Ugur Ozbek - Genetic Division of Experimental Research Institute of Medicine, Istanbul University

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Papers共 291 篇Author StatisticsCo-AuthorSimilar Experts

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Clinical Classification and Molecular Interpretation of Hereditary Cancer Patients with Germline Pathogenic Tp53 Variations

Nihat Bugra Agaoglu,Busra Unal,Gizem Onder,Ozkan Ozdemir, Ufuk Amanvermez,Merve Acıkel Elmas,Merve Gokbayrak, Cansu Ugurtas,Naci Cine,Ugur Ozbek,Özden Hatırnaz Ng

crossref（2024）

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Rapid genome sequencing for critically ill infants: an inaugural pilot study from Turkey

Bengisu Guner Yilmaz,Ozlem Akgun-Dogan, Ozkan Ozdemir,Bayram Yuksel, Ozden Hatirnaz Ng, Kaya Bilguvar,Beril Ay, Gulsah Sebnem Ozkose, Eylul Aydin, Ayca Yigit, Aybike Bulut, Fatma Nisa Esen,

Frontiers in pediatrics (2024): 1412880-1412880

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Betulin Stimulates Osteogenic Differentiation of Human Osteoblasts-Loaded Alginate-Gelatin Microbeads

Mehmet Ali Karaca,Derya Dilek Kancagi,Ugur Ozbek,Ercument Ovali,Ozgul Gok

Bioengineering (Basel, Switzerland)no. 6 (2024)

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Impact of TP53 gene variants on prognosis and survival of childhood acute lymphoblastic leukemia

Sinem Firtina,Yucel Erbilgin,Ozden Hatirnaz Ng,Serap Karaman,Zeynep Karakas,Tulin Tiraje Celkan,Sema Aylan Gelen,Yildiz Yildirmak,Ugur Ozbek,Muge Sayitoglu

Scandinavian journal of clinical and laboratory investigationno. 3 (2023): 187-193

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Pb2401: determining molecular background of a group of childhood leukemia/lymphoma patients with positive family history from türkiye

Graziano Onder, Ufuk Amanvermez,Cengiz Canpolat,Fatih Erbey,Davut Albayrak,Elif İnce,Gül Nihal Özdemir,Yunus Murat Akçabelen,Neşe Yaralı,Namık Özbek, İkbal Ok-Bozkaya,Turan Bayhan,

HemaSphere（2023）

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Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators

Savino Sciascia,Dario Roccatello,Marco Salvatore,Claudio Carta,Laura L. Cellai,Gianluca Ferrari,Aimè Lumaka,Aimè Lumaka,Stephen Groft,Yasemin Alanay,Maleeha Azam, Gareth Baynam,

Frontiers in Public Health (2023)

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Memantine and SKF82958 but not an enriched environment modulate naloxone-precipitated morphine abstinence syndrome without affecting hippocampal tPA mRNA levels in rats

Abdurrahman Aslan, Özden Hatırnaz-Ng,Orçun Taşar,Uğur Özbek, Pınar Yamantürk-Çelik

Pharmacology, biochemistry, and behavior (2023): 173688-173688

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Obstacles and expectations of rare disease patients and their families in Türkiye: ISTisNA project survey results

Ozden Hatirnaz Ng,Ilayda Sahin,Yucel Erbilgin,Ozkan Ozdemir,Emrah Yucesan,Nazli Erturk,Merve Yemenici,Ozlem Akgun Dogan,Sibel Aylin Ugur Iseri,Ilhan Satman,Yasemin Alanay,Ugur Ozbek

Frontiers in public health（2023）

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From patient to function: modeling CRIM1 in xenopus tropicalis

Ozlem Akgun Dogan,Stephen Viviano,Ozden Hatirnaz Ng,Nihat Bugra Agaoglu,Weizhen Ji,Lauren Jeffries,Ugur Ozbek,Saquib Lakhani,Mustafa Khokha,Engin Deniz,Yasemin Alanay

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 656-657

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Two rare autosomal recessive neurological disorders identified by combined genetic approaches in a single consanguineous family with multiple offspring

Seda Susgun,Emrah Yucesan,Beyza Goncu, Sevde Hasanoglu Sayin,Umit Yasar Kina,Cemil Ozgul,Omer Faruk Duzenli,Ozcan Kocaturk,Mustafa Calik,Ugur Ozbek,Sibel Aylin Ugur Iseri

Neurological Sciencesno. 5 (2023): 1-7

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