıp Dergisi, 2022, v. 14, n. 2, p. 120, doi. 10.14744/iksstd.2021.29494
    By:
    • Sarıman, Melda;
    • Karaçam, Büşra;
    • Ayer, Mesut;
    • Ekmekci, Sema Sırma;
    • Suer, İlknur;
    • Çefle, Kıvanç;
    • Palanduz, Şükrü;
    • Öztürk, Şükrü;
    • Nalçacı, Meliha;
    • Abacı, Neslihan
    Publication type:
    Article
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    A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23–q24.

    Published in:
    European Journal of Human Genetics, 2007, v. 15, n. 8, p. 889, doi. 10.1038/sj.ejhg.5201844
    By:
    • Deglincerti, Alessia;
    • De Giorgio, Roberto;
    • Cefle, Kivanc;
    • Devoto, Marcella;
    • Pippucci, Tommaso;
    • Castegnaro, Giovanni;
    • Panza, Emanuele;
    • Barbara, Giovanni;
    • Cogliandro, Rosanna F;
    • Mungan, Zeynel;
    • Palanduz, Sukru;
    • Corinaldesi, Roberto;
    • Romeo, Giovanni;
    • Seri, Marco;
    • Stanghellini, Vincenzo
    Publication type:
    Article
    12

    Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes.

    Published in:
    European Journal of Human Genetics, 2003, v. 11, n. 11, p. 858, doi. 10.1038/sj.ejhg.5201050
    By:
    • Türkmen, Seval;
    • Gillessen-Kaesbach, Gabriele;
    • Meinecke, Peter;
    • Albrecht, Beate;
    • Neumann, Luitgard M.;
    • Hesse, Volker;
    • Palanduz, Sükrü;
    • Balg, Stefanie;
    • Majewski, Frank;
    • Fuchs, Sigrun;
    • Zschieschang, Petra;
    • Greiwe, Monika;
    • Mennicke, Kirsten;
    • Kreuz, Friedmar R.;
    • Dehmel, Harald J.;
    • Rodeck, Burkhard;
    • Kunze, Jürgen;
    • Tinschert, Sigrid;
    • Mundlos, Stefan;
    • Horn, Denise
    Publication type:
    Article
    13

    Evaluation of TMED9, DNAJC1, LMAN2, COPE and KDELR1 Biomarkers in Patients with Monoclonal Gammopathy of Undetermined Significance and Multiple Myeloma.

    Published in:
    UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2023, v. 33, n. 2, p. 92, doi. 10.4999/uhod.236990
    By:
    • SARIMAN, Melda;
    • SALMAN YAYLAZ, Burcu;
    • YABACI TAK, Aysegul;
    • AYER, Mesut;
    • SIRMA EKMEKCI, Sema;
    • SUER, Ilknur;
    • CEFLE, Kivanc;
    • PALANDUZ, Sukru;
    • OZTURK, Sukru;
    • NALCACI, Meliha;
    • ABACI, Neslihan
    Publication type:
    Article
    14

    Dysregulation of MS4A3 and PRDX5 Gene Expression in Multiple Myeloma Patients.

    Published in:
    UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2021, v. 31, n. 4, p. 205, doi. 10.4999/uhod.215420
    By:
    • SUER, Ilknur;
    • ADAY, Aynur;
    • SARIMAN, Melda;
    • AYER, Mesut;
    • HINDILERDEN, Ipek Yonal;
    • EKMEKCI, Sema Sirma;
    • ABACI, Neslihan;
    • PALANDUZ, Sukru;
    • CEFLE, Kıvanc;
    • OZTURK, Sukru
    Publication type:
    Article
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    Clinical Images in Oral Medicine and Maxillofacial Radiology.

    Published in:
    Quintessence International, 2001, v. 32, n. 9, p. 748
    By:
    • Yalçin, Serhat;
    • Aybar, Buket;
    • Palandüz, Sükrü;
    • Haznedaroglu, Faruk;
    • Yazar, Taha Tekin;
    • Emes, Yusuf;
    • Terezhalmy, Geza T.;
    • Riley, Catherine K.;
    • Moore, William S.
    Publication type:
    Article
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    Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey.

    Published in:
    American Journal of Medical Genetics. Part A, 2021, v. 185, n. 8, p. 2488, doi. 10.1002/ajmg.a.62261
    By:
    • Berkay, Ezgi Gizem;
    • Elkanova, Leyla;
    • Kalaycı, Tuğba;
    • Uludağ Alkaya, Dilek;
    • Altunoğlu, Umut;
    • Cefle, Kıvanç;
    • Mıhçı, Ercan;
    • Nur, Banu;
    • Taşdelen, Elifcan;
    • Bayramoğlu, Zuhal;
    • Karaman, Volkan;
    • Toksoy, Güven;
    • Güneş, Nilay;
    • Öztürk, Şükrü;
    • Palandüz, Şükrü;
    • Kayserili, Hülya;
    • Tüysüz, Beyhan;
    • Uyguner, Zehra Oya
    Publication type:
    Article
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    Atrial and Ventricular Arryhthmogenic Potential in Turner Syndrome.

    Published in:
    Pacing & Clinical Electrophysiology, 2008, v. 31, n. 9, p. 1140, doi. 10.1111/j.1540-8159.2008.01154.x
    By:
    • SOZEN, AHMET B.;
    • CEFLE, KIVANÇ;
    • KUDAT, HASAN;
    • OZTURK, SUKRU;
    • OFLAZ, HUSEYIN;
    • PAMUKCU, BURAK;
    • AKKAYA, VAKUR;
    • ISGUVEN, PINAR;
    • PALANDUZ, SUKRU;
    • OZCAN, MUSTAFA;
    • GOREN, TANER;
    • GUVEN, OZEN
    Publication type:
    Article
    44

    WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.

    Published in:
    Human Mutation, 2017, v. 38, n. 1, p. 7, doi. 10.1002/humu.23128
    By:
    • Yokote, Koutaro;
    • Chanprasert, Sirisak;
    • Lee, Lin;
    • Eirich, Katharina;
    • Takemoto, Minoru;
    • Watanabe, Aki;
    • Koizumi, Naoko;
    • Lessel, Davor;
    • Mori, Takayasu;
    • Hisama, Fuki M.;
    • Ladd, Paula D.;
    • Angle, Brad;
    • Baris, Hagit;
    • Cefle, Kivanc;
    • Palanduz, Sukru;
    • Ozturk, Sukru;
    • Chateau, Antoinette;
    • Deguchi, Kentaro;
    • Easwar, T.K.M;
    • Federico, Antonio
    Publication type:
    Article
    45

    Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.

    Published in:
    Human Mutation, 2012, v. 33, n. 8, p. 1175, doi. 10.1002/humu.22111
    By:
    • Diggle, Christine P.;
    • Parry, David A.;
    • Logan, Clare V.;
    • Laissue, Paul;
    • Rivera, Carolina;
    • Restrepo, Carlos Martín;
    • Fonseca, Dora J.;
    • Morgan, Joanne E.;
    • Allanore, Yannick;
    • Fontenay, Michaela;
    • Wipff, Julien;
    • Varret, Mathilde;
    • Gibault, Laure;
    • Dalantaeva, Nadezhda;
    • Korbonits, Márta;
    • Zhou, Bowen;
    • Yuan, Gang;
    • Harifi, Ghita;
    • Cefle, Kivanc;
    • Palanduz, Sukru
    Publication type:
    Article
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