Tayfun Ozcelik : rechercher sur Z-Library

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1

Neuro-ophthalmologic findings in humans with quadrupedal locomotion

Sarac, Ozge, Gulsuner, Suleyman, Yildiz-Tasci, Yelda, Ozcelik, Tayfun, Kansu, Tulay

Journal:

Ophthalmic Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 637 KB

english, 2012

2

Genomic landscape of the Greater Middle East

Özçelik, Tayfun, Onat, Onur Emre

Journal:

Nature Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 1.63 MB

english, 2016

3

Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder

Patke, Alina, Murphy, Patricia J., Onat, Onur Emre, Krieger, Ana C., Özçelik, Tayfun, Campbell, Scott S., Young, Michael W.

Journal:

Année:

2017

Langue:

english

Fichier:

PDF, 5.19 MB

english, 2017

4

The SOCS-1 gene methylation in chronic myeloid leukemia patients

Ozden Hatirnaz, Umit Ure, Cem Ar, Cemaliye Akyerli, Teoman Soysal, Burhan Ferhanoğlu, Tayfun Özçelik, Ugur Ozbek

Journal:

American Journal of Hematology

Année:

2007

Langue:

english

Fichier:

PDF, 77 KB

english, 2007

5

Skewed X chromosome inactivation in blood cells of women with scleroderma

Zeynep Özbalkan, Sevgi Baǧışlar, Sedat Kiraz, Cemaliye Boylu Akyerli, Hüseyin T. E. Özer, Şule Yavuz, A. Merih Birlik, Meral Çalgüneri, Tayfun Özçelik

Journal:

Arthritis & Rheumatism

Année:

2005

Langue:

english

Fichier:

PDF, 170 KB

english, 2005

6

Reply

Zeynep Özbalkan, Sedat Kiraz, Meral Çalgüneri, Sevgi Bağişlar, Cemaliye Boylu Akyerli, Hüseyin T. C. Özer, Şule Yavuz, A. Merih Birlik, Tayfun Özçelik

Journal:

Arthritis & Rheumatism

Année:

2005

Langue:

english

Fichier:

PDF, 42 KB

english, 2005

7

Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritis

Elif Uz, Chigdem Mustafa, Rezan Topaloglu, Yelda Bilginer, Ali Dursun, Ozgur Kasapcopur, Seza Ozen, Aysin Bakkaloglu, Tayfun Ozcelik

Journal:

Arthritis & Rheumatism

Année:

2009

Langue:

english

Fichier:

PDF, 50 KB

english, 2009

8

Echinococcus against cancer: Why not?

Hikmet Akgül, Mesut Tez, Aliekrem E. Ünal, Mehmet Keşkek, İskender Sayek, Tayfun Özçelik

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 61 KB

english, 2003

9

Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients

A. Esra Manguoǧlu, Güven Lüleci, Tayfun Özçelik, Taner Çolak, Hagit Schayek, Mustafa Akaydın, Eitan Friedman

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 47 KB

english, 2003

10

Changes in cyclic nucleotides during the calcium paradox in the isolated rat heart

Yusuf E. Karakullukçu, Tayfun Özçelik, Nuran Gökhan

Journal:

Pflügers Archiv European Journal of Physiology

Année:

1987

Langue:

english

Fichier:

PDF, 777 KB

english, 1987

11

p53 codon 72 polymorphism in bladder cancer – no evidence of association with increased risk or invasiveness

Gökçe A. Törüner, Ahmet Uçar, Mesut Tez, Mesut Çetinkaya, Haluk Özen, Tayfun Özçelik

Journal:

Année:

2001

Langue:

english

Fichier:

PDF, 81 KB

english, 2001

12

Analysis ofMYHTyr165Cys and Gly382Asp variants in childhood leukemias

Cemaliye Boylu Akyerli, Ugur Özbek, Müge Aydin-Sayitoglu, Sema Sirma, Tayfun Özçelik

Journal:

Journal of Cancer Research and Clinical Oncology

Année:

2003

Langue:

english

Fichier:

PDF, 148 KB

english, 2003

13

Extremely skewed X-chromosome inactivation is increased in pre-eclampsia

Elif Uz, Ismail Dolen, Atakan R. Al, Tayfun Ozcelik

Journal:

Année:

2007

Langue:

english

Fichier:

PDF, 287 KB

english, 2007

14

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy

Luis E. Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, Ali K. Ozturk, Jennifer A. Moliterno, Ozdem Erturk, Fatih Bayrakli, Baris Korkmaz, Michael L. DiLuna, Katsuhito Yasuno, Kaya Bilguvar, Tayfun Ozcelik,

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 333 KB

english, 2010

15

Skewed X-Chromosome Inactivation in Scleroderma

Elif Uz, Laurence S. Loubiere, Vijayakrishna K. Gadi, Zeynep Ozbalkan, Jeffrey Stewart, J. Lee Nelson, Tayfun Ozcelik

Journal:

Clinical Reviews in Allergy & Immunology

Année:

2008

Langue:

english

Fichier:

PDF, 75 KB

english, 2008

16

X Chromosome Inactivation and Female Predisposition to Autoimmunity

Journal:

Clinical Reviews in Allergy & Immunology

Année:

2008

Langue:

english

Fichier:

PDF, 85 KB

english, 2008

17

Collaborative genomics for human health and cooperation in the Mediterranean region

Journal:

Current Opinion in Biotechnology

Année:

2011

Langue:

english

Fichier:

PDF, 72 KB

english, 2011

18

Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion

Sevgi BAGISLAR, Isik USTUNER, Bora CENGIZ, Feride SOYLEMEZ, Cemaliye Boylu AKYERLI, Serdar CEYLANER, Gulay CEYLANER, Aynur ACAR, Tayfun OZCELIK

Journal:

Australian and New Zealand Journal of Obstetrics and Gynaecology

Année:

2006

Langue:

english

Fichier:

PDF, 81 KB

english, 2006

19

Myocardial Tissue Velocities in Neonates

Filiz Ekici, Semra Atalay, Nazire Ozcelik, Tayfun Uçar, Erdal Yılmaz, Ercan Tutar

Journal:

Echocardiography

Année:

2007

Langue:

english

Fichier:

PDF, 144 KB

english, 2007

20

Trembler mouse carries a point mutation in a myelin gene

Suter, Ueli, Welcher, Andrew A., Özcelik, Tayfun, Snipes, G. Jackson, Kosaras, Bela, Francke, Uta, Billings-Gagliardi, Susan, Sidman, Richard L., Shooter, Eric M.

Journal:

Année:

1992

Fichier:

PDF, 653 KB

1992

21

Uncovering the complex mysteries of mosaicism

Özçelik, Tayfun

Journal:

Année:

2002

Langue:

english

Fichier:

PDF, 28 KB

english, 2002

22

Collaborative genomics for human health and cooperation in the Mediterranean region

Özçelik, Tayfun, Kanaan, Moien, Avraham, Karen B, Yannoukakos, Drakoulis, Mégarbané, André, Tadmouri, Ghazi O, Middleton, Lefkos, Romeo, Giovanni, King, Mary-Claire, Levy-Lahad, Ephrat

Journal:

Nature Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 144 KB

english, 2010

23

Molecular evolution of the human interleukin–8 receptor gene cluster

Ahuja, Sunil K., Özçelik, Tayfun, Milatovitch, Athena, Francke, Uta, Murphy, Philip M.

Journal:

Nature Genetics

Année:

1992

Fichier:

PDF, 649 KB

1992

24

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region

Leff, Stuart E., Brannan, Camilynn I., Reed, Martha L., Özçelik, Tayfun, Francke, Uta, Copeland, Neal G., Jenkins, Nancy A.

Journal:

Nature Genetics

Année:

1992

Fichier:

PDF, 861 KB

1992

25

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region

Özçelik, Tayfun, Leff, Stuart, Robinson, Wendy, Donlon, Tim, Lalande, Marc, Sanjines, Elvira, Schinzel, Albert, Francke, Uta

Journal:

Nature Genetics

Année:

1992

Fichier:

PDF, 716 KB

1992

26

Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity

Ozcelik, Tayfun, Uz, Elif, Akyerli, Cemaliye B, Bagislar, Sevgi, Mustafa, Chigdem A, Gursoy, Alptekin, Akarsu, Nurten, Toruner, Gokce, Kamel, Nuri, Gullu, Sevim

Journal:

European Journal of Human Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 132 KB

english, 2006

27

Human chromosome 19 contains the neurotrophin-5 gene locus and three related genes that may encode novel acidic neurotrophins

Lucy R. Berkemeier, Tayfun Özçelik, Uta Francke, Arnon Rosenthal

Journal:

Somatic Cell and Molecular Genetics

Année:

1992

Langue:

english

Fichier:

PDF, 1.29 MB

english, 1992

28

Polymorphisms of glutathioneS-transferase genes (GSTM1,GSTP1andGSTT1) and bladder cancer susceptibility in the Turkish population

Gökçe A. Törüner, Cemaliye Akyerli, Ahmet Uçar, Tuncay Akı, Necmettin Atsu, Haluk Özen, Mesut Tez, Mesut Çetinkaya, Tayfun Özçelik

Journal:

Archives of Toxicology

Année:

2001

Langue:

english

Fichier:

PDF, 83 KB

english, 2001

29

Endothelial progenitor cells display clonal restriction in multiple myeloma

Marc Braunstein, Tayfun Özçelik, Sevgi Bağişlar, Varsha Vakil, Eric LP Smith, Kezhi Dai, Cemaliye B Akyerli, Olcay A Batuman

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 496 KB

english, 2006

30

cDNA Cloning of the Two Subunits of Human CAAX Farnesyltransferase and Chromosomal Mapping of FNTA and FNTB Loci and Related Sequences

Douglas A. Andres, Athena Milatovich, Tayfun Özçelik, Janet M. Wenzlau, Michael S. Brown, Joseph L. Goldstein, Uta Francke

Journal:

Année:

1993

Fichier:

PDF, 544 KB

1993

31

HER2 and proliferation of wound-induced breast carcinoma

Mesut Tez, Erdal Göçmen, Tayfun Özçelik

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 55 KB

english, 2003

32

Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with time

Feza Deymeer, Pıraye Serdaroğlu, Mehveş Poda, Yeşim Gülşen-Parman, Tayfun Özçelık, Coşkun Özdemır

Journal:

Neuromuscular Disorders

Année:

1997

Langue:

english

Fichier:

PDF, 372 KB

english, 1997

33

A retrospective comparison of allogeneic peripheral blood stem cell and bone marrow transplantation results from a single center: A focus on the incidence of graft-vs.-host disease and relapse

Celalettin Ustun, Onder Arslan, Meral Beksac, Haluk Koc, Gunhan Gurman, Tayfun Ozcelik, Buket Yilmaz, Osman Ilhan, Hamdi Akan, Muhit Ozcan, Taner Demirer, Akin Uysal, Nahide Konuk, Mutlu Arat, Imdat D

Journal:

Biology of Blood and Marrow Transplantation

Année:

1999

Langue:

english

Fichier:

PDF, 176 KB

english, 1999

34

Two Males with SRY-Positive 46,XX Testicular Disorder of Sex Development

Gunes, Sezgin, Asci, Ramazan, Okten, Gülsen, Atac, Fatih, Onat, Onur E., Ogur, Gonul, Aydin, Oguz, Ozcelik, Tayfun, Bagci, Hasan

Journal:

Systems Biology in Reproductive Medicine

Année:

2013

Langue:

english

Fichier:

PDF, 300 KB

english, 2013

35

Disruption of HDX gene in premature ovarian failure

Okten, Gülsen, Gunes, Sezgin, Onat, Onur Emre, Tukun, Ajlan, Ozcelik, Tayfun, Kocak, Idris

Journal:

Systems Biology in Reproductive Medicine

Année:

2013

Langue:

english

Fichier:

PDF, 225 KB

english, 2013

36

2012 William Allan Award Introduction: Uta Francke1

Özçelik, Tayfun

Journal:

The American Journal of Human Genetics

Année:

2013

Langue:

english

Fichier:

PDF, 121 KB

english, 2013

37

Chromosomal mapping of brain-derived neurotrophic factor and neurotrophin-3 genes in man and mouse

Özçelik, Tayfun, Rosenthal, Arnon, Francke, Uta

Journal:

Année:

1991

Langue:

english

Fichier:

PDF, 2.75 MB

english, 1991

38

Dlx2 (Tes1), a homeobox gene of the Distal-less family, assigned to conserved regions on human and mouse chromosomes 2

Özçelik, Tayfun, Porteus, Matthew H., Rubenstein, John L.R., Francke, Uta

Journal:

Année:

1992

Langue:

english

Fichier:

PDF, 896 KB

english, 1992

39

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

Ibraghimov-Beskrovnaya, Oxana, Milatovich, Athena, Ozcelik, Tayfun, Yang, Bin, Koepnick, Kevin, Francke, Uta, Campbell, Kevin P.

Journal:

Human Molecular Genetics

Année:

1993

Langue:

english

Fichier:

PDF, 5.54 MB

english, 1993

40

Rupture of the Hydatid Disease of the Liver into the Biliary Tracts

Paksoy, Melih, Karahasanoglu, Tayfun, Carkman, Sinan, Giray, Serdar, Senturk, Hakan, Ozcelik, Faik, Erguney, Sabri

Journal:

Digestive Surgery

Année:

1998

Langue:

english

Fichier:

PDF, 204 KB

english, 1998

41

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

Emre Onat, Onur, Gulsuner, Suleyman, Bilguvar, Kaya, Nazli Basak, Ayse, Topaloglu, Haluk, Tan, Meliha, Tan, Uner, Gunel, Murat, Ozcelik, Tayfun

Journal:

European Journal of Human Genetics

Année:

2013

Langue:

english

Fichier:

PDF, 999 KB

english, 2013

42

Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy

Topçu, Meral, Akyerli, Cemaliye, Sayı, Ayça, Törüner, Gökçe A, Koçoğlu, Süha R, Cimbiş, Mine, Özçelik, Tayfun

Journal:

European Journal of Human Genetics

Année:

2002

Langue:

english

Fichier:

PDF, 161 KB

english, 2002

43

Characterization of a novel zebrafish (Danio rerio) gene,wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ)

Doldur-Balli, Fusun, Ozel, Mehmet Neset, Gulsuner, Suleyman, Tekinay, Ayse B., Ozcelik, Tayfun, Konu, Ozlen, Adams, Michelle M.

Journal:

BMC Neuroscience

Année:

2015

Langue:

english

Fichier:

PDF, 2.34 MB

english, 2015

44

cDNA Cloning of a Liver Isoform of the Phosphorylase Kinase α Subunit and Mapping of the Gene to Xp22.2-p22.1, the Region of Human X-Linked Liver Glycogenosis

Jutta J. Davidson, Tayfun Ozcelik, Christiane Hamacher, Patrick J. Willems, Uta Francke and Manfred W. Kilimann

Journal:

Proceedings of the National Academy of Sciences

Année:

1992

Langue:

english

Fichier:

PDF, 1.18 MB

english, 1992

45

A7.9 Does Telomere Shortening in Women with Rheumatoid Arthritis Predict X Chromosome Inactivation Bias?

Kanaan, Sami Barna, Onat, Onur Emre, Balandraud, Nathalie, Azzouz, Doua F, Roudier, Jean, Ozcelik, Tayfun, Lambert, Nathalie C

Journal:

Annals of the Rheumatic Diseases

Année:

2013

Langue:

english

Fichier:

PDF, 71 KB

english, 2013

46

Medical genetics and genomic medicine in Turkey: a bright future at a new era in life sciences

Özçelik, Tayfun

Journal:

Molecular Genetics & Genomic Medicine

Année:

2017

Langue:

english

Fichier:

PDF, 3.00 MB

english, 2017

47

Homozygous LAMC3 mutation links to structural and functional changes in visual attention networks

Urgen, Buse M., Topac, Yasemin, Ustun, F. Seyhun, Demirayak, Pinar, Oguz, Kader K., Kansu, Tulay, Saygi, Serap, Ozcelik, Tayfun, Boyaci, Huseyin, Doerschner, Katja

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 2.88 MB

english, 2018

48

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis

Kanaan, Sami B., Onat, Onur E., Balandraud, Nathalie, Martin, Gabriel V., Nelson, J. Lee, Azzouz, Doua F., Auger, Isabelle, Arnoux, Fanny, Martin, Marielle, Roudier, Jean, Ozcelik, Tayfun, Lambert, Na

Journal:

Année:

2016

Langue:

english

Fichier:

PDF, 770 KB

english, 2016

49

Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation

Demirayak, Pinar, Onat, Onur Emre, Ors Gevrekci, Aslihan, Gulsuner, Suleyman, Uysal, Hilmi, Bilgen, Rengin, Doerschner, Katja, Ozcelik, Tayfun, Boyaci, Huseyin

Journal:

Diagnostic and Interventional Radiology

Année:

2018

Langue:

english

Fichier:

PDF, 2.11 MB

english, 2018

50

Multiscale analysis of SRYâpositive 46,XX testicular disorder of sex development: Presentation of nine cases

Akar, Omer Salih, Gunes, Sezgin, Abur, Ummet, Altundag, Engin, Asci, Ramazan, Onat, Onur Emre, Ozcelik, Tayfun, Ogur, Gonul

Journal:

Année:

2020

Fichier:

PDF, 1.22 MB

2020