Hilal Ozdag PhD
Hilal Ozdag PhD
Ankara University Biotechnology Institute
ankara.edu.tr üzerinde doğrulanmış e-posta adresine sahip
BaşlıkAlıntı yapanlarYıl
p300/CBP and cancer
NG Iyer, H Özdag, C Caldas
Oncogene 23 (24), 4225, 2004
5312004
EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer
L Hughes-Davies, D Huntsman, M Ruas, F Fuks, J Bye, SF Chin, J Milner, ...
Cell 115 (5), 523-535, 2003
4392003
Human MLH1 deficiency predisposes to hematological maligancy and neurofibromatosis type 1
MD Ricciardone, T Özçelik, B Cevher, H Özdağ, M Tuncer, A Gürgey, ...
Cancer Research 59 (2), 290-293, 1999
2541999
Differential expression of selected histone modifier genes in human solid cancers
H Özdağ, AE Teschendorff, AA Ahmed, SJ Hyland, C Blenkiron, L Bobrow, ...
BMC genomics 7 (1), 90, 2006
2512006
p300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels
NG Iyer, SF Chin, H Ozdag, Y Daigo, DE Hu, M Cariati, K Brindle, ...
Proceedings of the National Academy of Sciences 101 (19), 7386-7391, 2004
1552004
A 1 Mb minimal amplicon at 8p11–12 in breast cancer identifies new candidate oncogenes
MJ Garcia, JCM Pole, SF Chin, A Teschendorff, A Naderi, H Ozdag, ...
Oncogene 24 (33), 5235, 2005
1472005
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia
E Uz, Y Alanay, D Aktas, I Vargel, S Gucer, G Tuncbilek, F von Eggeling, ...
The American Journal of Human Genetics 86 (5), 789-796, 2010
982010
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia
M Tekin, BÖ Hişmi, S Fitoz, H Özdağ, FB Cengiz, A Sırmacı, İ Aslan, ...
The American Journal of Human Genetics 80 (2), 338-344, 2007
952007
Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours
H Özdağ, SJ Batley, A Försti, NG Iyer, Y Daigo, J Boutell, MJ Arends, ...
British journal of cancer 87 (10), 1162, 2002
632002
Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey
D Duman, A Sirmaci, FB Cengiz, H Ozdag, M Tekin
Genetic testing and molecular biomarkers 15 (1-2), 29-33, 2011
612011
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss
A Sırmacı, S Erbek, J Price, M Huang, D Duman, FB Cengiz, G Bademci, ...
The American Journal of Human Genetics 86 (5), 797-804, 2010
472010
Possible causes of chromosome instability: comparison of chromosomal abnormalities in cancer cell lines with mutations in BRCA1, BRCA2, CHK2 and BUB1
M Grigorova, JM Staines, H Ozdag, C Caldas, PAW Edwards
Cytogenetic and genome research 104 (1-4), 333-340, 2004
432004
Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis
G Yildiz, A Arslan-Ergul, S Bagislar, O Konu, H Yuzugullu, ...
PloS one 8 (5), e64016, 2013
382013
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations
A Sırmacı, D Duman, H Öztürkmen-Akay, S Erbek, A İncesulu, ...
International journal of pediatric otorhinolaryngology 73 (5), 699-705, 2009
382009
Recurrent and private MYO15A mutations are associated with deafness in the Turkish population
FB Cengiz, D Duman, A Sırmacı, S Tokgöz-Yilmaz, S Erbek, ...
Genetic testing and molecular biomarkers 14 (4), 543-550, 2010
322010
Germ line< i> BRCA1</i> and< i> BRCA2</i> gene mutations in Turkish breast cancer patients
H Özdag, M Tez, I Sayek, M Müslümanoglu, O Tarcan, F Içli, M Öztürk, ...
European Journal of Cancer 36 (16), 2076-2082, 2000
272000
A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia
A Sırmacı, H Öztürkmen‐Akay, S Erbek, A Incesulu, D Duman, ...
Clinical genetics 75 (6), 562-567, 2009
182009
A Novel (δβ)°-Thalassemia due to a∼ 30-kb Deletion Observed in a Turkish Family
R Öner, C Öner, G Erdem, H Balkan, H Özdağ, M Erkan, F Gümrük, ...
Acta haematologica 96 (4), 232-236, 1996
111996
Behçet's: A disease or a syndrome? Answer from an expression profiling study
AK Oğuz, ST Yılmaz, ÇŞ Oygür, T Çandar, I Sayın, SS Kılıçoğlu, İ Ergün, ...
PloS one 11 (2), e0149052, 2016
102016
From RNA isolation to microarray analysis: comparison of methods in FFPE tissues
N Belder, Ö Coskun, BD Erdogan, O Ilk, B Savas, A Ensari, H Özdağ
Pathology-Research and Practice 212 (8), 678-685, 2016
92016
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20