2. academic degrees - Bilkent University - Faculty of Science

More documents

Recommendations

Info

$SET 7 MATH 543: FUCHSIAN DIFFERENTIAL EQUATIONS ...$

$MATH 225: DIFFERENTIAL EQUATIONS AND LINEAR ALGEBRA ...$

8. ARTISTIC & SCIENTIFIC EXHIBITS, PRESENTATIONS 2011 Miami 2011 Winter Symposium: Epigenetics in Development and Disease, which is organized by University of Miami, Nature Group and Scripps Florida has selected “Chromatin Iznik chini by Tayfun Özçelik” as the banner of the congress (http://www.nature.com/natureconferences/miami/MWS2011/index.html) 2009 Co-organizer of the exhibit “Darwin Now” British Council and Bilkent University, Bilkent, Ankara 2006 Co-curator of the exhibit “James D Watson: Journey to the World of DNA” Cold Spring Harbor Laboratories and Bilkent University, Bilkent, Ankara 2007 Ozcelik T., “Fugitives of Destiny” Nature Genetics 39 (2): Cover art 2005 Ozcelik T., “LIFE” Nature Genetics 37 (11): Cover art 2005 Ozcelik T., “Chromatin” Nature Genetics 37 (4): Cover art 2003 Ozcelik T., “Half chromatid mutation” Nature Genetics 34 (4): Cover art 9. TEACHING Graduate Courses: Human Genet. (MBG 601, 1995-present) Special Topics in Genetics I & II (MBG 612 & 613, 2002-2003) Advances in Molecular Genetics (MBG 507, 1996-present) Special Topics in Molecular Biology I & II (MBG 509 & 510, 2002-2003) Medical Genetics (Istanbul University, 1993-1995) Molecular Genetics (Istanbul University, 1993-1995) Human Genetics (Bogazici University, 1995-1996) Undergraduate Courses: Introduction to Modern Biology (MBG 110, 2001-present) Biology I & II (MBG 101 & 102, 1995-2000) Genetic Engineering and Biotechnology (MBG 415, 2001-2002) Introduction to Human Genetics (MBG 488, 2000-present) 10. GRADUATE SUPERVISION PhD Bilkent University Merve Gulsah Dal, “to be determined”, in progress Fusun Doldur, “to be determined”, in progress Chigdem Mustafa, “X-chromosome inactivation in pediatric diseases”, in progress Emre Onat, “Molecular genetics studies on Rett syndrome”, in progress Suleyman Gulsuner, “Identification of the molecular bases of quadrupedal locomotion”, in progress Elif Uz, “X-chromosome inactivation & female predisposition to autoimmunity”, 2008 Cemaliye Akyerli, “Alfa-interferon signalling pathway in CML”, 2005 Gokce Toruner,“Identification of new genes in bladder cancer”, 2001 Hilal Ozdag, “Molecular bases of hereditary breast cancer in Turkey”, 2000 Istanbul University Ali C. Hatemi, “Bazi kardiyovaskuler hastaliklarin molekuler genetik incelemesi”, 1994 Fahri Akbas, “Uçlu nukleotid artisina bagli norolojik hastaliklar”, 1996 Ugur Ozbek, “Noroblastom'da N-myc gen amplifikasyonu”, 1995 MSc Bilkent University Melda Kantar, “X-inactivation in Sjogrens syndrome”, 2008 Safak Caglayan, “Genetic studies of quadrupedal walking in humans”, 2008 Chigdem Mustafa, “Extremely skewed X-inactivation in JIA”, 2007 Emre Onat, “Rett syndrome and X-linked gene expression”, 2006 Akin Sevinc, “RNASEL Arg462 Gly variant in breast cancer”, 2003 Ayca Sayi, “Analysis of MECP2 gene mutations in Turkish Rett syndrome patients”, 2001 Buket Yilmaz, “Establishment of rapid screening techniques for hematological malignancies”, 1998 Emre Oktem, “Establishment of a rapid mutation detection technique for screening of the BRCA1 and BRCA2 genes”, 1997 Korkut Vata, “Development of a non-radioactive diagnostic test for the detection of microsatellite instability in colon cancer”, 1997 4
Istanbul University Naci Cine, “Fenilketonurili hastalarin DNA analizi ile dogum oncesi tanisi”, 1996 Mehves Poda, “Spinal muskuler atrofilerin molekuler temelinin Turk toplumunda belirlenmesi”, 1995 Burcak Vural, “Bazi genomik lokuslarin allel ve genotip frekanslarinin Turk toplumunda belirlenmesi”, 1995 11. PATENTS 1992 Method for the diagnosis of Prader-Willi syndrome, USA patent no 08/161, 012 12. SCHOLARLY PUBLICATIONS Specialty in Medical Genetics Dissertation SYP1 ve SYP2 genlerinin kromozomal lokalizasyonlari, 8/1990, Advisor: Uta Francke, Stanford University. Chapters in books 1. A. B. Tekinay, T. Tekinay, H. T. Özçelik. “Nanobiyoteknoloji” in Moleküler Parazitoloji” (Edited by MA Özcel, M. Tanyüksel, H. Eren), pp. 201-214, Türkiye Parazitoloji Derneği Yayın No:22, İzmir: Meta Basım Matbaacılık, (2009) ISBN 978-975-94646-9-1. 2. Ozcelik T. “Molekuler Genetikte Temel Kavramlar” in OBSTETRİK: Maternal·Fetal Tip ve Perinatoloji (Edited by MS Beksac, N. Demir, A. Koc). pp. 641-51, Ankara: Medical Network, (2001). 3. Huner G, Demirkol M, Cine N, Baykal T, Carbat G, Caliskan M, Aydinli N, Ozmen M, Seckin Y, Ozcelik T. “The PAH Splicing Mutation IVS10nt546 in Late Diagnosed PKU Patients is Associated with Hypsarrytmia”, “Diagnosis and Treatment of Inborn Errors of Metabolism: Contributions to an Equal Opportunity for Children in Asia and Europe” M. Demirkol and Y.S. Shin .eds., 79-84, Published by the Turkish Society for PKU. Istanbul Branch, (1996). 4. Ozcelik T, Cine N, Huner G, Baykal T, Sarbat G, Demirkol M. “Molecular Genetic Approaches to the Diagnosis of Phenylketonuria in Istanbul”, “Diagnosis and Treatment of Inborn Errors of Metabolism: Contributions to an Equal Opportunity for Children in Asia and Europe” M. Demirkol and Y.S. Shin.eds., 73-78, Published by the Turkish Society for PKU. Istanbul Branch, (1996). Reviews 1. Ozcelik T. “Farmakogenetik” Dokuz Eylul Tip Fak Der, (2001). 2. Ozcelik T. “Adli Amaçli DNA analizleri” Hacettepe Tip Derg 27(2): 50-5 (1996). 3. Ozcelik T. “DNA polimorfizminin Tip'da kullanimi” Hacettepe Tip Derg 27(1): 72-6 (1996). 4. Ozcelik T. “Noromuskuler hastaliklara neden olan genler ve tani testleri” Klinik Gelisim 8: 3728-42 (1995). 5
Page 1 and 2: 1. PERSONAL DATA CURRICULUM VITAE T
Page 3: 2002 “Rett syndrome and related d
Page 7 and 8: X-chromosome inactivation and femal
Page 9 and 10: 41. Ustun C, Arslan O, Beksac M, Ko
Page 11 and 12: acetylcholine added perfusion in ca

2. academic degrees - Bilkent University - Faculty of Science

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?